Advanced Materials, ISSN 0935-9648, 03/2018, Volume 30, Issue 10, pp. 1705969 - n/a
A fused tris(thienothiophene) (3TT) building block is designed and synthesized with strong electron‐donating and molecular packing properties, where three...
organic solar cells | semitransparent | tris(thieno[3,2‐b]thiophene) | nonfullerene acceptors | near‐infrared absorption | tris(thieno[3,2-b]thiophene) | near-infrared absorption | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | tris(thieno[3, 2-b]thiophene) | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | POLYMER | GAP | LAYER | EFFICIENCY | Solar cells | Solar batteries | Thiophene | Photovoltaic cells | Mixtures | Energy conversion | Infrared absorption | Electron mobility | Molecular orbitals | Malononitrile | Chemical synthesis | Electrons
organic solar cells | semitransparent | tris(thieno[3,2‐b]thiophene) | nonfullerene acceptors | near‐infrared absorption | tris(thieno[3,2-b]thiophene) | near-infrared absorption | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | tris(thieno[3, 2-b]thiophene) | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | POLYMER | GAP | LAYER | EFFICIENCY | Solar cells | Solar batteries | Thiophene | Photovoltaic cells | Mixtures | Energy conversion | Infrared absorption | Electron mobility | Molecular orbitals | Malononitrile | Chemical synthesis | Electrons
Journal Article
Advanced Materials, ISSN 0935-9648, 08/2017, Volume 29, Issue 31, pp. 1701308 - n/a
A fused hexacyclic electron acceptor, IHIC, based on strong electron‐donating group dithienocyclopentathieno[3,2‐b]thiophene flanked by strong...
organic solar cells | fused‐ring electron acceptors | nonfullerene acceptors | dithienocyclopentathieno[3,2‐b]thiophene | near‐infrared absorption | dithienocyclopentathieno[3,2-b]thiophene | fused-ring electron acceptors | near-infrared absorption | PHYSICS, CONDENSED MATTER | 3D STRUCTURE | DESIGN | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | NON-FULLERENE | CHEMISTRY, MULTIDISCIPLINARY | CATHODE | SMALL MOLECULAR ACCEPTOR | PHOTOVOLTAIC APPLICATIONS | POLYMER | LAYER | COPOLYMER | ELECTRON-ACCEPTORS | Solar cells | Solar batteries | Thiophene | Near infrared radiation | Polymer blends | Photovoltaic cells | Efficiency | Infrared absorption | Electron mobility | Energy conversion efficiency
organic solar cells | fused‐ring electron acceptors | nonfullerene acceptors | dithienocyclopentathieno[3,2‐b]thiophene | near‐infrared absorption | dithienocyclopentathieno[3,2-b]thiophene | fused-ring electron acceptors | near-infrared absorption | PHYSICS, CONDENSED MATTER | 3D STRUCTURE | DESIGN | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | NON-FULLERENE | CHEMISTRY, MULTIDISCIPLINARY | CATHODE | SMALL MOLECULAR ACCEPTOR | PHOTOVOLTAIC APPLICATIONS | POLYMER | LAYER | COPOLYMER | ELECTRON-ACCEPTORS | Solar cells | Solar batteries | Thiophene | Near infrared radiation | Polymer blends | Photovoltaic cells | Efficiency | Infrared absorption | Electron mobility | Energy conversion efficiency
Journal Article
Applied Physics Letters, ISSN 0003-6951, 06/2014, Volume 104, Issue 25, p. 251110
We consider a mirror-symmetric resonator with two ports. We show that, when excited from a single port, complete absorption can be achieved through critical...
