Academic literature on the topic 'Molecular Photonics'

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Journal articles on the topic "Molecular Photonics"

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Zhang, Chuang, Chang-Ling Zou, Yan Zhao, Chun-Hua Dong, Cong Wei, Hanlin Wang, Yunqi Liu, Guang-Can Guo, Jiannian Yao, and Yong Sheng Zhao. "Organic printed photonics: From microring lasers to integrated circuits." Science Advances 1, no. 8 (September 2015): e1500257. http://dx.doi.org/10.1126/sciadv.1500257.

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A photonic integrated circuit (PIC) is the optical analogy of an electronic loop in which photons are signal carriers with high transport speed and parallel processing capability. Besides the most frequently demonstrated silicon-based circuits, PICs require a variety of materials for light generation, processing, modulation, and detection. With their diversity and flexibility, organic molecular materials provide an alternative platform for photonics; however, the versatile fabrication of organic integrated circuits with the desired photonic performance remains a big challenge. The rapid development of flexible electronics has shown that a solution printing technique has considerable potential for the large-scale fabrication and integration of microsized/nanosized devices. We propose the idea of soft photonics and demonstrate the function-directed fabrication of high-quality organic photonic devices and circuits. We prepared size-tunable and reproducible polymer microring resonators on a wafer-scale transparent and flexible chip using a solution printing technique. The printed optical resonator showed a quality (Q) factor higher than 4 × 105, which is comparable to that of silicon-based resonators. The high material compatibility of this printed photonic chip enabled us to realize low-threshold microlasers by doping organic functional molecules into a typical photonic device. On an identical chip, this construction strategy allowed us to design a complex assembly of one-dimensional waveguide and resonator components for light signal filtering and optical storage toward the large-scale on-chip integration of microscopic photonic units. Thus, we have developed a scheme for soft photonic integration that may motivate further studies on organic photonic materials and devices.
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Wada, Kazumi. "A New Approach of Electronics and Photonics Convergence on Si CMOS Platform: How to Reduce Device Diversity of Photonics for Integration." Advances in Optical Technologies 2008 (July 7, 2008): 1–7. http://dx.doi.org/10.1155/2008/807457.

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Integrated photonics via Si CMOS technology has been a strategic area since electronics and photonics convergence should be the next platform for information technology. The platform is recently referred to as “Si photonics” that attracts much interest of researchers in industries as well as academia in the world. The main goal of Si Photonics is currently to reduce material diversity of photonic devices to pursuing CMOS-compatibility. In contrast, the present paper proposes another route of Si Photonics, reducing diversity of photonic devices. The proposed device unifying functionality of photonics is a microresonator with a pin diode structure that enables the Purcell effect and Franz-Keldysh effect to emit and to modulate light from SiGe alloys.
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Lewis, Frederick D. "DNA Molecular Photonics¶†." Photochemistry and Photobiology 81, no. 1 (2005): 65. http://dx.doi.org/10.1562/2004-09-01-ir-299.1.

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Gurinovich, G. P. "Molecular-oxygen photonics." Journal of Applied Spectroscopy 54, no. 3 (March 1991): 243–49. http://dx.doi.org/10.1007/bf00673423.

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Plotnikov, V. G. "Theoretical molecular photonics." Russian Journal of Physical Chemistry A 88, no. 11 (October 10, 2014): 1849–60. http://dx.doi.org/10.1134/s0036024414110120.

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Lewis, Frederick D. "DNA Molecular Photonics¶†." Photochemistry and Photobiology 81, no. 1 (May 23, 2007): 65–72. http://dx.doi.org/10.1111/j.1751-1097.2005.tb01523.x.

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Wu, Xiaozhong, and Qinglei Guo. "Bioresorbable Photonics: Materials, Devices and Applications." Photonics 8, no. 7 (June 25, 2021): 235. http://dx.doi.org/10.3390/photonics8070235.

