Del Mar Photonics - Newsletter Fall 2010 - Newsletter Winter 2010
Femtosecond Nanotubes
Brochures to present at the expo:
Brochures to present at the exhibition:
Product Data Sheets
Pulse 
strecher/compressor
Avoca SPIDER system
Buccaneer femtosecond 
fiber lasers with SHG Second Harmonic Generator
Cannon Ultra-Broadband Light 
Source
Cortes Cr:Forsterite 
Regenerative Amplifier
Infrared 
cross-correlator CCIR-800
Cross-correlator Rincon
Femtosecond Autocorrelator 
IRA-3-10
Kirra Faraday Optical Isolators
Mavericks femtosecond 
Cr:Forsterite laser
OAFP optical attenuator
Pearls femtosecond fiber laser 
(Er-doped fiber, 1530-1565 nm)
Pismo pulse picker
Reef-M femtosecond scanning 
autocorrelator for microscopy
Reef-RTD scanning 
autocorrelator
Reef-SS single shot 
autocorrelator
Femtosecond Second Harmonic Generator
Spectrometer ASP-100M
Spectrometer ASP-150C
Spectrometer ASP-IR
Tamarack and Buccaneer 
femtosecond fiber lasers (Er-doped fiber, 1560+/- 10nm)
Teahupoo femtosecond Ti:Sapphire regenerative amplifier
Femtosecond 
third harmonic generator
Tourmaline femtosecond fiber 
laser (1054 nm)
Tourmaline TETA Yb 
femtosecond amplified laser system
Tourmaline Yb-SS 
femtosecond solid state laser system 
Trestles CW Ti:Sapphire 
laser
Trestles femtosecond 
Ti:Sapphire laser
Trestles Finesse 
femtosecond lasers system integrated with DPSS pump laser
Wedge Ti:Sapphire multipass amplifier
    Multi-terawatt 
    lasers overview
    Hydrogen Thyratrons -
    Deuterium Thyratrons -
    Untriggered 
    Spask Gaps - 
    Triggered Spask Gaps - X-ray tube
    Rincon 800 third-order 
    scanning cross-correlator for aligning 20 Terawatt Ti:Sapphire laser
    MCP + phosphorous screen for imaging of XUV radiation (14eV- 160-eV) in high harmonics experiments
    
    Femtosecond autocorrelator Reef-RTD 700-1300 nm
    New Trestles fs/CW laser system 
    which can be easily switched from femtosecond mode to CW and back.
    
    Femtosecond Two-stage Amplifier System Wedge-XL (table-top terawatt system) 
    - pdf
    CORTES-800 40 TERAWATT LASER 
    SYSTEM
    New Beacon Femtosecond 
    Fluoresscence Upconversion System
    
    Tamarack C1560 femtosecond fiber laser
    Pacifica THz Time Domain Spectrometer
    
    Wedge TiSapphire Multipass Amplifier
    New Hatteras femtosecond transient 
    absorption system
    Photon Scanning Tunneling Microscope 
    - Power Point presentation (use read-only 
    mode)
    Atomic 
    Force Microscope AFM HERON -
    
    sample quotes
    Near-field 
    Scanning Optical Microscope (NSOM) for nano-characterization and 
    nanomanufacturing
    
    Yb-based high-energy fiber laser system kit, model Tourmaline 
    Yb-ULRepRate-07
    
    Ytterbium-doped Femtosecond Solid-State Laser Tourmaline Yb-SS400
    
    Pismo pulse picker for 1500-1600nm range
Del Mar Photonics Product brochures - Femtosecond products data sheets (zip file, 4.34 Mbytes) - Del Mar Photonics
    New Beacon Femtosecond 
    Fluoresscence Upconversion System
    
    Tamarack C1560 femtosecond fiber laser
    Pacifica THz Time Domain Spectrometer
    ĀNUENUE - patented miniature Holographic Fourier 
    Transform Spectrometer for the UV/Visible/NIR
    New!
    Holographic Fourier Transform Spectrometer for THz Region
    
    Wedge TiSapphire Multipass Amplifier
    New Hatteras femtosecond transient 
    absorption system
    Photon Scanning Tunneling Microscope 
    - Power Point presentation (use read-only 
    mode)
    Atomic 
    Force Microscope AFM HERON -
    
    sample quotes
    Near-field 
    Scanning Optical Microscope (NSOM) for nano-characterization and 
    nanomanufacturing
    
    Yb-based high-energy fiber laser system kit, model Tourmaline 
    Yb-ULRepRate-07
    
    Ytterbium-doped Femtosecond Solid-State Laser Tourmaline Yb-SS400
    
    Pismo pulse picker for 1500-1600nm range
Trestles Finesse Ti:Sapphire oscillator -
    DPSS 5W green laser 
    - DPSS 4W green laser
    SAM-1550 -
    SAM-1040 -
    SAM-1064 -
    SAM-1300 -
    
    PCA-40-05-10-800-h - LiNbO3
    
    Laser Power Meters -
    DMP12 -
    UP 
    
    High-resolution laser spectrometer -
New!
    
    Super-frequency-stable Ti:Sapphire laser TIS-SF-777 now has an absolute 
    linewidth < 10 kHz rms - New!
Trestles Femtosecond Ti:Sapphire 
laser - Trestles 50 Manual -
pump options
Trestles 20 Manual -
20/50/100 fs oscillators - FemtoStart -
safety
Trestles Finesse Ti:Sapphire oscillator -
Q&A 
- LQ
Wedge-M Multipass Ti:Sapphire Amplifier
    Amplified Ti:Sapphire System Teahupoo
Choose what is right for you!
featured on Optics.org
Trestles CW 
Ti:Sapphire laser (40GHz - 20GHz - 2GHz linewidth)
Mavericks Femtosecond Cr:Forsterite 
laser (around 1250 nm)
Multiphoton Imaging with Mavericks - 
introductory brochure
 