GRAPHENE | RADIATION | PHYSICS, APPLIED | NEAR INFRARED RADIATION | SYMMETRY | RESONANCE | RESONATORS | CRYSTALS | CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY | ABSORPTION
GRAPHENE | RADIATION | PHYSICS, APPLIED | NEAR INFRARED RADIATION | SYMMETRY | RESONANCE | RESONATORS | CRYSTALS | CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY | ABSORPTION
Journal Article
Advanced Functional Materials, ISSN 1616-301X, 08/2018, Volume 28, Issue 33, pp. 1802324 - n/a
A novel acceptor–donor–acceptor (A–D–A) type electron acceptor 6TIC‐4F with terthieno[3,2‐b]thiophene (6T) as the core unit is rationally designed and...
organic solar cells | X‐ray diffraction | nonfullerene acceptors | near‐infrared semiconductors | X-ray diffraction | near-infrared semiconductors | PHYSICS, CONDENSED MATTER | DESIGN | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | NON-FULLERENE ACCEPTORS | CHEMISTRY, PHYSICAL | LOW ENERGY-LOSSES | 13-PERCENT EFFICIENCY | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | BAND-GAP | PHASE-SEPARATION | POLYMER | Solar cells | Thiophene | Semiconductors | Solar batteries | Analysis | Organic chemistry | Absorption | Photovoltaic cells | Crystallography | Energy conversion efficiency
organic solar cells | X‐ray diffraction | nonfullerene acceptors | near‐infrared semiconductors | X-ray diffraction | near-infrared semiconductors | PHYSICS, CONDENSED MATTER | DESIGN | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | NON-FULLERENE ACCEPTORS | CHEMISTRY, PHYSICAL | LOW ENERGY-LOSSES | 13-PERCENT EFFICIENCY | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | BAND-GAP | PHASE-SEPARATION | POLYMER | Solar cells | Thiophene | Semiconductors | Solar batteries | Analysis | Organic chemistry | Absorption | Photovoltaic cells | Crystallography | Energy conversion efficiency
Journal Article
Postharvest Biology and Technology, ISSN 0925-5214, 08/2017, Volume 130, pp. 56 - 63
Quality attributes of fruit determine its acceptability by the retailer and consumer. The objective of this work was to investigate the potential of absorption...
Non-destructive | Absorption | Pear | Quality | Scattering | AGRONOMY | APPLE FRUIT | FOOD SCIENCE & TECHNOLOGY | TISSUE | RESOLVED REFLECTANCE SPECTROSCOPY | OPTICAL-PROPERTIES | MODEL | PREDICTION | DENSITY WAVE SPECTROSCOPY | HORTICULTURE | NEAR-INFRARED SPECTROSCOPY | CHLOROPHYLL | Usage | Conferences, meetings and seminars | Conferences and conventions | Light | Optical properties | Chlorophyll | Islamic law
Non-destructive | Absorption | Pear | Quality | Scattering | AGRONOMY | APPLE FRUIT | FOOD SCIENCE & TECHNOLOGY | TISSUE | RESOLVED REFLECTANCE SPECTROSCOPY | OPTICAL-PROPERTIES | MODEL | PREDICTION | DENSITY WAVE SPECTROSCOPY | HORTICULTURE | NEAR-INFRARED SPECTROSCOPY | CHLOROPHYLL | Usage | Conferences, meetings and seminars | Conferences and conventions | Light | Optical properties | Chlorophyll | Islamic law
Journal Article
Journal of Nanoparticle Research, ISSN 1388-0764, 11/2018, Volume 20, Issue 11, pp. 1 - 9
Based on a liquid phase decomposition reaction, WO3 − x nanorods with different dimensions were synthesized by varying the organic acid to amine ratio in the...