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Bio-photonic devices that utilize the interaction between light and biological substances have been emerging as an important tool for clinical diagnosis and/or therapy. At the same time, implanted biodegradable photonic devices can be disintegrated and resorbed after a predefined operational period, thus avoiding the risk and cost associated with the secondary surgical extraction. In this paper, the recent progress on biodegradable photonics is reviewed, with a focus on material strategies, device architectures and their biomedical applications. We begin with a brief introduction of biodegradable photonics, followed by the material strategies for constructing biodegradable photonic devices. Then, various types of biodegradable photonic devices with different functionalities are described. After that, several demonstration examples for applications in intracranial pressure monitoring, biochemical sensing and drug delivery are presented, revealing the great potential of biodegradable photonics in the monitoring of human health status and the treatment of human diseases. We then conclude with the summary of this field, as well as current challenges and possible future directions.
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Venturi, Margherita, Vincenzo Balzani, Roberto Ballardini, Alberto Credi, and M. Teresa Gandolfi. "Towards molecular photochemionics." International Journal of Photoenergy 6, no. 1 (2004): 1–10. http://dx.doi.org/10.1155/s1110662x04000017.

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In the last few years there has been a great interest in developing electronics at a molecular level (molecular electronics), e.g. to construct miniaturized electric circuits that would be much smaller than the corresponding micron-scale digital logic circuits fabricated on conventional solid-state semiconductor chips. An alternative possibility to the use of electron fluxes as a means for information processing (electronics) is that of using optical beams (photonics), but up until now scarce attention has been devoted to the possibility of developing photonics at the molecular level. In this paper we review some recent achievements in the design and construction of molecular-level systems that are capable of transferring, switching, collecting, storing, and elaborating light signals. The combination of molecular photonics with chemionics can lead to a wealth of molecular-level devices capable of information processing.
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Saikin, Semion K., Alexander Eisfeld, Stéphanie Valleau, and Alán Aspuru-Guzik. "Photonics meets excitonics: natural and artificial molecular aggregates." Nanophotonics 2, no. 1 (February 1, 2013): 21–38. http://dx.doi.org/10.1515/nanoph-2012-0025.

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AbstractOrganic molecules store the energy of absorbed light in the form of charge-neutral molecular excitations – Frenkel excitons. Usually, in amorphous organic materials, excitons are viewed as quasiparticles, localized on single molecules, which diffuse randomly through the structure. However, the picture of incoherent hopping is not applicable to some classes of molecular aggregates – assemblies of molecules that have strong near-field interaction between electronic excitations in the individual subunits. Molecular aggregates can be found in nature, in photosynthetic complexes of plants and bacteria, and they can also be produced artificially in various forms including quasi-one dimensional chains, two-dimensional films, tubes, etc. In these structures light is absorbed collectively by many molecules and the following dynamics of molecular excitation possesses coherent properties. This energy transfer mechanism, mediated by the coherent exciton dynamics, resembles the propagation of electromagnetic waves through a structured medium on the nanometer scale. The absorbed energy can be transferred resonantly over distances of hundreds of nanometers before exciton relaxation occurs. Furthermore, the spatial and energetic landscape of molecular aggregates can enable the funneling of the exciton energy to a small number of molecules either within or outside the aggregate. In this review we establish a bridge between the fields of photonics and excitonics by describing the present understanding of exciton dynamics in molecular aggregates.
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Xiang, Bo, Raphael F. Ribeiro, Yingmin Li, Adam D. Dunkelberger, Blake B. Simpkins, Joel Yuen-Zhou, and Wei Xiong. "Manipulating optical nonlinearities of molecular polaritons by delocalization." Science Advances 5, no. 9 (September 2019): eaax5196. http://dx.doi.org/10.1126/sciadv.aax5196.

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Optical nonlinearities are key resources in the contemporary photonics toolbox, relevant to quantum gate operations and all-optical switches. Chemical modification is often used to control the nonlinear response of materials at the microscopic level, but on-the-fly manipulation of such response is challenging. Tunability of optical nonlinearities in the mid-infrared (IR) is even less developed, hindering its applications in chemical sensing or IR photonic circuitry. Here, we report control of vibrational polariton coherent nonlinearities by manipulation of macroscopic parameters such as cavity longitudinal length or molecular concentration. Further two-dimensional IR investigations reveal that nonlinear dephasing provides the dominant source of the observed ultrafast polariton nonlinearities. The reported phenomena originate from the nonlinear macroscopic polarization stemming from strong coupling between microscopic molecular excitations and a macroscopic photonic cavity mode.
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Dissertations / Theses on the topic "Molecular Photonics"

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Gray, David. "Molecular organic photonics." Thesis, Durham University, 1994. http://etheses.dur.ac.uk/5593/.