Program and Notes
Acoustooptical delay lines for femtosecond pulse shaping based on crystal 
materials with strong acoustic anisotropy 
Paper 7789-8 of Conference 7789
Date: Monday, 02 August 2010
Author(s): Vladimir Y. Molchanov, Sergey I. Chizhikov, National Univ. of Science 
and Technology (Russian Federation); Oleg Y. Makarov, Molecular Technology GmbH 
(Germany); Efim A. Khazanov, Vladislav N. Ginzburg, Institute of Applied Physics 
(Russian Federation)
The femtosecond pulse quality in a laser system is determined by a 
non-compensated high-order dispersion and spectral deformation of the amplifier. 
A dispersive device that modifies the spectral amplitude and phase of the 
femtosecond pulse should be used to improve the duration of the compressed pulse 
and suppress the prepulses. The application of acoustoopical dispersive delay 
lines is considered. Different modifications of delay lines are compared and the 
types of devices used to shape femtosecond pulses are discussed. Different 
experimental dispersive delay lines were fabricated and investigated.
Ablation of silicon by focusing a femtosecond laser through a subwavelength 
annular aperture structure 
Paper 7789-21 of Conference 7789
Date: Monday, 02 August 2010
Author(s): Yuh-Yan Yu, National Taiwan Univ. (Taiwan); Chin-Kai Chang, Ming-Wei 
Lai, Industrial Technology Research Institute (Taiwan); Long-Sun Huang, 
Chih-Kung Lee, National Taiwan Univ. (Taiwan)
We examined the effect of using laser energy on the ablation of silicon with a 
Ti:sapphire femtosecond laser. The femtosecond laser was focused through an 
oxide-metal-oxide film engraved with a subwavelength annular aperture structure 
to create a quasi-Bessel beam for long depth of focus machining. The 
experimental results showed that the silicon can be ablated with an extremely 
low input ablation threshold, which was in the order of 0.3 J/cm2 for a pulse 
duration of around 130 femtoseconds. The depth of focus and the focal spot of 
the SAA structure were simulated using finite-difference time domain 
calculations. The far-field laser beam which propagated through the SAA 
structure possessed both a sub-micron focal spot, long depth of focus, and high 
focus intensity. The results show that this kind of system has good potential 
when silicon machining is required, which is particularly true for creating high 
aspect ratio surface structures.
Generation of femtosecond Bessel type pulses using multi-ring circular-slit 
diaphragm 
Paper 7789-29 of Conference 7789
Date: Monday, 02 August 2010
Author(s): Vladimir Belyi, Svetlana N. Kurilkina, Elena Ushakova, B.I. Stepanov 
Institute of Physics (Belarus)
It is shown that using a multi-ring circularly-slit diaphragm placed in focal 
plane of lens, it is possible to form pulsed beams of Bessel type characterized 
by a narrow central maximum and essential suppression of lateral maxima in the 
radial intensity distribution. It has been established that with increasing 
radius and number of diaphragm rings, the narrowing of central maximum with 
accompanying essential decrease of lateral maxima takes place. When a Gaussian 
pulse falls on two-ring diaphragm at a definite distance from lens, a weak 
satellite is found to appear in the formed femtosecond beam. At the same time 
the beam-pulse formed using three-ring diaphragm has the envelope with two 
distinguished maxima, one of which decreases when moving off the lens.
Fabrication of Raman biochip prototype by femtosecond laser micromachining 
Paper 7759-42 of Conference 7759
Date: Tuesday, 03 August 2010
Author(s): Zenghui Zhou, Jian Xu, Fei He, Yang Liao, Ya Cheng, Zhizhan Xu, 
Shanghai Institute of Optics and Fine Mechanics (China); Koji Sugioka, Katsumi 
Midorikawa, RIKEN (Japan)
A nanoscale surface-enhanced Raman scattering (SERS) substrate is fabricated by 
fs laser reduction and deposition. The conductive silver microstructures are 
also deposited in fs laser irradiated area on the glass surfaces. Based on this 
approach, we integrate the microelectronic circuit and micro-Raman substrate 
into a microfluidic chamber and form a prototype of Raman biochip for 
biosensing. Enhancement of Raman signal and control of temperature of the sensor 
are both achieved. This technique provides a great potential for integrating 
microelectronics and micro-Raman sensors on a single glass chip.l>
Femtosecond optical Kerr gating using nonlinear photonic crystal fiber 
Paper 7775-51 of Conference 7775
Date: Wednesday, 04 August 2010
Author(s): Qian Xu, Kebin Shi, Zhiwen Liu, The Pennsylvania State Univ. (United 
States)
We experimentally investigated optical Kerr gating effect by co-propagating a 
pump beam and a weak signal beam in a nonlinear photonic crystal fiber. It is 
shown that optical Kerr gating can be observed by using femtosecond pump pulses 
with only a few milliwatts of average power.
Widefield multiphoton excited fluorescence microscopy for animal study in vivo
Paper 7765-32 of Conference 7765
Date: Wednesday, 04 August 2010
Author(s): Shean-Jen Chen, Li-Chung Cheng, Chia-Yuan Chang, Hung-Wei Su, 
National Cheng Kung Univ. (Taiwan)
A widefield multiphoton excited fluorescence microscope with a simultaneously 
spatial and temporal focusing technique has been developed to provide fast 
three-dimensional (3D) multiphoton fluorescence images fro animal study in vivo. 
Unlike conventional multiphoton microscopy based on pixel by pixel scanning 
technique, the wide-field multiphoton microscope only scans one dimension, 
z-axis, to construct a 3D image. By using a Ti:sapphire femtosecond laser 
oscillator as a seed laser for the femtosecond laser amplifier with a repetition 
rate of 10 kHz, we raise the average power from 1.0 to 4.2 W, which is enough 
power to excite the fluorescence in the area over 100 μm x 100 μm. The 
fluorescence image signal is detected by an EM CCD, which frame rate might rise 
up to 1 kHz according to the efficiency of fluorophore, so the widefield 
multiphoton microscopy can provide very fast imaging fro animal study in vivo 
such as monitoring brain neuron activity and liver metabolism.
Near-field imaging with a localized nonlinear light source (Keynote 
Presentation) (Keynote Presentation)
Paper 7757-4 of Conference 7757
Date: Sunday, 01 August 2010
Author(s): Lukas Novotny, Stefano Palomba, Univ. of Rochester (United States)
We demonstrate high-resolution near-field imaging and spectroscopy using the 
nonlinear optical response of a gold nanoparticle pair as an excitation photon 
source. Femtosecond pulses of frequencies f1 and f2 are used to induce a 
nonlinear polarization at the four wave mixing (4WM) frequency 2 f1 − f2 in the 
junction of the nanoparticle dimer. The nonlinear response leads to localized 
photon emission, which is employed as an excitation source for fluorescence and 
extinction imaging. The principle of this imaging technique is demonstrated for 
samples of fluorescent nanospheres and tubular J-aggregates
Tomography with random snapshots of faint non-stationary objects 
Paper 7800-1 of Conference 7800
Date: Monday, 02 August 2010
Author(s): Abbas Ourmazd, Peter Schwander, Univ. of Wisconsin-Milwaukee (United 
States); Dimitris Giannakis, Courant Institute of Mathematical Sciences (United 
States); George N. Phillips, Jr., Univ. of Wisconsin-Madison (United States)
A new generation of powerful algorithms is poised to enable the determination of 
the structure and evolution of objects ranging from single molecules to beating 
hearts and breathing lungs. At one extreme, new algorithms are paving the way to 
atomic-level mapping of the conformations of biological molecules with 
femtosecond time resolution. At the other, they are driving ultra-low-dose 
tomography of non-stationary, faintly scattering macroscopic objects. We 
describe how such approaches can be used to reconstruct the structure and 
conformational continuum of individual molecules, viruses, and potentially 
living cells.
Supercontinuum generation using small core photonic crystal fibers 
Paper 7781-21 of Conference 7781
Date: Monday, 02 August 2010
Author(s): Luiz C. Barbosa, Enver F. Chillcce, Italo O. Mazali, Univ. Estadual 
de Campinas (Brazil)
In this work we study the supercontinuum generaton using small core silica 
photonic crystal fibers (PCFs). The core of the PCFs varying from 1.0 to 2.0 µm 
was possible changing the external fiber diameter. The PCFs have structures 
which consist of small hollows. The supercontinum light, that extends from blue 
to near infra-red region, was obtained using a femtosecond 785 nm Ti:Saphire 
laser. The blue light generated is very intense, which could be used to 
fluorescence applications as biological.
Three-dimensional polymer microdevices with gold nanorods 
Paper 7757-123 of Conference 7757
Date: Monday, 02 August 2010
Author(s): Shean-Jen Chen, Wen-Shuo Kuo, Chi-Hsiang Lien, National Cheng Kung 
Univ. (Taiwan)
In this study, nonlinear multiphoton photocrosslinking and photopolymerization 
of rose bengal and trimethylolpropane triacrylate monomers in solution have been 
used to direct the three-dimension (3D) assembly of microdevices; moreover, we 
also presents the first example of containing gold nanorods within the 
photopolymerization. The experimental results show that the two-photon excited 
photopolymerization containing the nanorods improves more efficiently of 
decreasing the power density of femtosecond laser, and also provides a great 
diversity of optical properties. The doped nanorods with two-photon luminescence 
act as label molecules for internal microdiagnosis of 3D polymer microdevices.
Nanojoining as interconnect and packaging technologies for nanodevices 
Paper 7764-12 of Conference 7764
Date: Tuesday, 03 August 2010
Author(s): Norman Y. Zhou, Univ. of Waterloo (Canada)
Joining, whether at nano-, micro- or macro-scale, is an essential part of 
man-made product manufacturing and assembly, providing mechanical coupling and 
support, electrical connection or insulation, environmental protection, etc. 
Nanojoining, also termed nanobonding, nanowelding, nanobrazing, nanosoldering, 
etc., has attracted growing interests in the past few years as emerging 
interconnect and packaging technologies for nanodevices and nanosystems. A 
number of nanojoining techniques have been developed and will be described, 
namely, femtosecond laser welding of Au nanoparticles, low temperature bonding 
using Ag nanoparticles, and brazing of carbon nano-tubes (CNTs).
Experimental observation of the Laue diffraction in one-dimensional photonic 
crystals 
Paper 7755-23 of Conference 7755
Date: Wednesday, 04 August 2010
Author(s): Sergey E. Svyakhovskiy, Anton I. Maydykovskiy, Ilya E. Razdolski, 
Tatiana V. Murzina, Alexander A. Skorynin, Boris I. Mantsyzov, Oleg A. 
Aktsipetrov, Moscow State Univ. (Russian Federation)
Theoretically predicted that the femtosecond laser pulse propagating in the 
linear photonic crystal (PC) in case of the Bragg diffraction at the Laue scheme 
is separated into two, called the transmitted and the diffracted pulses. Each of 
them, in turn, is separated into two pulses with different propagation velocity, 
which is associated with redistribution of the field of an initial pulse between 
the layers of PC. In this work we experimentally observed spatial laser pulse 
splitting into two beams in a PC made of porous silicon. Direction and intensity 
of transmitted and diffracted beams coincides with theoretically predicted.
Spatio-temporal control of fields around nano-antennas 
Paper 7757-16 of Conference 7757
Date: Sunday, 01 August 2010
Author(s): Daan Brinks, Marta Castro Lopez, Alberto G. Curto, Richard Hildner, 
Tim H. Taminiau, Niek F. van Hulst, ICFO - Instituto de Ciencias Fotónicas 
(Spain)
Nano-antennas concentrate electromagnetic fields in sub-diffraction limited 
hotspots, whose position in time and space depends on the antenna-structure and 
the incoming electromagnetic field. Antennas can therefore be combined with 
ultrafast pulses to address femtosecond processes in nanometric volumes, 
provided one takes into account and compensates for the dispersion of the 
antenna-structures. We adapt the field of an excitation pulse to the dispersion 
and resonances of an optical gap-antenna. This way we change and enhance the 
localization of hotspots, while at the same time obtaining quantitative 
information about the field dynamics around the structure. Our latest 
experimental results will be presented.
Two-photon spectroscopy allows for probing of the pi-conjugation pathway in 
tetrapyrolles 
Paper 7774-20 of Conference 7774
Date: Monday, 02 August 2010
Author(s): Nikolay S. Makarov, Mikhail Drobizhev, Montana State Univ. (United 
States); Elena A. Makarova, Evgeny A. Lukyanets, Institute of Biochemistry and 
Physiology of Plants and Microorganisms (Russian Federation); Aleksander K. 
Rebane, Montana State Univ. (United States)