Materials Science | Near-infrared shielding | Physical Chemistry | Optics, Lasers, Photonics, Optical Devices | Characterization and Evaluation of Materials | Optics | WO 3 − x | Inorganic Chemistry | Localized surface plasmon resonance | Solar control film | Nanorod | Nanotechnology | THIN-FILMS | MATERIALS SCIENCE, MULTIDISCIPLINARY | SIZE | NANOCRYSTALS | WO3-x | OPTICAL-PROPERTIES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | SILVER NANOPARTICLES | TUNGSTEN-OXIDE NANORODS | SHAPE | SURFACE-PLASMON RESONANCE | NANOWIRES | Liquid phases | Decomposition reactions | Infrared absorption | I.R. radiation | Tungsten oxides | Shielding | Infrared spectra | Near infrared radiation | Phase decomposition | Absorption | Acids | Surface plasmon resonance | Chemical synthesis | Nanorods
Materials Science | Near-infrared shielding | Physical Chemistry | Optics, Lasers, Photonics, Optical Devices | Characterization and Evaluation of Materials | Optics | WO 3 − x | Inorganic Chemistry | Localized surface plasmon resonance | Solar control film | Nanorod | Nanotechnology | THIN-FILMS | MATERIALS SCIENCE, MULTIDISCIPLINARY | SIZE | NANOCRYSTALS | WO3-x | OPTICAL-PROPERTIES | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | SILVER NANOPARTICLES | TUNGSTEN-OXIDE NANORODS | SHAPE | SURFACE-PLASMON RESONANCE | NANOWIRES | Liquid phases | Decomposition reactions | Infrared absorption | I.R. radiation | Tungsten oxides | Shielding | Infrared spectra | Near infrared radiation | Phase decomposition | Absorption | Acids | Surface plasmon resonance | Chemical synthesis | Nanorods
Journal Article
Physical Chemistry Chemical Physics, ISSN 1463-9076, 07/2008, Volume 10, Issue 30, pp. 4410 - 4419
The high resolution absorption spectrum of methane has been recorded at liquid nitrogen temperature by direct absorption spectroscopy between 1.30 and 1.70 mm...
VIBRATIONAL OVERTONE BAND | TRANSITION | GROUND-STATE | CW-CAVITY RING | HIGH-RESOLUTION | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | COEFFICIENTS | CHEMISTRY, PHYSICAL | JET EXPANSIONS | SPECTROSCOPIC DATABASE | (CH4)-C-12 | REGION | Methane - chemistry | Cold Temperature | Temperature | Absorption | Spectroscopy, Near-Infrared | Instrumentation and Detectors | Optics | Physics
VIBRATIONAL OVERTONE BAND | TRANSITION | GROUND-STATE | CW-CAVITY RING | HIGH-RESOLUTION | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | COEFFICIENTS | CHEMISTRY, PHYSICAL | JET EXPANSIONS | SPECTROSCOPIC DATABASE | (CH4)-C-12 | REGION | Methane - chemistry | Cold Temperature | Temperature | Absorption | Spectroscopy, Near-Infrared | Instrumentation and Detectors | Optics | Physics
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2018, Volume 24, Issue 72, pp. 19341 - 19347
Four stable boron dipyrromethene (BODIPY)‐ and porphyrin‐based bis‐arylamine diradical dications were synthesized by two‐electron oxidation of their neutral...
dyes/pigments | porphyrinoids | BODIPYs | near-infrared absorption | radical ions | OXIDATION | BIS(TRIARYLAMINE) DICATIONS | DIMERS | CHEMISTRY, MULTIDISCIPLINARY | SINGLET | TAPES | FLUORESCENT | ELECTRON-TRANSFER | RADICAL-CATION | OPEN-SHELL CHARACTER | DERIVATIVES | Boron | Dyes | Absorption | Wavelengths | Infrared absorption | Chromophores | Oxidation | Absorption spectra | Chemical synthesis
dyes/pigments | porphyrinoids | BODIPYs | near-infrared absorption | radical ions | OXIDATION | BIS(TRIARYLAMINE) DICATIONS | DIMERS | CHEMISTRY, MULTIDISCIPLINARY | SINGLET | TAPES | FLUORESCENT | ELECTRON-TRANSFER | RADICAL-CATION | OPEN-SHELL CHARACTER | DERIVATIVES | Boron | Dyes | Absorption | Wavelengths | Infrared absorption | Chromophores | Oxidation | Absorption spectra | Chemical synthesis
Journal Article
Applied Physics Letters, ISSN 0003-6951, 04/2014, Volume 104, Issue 14, p. 141102
We report on the demonstration of a femtosecond all-optical modulator providing, without nonlinearity and therefore at arbitrarily low intensity, ultrafast...