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The work presented in this thesis is derived from experimentation in the field of molecular organic photonics. This is done from the standpoint that devices cannot be understood without recourse to the molecular properties and vice versa. A background of nonlinear optics and a brief introduction to the origins of molecular organic nonlinearity is given to aid understanding of the main points of the argument. The dipole moment of several organics was calculated using a simple capacitance method which has been successfully applied to reactive species. These dipole moment results were necessary in the extraction of βʷ from the µβʷ extracted from the EFISH technique. This experiment was performed at 1.064µm and 1.907µm with the latter wavelength being applied to the first in a new class of organic molecules. Results of the work on a number of techniques relevant to thin film devices are also presented. This culminated in an amplitude modulator case study that brought all the techniques together. Finally a discussion on the links between molecular and device related properties justifies the approach taken.
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Keogh, Gary Peter. "The application of coherent Raman scattering to molecular photonics." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243375.

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McKee, Erik. "Femtosecond Filament Interaction as a Probe for Molecular Alignment." Master's thesis, University of Central Florida, 2013. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/5991.

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Femtosecond laser filamentation is a highly nonlinear propagation mode. When a laser pulse propagates with a peak power exceeding a critical value Pcr (5 GW at 800 nm in air), the Kerr effect tends to collapse the beam until the intensity is high enough to ionize the medium, giving rise to plasma defocusing. A dynamic competition between these two effects takes place leaving a thin and weakly ionized plasma channel in the trail of the pulse. When an ultrafast laser pulse interacts with molecules, it will align them, spinning them about their axis of polarization. As the quantum rotational wave packet relaxes, the molecules will experience periodic field-free alignment. Recent work has demonstrated the effect of molecular alignment on laser filamentation of ultra-short pulses. Revival of the molecular alignment can modify filamentation parameters as it can locally modify the refractive index and the ionization rate. In this thesis, we demonstrate with simulations and experiments that these changes in the filament parameters (collapse distance and filament plasma length) can be used to probe molecular alignment in CO2.
M.S.
Masters
Optics and Photonics
Optics and Photonics
Optics
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Liu, Yuan. "Development of laser spectroscopy for elemental and molecular analysis." Doctoral diss., University of Central Florida, 2013. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/5978.

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Laser-Induced Breakdown Spectroscopy (LIBS) and Raman spectroscopy are still growing analytical and sensing spectroscopic techniques. They significantly reduce the time and labor cost in analysis with simplified instrumentation, and lead to minimal or no sample damage. In this dissertation, fundamental studies to improve LIBS analytical performance were performed and its fusion with Raman into one single sensor was explored. On the fundamental side, Thomson scattering was reported for the first time to simultaneously measure the electron density and temperature of laser plasmas from a solid aluminum target at atmospheric pressure. Comparison between electron and excitation temperatures brought insights into the verification of local thermodynamic equilibrium condition in laser plasmas. To enhance LIBS emission, Microwave-Assisted LIBS (MA-LIBS) was developed and characterized. In MA-LIBS, a microwave field extends the emission lifetime of the plasma and stronger time integrated signal is obtained. Experimental results showed sensitivity improvement (more than 20-fold) and extension of the analytical range (down to a few tens of ppm) for the detection of copper traces in soil samples. Finally, laser spectroscopy systems that can perform both LIBS and Raman analysis were developed. Such systems provide two types of complimentary information – elemental composition from LIBS and structural information from Raman. Two novel approaches were reported for the first time for LIBS-Raman sensor fusion: (i) an Ultra-Violet system which combines Resonant Raman signal enhancement and high ablation efficiency from UV radiation, and (ii) a Ti:Sapphire laser based NIR system which reduces the fluorescence interference in Raman and takes advantage of femtosecond ablation for LIBS.
Ph.D.
Doctorate
Optics and Photonics
Optics and Photonics
Optics
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Jemli, Khaoula. "Synthése et auto-assemblage de molécules de pérovskite pour la photonique et le marquage." Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLN009/document.