Two-dimensionally extended, branched, pi-electron structure provides 
tetrapyrrolic molecules their unique optical properties, which makes them 
attractive for photonics applications. The knowledge of the structure and the 
symmetry of the pi-electron conjugation pathway thus presents an important task 
for understanding of the optical properties of tetrapyrroles. Here we study 
femtosecond two-photon absorption (2PA) and excited-state absorption spectra of 
metal-free centrosymmetrical tetra-tert-butyl-phthalocyanine and formally 
non-centrosymmetrical tribenzo-tetraazachlorin. We show that both molecules 
contain a strong 2PA transition near 940 nm, which is absent in corresponding 
one-photon absorption spectra. This observation imply, in accordance with 
previous quantum-chemical calculations, that the main pi-conjugation pathway of 
phthalocyanines excludes the outer parts of the pyrrolenine rings.
Ultra-fast dynamics of spin and orbital magnetic moments of CoPd alloys probed 
by time resolved x-ray magnetic circular dichroism 
Paper 7760-21 of Conference 7760
Date: Tuesday, 03 August 2010
Author(s): Eric Beaurepaire, Christine Boeglin, Valérie Halté, Jean-Yves Bigot, 
Victor Lopez-Flores, Jacek Arabski, Institut de Physique et Chimie des Matériaux 
de Strasbourg (France); Christian Stamm, Nikolaus Pontius, Hermann Dürr, 
Helmholtz-Zentrum Berlin für Materialien und Energie GmbH (Germany)
Ultrashort optical laser pulses (60 fs) have been used to change the 
magnetization of a ferromagnetic CoPd alloy film, and probe its dynamics with 
circularly polarized femtosecond X-ray pulses (100 fs), measuring the magnetic 
dichroism at Co L2,3 edges. The use of sum rules allows disentangling for the 
first time, the spin and orbital components of the magnetic moment. We show that 
the dynamics of L and S are different. Our results show that the mechanism 
responsible for the ultrafast laser induced demagnetization requires the concept 
of spin-orbit interaction, and that the magneto-crystalline anisotropy energy is 
an important quantity to consider.
Role of carrier diffusion and picosecond exciton kinetics in nonproportionality 
of scintillator light yield 
Paper 7805-19 of Conference 7805
Date: Tuesday, 03 August 2010
Author(s): Richard T. Williams, Joel Q. Grim, Qi Li, Wake Forest Univ. (United 
States); William W. Moses, Lawrence Berkeley National Lab. (United States)
Numerical modeling of carrier diffusion and drift in the strong concentration 
gradient surrounding the track of an energetic electron in the 
femtosecond-picosecond time domain shows that hole and electron mobilities can 
exert a controlling influence on whether subsequent recombination kinetics are 
1st or 2nd order, and what the effective volume density of recombinations is, as 
it affects nonradiative 2nd and 3rd order decay processes. These affect the 
shape of both the low- and high-dE/dx ends of the light-yield curve of a 
scintillator. We report time-resolved measurements of recombination kinetics at 
the high excitation densities appropriate to track ends and the picosecond 
population dynamics of excitons and activators in CsI:Tl.
Non-adiabatic change in frequency of light trapped in a GaAs-AlAs microcavity
Paper 7756-13 of Conference 7756
Date: Tuesday, 03 August 2010
Author(s): Philip J. Harding, Univ. Twente (Netherlands); Huib J. Bakker, Alex 
Hartsuiker, FOM Institute for Atomic and Molecular Physics (Netherlands); Julien 
Claudon, Commissariat à l'Énergie Atomique (France); Allard P. Mosk, Univ. 
Twente (Netherlands); Jean-Michel Gérard, Commissariat à l'Énergie Atomique 
(France); Willem L. Vos, Univ. Twente (Netherlands)
We study frequency-resolved femtosecond pump-probe reflectivity of a planar 
GaAs-AlAs microcavity. About 8 ps after a pump pulse, we observe a strong excess 
probe reflectivity. Light trapped in the cavity accumulates a phase change due 
to a time-dependent refractive index, resulting in a change in frequency by more 
than 5 linewidths away from the cavity resonance. The frequency change is 
non-adiabatic as the wave function changes shape in time and the rate of change 
of the cavity resonance is fast. An analytical model predicts dynamics in 
agreement with experiments, and points to crucial parameters that control future 
applications.
Orientation determination for 3D single molecule diffraction imaging 
Paper 7800-25 of Conference 7800
Date: Tuesday, 03 August 2010
Author(s): Chao Yang, Stefano Marchesini, Lawrence Berkeley National Lab. 
(United States)
The latest development of ultrafast free electron laser makes it possible to 
perform single molecule diffraction imaging. In such an experiment, 
two-dimensional diffraction images of randomly oriented molecules of the same 
type can be captured within femtosecond exposure time. To deduce the 3D 
structure of the molecule at high resolution, we must solve two challenging 
problems: 1) the determination of the relative orientations of 2D images; 2) 
phase retrieval of a reconstructed 3D diffraction pattern. We will focus on the 
first problem and discuss the use of common curve detection techniques to deduce 
the relative orientation of 2D diffraction images.
Upconversion as a tool for characterization and preparation of photonic quantum 
states 
Paper 7815-9 of Conference 7815
Date: Wednesday, 04 August 2010
Author(s): Alfred B. U'Ren, Univ. Nacional Autónoma de México (Mexico); Kevin A. 
O'Donnell, Ctr. de Investigación Científica y de Educación Superior de Ensenada 
(Mexico)
There are few ways of characterizing photon wavepackets on an ultrafast 
time-scale. While femtosecond resolution can be necessary, optical detectors 
have a slower response by several orders of magnitude. One way of overcoming 
this limitation is with Hong-Ou-Mandel interference. Another possible ultrafast 
characterization method is to introduce a controlled delay between generated 
signal and idler photons, overlap them spatially in a nonlinear crystal, and 
detect the sum-frequency photon, in analogy to the autocorrelation of classical 
laser pulses. We present experimental results where we demonstrate this latter 
principle and discuss extensions of this work for the preparation of photonic 
quantum states.
Dynamic complex optical fields for optical manipulation, 3D microscopy, and 
photostimulation of neurotransmitters 
Paper 7762-64 of Conference 7762
Date: Wednesday, 04 August 2010
Author(s): Vincent R. Daria, Christian Stricker, John Bekkers, Steve Redman, 
Hans-Albert Bachor, The Australian National Univ. (Australia)
We demonstrate a multi-functional system capable of multiple-site two-photon 
excitation of photo-sensitive compounds as well as transfer of optical 
mechanical properties on an array of mesoscopic particles. We use holographic 
projection of a single Ti:Sapphire laser operating in femtosecond pulse mode to 
show that the projected three-dimensional light patterns have sufficient 
spatiotemporal photon density for multi-site two-photon excitation of biological 
fluorescent markers and caged neurotransmitters. Using the same laser operating 
in continuous-wave mode, we can use the same light patterns for non-invasive 
transfer of both linear and orbital angular momentum on a variety of mesoscopic 
particles. The system also incorporates high-speed scanning using acousto-optic 
modulators to rapidly render 3D images of neuron samples via two-photon 
microscopy.
Fundamental understanding of the ordered heterojunction hybrid systems from in 
situ polymerization for photovoltaics 
Paper 7777-75 of Conference 7777
Date: Wednesday, 04 August 2010
Author(s): Tingting Xu, Xingzhong Yan, South Dakota State Univ. (United States); 
Jing-Shun Huang, Ching-Fuh Lin, National Taiwan Univ. (Taiwan); David W. 
Galipeau, Qiquan Qiao, South Dakota State Univ. (United States)
Ordered heterojunction hybrid systems from in-situ polymerization is one of the 
promising technologies to achieve high efficiency because it has an optimized 
structure to increase the exciton dissociation and charge transport. Here, 
in-situ electrochemical polymerization of a polythiophene (P3HT) into vertical 
aligned ZnO nanorods was prepared through a novel silane linker. Through the 
UV-visible absorption measuremen, it was found that this ordered hybrid system 
had a comparable absorption with the other methods including the physical 
filtration of P3HT into the nanorod template. The femtosecond fluorescence 
up-conversion (FFU) technique was used to probe the dynamics of vibrational 
relaxation processes, intra-chain (intramolecular) and inter-chain 
(intermolecular) energy transfer between segments, self-trapping of excitons, 
and/or charge transfer dynamics of the in-situ polymerized hybrid system and 
their application photovoltaics.
Course: Nanoplasmonics
Date: Thursday, 05 August 2010
Instructor(s): Mark I. Stockman, Georgia State Univ. (United States)
Nanooptics deals with optical phenomena and spectroscopy on the nanoscale, i.e., 
in the regions of space whose size is much smaller than the light wavelength. 
While electromagnetic waves cannot be localized in the regions with sizes 
significantly less than half wavelength, nanooptics is based on electric fields 
oscillating at optical frequency. From the positions of the interaction with 
matter and spectroscopy, such local optical fields mostly produce the same type 
of responses as electromagnetic waves. Elementary excitations that are carriers 
of energy and coherence in nanooptics are surface plasmons (SPs). These local 
fields cause a wealth of gigantically enhanced optical phenomena of which the 
surface enhanced Raman scattering (SERS) is the most studied and widely known. 
This one-day course will encompass the fundamental properties and applications 
of the surface plasmonics at the nanoscale. It will include coherent effects 
associated with phase memory of the SPs, in particular, coherent control of 
nanooptical phenomena. Nonlinear processes such as generation of harmonics and 
two-photon excitation by nanoscale fields will also be covered. Ultrafast 
(femtosecond and attosecond) phenomena are within the scope of this course. We 
will also include quantum phenomena associated with properties of surface 
plasmons as quantum quasiparticles such as quantum generation and fluctuations. 
Along with fundamental properties of SPs, we will consider many applications of 
nanoplasmonics, in particular, detection of ultrasmall amounts of chemical and 
biological compounds, scanning near-field optical microscopes or SNOMs, and 
nanolithography.
Interfacial charge transfer excitations for optical applications: A case of 
molecule-metal and molecule-semiconductor nanoclusters 
Paper 7758-1 of Conference 7758
Date: Wednesday, 04 August 2010
Author(s): Ramakrishna Guda, Western Michigan Univ. (United States)
Optical excitations in donor-acceptor systems in organic molecules, polymers, 
nanomaterials and molecule-nanomaterial interface are under intense research 
both because of their fundamental interest as well as applications in 
photo-voltaics, nonlinear optics and sensors. One of the important applications 
is in solar energy conversion especially the ones related to dye-sensitized 
solar cells1 and organic bulk heterojunction solar cells2. These systems are 
considered cost-effective alternatives to silicon based solar cells. Vital 
aspect of these devices is the photo-induced electron transfer where the 
photo-excited donor transfers the electron to the acceptor. Our strategy is to 
use the interfacial charge transfer excitons where the excitation leads directly 
to an electron on the acceptor and hole in the donor without loss as heat due to 
photo-induced electron transfer3, 4. If this energy can be converted without 
loss as heat, the solar cell efficiencies can be increased by as high as 5%. 
Dynamics of direct charge transfer excitations in small molecule-TiO2 
nanoparticles5 and chromophore functionalized TiO2, ZnO and ZrO2 nanoparticles 
are investigated6. Interesting localization and delocalization of the charge 
transfer excitations are observed which can provide insights in designing better 
dye molecules which can improve the solar energy conversion efficiency. In 
addition, chromophore-gold cluster composites are being investigated which have 
shown directional photo-induced electron transfer and interfacial charge 
transfer excitations. Femtosecond fluorescence upconversion and transient 
measurements measurements are being utilized to follow such charge transfer 
excitations and the consequent localization and delocalization pathways. Present 
results also show the potential of these systems as better nonlinear optical 
materials especially in relation to optical limiting. References 1. Gratzel, M 
Nature 2001, 414, 338. 2. Dennler, G.; Scharber, M.; Brabec, C. J. Adv. Mater. 
2009, 21, 1323. 3. Tae, E. L.; Lee, S. H.; Lee, K.; Yoo, S. S.; Kang, E. J.; 