PHYSICS, APPLIED | NETWORKS | Femtosecond | Femtosecond pulses | Electronic devices | Data processing | Switching theory | Metamaterials | Near infrared radiation | Luminous intensity | Absorption | Optical switching | Modulation | Coherence | Optical data processing | Physics - Optics
PHYSICS, APPLIED | NETWORKS | Femtosecond | Femtosecond pulses | Electronic devices | Data processing | Switching theory | Metamaterials | Near infrared radiation | Luminous intensity | Absorption | Optical switching | Modulation | Coherence | Optical data processing | Physics - Optics
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2016, Volume 55, Issue 7, pp. 2387 - 2391
Large increases in molecular two‐photon absorption, the onset of measurable molecular three‐photon absorption, and record molecular four‐photon absorption in...
optically active materials | nonlinear optics | ruthenium | dendrimers | photonics | DESIGN | 2-PHOTON ABSORPTION | DISPERSION | CHEMISTRY, MULTIDISCIPLINARY | NONLINEAR-OPTICAL PROPERTIES | ALKYNYLRUTHENIUM DENDRIMERS | 3-PHOTON ABSORPTION | METAL-COMPLEXES | Dendrimers | Optical properties | Linkages | Transparency | Ruthenium | Metals | Solubility | I.R. radiation | Telecommunications | Photon absorption | Biological activity | Near infrared radiation | Absorption | Multiphoton absorption | Cross sections
optically active materials | nonlinear optics | ruthenium | dendrimers | photonics | DESIGN | 2-PHOTON ABSORPTION | DISPERSION | CHEMISTRY, MULTIDISCIPLINARY | NONLINEAR-OPTICAL PROPERTIES | ALKYNYLRUTHENIUM DENDRIMERS | 3-PHOTON ABSORPTION | METAL-COMPLEXES | Dendrimers | Optical properties | Linkages | Transparency | Ruthenium | Metals | Solubility | I.R. radiation | Telecommunications | Photon absorption | Biological activity | Near infrared radiation | Absorption | Multiphoton absorption | Cross sections
Journal Article
Astrophysical Journal, ISSN 0004-637X, 02/2015, Volume 800, Issue 1, pp. 56 - 17
We report the identification of an unusual absorption-line system in the quasar SDSS J080248.18+551328.9 and present a detailed study of the system,...
Quasars: absorption lines | Quasars: individual (SDSS J080248.18+551328.9) | Quasars: emission lines | quasars: emission lines | quasars: absorption lines | LARGE TELESCOPE OBSERVATIONS | STAR-FORMATION | HOST GALAXIES | quasars: individual (SDSS J080248.18+551328.9) | ACTIVE GALACTIC NUCLEI | SPECTRAL ENERGY-DISTRIBUTIONS | DIGITAL SKY SURVEY | ASTRONOMY & ASTROPHYSICS | MOLECULAR GAS | SEYFERT-1 GALAXIES | STELLAR POPULATION | DATA RELEASE | Quasars | Seyfert galaxies | Construction | Absorption | Galaxies | Black holes (astronomy) | Density | Balmer series | Physics - Astrophysics of Galaxies | EXCITED STATES | RED SHIFT | ABSORPTION SPECTRA | BLACK HOLES | DENSITY | BALMER LINES | HYDROGEN | NEAR INFRARED RADIATION | PHOTOIONIZATION | QUASARS | ASTROPHYSICS, COSMOLOGY AND ASTRONOMY | INFRARED SPECTRA | STELLAR WINDS | GALAXIES | MULTIPLETS
Quasars: absorption lines | Quasars: individual (SDSS J080248.18+551328.9) | Quasars: emission lines | quasars: emission lines | quasars: absorption lines | LARGE TELESCOPE OBSERVATIONS | STAR-FORMATION | HOST GALAXIES | quasars: individual (SDSS J080248.18+551328.9) | ACTIVE GALACTIC NUCLEI | SPECTRAL ENERGY-DISTRIBUTIONS | DIGITAL SKY SURVEY | ASTRONOMY & ASTROPHYSICS | MOLECULAR GAS | SEYFERT-1 GALAXIES | STELLAR POPULATION | DATA RELEASE | Quasars | Seyfert galaxies | Construction | Absorption | Galaxies | Black holes (astronomy) | Density | Balmer series | Physics - Astrophysics of Galaxies | EXCITED STATES | RED SHIFT | ABSORPTION SPECTRA | BLACK HOLES | DENSITY | BALMER LINES | HYDROGEN | NEAR INFRARED RADIATION | PHOTOIONIZATION | QUASARS | ASTROPHYSICS, COSMOLOGY AND ASTRONOMY | INFRARED SPECTRA | STELLAR WINDS | GALAXIES | MULTIPLETS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2008, Volume 47, Issue 13, pp. 2439 - 2442
The best of both worlds: Multifunctional Fe3O4@polymer@Au shell nanoparticles (see scheme; Fe3O4 is black, polymer is blue, gold shell is brown) display good...