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Cette thèse s’inscrit dans la conjoncture actuelle de la recherche et du développement des matériaux pour les énergies renouvelables et dispositifs optoélectroniques à bas coût. Nous avons développées des nouveaux matériaux de pérovskites 2D et 3D afin d’exploiter leurs propriétés originales dans le but de les intégrer dans un second temps dans des dispositifs photoniques et photovoltaïques. Le travail d’ingénierie moléculaire sur la flexibilité des pérovskites 2D a permis de moduler le gap optique, d’extraire des informations sur les propriétés excitonique ainsi que l’activation de la photoluminescence. Quant à la flexibilité de la mise en forme des nouvelles pistes ont été initiées. L’étude de cette pérovskite 3D spécialement MAPI est très utile pour les applications photovoltaïques. La connaissance des propriétés optiques, structurales et de transport est une clé majeure pour l’augmentation des rendements et la stabilité de ces cellules
This thesis is involved in the current situation of research and development of materials for renewable energy and optoelectronic devices at low cost.We have developed new 2D and 3D perovskite materials to exploit their unique properties in order to integrate them in a second time in photonic and photovoltaic devices. The molecular engineering work on flexibility perovskites 2D allowed to modulate the optical gap, to extract information about the properties excitonqiue as well as activation of the photoluminescence. As to the flexibility of the layout of the new tracks were initiated.The study of this 3D perovskite especially MAPI is very useful for photovoltaic applications. The knowledge of the optical properties, structural and transport is a major key to increased yields and stability of these cells
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McDougall, Craig. "Advanced photonic methodologies for the 'in vitro' manipulation of cellular systems." Thesis, University of St Andrews, 2011. http://hdl.handle.net/10023/1876.

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This thesis investigates the application of a variety of optical techniques for the manipulation of single cells and their local micro-environment. The methodologies developed provide enhanced control over a single cell under study affording exquisite spatial and temporal control over biological processes of interest. The work presented within the thesis can be split into three distinct categories. The first of these provides an investigation in light activated “caged” molecular probes. This work generated several new compounds which were then applied to providing control over processes involved in pain, mitochondrial intracellular signalling and memory processes in the central nervous system. Application of caged neurotransmitters then demonstrates the first in vitro wavelength orthogonal photolysis of biologically relevant substances. Such a technique has great potential in the study of fundamental interactions within the processes underpinning memory and cognitive function. Secondly the application of optical injection techniques for the introduction of membrane impermeable species of interest is presented. An exploration of laser sources and optical systems has yielded two new strategies for optical injection. The targeted introduction of fluorescent stains, nucleic acids and gold nanoparticles to the interior of live mammalian cells demonstrates the power of these techniques. Thirdly, an investigation in optical trapping and optical injection provides simplified micromanipulation techniqes for application to biological studies. The use of capillaries as reservoirs for reagents of interest has realised a procedure for the reduction of large-scale chemical assays to a single cell level in static flow. When this technique is combined with intelligent control over the trapping laser source’s temporal behaviour, the interaction with the sample under study can be tailored for biological amiability or sample ablation. In this way a single laser source can be employed for the optical trapping and nanosurgery of a biological sample. A final study is presented demonstrating initial results for the targeted optical injection of caged compounds into mammalian cells. This methodology draws on the strengths of optical injection and caging technologies and presents a significant step forward in the level of control afforded over a biological system under study by optical techniques. The studies presented highlight the level of control and flexibility afforded by the application of optical manipulation and excitation strategies. Such optical methodologies extend the photonic tools available for enhanced studies in the life sciences.
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Zandbergen, Sander, and Sander Zandbergen. "Light-Matter Interactions in Various Semiconductor Systems." Diss., The University of Arizona, 2017. http://hdl.handle.net/10150/624528.