Yoon, K. B. J. Phys. Chem. B 2005, 109, 22513. 4. Schmidtke, J. P.; Friend, R. 
H.; Silva, C. Phys. Rev. Lett. 2008, 100, 157401 5. Varaganti, S.; Ramakrishna, 
G. J Phys Chem (submitted). 6. Varaganti,S.; Gessesse, M.; Obare, S.; 
Ramakrishna, G. Proc SPIE 2009, 741309, 741309/01-10.
The role of polarization pulse shaping in ultrafast nanooptics: adaptive and 
deterministic control mechanisms 
Paper 7757-12 of Conference 7757
Date: Sunday, 01 August 2010
Author(s): Walter Pfeiffer, Univ. Bielefeld (Germany)
Recent theoretical investigations as well as experiments have shown that the 
polarization degree of freedom of the incident light is essential to manipulate 
and control nanophotonic excitations on an ultrashort time scale and at a length 
scale below the diffraction limit. The present status of knowledge is reviewed 
and a qualitative discussion of the different control mechanisms is presented. 
To some extend deterministic rules are applicable to realize particular 
nanophotonic excitations as it is shown for spatial contrast reversal.
Spaser as nanoscale optical generator and ultrafast nano-amplifier 
Paper 7754-16 of Conference 7754
Date: Monday, 02 August 2010
Author(s): Mark I. Stockman, Georgia State Univ. (United States)
Nanoplasmonics deals with collective electron dynamics on the surface of metal 
nanostructures, which arises as a result of excitations called surface plasmons. 
The surface plasmons localize and concentrate optical energy in nanoscopic 
regions creating highly enhanced local optical fields. They undergo ultrafast 
dynamics with timescales as short as a few hundred attoseconds. We will review 
the numerous existing applications of nanoplasmonics: nanoantennas for 
photovoltaic cells and LEDs, nanoplasmonic labels, tests, and sensors for 
biology, medicine, industry, environmental monitoring and defense, 
ultramicroscopy, plasmonics-assisted magnetic recording, nanoshell-mediated 
cancer treatment, etc. From the latest developments and original work in 
nanoplasmonics, we will concentrate on the SPASER as a quantum nanoscale optical 
generator and ultrafast nanoamplifier of local fields.
Chalcogenide photonic integrated circuits for ultrafast nonlinear optics 
Paper 7756-18 of Conference 7756
Date: Tuesday, 03 August 2010
Author(s): Benjamin J. Eggleton, The Univ. of Sydney (Australia)
This paper reviews our recent progress in developing dispersion engineered 
highly nonlinear chalcogwnide circuits for all-optical processing. Highlights of 
this research include recent demonstrations of >Tera/baud per second optical 
switching and waveform analysis.
Pulse laser driven ultrafast micro and nanofluidics system 
Paper 7759-36 of Conference 7759
Date: Tuesday, 03 August 2010
Author(s): Pei-Yu Chiou, Univ. of California, Los Angeles (United States)
A tightly focused laser beam is capable of disrupting water medium directly and 
inducing localized hot plasma for rapid heating and creating cavitation bubbles. 
These bubbles expand at speeds up to hundred meters per second in the micro and 
nanometer scale. Through proper engineering designs, such ultrafast microfluidic 
phenomena can be utilized for actuating ultrafast microfluidic devices to enable 
new functionalities not possible with conventional microfluidic devices.
Electron and XUV light emission probes of ultrafast nano-localized plasmonic 
fields 
Paper 7757-47 of Conference 7757
Date: Wednesday, 04 August 2010
Author(s): Matthias F. Kling, Max-Planck-Institut für Quantenoptik (Germany)
Recent advantages in laser technology have paved the way for a full control of 
the waveform of optical fields. The use of metallic nanostructures for 
high-harmonic generation (HHG) via nanoplasmonic field enhancement offers a 
route for the production of ultrashort XUV pulses. We have theoretically studied 
the influence of the sub-cycle field evolution of the driving laser field on the 
generated plasmonic fields and found feasible conditions for the generation of 
single attosecond pulses. These results together with first experimental work on 
HHG from nanostructures will be presented. We will furthermore present results 
on the characterization of nanolocalized plasmonic fields utilizing 
time-of-flight photoelectron emission microscopy (TOF-PEEM).
Probing ultrafast nano-localised plasmonic fields via XUV light generation 
Paper 7757-48 of Conference 7757
Date: Wednesday, 04 August 2010
Author(s): Sarah L. Stebbings, Frederik Süßmann, Ying Ying Yang, 
Max-Planck-Institut für Quantenoptik (Germany); Roswitha Graf, Alexander 
Apolonskiy, Ludwig-Maximilians-Univ. München (Germany); Alexander 
Weber-Bargioni, Lawrence Berkeley National Lab. (United States); Mark I. 
Stockman, Georgia State Univ. (United States); Ferenc Krausz, Matthias F. Kling, 
Max-Planck-Institut für Quantenoptik (Germany)
The use of nanostructure arrays, such as bow-tie-like antennae, offer a 
promising route to ultrashort XUV pulses via plasmonic enhanced high harmonic 
generation at relatively low laser intensities. By performing a systematic 
theoretical investigation, the optimal conditions for the generation of single 
XUV pulses via nanoplasmonic field enhancement have been identified. Both the 
experimental and theoretical results of this work will be presented at the 
conference.
Photodetector behavior in the presence of ultrafast laser irradiance 
Paper 7780A-7 of Conference 7780A
Date: Wednesday, 04 August 2010
Author(s): Michael K. Rafailov, Richer LLC (United States)
Ultra-fast laser is able to change optical state of semiconductor. These changes 
are time-dependent and completely reversible: ultra-fast laser "bleaches" 
semiconductor and therefore temporally changes detector's optical 
characteristics. Practically, ultra-fast laser allows remote control of 
fundamental properties of semiconductor and therefore, temporal alteration of 
photodetector's characteristics - such as responsivity and detectivity as well 
as response time and response spectral bandwidth. However, with excessive energy 
transfer that can follow bleaching the effect may be masked by thermal noise or 
even lattice disorder. In this paper we will discuss some foundations of 
ultra-fast laser bandgap photonics in connection to ultra-fast low energy per 
pulse laser.
Electrical polaritonic control of ultrafast optical amplification in 
semiconductor microcavities 
Paper 7756-33 of Conference 7756
Date: Wednesday, 04 August 2010
Author(s): Jeremy J. Baumberg, Gabriel Christmann, Univ. of Cambridge (United 
Kingdom); Pavlos Savvidis, Nikolaos Pelekanos, Zacharias Hatzopoulos, Simeon 
Tsintzos, Univ. of Crete (Greece); Chris Coulson, Cornelius Grossman, Univ. of 
Cambridge (United Kingdom)
Optical amplification in strongly-coupled semiconductor microcavities is the 
largest reported for any material. We report high-speed electronic control of 
ultrafast polariton amplification in an electrically-biased semiconductor 
microcavity which contains double-quantum wells. A >90% reduction of the 
parametric scattering gain is obtained by tuning the intracavity electric field 
to turn on inter-well resonant tunneling.
Ultrafast optical switching of nematic liquid crystal birefringence 
Paper 7775-47 of Conference 7775
Date: Wednesday, 04 August 2010
Author(s): Iam Choon Khoo, Justin Liou, Michael V. Stinger, The Pennsylvania 
State Univ. (United States)
The theory and experimental demonstrations of ultra-fast all-optical switching 
based on laser induced order parameter and birefringence changes with cw - 
nanosecond pulsed lasers at 400 nm - 1550 nm will be presented.
Ultrafast transient absorption microscopy studies of carrier dynamics in 
epitaxial graphene 
Paper 7758-35 of Conference 7758
Date: Thursday, 05 August 2010
Author(s): Libai Huang, Gregory V. Hartland, Huili Xing, Univ. of Notre Dame 
(United States)
Energy exchange between the electrons and phonons is particularly important to 
electron transport, and understanding this process will be vital for the 
realization of future graphene-based electronics. Epitaxial growth is a very 
promising approach for practical applications, as it has the ability to prepare 
graphene on a large scale and supported on a substrate. However, epitaxially 
grown graphene is highly inhomogeneous, with variations in the sample thickness 
occurring over length scale of a few micrometers. To pave the road for 
electronic devices based on epitaxial graphene, characterization methods with 
high spatial resolution are required. Here we present transient absorption 
microscopy as a novel tool to characterize graphene, and to interrogate the 
charge carrier dynamics. This technique has the ability to directly image 
carrier dynamics with a diffraction-limited spatial resolution and a time 
resolution of ~ 200 fs. The intensity of the transient absorption signal is 
shown to correlate with the number of graphene layers. The carrier cooling 
exhibits a bi-exponential decay, consisting of an instrument-response limited 
fast decay time 1 (< 0.2 ps) and a slower decay time 2. The fast and slow 
relaxation times were assigned to coupling between electrons and optical phonon 
modes and the hot phonon effect, respectively. The limiting value of the slow 
relaxation time at high pump intensity reflects the lifetime of the optical 
phonons. The contribution of the slow component to the overall decay was found 
to vary with spatial position in the sample. This is attributed to differences 
in coupling between the graphene and the substrate. These results point to 
transient absorption microscopy as a potentially important tool for 
characterizing graphene.
Modeling of non-adiabatic photoinduced dynamics and energy transfer in 
conjugated molecules 
Paper 7758-6 of Conference 7758
Date: Wednesday, 04 August 2010
Author(s): Sebastian Fernandez-Alberti, Univ. Nacional de Quilmes (Argentina); 
Valeria D. Kleiman, Adrian E. Roitberg, Univ. of Florida (United States); Sergei 
Tretiak, Los Alamos National Lab. (United States)
Prediction and understanding of photoinduced processes in molecular- and 
nano-materials is fundamental to a myriad of technological applications, ranging 
from sensing, imaging, solar energy harvesting, to future optoelectronic 
devices. This talk will overview several applications of recently developed 
excited state molecular dynamics framework incorporating non-adiabatic quantum 
transitions studying ultrafast dynamics and exciton transport in several 
conjugated molecular systems. Our calculations rely on the use of the Collective 
Electronic Oscillator (CEO) package accounting for many-body effects and actual 
potential energy surfaces of the excited states combined with the Tully's fewest 
switches algorithm for surface hopping probing non-adiabatic processes. Our 
analysis show intricate details of photoinduced vibronic relaxation and identify 
the conformational degrees of freedom leading to ultrafast energy transfer. This 
theoretical modeling allows to understand and to potentially manipulate energy 
transfer pathways in molecular materials suitable for solar energy conversion.
Upconversion as a tool for characterization and preparation of photonic quantum 
states 
Paper 7815-9 of Conference 7815
Date: Wednesday, 04 August 2010
Author(s): Alfred B. U'Ren, Univ. Nacional Autónoma de México (Mexico); Kevin A. 
O'Donnell, Ctr. de Investigación Científica y de Educación Superior de Ensenada 
(Mexico)
There are few ways of characterizing photon wavepackets on an ultrafast 
time-scale. While femtosecond resolution can be necessary, optical detectors 
have a slower response by several orders of magnitude. One way of overcoming 
this limitation is with Hong-Ou-Mandel interference. Another possible ultrafast 
characterization method is to introduce a controlled delay between generated 
signal and idler photons, overlap them spatially in a nonlinear crystal, and 
detect the sum-frequency photon, in analogy to the autocorrelation of classical 
laser pulses. We present experimental results where we demonstrate this latter 
principle and discuss extensions of this work for the preparation of photonic 
quantum states.
Terahertz nonlinear spectroscopy of free-carriers in direct bandgap 
semiconductors 
Paper 7763-11 of Conference 7763
Date: Sunday, 01 August 2010
Author(s): Luca Razzari, Francois Blanchard, Institut National de la Recherche 
Scientifique (Canada); Fuhai Su, Univ. of Alberta (Canada); Gargi Sharma, 
Institut National de la Recherche Scientifique (Canada); Ayesheshim K. 
Ayesheshim, Tyler L. Cocker, Lyubov V. Titova, Univ. of Alberta (Canada); Heidi 
C. Bandulet, Roberto Morandotti, Jean-Claude Kieffer, Tsuneyuki Ozaki, Institut 
National de la Recherche Scientifique (Canada); Matthew E. Reid, Univ. of 
Northern British Columbia (Canada); Frank A. Hegmann, Univ. of Alberta (Canada)
Ultrafast nonlinear processes have been extensively explored in the visible and 
