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  • 2000-2004  (3)
  • 1990-1994  (11)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 6200-6209 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The (2ν2,l=2←ν2), (2ν2,l=0←ν2), and (ν1+ν2←ν1) hot bands of H+3 were observed. The vibrationally hot ions were produced in a liquid nitrogen cooled 6 kHz ac discharge using gas mixtures of H2 and He. The spectra were detected in direct absorption using a newly extended tunable difference frequency spectrometer using both LiNbO3 and LiIO3 crystals as nonlinear optical elements. The range of this spectrometer is now ∼5300–∼1900 cm−1. The positions of the rovibrational transitions compare extremely well with the theoretical predictions of Miller and Tennyson. A vibrational temperature study of the discharge indicates a significant population inversion between the ν1 and ν2 levels.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 946-954 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We use time-, wavelength-, temperature-, polarization-resolved luminescence to elucidate the nature of the absorbing and "band edge'' luminescing states in 32 A(ring) diameter wurtzite CdSe quantum crystallites. Time-resolved emission following picosecond size-selective resonant excitation of the lowest excited state shows two components—a temperature insensitive 100 ps component and a microsecond, temperature sensitive component. The emission spectrum, showing optic phonon vibrational structure, develops a ∼70 wave number red shift as the fast component decays. Photoselection shows the slow component to be reverse polarized at 10 K, indicating this component to be the result of a hole radiationless transition. The 100 ps emitting state is repopulated thermally as temperature increases from 10 to 50 K. All available data are interpreted by postulating strong resonant mixing between a standing wave molecular orbital delocalized inside the crystallite and intrinsic surface Se lone pair states. The apparent exciton transition is assigned to a ∼130 wave number wide band of eigenstates with the hole localized principally on the surface. The band contains strongly emitting "doorway'' states and weakly emitting "background'' states. The hole becomes mobile among these states as T increases to 50 K. It is suggested that such resonant mixing may be general in II–VI and III–V crystallites.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 80 (2002), S. 2380-2382 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We study the effect of multiparticle interactions on optical gain and stimulated emission in close-packed solids of chemically synthesized CdSe nanocrystals (nanocrystal quantum dots). An analysis of pump-dependent nonlinear absorption signals indicates that the band-edge optical gain is due to multiparticle states with a dominant contribution from doubly excited nanocrystals (quantum-confined biexcitons). We observe that optical gain dynamics are due to the competition between ultrafast hole surface trapping and multiparticle Auger decay. We analyze the effect of intrinsic Auger recombination on optical gain lifetimes and gain pump intensity thresholds. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 81 (2002), S. 1303-1305 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We study different emission regimes in close-packed films of chemically synthesized CdSe nanoparticles [nanocrystal quantum dots (NQDs)]. We observe that the NQD photoluminescence is dominated by excitons and biexcitons, respectively, before and after the threshold for stimulated emission. Furthermore, we demonstrate the regime of microring lasing into sharp, whispering-gallery modes using NQD solids incorporated into microcapillary tubes. This result indicates a feasibility of miniature, solid-state laser devices based on chemically synthesized NQDs. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 65 (1994), S. 2795-2797 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A novel technique combining electrospray and organometallic chemical vapor deposition (OMCVD) has been developed for the synthesis of new II–VI quantum dot composites. CdSe nanocrystals (quantum dots) of selected size are dispersed in a pyridine/acetonitrile mixture. The nanocrystals are transferred by electrospray into the growth zone of an OMCVD reactor and codeposited on a ZnSe matrix grown from hydrogen selenide and diethyl zinc. Composites consisting of CdSe nanocrystals and an amorphous or polycrystalline ZnSe matrix have been deposited on glass substrates at temperatures of 150–250 °C. Room-temperature absorption and photoluminescence spectra show optical transitions characteristic of the initial nanocrystal dispersions. The emission wavelength may be tuned in a broad spectral region by incorporating nanocrystals of varying sizes. The composites have been characterized by Auger electron spectroscopy, high resolution transmission electron microscopy, and scanning transmission electron microscopy. © 1994 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 3297-3300 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Room temperature 31P magic angle sample spinning (MAS) nuclear magnetic resonance (NMR) is used to study the phosphine chalconide species coordinating the surface of CdSe nanocrystallites. Two surface species are identified: trioctylphosphine oxide (TOPO) and trioctylphosphine selenide (TOPSe). The TOPO coordinates Cd surface sites while trioctylphosphine (TOP) coordinates Se to produce surface TOPSe species. Chemical removal of TOPSe linkages produces CdSe nanocrystallites passivated exclusively with TOPO. A double resonance experiment (31P and 77Se) characterizes the TOPSe species. Quantitative studies indicate coordination to nearly all surface Cd atoms and allows the development of a model for the morphology of an average crystallite surface.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 30 (2000), S. 545-610 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Solution phase syntheses and size-selective separation methods to prepare semiconductor and metal nanocrystals, tunable in size from ~1 to 20 nm and monodisperse to 〈=5%, are presented. Preparation of monodisperse samples enables systematic characterization of the structural, electronic, and optical properties of materials as they evolve from molecular to bulk in the nanometer size range. Sample uniformity makes it possible to manipulate nanocrystals into close-packed, glassy, and ordered nanocrystal assemblies (superlattices, colloidal crystals, supercrystals). Rigorous structural characterization is critical to understanding the electronic and optical properties of both nanocrystals and their assemblies. At inter-particle separations 5-100 A, dipole-dipole interactions lead to energy transfer between neighboring nanocrystals, and electronic tunneling between proximal nanocrystals gives rise to dark and photoconductivity. At separations 〈5 A, exchange interactions cause otherwise insulating assemblies to become semiconducting, metallic, or superconducting depending on nanocrystal composition. Tailoring the size and composition of the nanocrystals and the length and electronic structure of the matrix may tune the properties of nanocrystal solid-state materials.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physical Chemistry 41 (1990), S. 477-496 
    ISSN: 0066-426X
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 115 (1993), S. 8706-8715 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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