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Semiconductors provide an interesting platform for studying light-matter interactions due to their unique electrically conductive behavior which can be deliberately altered in useful ways with the controlled introduction of confinement and doping, which changes the electronic band structure. This area of research has led to many important fundamental scientific discoveries that have in turn spawned a plethora of applications in areas such as photonics, microscopy, single-photon sources, and metamaterials. Silicon is the prevalent semiconductor platform for microelectronics because of its cost and electrical properties, while III-V materials are optimal for optoelectronics because of the ability to engineer a direct bandgap and create versatile heterojunctions by growing binary, ternary, or quaternary compounds.
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Konrad, Alexander [Verfasser], and Alfred J. [Akademischer Betreuer] Meixner. "Nano-photonics on luminescent molecular systems and metal particles in optical sub-wavelength microresonators / Alexander Konrad ; Betreuer: Alfred J. Meixner." Tübingen : Universitätsbibliothek Tübingen, 2016. http://d-nb.info/1198122153/34.

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Beaudoin, Bertrand Julien. "Homodyne High-harmonic Spectroscopy: Coherent Imaging of a Unimolecular Chemical Reaction." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23173.

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At the heart of high harmonic generation lies a combination of optical and collision physics entwined by a strong laser field. An electron, initially tunnel-ionized by the field, driven away then back in the continuum, finally recombines back to rest in its initial ground state via a radiative transition. The emitted attosecond (atto=10^-18) XUV light pulse carries all the information (polarization, amplitude and phase) about the photorecombination continuum-to-ground transition dipolar field. Photorecombination is related to the time-reversed photoionization process. In this perspective, high-harmonic spectroscopy extends well-established photoelectron spectroscopy, based on charged particle detection, to a fully coherent one, based on light characterization. The main achievement presented in this thesis is to use high harmonic generation to probe femtosecond (femto=10^-15) chemical dynamics for the first time. Thanks to the coherence imposed by the strong driving laser field, homodyne detection of attosecond pulses from excited molecules undergoing dynamics is achieved, the signal from unexcited molecules acting as the reference local oscillator. First, applying time-resolved high-harmonic spectroscopy to the photodissociation of a diatomic molecule, Br2 to Br + Br, allows us to follow the break of a chemical bond occurring in a few hundreds of femtoseconds. Second, extending it to a triatomic (NO2) lets us observe both the previously unseen (but predicted) early femtosecond conical intersection dynamics followed by the late picosecond statistical photodissociation taking place in the reaction NO2 to NO + O. Another important realization of this thesis is the development of a complementary technique to time-resolved high-harmonic spectroscopy called LAPIN, for Linked Attosecond Phase INterferometry. When combined together, time-resolved high-harmonic spectroscopy and LAPIN give access to the complex photorecombination dipole of aligned excited molecules. These achievements lay the basis for electron recollision tomographic imaging of a chemical reaction with unprecedented angstrom (1 angstrom= 0.1 nanometer) spatial resolution. Other contributions dedicated to the development of attosecond science and the generalization of high-harmonic spectroscopy as a novel, fully coherent molecular spectroscopy will also be presented in this thesis.
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Clavel, Michael Brian. "Tensile-Strained Ge/InₓGa₁₋ₓAs Heterostructures for Electronic and Photonic Applications." Thesis, Virginia Tech, 2015. http://hdl.handle.net/10919/78129.