near infrared frequency range, thanks to the availability of ultrashort pulses 
delivered by mode-locked lasers. Here, the combination of high intensities of 
excitation together with a very fine temporal resolution have shed new light on 
diverse aspects of condensed-matter dynamics [1]. On the other hand, this kind 
of phenomena has remained relatively unexplored in the terahertz (THz) spectral 
region (typically 0.1-10 THz), mainly because of the lack of sources delivering 
high-energy, fewcycle THz pulses. Nowadays, this kind of sources is becoming 
available [2,3], thus opening the route towards the understanding of new aspects 
of radiation-matter interaction. Nonlinear interactions at THz frequencies 
possess interesting properties and peculiarities: on one side, in this spectral 
range one can observe an intermediate regime in which both electronic and ionic 
motions contribute to the nonlinear dielectric function of a material. On the 
other side, the very low energy per photon associated to this radiation allows 
to neglect multiphoton interactions in semiconductors, thus opening up the 
possibility of observing drift-velocity-based nonlinearities owing to free 
carriers in this type of systems. While these processes were studied in the past 
using relatively long THz pulses (time duration of several tens of nanoseconds) 
[4,5], the above-mentioned new-generation of few-cycle THz sources allows now to 
explore their ultrafast nature and dynamics in the picosecond domain [6]. In 
particular, our investigation has been aimed at studying the ultrafast nonlinear 
dynamics of free carriers in semiconductors and at developing the proper tools 
for this new kind of THz spectroscopy. We have performed several nonlinear 
experiments on free-carriers in direct bandgap semiconductors at THz 
frequencies. Techniques as Z-scan [7], THz pump - THz probe [8], and optical 
pump - THz probe [9] have been employed to explore nonlinear interactions in 
both n-doped and photoexcited samples. The mechanism that dominates these 
nonlinearities is found to be intervalley scattering and a simple mathematical 
model adding this effect to a standard Drude-like response well explains our 
experimental results. References [1] S. Mukamel, Principles of nonlinear 
spectroscopy, Oxford University Press, (1999). [2] F. Blanchard et al., Opt. 
Exp. 15 (20), 13212 (2007). [3] K.-L. Yeh, Appl. Phys. Lett. 90, 171121 (2007). 
[4] A. Mayer and F. Keilmann, Phys. Rev. B 33, 6954 (1986). [5] A. Mayer and F. 
Keilmann, Phys. Rev. B 33, 6962 (1986). [6] J. Hebling et al., IEEE J. Sel. Top. 
Quant. Electron. 14, 345 (2008). [7] L. Razzari et al., Phys. Rev. B 79, 193204 
(2009). [8] F. Blanchard et al., in preparation. [9] F.H. Su et al., Opt. Exp. 
17 (12), 9620 (2009).
Nanocrystal lasing in the Auger-recombination-free regime using engineered 
heterostructures 
Paper 7756-23 of Conference 7756
Date: Wednesday, 04 August 2010
Author(s): Victor I. Klimov, Los Alamos National Lab. (United States)
Nanocrystal quantum dots show high photoluminescence quantum yields and 
size-dependent emission colors tunable through the quantum-confinement effect. 
Despite their favorable light-emitting properties, nanocrystals are difficult to 
use in lasing because of fast optical-gain decay induced by nonradiative Auger 
recombination. In this talk, I will discuss several approaches for resolving the 
problem of ultrafast Auger recombination by using engineered carrier-carrier 
interactions in various types of heterostructured nanocrystals.
Performance of a Schwarzschild imaging microscope for plasma diagnostics 
Paper 7801-15 of Conference 7801
Date: Sunday, 01 August 2010
Author(s): Xin Wang, Baozhong Mu, Yi Huang, Zirong Zhai, Shengzhen Yi, Li Jiang, 
Jingtao Zhu, Zhanshan Wang, Tongji Univ. (China)
Schwarzschild microscope system has been essential diagnostics in the intense 
ultrafast laser-matter interaction research. A Schwarzschild type plasma 
diagnostics system with numerical aperture of 0.1 and a magnification of 10 has 
been designed, component fabricated, system assembled and experimental tested. A 
Q-switched Nd:YAG laser at 1064 nm with a pulsed energy of 1 J was used to 
ablate copper target to produce EUV emission above 10 nm. Mo/Si multilayers with 
a thickness period of 9.5 nm and 30 layers pairs are deposited by magnetron 
sputtering as a normal-incidence reflection coating at 18.2 nm and 5% bandwidth. 
Since the spatial resolution of the microscope is limited by the CCD camera, LiF 
is employed as the detector to achieve the sub-micron resolution for a field of 
view of 2 mm using 600# copper mesh (bar width is 5μm) and 500lp/mm 
transmittance grating as the object.
Spatio-temporal control of fields around nano-antennas 
Paper 7757-16 of Conference 7757
Date: Sunday, 01 August 2010
Author(s): Daan Brinks, Marta Castro Lopez, Alberto G. Curto, Richard Hildner, 
Tim H. Taminiau, Niek F. van Hulst, ICFO - Instituto de Ciencias Fotónicas 
(Spain)
Nano-antennas concentrate electromagnetic fields in sub-diffraction limited 
hotspots, whose position in time and space depends on the antenna-structure and 
the incoming electromagnetic field. Antennas can therefore be combined with 
ultrafast pulses to address femtosecond processes in nanometric volumes, 
provided one takes into account and compensates for the dispersion of the 
antenna-structures. We adapt the field of an excitation pulse to the dispersion 
and resonances of an optical gap-antenna. This way we change and enhance the 
localization of hotspots, while at the same time obtaining quantitative 
information about the field dynamics around the structure. Our latest 
experimental results will be presented.
Ultra-fast dynamics of spin and orbital magnetic moments of CoPd alloys probed 
by time resolved x-ray magnetic circular dichroism 
Paper 7760-21 of Conference 7760
Date: Tuesday, 03 August 2010
Author(s): Eric Beaurepaire, Christine Boeglin, Valérie Halté, Jean-Yves Bigot, 
Victor Lopez-Flores, Jacek Arabski, Institut de Physique et Chimie des Matériaux 
de Strasbourg (France); Christian Stamm, Nikolaus Pontius, Hermann Dürr, 
Helmholtz-Zentrum Berlin für Materialien und Energie GmbH (Germany)
Ultrashort optical laser pulses (60 fs) have been used to change the 
magnetization of a ferromagnetic CoPd alloy film, and probe its dynamics with 
circularly polarized femtosecond X-ray pulses (100 fs), measuring the magnetic 
dichroism at Co L2,3 edges. The use of sum rules allows disentangling for the 
first time, the spin and orbital components of the magnetic moment. We show that 
the dynamics of L and S are different. Our results show that the mechanism 
responsible for the ultrafast laser induced demagnetization requires the concept 
of spin-orbit interaction, and that the magneto-crystalline anisotropy energy is 
an important quantity to consider.
Orientation determination for 3D single molecule diffraction imaging 
Paper 7800-25 of Conference 7800
Date: Tuesday, 03 August 2010
Author(s): Chao Yang, Stefano Marchesini, Lawrence Berkeley National Lab. 
(United States)
The latest development of ultrafast free electron laser makes it possible to 
perform single molecule diffraction imaging. In such an experiment, 
two-dimensional diffraction images of randomly oriented molecules of the same 
type can be captured within femtosecond exposure time. To deduce the 3D 
structure of the molecule at high resolution, we must solve two challenging 
problems: 1) the determination of the relative orientations of 2D images; 2) 
phase retrieval of a reconstructed 3D diffraction pattern. We will focus on the 
first problem and discuss the use of common curve detection techniques to deduce 
the relative orientation of 2D diffraction images.
Surface plasmon enhancement of third-generation conversion processes 
Paper 7772-32 of Conference 7772
Date: Wednesday, 04 August 2010
Author(s): Jao van de Lagemaat, Allison C. Kanarr, Thomas H. Reilly III, Justin 
C. Johnson, National Renewable Energy Lab. (United States)
In this presentation, I will describe a study of surface plasmon/exciton 
hybridization with the aim of enhancing third-generation photoconversion 
processes that have the theoretical capability of breaking the Shockley-Queisser 
limit. Pentacene is a candidate for such a process called singlet fission, in 
which a singlet exciton breaks up in two separate triplet excitons. We will show 
results of ultrafast spectroscopy of pentacene on plasmonically active systems. 
These measurements show altered excited state kinetics and show evidence of 
enhanced formation of triplets indicating that hybridizing surface plasmons with 
molecular states is a promising avenue of controlling energy conversion 
pathways.
Detection of nucleic acids with graphene nanopores: ab initio characterization 
of a novel sequencing device 
Paper 7758-15 of Conference 7758
Date: Wednesday, 04 August 2010
Author(s): Tammie Nelson, Bo Zhang, Oleg V. Prezhdo, Univ. of Washington (United 
States)
We report an ab initio study of the interaction of two nucleobases, cytosine and 
adenine, with a novel graphene nanopore device for detecting the base sequence 
of a single-stranded nucleic acid (ssDNA or RNA). The nucleobases were inserted 
into a pore in a graphene nanoribbon, and the electrical current and conductance 
spectra were calculated as functions of voltage applied across the nanoribbon. 
The conductance spectra and charge densities were analyzed in the presence of 
each nucleobase in the graphene nanopore. The results indicate that, due to 
significant differences in the conductance spectra, the proposed device has 
adequate sensitivity to discriminate between different nucleotides. Moreover, we 
show that the nucleotide conductance spectra are not affected by its orientation 
inside the graphene nanopore. The proposed technique may be extremely useful for 
real applications in developing ultrafast, low cost DNA sequencing methods.
Course: Nanoplasmonics
Date: Thursday, 05 August 2010
Instructor(s): Mark I. Stockman, Georgia State Univ. (United States)
Nanooptics deals with optical phenomena and spectroscopy on the nanoscale, i.e., 
in the regions of space whose size is much smaller than the light wavelength. 
While electromagnetic waves cannot be localized in the regions with sizes 
significantly less than half wavelength, nanooptics is based on electric fields 
oscillating at optical frequency. From the positions of the interaction with 
matter and spectroscopy, such local optical fields mostly produce the same type 
of responses as electromagnetic waves. Elementary excitations that are carriers 
of energy and coherence in nanooptics are surface plasmons (SPs). These local 
fields cause a wealth of gigantically enhanced optical phenomena of which the 
surface enhanced Raman scattering (SERS) is the most studied and widely known. 
This one-day course will encompass the fundamental properties and applications 
of the surface plasmonics at the nanoscale. It will include coherent effects 
associated with phase memory of the SPs, in particular, coherent control of 
nanooptical phenomena. Nonlinear processes such as generation of harmonics and 
two-photon excitation by nanoscale fields will also be covered. Ultrafast 
(femtosecond and attosecond) phenomena are within the scope of this course. We 
will also include quantum phenomena associated with properties of surface 
plasmons as quantum quasiparticles such as quantum generation and fluctuations. 
Along with fundamental properties of SPs, we will consider many applications of 
nanoplasmonics, in particular, detection of ultrasmall amounts of chemical and 
biological compounds, scanning near-field optical microscopes or SNOMs, and 
nanolithography.
State-resolved exciton dynamics in quantum dots 
Paper 7758-27 of Conference 7758
Date: Thursday, 05 August 2010
Author(s): Patanjali Kambhampati, McGill Univ. (Canada)
The semiconductor quantum dot is one of the canonical systems in nanoscience. 
Whereas the nanometer size of these materials is obvious, the richer and more 
meaningful issue is the presence of quantum confinement effects conferred by 
virtue of size. One may qualitatively describe quantum dot electronic structure 
like the textbook particle in a sphere. However, this simple picture misses the 
vast majority of the processes which ultimately control the functionality of the 
quantum dot. Our goal is to obtain a detailed picture of the rich inner workings 
of the quantum dot. We introduce a mixed time/frequency domain ultrafast 
spectroscopic approach which we denote State-Resolved Exciton Dynamics. We have 
applied this approach to resolve several long standing issues central to quantum 
dot science: 1) Hot exciton relaxation dynamics: radiationless transitions on 
the nanoscale 2) Optical gain: recovering predictions from theory and revealing 
new physics 3) Electronic structure of multiexcitons: creation of an artificial 