gold | magnetic properties | nanostructures | photothermal ablation | NIR absorption | Photothermal ablation | Gold | Nanostructures | Magnetic properties | CELLS | MICROSPHERES | NANOCRYSTALS | NANOCAGES | NANORODS | CHEMISTRY, MULTIDISCIPLINARY | GOLD NANOSHELLS | DELIVERY | PHOTOTHERMAL THERAPY | RESONANCES | Particle Size | Absorption | Nanoparticles - chemistry | Nanotechnology - methods | Magnetic Resonance Imaging - methods | Models, Molecular | Ferric Compounds - chemistry | Spectroscopy, Near-Infrared - methods | Magnetics
gold | magnetic properties | nanostructures | photothermal ablation | NIR absorption | Photothermal ablation | Gold | Nanostructures | Magnetic properties | CELLS | MICROSPHERES | NANOCRYSTALS | NANOCAGES | NANORODS | CHEMISTRY, MULTIDISCIPLINARY | GOLD NANOSHELLS | DELIVERY | PHOTOTHERMAL THERAPY | RESONANCES | Particle Size | Absorption | Nanoparticles - chemistry | Nanotechnology - methods | Magnetic Resonance Imaging - methods | Models, Molecular | Ferric Compounds - chemistry | Spectroscopy, Near-Infrared - methods | Magnetics
Journal Article
Journal of Physics Condensed Matter, ISSN 0953-8984, 05/2016, Volume 28, Issue 28, pp. 285801 - 285805
Tuning a semiconductor nanomaterial with large three-photon absorption (3PA) cross section in the near infrared and investigating the relationship between the...
three-photon absorption | photo-induced dipole moment | intrinsic dipole moment | Nanorod | PHYSICS, CONDENSED MATTER | nanorod | SEMICONDUCTOR QUANTUM DOTS | NANOCRYSTALS | MULTIPHOTON ABSORPTION | NONLINEAR REFRACTION | Near infrared radiation | Absorption | Semiconductors | Condensed matter | Nanostructure | Cross sections | Nanorods | Tuning
three-photon absorption | photo-induced dipole moment | intrinsic dipole moment | Nanorod | PHYSICS, CONDENSED MATTER | nanorod | SEMICONDUCTOR QUANTUM DOTS | NANOCRYSTALS | MULTIPHOTON ABSORPTION | NONLINEAR REFRACTION | Near infrared radiation | Absorption | Semiconductors | Condensed matter | Nanostructure | Cross sections | Nanorods | Tuning
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2013, Volume 52, Issue 33, pp. 8561 - 8565
Biradicaloids based on quinoidal rylenes! Soluble and stable tetracyanoquaterrylenequinodimethane (QR‐CN) and tetracyanohexarylenequinodimethane (HR‐CN) were...
biradicaloids | quaterrylene | hexarylene | near‐infrared dyes | polycyclic hydrocarbons | near-infrared dyes | GRAPHENE NANORIBBONS | 2-PHOTON ABSORPTION | OPEN-SHELL | CHEMISTRY, MULTIDISCIPLINARY | MOLECULES | QUINOIDAL OLIGOTHIOPHENES | KEKULE STRUCTURES | CHARACTER | CLOSED-SHELL | HYDROCARBON | ELECTRONIC-STRUCTURE | Ground state
biradicaloids | quaterrylene | hexarylene | near‐infrared dyes | polycyclic hydrocarbons | near-infrared dyes | GRAPHENE NANORIBBONS | 2-PHOTON ABSORPTION | OPEN-SHELL | CHEMISTRY, MULTIDISCIPLINARY | MOLECULES | QUINOIDAL OLIGOTHIOPHENES | KEKULE STRUCTURES | CHARACTER | CLOSED-SHELL | HYDROCARBON | ELECTRONIC-STRUCTURE | Ground state
Journal Article