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The continued scaling of feature size in silicon (Si)-based complimentary metal-oxide-semiconductor (CMOS) technology has led to a rapid increase in compute power. Resulting from increases in device densities and advances in materials and transistor design, integrated circuit (IC) performance has continued to improve while operational power (VDD) has been substantially reduced. However, as feature sizes approach the atomic length scale, fundamental limitations in switching characteristics (such as subthreshold slope, SS, and OFF-state power dissipation) pose key technical challenges moving forward. Novel material innovations and device architectures, such as group IV and III-V materials and tunnel field-effect transistors (TFETs), have been proposed as solutions for the beyond Si era. TFETs benefit from steep switching characteristics due to the band-to-band tunneling injection of carriers from source to channel. Moreover, the narrow bandgaps of III-V and germanium (Ge) make them attractive material choices for TFETs in order to improve ON-state current and reduce SS. Further, Ge grown on InₓGa₁₋ₓAs experiences epitaxy-induced strain (ε), further reducing the Ge bandgap and improving carrier mobility. Due to these reasons, the ε-Ge/InₓGa₁₋ₓAs system is a promising candidate for future TFET architectures. In addition, the ability to tune the bandgap of Ge via strain engineering makes ε-Ge/InₓGa₁₋ₓAs heterostructures attractive for nanoscale group IV-based photonics, thereby benefitting the monolithic integration of electronics and photonics on Si. This research systematically investigates the material, optical, and heterointerface properties of ε-Ge/InₓGa₁₋ₓAs heterostructures on GaAs and Si substrates. The effect of strain on the heterointerface band alignment is comprehensively studied, demonstrating the ability to modulate the effective tunneling barrier height (Ebeff) and thus the threshold voltage (VT), ON-state current, and SS in future ε-Ge/InₓGa₁₋ₓAs TFETs. Further, band structure engineering via strain modulation is shown to be an effective technique for tuning the emission properties of Ge. Moreover, the ability to heterogeneously integrate these structures on Si is demonstrated for the first time, indicating their viability for the development of next-generation high performance, low-power logic and photonic integrated circuits on Si.
Master of Science
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Books on the topic "Molecular Photonics"

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Hideharu, Ushiki, and Winnik Françoise M, eds. Molecular photonics: Fundamentals and practical aspects. Tokyo: Kodansha, 2000.

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Thin-film organic photonics: Molecular layer deposition and applications. Boca Raton: Taylor & Francis, 2011.

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J, Zyss, Garnier F, European Materials Research Society. Meeting, and International Conference on Applied Materials (1997 : Strasbourg, France), eds. Materials, physics and devices for molecular electronics and photonics: Proceedings of Symposium M on Materials, Physics and Devices for Molecular Electronics and Photonics of the 1997 ICAM/E-MRS Spring Conference, Strasbourg, France, June 16-20, 1997. Amsterdam, Netherlands: Elsevier, 1997.

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L, Derbov Vladimir, Melnikov Leonid A, Babkov L. M, Saratovskiĭ gosudarstvennyĭ universitet im. N.G. Chernyshevskogo., Russia (Federation) Ministerstvo obrazovanii͡a︡, Society of Photo-optical Instrumentation Engineers. Russian Chapter., Society of Photo-optical Instrumentation Engineers., Workshop on Laser Physics and Photonics (2001 : Saratov, Russia), and Workshop on Spectroscopy and Molecular Modeling (2001 : Saratov, Russia), eds. Laser physics and photonics, spectroscopy, and molecular modeling II: Saratov Fall Meeting 2001 : 2-5 October 2001, Saratov, Russia. Bellingham, Washington: SPIE, 2002.

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Saratov Fall Meeting (2001 Saratov, Russia). Laser physics and photonics, spectroscopy, and molecular modeling II: Saratov Fall meeting 2001 : 2-5 October, 2001, Saratov, Russia. Edited by Derbov Vladimir L, Melnikov Leonid A, Babkov L. M, Saratovskiĭ gosudarstvennyĭ universitet im. N.G. Chernyshevskogo, Russia (Federation) Ministerstvo obrazovanii︠a︡, Society of Photo-optical Instrumentation Engineers. Russian Chapter., and Society of Photo-optical Instrumentation Engineers. Bellingham, Washingtomn: SPIE, 2001.

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Saratov Fall Meeting (2003 Saratov, Russia). Laser physics and photonics, spectroscopy, and molecular modeling IV: Saratov Fall Meeting 2003 : 7-10 October, 2003, Saratov, Russia. Edited by Derbov Vladimir L, Melinkov Leonid A, Babkov L. M, Saratovskiĭ gosudarstvennyĭ universitet im. N.G. Chernyshevskogo., Society of Photo-optical Instrumentation Engineers. Russian Chapter., and Society of Photo-optical Instrumentation Engineers. Bellingham, Wash: SPIE, 2004.