periodic table 4) electron-phonon interactions: quantizing piezoelectricity The 
power of this approach is reflected by our ability to predict aspects of 
unrelated experiments, e.g. single dot blinking and multiple exciton generation. 
In addition to the basic science of excitons in nanoscale materials, these 
fundamental results have advanced the design principles for a broad range of 
applications including: LEDs, lasers, solar cells, THz radiation sources, 
piezoelectrics, and non-classical light.
Excitation dynamics in nanoscale materials for solar energy harvesting 
Paper 7758-28 of Conference 7758
Date: Thursday, 05 August 2010
Author(s): Oleg V. Prezhdo, Univ. of Washington (United States)
Design of novel materials for energy harvesting and storage requires an 
understanding of the dynamical response on the nanometer scale. A great deal of 
experimental and theoretical work has been devoted to characterizing the 
excitation, charge, spin, and vibrational dynamics in quantum dots, conducting 
polymers, carbon nanotubes, inorganic semiconductors and molecular chromophores. 
We have developed state-of-the-art non-adiabatic molecular dynamics techniques 
and implemented them within time-dependent density functional theory in order to 
model the ultrafast processes in these materials at the atomistic level and in 
real time. Quantum dots (QD) are quasi-zero dimensional structures with a unique 
combination of molecular and bulk properties. As a result, QDs exhibit new 
physical phenomena such as the electron-phonon relaxation bottleneck and 
efficient carrier multiplication, which have the potential to greatly increase 
the efficiency of solar cells. Photoinduced charge separation across 
molecular/bulk interfaces drives the dye-sensitized semiconductor solar cell. A 
subject of active research, it creates many challenges due to the stark 
differences between the quantum states of molecular and periodic systems, as 
well as the different sets of theories and experimental tools used by physicists 
and chemists. Our time-domain atomistic simulations create a detailed picture of 
these materials. By comparing and contrasting their properties, we provide a 
unifying description of quantum dynamics on the nanometer scale, resolve several 
highly debated issues, and generate theoretical guidelines for development of 
novel systems for energy harvesting and storage.
Widefield multiphoton excited fluorescence microscopy for animal study in vivo
Paper 7765-32 of Conference 7765
Date: Wednesday, 04 August 2010
Author(s): Shean-Jen Chen, Li-Chung Cheng, Chia-Yuan Chang, Hung-Wei Su, 
National Cheng Kung Univ. (Taiwan)
A widefield multiphoton excited fluorescence microscope with a simultaneously 
spatial and temporal focusing technique has been developed to provide fast 
three-dimensional (3D) multiphoton fluorescence images fro animal study in vivo. 
Unlike conventional multiphoton microscopy based on pixel by pixel scanning 
technique, the wide-field multiphoton microscope only scans one dimension, 
z-axis, to construct a 3D image. By using a Ti:sapphire femtosecond laser 
oscillator as a seed laser for the femtosecond laser amplifier with a repetition 
rate of 10 kHz, we raise the average power from 1.0 to 4.2 W, which is enough 
power to excite the fluorescence in the area over 100 μm x 100 μm. The 
fluorescence image signal is detected by an EM CCD, which frame rate might rise 
up to 1 kHz according to the efficiency of fluorophore, so the widefield 
multiphoton microscopy can provide very fast imaging fro animal study in vivo 
such as monitoring brain neuron activity and liver metabolism.
Multiphoton excited whispering gallery mode ultraviolet lasing from ZnO 
nano-multipods 
Paper 7755-3 of Conference 7755
Date: Sunday, 01 August 2010
Author(s): Gaurav Shukla, Alika Khare, Indian Institute of Technology Guwahati 
(India)
For c-axis oriented hexagonal ZnO nanodisks, microrods, and nano-multipods, the 
lasing action can originate from whispering-gallery mode (WGM) cavity, in which 
the light wave propagates circularly in the inner walls due to multiple total 
internal reflections at the resonator's boundary. In this work, growth of ZnO 
nano-multipods on ZnO seed layer using a two step hydrothermal process followed 
by high temperature annealing is reported. Under excitation of a nanosecond 
pulsed laser with 1064 nm wavelength, UV lasing emission from ZnO nano-multipods 
was obtained. The UV lasing emission, resonant conditions, and laser mode 
characteristics will be discussed using whispering-gallery mode mechanism.
3D microstructures of functional materials fabricated by multiphoton processing
Paper 7774-16 of Conference 7774
Date: Monday, 02 August 2010
Author(s): Xuan-Ming Duan, Xian-Zi Dong, Feng Jin, Wei-Qiang Chen, Zhen-Sheng 
Zhao, Technical Institute of Physics and Chemistry (China)
Multi-photon process of nonlinear optical materials provides an excellent 
opportunity for nanolithography with laser direct writing technique, which can 
achieve not only nanometer scale resolution but also microstructure fabrication 
in three-dimensions. In this paper, we will report the latest progresses on the 
resolution of nanometer scale and 3D microstructures of functional materials 
fabricated by multi-photon processing in our laboratory. The fabrication 
resolution is downed to less than 50 nm. The fabricated 3D microstructures of 
active materials, semiconductor-polymer nanocomposites exhibit excellent 
properties such as ultra-low lasing threshold, tunable photonic bandgap and so 
on.
Widefield multiphoton excited fluorescence microscopy with adaptive optics 
Paper 7765-33 of Conference 7765
Date: Wednesday, 04 August 2010
Author(s): Shean-Jen Chen, Chia-Yuan Chang, Li-Chung Cheng, Hung-Wei Su, 
National Cheng Kung Univ. (Taiwan)
This paper demonstrates the first integration for widefield multiphoton excited 
fluorescence microscopy with adaptive optics to image mice in vivo. According to 
distorted wavefront collected by defined image sharpness parameters, deformable 
mirror is used to correct the distortion in real time. The adaptive optics 
device corrects uniformity and system misalignment first and then reduces 
biospecimen distortion to ensure perfect temporal focusing.
Entanglement-enhanced measurement of a completely unknown phase 
Paper 7815-36 of Conference 7815
Date: Thursday, 05 August 2010
Author(s): B. L. Higgins, G. Y. Xiang, Griffith Univ. (Australia); D. W. Berry, 
Univ. of Waterloo (Canada); H. M. Wiseman, G. J. Pryde, Griffith Univ. 
(Australia)
Obtaining uncertainty in an estimate of an optical phase shift below the 
standard quantum limit (SQL) requires employing nonclassical properties of 
quantum mechanics, such as multiphoton entangled NOON states. Measurement of a 
phase anywhere within 0 to 2π, however, additionally requires nontrivial quantum 
control. Furthermore, the experimental construction of NOON states is 
notoriously difficult. We present an adaptive phase measurement scheme using 
entangled multiphoton states. We take a "bottom-up" approach by constructing an 
experimental measurement protocol tailored to available states, employing 
precharacterization of the apparatus and optimising feedback to achieve sub-SQL 
measurement of a random phase.
Three-dimensional polymer microdevices with gold nanorods 
Paper 7757-123 of Conference 7757
Date: Monday, 02 August 2010
Author(s): Shean-Jen Chen, Wen-Shuo Kuo, Chi-Hsiang Lien, National Cheng Kung 
Univ. (Taiwan)
In this study, nonlinear multiphoton photocrosslinking and photopolymerization 
of rose bengal and trimethylolpropane triacrylate monomers in solution have been 
used to direct the three-dimension (3D) assembly of microdevices; moreover, we 
also presents the first example of containing gold nanorods within the 
photopolymerization. The experimental results show that the two-photon excited 
photopolymerization containing the nanorods improves more efficiently of 
decreasing the power density of femtosecond laser, and also provides a great 
diversity of optical properties. The doped nanorods with two-photon luminescence 
act as label molecules for internal microdiagnosis of 3D polymer microdevices.
The 3D structure with gradient spiral lattices exhibits a completely different 
phenomenon on light propagation: these gradient 3D photonic structures may be 
beneficial for developing polymer based optoelectronic devices and integrated 
systems 
Paper 7774-18 of Conference 7774
Date: Monday, 02 August 2010
Author(s): Zhen-Sheng Zhao, Xian-Zi Dong, Xuan-Ming Duan, Technical Institute of 
Physics and Chemistry (China)
Multiphoton photopolymerization (MPP) is an emerging technique for the 
fabrication of three-dimensional (3D) microstructures. Here, we report the 
fabrication and properties of 3D photonic structures consisting of gradient 
lattices. The properties of 3D structures were experimentally confirmed by 
experimentals and FDTD calculations. The 3D structure with gradient quasidiamond 
lattices could effectively expand the width of the PBG. The 3D structure with 
gradient spiral lattices exhibits a completely different phenomenon on light 
propagation. These gradient 3D photonic structures may be beneficial for 
developing polymer based optoelectronic devices and integrated systems. The 
details will be reported on the conference.
Terahertz nonlinear spectroscopy of free-carriers in direct bandgap 
semiconductors 
Paper 7763-11 of Conference 7763
Date: Sunday, 01 August 2010
Author(s): Luca Razzari, Francois Blanchard, Institut National de la Recherche 
Scientifique (Canada); Fuhai Su, Univ. of Alberta (Canada); Gargi Sharma, 
Institut National de la Recherche Scientifique (Canada); Ayesheshim K. 
Ayesheshim, Tyler L. Cocker, Lyubov V. Titova, Univ. of Alberta (Canada); Heidi 
C. Bandulet, Roberto Morandotti, Jean-Claude Kieffer, Tsuneyuki Ozaki, Institut 
National de la Recherche Scientifique (Canada); Matthew E. Reid, Univ. of 
Northern British Columbia (Canada); Frank A. Hegmann, Univ. of Alberta (Canada)
Ultrafast nonlinear processes have been extensively explored in the visible and 
near infrared frequency range, thanks to the availability of ultrashort pulses 
delivered by mode-locked lasers. Here, the combination of high intensities of 
excitation together with a very fine temporal resolution have shed new light on 
diverse aspects of condensed-matter dynamics [1]. On the other hand, this kind 
of phenomena has remained relatively unexplored in the terahertz (THz) spectral 
region (typically 0.1-10 THz), mainly because of the lack of sources delivering 
high-energy, fewcycle THz pulses. Nowadays, this kind of sources is becoming 
available [2,3], thus opening the route towards the understanding of new aspects 
of radiation-matter interaction. Nonlinear interactions at THz frequencies 
possess interesting properties and peculiarities: on one side, in this spectral 
range one can observe an intermediate regime in which both electronic and ionic 
motions contribute to the nonlinear dielectric function of a material. On the 
other side, the very low energy per photon associated to this radiation allows 
to neglect multiphoton interactions in semiconductors, thus opening up the 
possibility of observing drift-velocity-based nonlinearities owing to free 
carriers in this type of systems. While these processes were studied in the past 
using relatively long THz pulses (time duration of several tens of nanoseconds) 
[4,5], the above-mentioned new-generation of few-cycle THz sources allows now to 
explore their ultrafast nature and dynamics in the picosecond domain [6]. In 
particular, our investigation has been aimed at studying the ultrafast nonlinear 
dynamics of free carriers in semiconductors and at developing the proper tools 
for this new kind of THz spectroscopy. We have performed several nonlinear 
experiments on free-carriers in direct bandgap semiconductors at THz 
frequencies. Techniques as Z-scan [7], THz pump - THz probe [8], and optical 
pump - THz probe [9] have been employed to explore nonlinear interactions in 
both n-doped and photoexcited samples. The mechanism that dominates these 
nonlinearities is found to be intervalley scattering and a simple mathematical 
model adding this effect to a standard Drude-like response well explains our 
experimental results. References [1] S. Mukamel, Principles of nonlinear 
spectroscopy, Oxford University Press, (1999). [2] F. Blanchard et al., Opt. 
Exp. 15 (20), 13212 (2007). [3] K.-L. Yeh, Appl. Phys. Lett. 90, 171121 (2007). 
[4] A. Mayer and F. Keilmann, Phys. Rev. B 33, 6954 (1986). [5] A. Mayer and F. 
Keilmann, Phys. Rev. B 33, 6962 (1986). [6] J. Hebling et al., IEEE J. Sel. Top. 
Quant. Electron. 14, 345 (2008). [7] L. Razzari et al., Phys. Rev. B 79, 193204 
(2009). [8] F. Blanchard et al., in preparation. [9] F.H. Su et al., Opt. Exp. 
17 (12), 9620 (2009).
 