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Saratov Fall Meeting (2006 Saratov, Russia). Laser physics and photonics, spectroscopy and molecular modeling VII: Saratov Fall Meeting 2006 : 26-29 September 2006, Saratov, Russia. Edited by Derbov Vladimir L, Melnikov Leonid A, Babkov, L. M. (Lev Mikhaĭlovich), Saratovskiĭ gosudarstvennyĭ universitet im. N.G. Chernyshevskogo, Rossiĭskai︠a︡ akademii︠a︡ estestvennykh nauk. Saratovskoe regionalʹnoe otdelenie, Russian Society for Photobiology, Rossiĭskai︠a︡ akademii︠a︡ nauk. Saratov Science Center, Rossiĭskiĭ fond fundamentalʹnykh issledovaniĭ, and Society of Photo-optical Instrumentation Engineers. Bellingham, Wash: SPIE, 2006.

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Derbov, Vladimir L., and L. M. Babkov. Laser physics and photonics, spectroscopy, and molecular modeling V: Saratov Fall Meeting 2004 : 21-24 September 2004, Saratov, Russia. Edited by Melinkov Leonid A, Saratovskiĭ gosudarstvennyĭ universitet im. N.G. Chernyshevskogo, Rossiĭskai︠a︡ akademii︠a︡ estestvennykh nauk. Saratovskoe regionalʹnoe otdelenie, Society of Photo-optical Instrumentation Engineers. Russian Chapter, Society of Photo-optical Instrumentation Engineers, and Saratov Fall Meeting (2004 : Saratov, Russia). Bellingham, Wash: SPIE, 2005.

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service), SpringerLink (Online, ed. Optical Cooling Using the Dipole Force. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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International Workshop and Fall School for Young Scientists and Students on Optics, Laser Physics, and Biophysics. Laser physics and photonics, spectroscopy, and molecular modeling III: Coherent optics of ordered and random media III ; 1-4 October 2002, Saratov, Russia. Bellingham, WA: SPIE, 2003.

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Book chapters on the topic "Molecular Photonics"

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Yoshimura, Tetsuzo. "Thin-Film Molecular Nanophotonics." In Photonics, 261–310. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119011750.ch8.

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Ehrenfreund, Eitan, and Z. Valy Vardeny. "Magnetic Control of Spin in Molecular Photonics." In Photonics, 221–59. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119011750.ch7.

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Nagamura, Toshihiko. "Femtosecond Molecular Photonics Materials." In Springer Series in Photonics, 376–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58469-5_29.

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Buckup, Tiago, Marcus Motzkus, and Jürgen Hauer. "Coherent Control for Molecular Ultrafast Spectroscopy." In Extreme Photonics & Applications, 37–55. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-3634-6_3.

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Strukov, Dmitri B. "Hybrid Semiconductor-Molecular Integrated Circuits for Digital Electronics: CMOL Approach." In Nanoelectronics and Photonics, 15–57. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-76499-3_4.

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Li, Jianyou, Hadis Morkoç, and Arup Neogi. "Self-Assembled Guanosine-Based Nanoscale Molecular Photonic Devices." In Nanoscale Photonics and Optoelectronics, 77–99. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-7587-4_5.

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Lugli, Paolo, Simone Locci, Christoph Erlen, and Gyorgy Csaba. "Molecular Electronics: Challenges and Perspectives." In Nanotechnology for Electronics, Photonics, and Renewable Energy, 1–40. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-7454-9_1.

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Prasad, Paras N. "Photonics and Nonlinear Optics — Materials and Devices." In Lower-Dimensional Systems and Molecular Electronics, 563–72. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2088-1_67.

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Watanabe, T., H. Yamamoto, T. Hosomi, and S. Miyata. "New Molecular Design for Noncentrosymmetric Crystal Structures: Lambda Shape Molecules for Frequency Doubling." In Organic Molecules for Nonlinear Optics and Photonics, 151–59. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3370-8_10.

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Hasan, T., V. Scardaci, P. H. Tan, F. Bonaccorso, A. G. Rozhin, Z. Sun, and A. C. Ferrari. "Nanotube and Graphene Polymer Composites for Photonics and Optoelectronics." In Molecular- and Nano-Tubes, 279–354. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-9443-1_9.

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Conference papers on the topic "Molecular Photonics"

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Sclafani, M., M. G. Pullen, B. Wolter, A. T. Lee, M. Baudisch, M. Hemmer, A. Senftleben, et al. "Molecular structure from aligned polyatomic molecules using laser-induced electron diffraction." In 2015 Photonics North. IEEE, 2015. http://dx.doi.org/10.1109/pn.2015.7292472.

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Gangopadhyay, Palash, Guy Koeckelberghs, and André Persoons. "Molecular magneto-optics." In SPIE Organic Photonics + Electronics, edited by Jean-Michel Nunzi. SPIE, 2014. http://dx.doi.org/10.1117/12.2061841.

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Peng, J., Z. Zhao, S. Boscolo, C. Finot, S. Sugavanam, D. Churkin, and H. Zheng. "Dissipative Optical Breather Molecular Complexes." In Nonlinear Photonics. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/np.2020.nptu3d.2.

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Asselberghs, Inge, Gunther Hennrich, Jon McCleverty, Leila Boubekeur-Lecaque, Benjamin J. Coe, and Koen Clays. "Organic materials for molecular switching." In Photonics Europe, edited by Paul L. Heremans, Michele Muccini, and Eric A. Meulenkamp. SPIE, 2008. http://dx.doi.org/10.1117/12.779751.

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Sanders, Jack, and Glenn Rosecrans. "GOES-12 molecular contamination." In SPIE Optics + Photonics, edited by O. Manuel Uy, Sharon A. Straka, John C. Fleming, and Michael G. Dittman. SPIE, 2006. http://dx.doi.org/10.1117/12.682006.

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Fujii, Ayako, and Akito Ishida. "Surface plasmon enhanced excitation of photofunctional molecules in nanospace towards molecular plasmonics." In Optics & Photonics 2005, edited by Mark I. Stockman. SPIE, 2005. http://dx.doi.org/10.1117/12.618204.

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Gu, Claire, Xuan Yang, Jin Zhang, Rebecca Newhouse, and Liangcai Cao. "Fiber sensors for molecular detection." In Photonics Asia 2010, edited by Feijun Song, Shiquan Tao, Francis T. S. Yu, Suganda Jutamulia, Kees A. Schouhamer Immink, and Keiji Shono. SPIE, 2010. http://dx.doi.org/10.1117/12.872469.

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Chen, Juan, Klara Stefflova, Soungkyoo Kim, Hui Li, Diane Marotta, Britton Chance, Jerry D. Glickson, and Gang Zheng. "Molecular beacon-based photodynamic therapy." In Photonics Asia 2004, edited by Britton Chance, Mingzhe Chen, Arthur E. T. Chiou, and Qingming Luo. SPIE, 2005. http://dx.doi.org/10.1117/12.573915.

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Gehrig, Edeltraud, and Ortwin Hess. "Spatio-temporal dynamics of optical molecular motors." In Photonics Europe, edited by Michel D. Faupel and Patrick Meyrueis. SPIE, 2004. http://dx.doi.org/10.1117/12.544648.

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Intes, X. "Mesoscopic fluorescence molecular tomography." In 2017 IEEE Photonics Conference (IPC). IEEE, 2017. http://dx.doi.org/10.1109/ipcon.2017.8116286.

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Reports on the topic "Molecular Photonics"

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Prasad, Paras N. Photonics and Nonlinear Optics With Molecular and Polymeric Materials. Fort Belvoir, VA: Defense Technical Information Center, October 1999. http://dx.doi.org/10.21236/ada371534.

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Jain, Aditya. Photonic molecules for subwavelength light confinement design and applications. Office of Scientific and Technical Information (OSTI), December 2016. http://dx.doi.org/10.2172/1417977.

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Reif, John H., Erik A. Schultes, and Harish Chandran. AFSOR Bio-X: Encapsulated DNA-Based Molecular Autonomous Sensing Devices With Photonic I/O. Fort Belvoir, VA: Defense Technical Information Center, January 2009. http://dx.doi.org/10.21236/ada513915.

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Kimura, Mineo. Correlation between shape resonance energies and C-C bond length in carbon-containing molecules: Elastic electron scattering and carbon K-shell excitation by photons. Office of Scientific and Technical Information (OSTI), June 1994. http://dx.doi.org/10.2172/10159440.

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