Del Mar Photonics - Newsletter Fall 2010 - Newsletter Winter 2010
Del Mar Photonics is involved in research of CNTs, graphene nanoplatelets and graphene materials, develops advanced multifunctional materials for variety of applications as well as research instrumentation for characterization of the above.
We currently we can offer:
1) Graphene nanoplatelets: the stack of multi-layer graphene sheets with high 
aspect ratio, diameter: 0.5-20 µm, 
thickness: 5-25 nm.
2) Graphene materials: Graphene Powder, Graphene Oxide Powder, Graphene 
Suspension. 
3) Carbon Nanotubes.
 
Contact our application team to discuss your requirements for high-performance nanocomposite materials, display materials, sensing materials, ultracapacitors, batteries, energy storage and other area to improve electrical, thermal, barrier, or mechanical properties by using low-cost nano-additive.
Graphene nanoplatelets are the stack of multi-layer graphene sheets including platelet morphology, with characteristics as follows:
| Physical Properties | |||||
| Diameter | Thickness | Specific Surface Area | Density | Electrical Conductivity | Tensile Strength | 
| 0.5 - 20 µm | 5 - 25 nm | 40-60 m2/g | ~2.25 g/cm3 | 8000-10000 S/m | 5 GPa | 
| Bulk Characteristics | ||||
| Appearance | Carbon content | Bulk density | Water Content | Residual impurities | 
| A black and grey powder | >99.5% | ~0.30 g/ml | <0.5 wt% | <0.5 wt% | 
Request a quote for graphene nanoplatelets
Applications:
The high performance composite additives in PPO, POM, PPS, PC, ABS, 
PP, PE, PS, Nylon and rubbers.
To improve composite tensile strength, stiffness, corrosion resistance, abrasion 
resistance and anti-static and lubricant properties.
Mechanical properties modifications.
Conductivity modification.
Fuel tank coating.
In electronic enclosures add electrical conductivity to polymers at low 
densities of 3 to 5 wt%. 
Adding EMI or RFI shielding capabilities to a variety of polymers.
Automotive parts: a composite with nanoplatelets can be painted 
electrostatically, thereby saving costs.
Aerospace: graphite has long been used in aerospace composites. Nanoplatelets 
can be combined with other additives to reinforce stiffness, add electrical 
conductivity, EMI shielding, etc.
Appliances: fortified polymers provide superior thermal and electrical 
conductivity, thereby saving the costs of separate heat dissipation mechanisms.
Sporting goods: graphite-based composites are stronger and stiffer and lighter 
than comparable materials.
Coatings and paints: graphene nanoplatelets can be dispersed in a wide variety 
of materials to add electrical conductivity and surface durability.
Batteries: graphene nanoplatelets increase the effectiveness of Lithium-ion 
batteries when used to formulate electrodes.
Fuel cells: both bi-polar plate and electrode efficiencies can be improved.
Del Mar Photonics develops advanced instrumentation for research of CNTs, graphene nanoplatelets and graphene materials including lasers for broadband spectroscopy, femtosecond transient absorption and fluorescence measurements.
    T&D Scan high 
    resolution Laser Spectrometer based on broadly tunable CW laser
    
    CW single-frequency ring Dye laser
    
    Beacon Femtosecond Optically Gated Fluorescence Kinetic Measurement System
    New Hatteras femtosecond transient 
    absorption system
    Photon Scanning Tunneling Microscope 
     
Graphene is a one-atom-thick planar sheet of sp2-bonded carbon atoms that are 
densely packed in a honeycomb crystal lattice. The term Graphene was coined as a 
combination of graphite and the suffix -ene by Hanns-Peter Boehm,[1][2] who 
described single-layer carbon foils in 1962.[3] Graphene is most easily 
visualized as an atomic-scale chicken wire made of carbon atoms and their bonds. 
The crystalline or "flake" form of graphite consists of many graphene sheets 
stacked together.
The carbon-carbon bond length in graphene is about 0.142 nm. Graphene sheets 
stack to form graphite with an interplanar spacing of 0.335 nm, which means that 
a stack of 3 million sheets would be only one millimeter thick. Graphene is the 
basic structural element of some carbon allotropes including graphite, charcoal, 
carbon nanotubes, and fullerenes. It can also be considered as an indefinitely 
large aromatic molecule, the limiting case of the family of flat polycyclic 
aromatic hydrocarbons. The Nobel Prize in Physics for 2010 was awarded to Andre 
Geim and Konstantin Novoselov "for groundbreaking experiments regarding the 
two-dimensional material graphene".[4]
Graphene is a flat monolayer of carbon atoms tightly packed into a two-dimensional (2D) honeycomb lattice, and is a basic building block for graphitic materials of all other dimensionalities. It can be wrapped up into 0D fullerenes, rolled into 1D nanotubes or stacked into 3D graphite.[5]
References
[1] H. P. Boehm, R. Setton, E. Stumpp (1994). "Nomenclature and terminology of 
graphite intercalation compounds". Pure and Applied Chemistry 66 (9): 1893–1901. 
doi:10.1351/pac199466091893.
[2] H. C. Schniepp, J.-L. Li, M. J. McAllister, H. Sai, M. Herrera-Alonso, D. H. 
Adamson, R. K. Prud’homme, R. Car, D. A. Saville, I. A. Aksay (2006). 
"Functionalized Single Graphene Sheets Derived from Splitting Graphite Oxide". 
The Journal of Physical Chemistry B 110 (17): 8535–8539. doi:10.1021/jp060936f. 
PMID 16640401.
[3] H. P. Boehm, A. Clauss, G. O. Fischer, U. Hofmann (1962). "Das 
Adsorptionsverhalten sehr dünner Kohlenstoffolien". Zeitschrift für anorganische 
und allgemeine Chemie 316 (3-4): 119–127. doi:10.1002/zaac.19623160303.
[4] Nobel Foundation announcement
[5]  Geim, A. K. and Novoselov, K. S. (2007). "The rise of 
graphene". Nature Materials 6 (3): 183–191. doi:10.1038/nmat1849. PMID 17330084.
Carbon nanotubes (CNTs; also known as buckytubes) are allotropes of carbon 
with a cylindrical nanostructure. Nanotubes have been constructed with 
length-to-diameter ratio of up to 132,000,000:1,[1] which is significantly 
larger than any other material. These cylindrical carbon molecules have novel 
properties which make them potentially useful in many applications in 
nanotechnology, electronics, optics, and other fields of materials science, as 
well as potential uses in architectural fields. They may also have applications 
in the construction of body armor. They exhibit extraordinary strength and 
unique electrical properties, and are efficient thermal conductors.
Nanotubes are members of the fullerene structural family, which also includes 
the spherical buckyballs. The ends of a nanotube may be capped with a hemisphere 
of the buckyball structure. Their name is derived from their size, since the 
diameter of a nanotube is on the order of a few nanometers (approximately 
1/50,000th of the width of a human hair), while they can be up to 18 centimeters 
in length (as of 2010).[1] Nanotubes are categorized as single-walled nanotubes 
(SWNTs) and multi-walled nanotubes (MWNTs).
Chemical bonding in nanotubes is described by applied quantum chemistry, 
specifically, orbital hybridization. The chemical bonding of nanotubes is 
composed entirely of sp2 bonds, similar to those of graphite. These bonds, which 
are stronger than the sp3 bonds found in diamonds, provide nanotubules with 
their unique strength. Moreover, nanotubes naturally align themselves into 
"ropes" held together by Van der Waals forces.
[1] Wang, X.; Li, Q.; Xie, J.; Jin, Z.; Wang, J.; Li, Y.; Jiang, K.; Fan, S. (2009). "Fabrication of Ultralong and Electrically Uniform Single-Walled Carbon Nanotubes on Clean Substrates". Nano Letters 9 (9): 3137–3141. doi:10.1021/nl901260b. PMID 19650638.

Del Mar Photonics, Inc.
4119 Twilight Ridge
San Diego, CA 92130
tel: (858) 876-3133
fax: (858) 630-2376
    Skype: delmarphotonics
sales@dmphotonics.com 
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