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  • 1
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    Nonlinear delayed symmetry breaking in a solid excited by hard x-ray free electron laser pulses (2015)
    American Institute of Physics (AIP)
    Details
    Publication Date: 2015-04-14
    Description: We have studied the ultrafast changes of electronic states in bulk ZnO upon intense hard x-ray excitation from a free electron laser. By monitoring the transient anisotropy induced in an optical probe beam, we observe a delayed breaking of the initial c-plane symmetry of the crystal that lasts for several picoseconds. Interaction with the intense x-ray pulses modifies the electronic state filling in a manner inconsistent with a simple increase in electronic temperature. These results may indicate a way to use intense ultrashort x-ray pulses to investigate high-energy carrier dynamics and to control certain properties of solid-state materials.
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
    Published by American Institute of Physics (AIP)
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  • 2
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    Nanothermal characterization of amorphous and crystalline phases in chalcogenide thin films with scanning thermal microscopy (2014)
    American Institute of Physics (AIP)
    Details
    Publication Date: 2014-10-03
    Description: The thermal properties of amorphous and crystalline phases in chalcogenide phase change materials (PCM) play a key role in device performance for non-volatile random-access memory. Here, we report the nanothermal morphology of amorphous and crystalline phases in laser pulsed GeTe and Ge 2 Sb 2 Te 5 thin films by scanning thermal microscopy (SThM). By SThM measurements and quantitative finite element analysis simulations of two film thicknesses, the PCM thermal conductivities and thermal boundary conductances between the PCM and SThM probe are independently estimated for the amorphous and crystalline phase of each stoichiometry.
    Print ISSN: 0021-8979
    Electronic ISSN: 1089-7550
    Topics: Physics
    Published by American Institute of Physics (AIP)
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  • 3
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    Photoelectron spectroscopic and theoretical study of the [HPd(η2-H2)]− cluster anion (2015)
    American Institute of Physics (AIP)
    Details
    Publication Date: 2015-09-05
    Description: Anion photoelectron spectroscopic and theoretical studies were conducted for the PdH − and PdH 3 − cluster anions. Experimentally observed electron affinities and vertical detachment energies agree well with theoretical predictions. The PdH 3 − anionic complex is made up of a PdH − sub-anion ligated by a H 2 molecule, in which the H–H bond is lengthened compared to free H 2 . Detailed molecular orbital analysis of PdH − , H 2 , and PdH 3 − reveals that back donation from a d -type orbital of PdH − to the σ* orbital of H 2 causes the H–H elongation, and hence, its activation. The H 2 binding energy to PdH − is calculated to be 89.2 kJ/mol, which is even higher than that between CO and Pd. The unusually high binding energy as well as the H–H bond activation may have practical applications, e.g., hydrogen storage and catalysis.
    Print ISSN: 0021-9606
    Electronic ISSN: 1089-7690
    Topics: Chemistry and Pharmacology , Physics
    Published by American Institute of Physics (AIP)
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  • 4
    Electronic Resource
    Electronic Resource
    Collisional relaxation of DF(v=1) and HF(v=1) by the DF dimer (1987)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 1340-1347 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Overtone vibration-laser double resonance measurements determine the vibrational relaxation rates of DF(v=1) and HF(v=1) by the DF dimer. Both monomers are efficiently relaxed by the dimer at a rate that is 20% of the gas kinetic rate. The similarity of the rate constants for the two systems, which have very different energy defects, indicates that the relaxation occurs by collision complex formation and energy redistribution, rather than direct vibration-to-vibration energy transfer from the monomer to the dimer.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.452222
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  • 5
    Electronic Resource
    Electronic Resource
    State-to-state vibrational energy transfer in DF(v=1–3) (1990)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 3207-3214 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Overtone vibration–laser double resonance studies of DF(v=1–3) energy transfer yield self-relaxation rate constants for v=1, 2 and 3 of k1=(0.37±0.06)×10−12 cm3 mol−1 s−1, k2=(22.0±2.0)×10−12 cm3 mol−1 s−1, and k3=(17.0±1.8)×10−12 cm3 mol−1 s−1, respectively. The approach also directly measures the relative importance of vibration-to-vibration (V–V) and vibration-to-translation-and-rotation (V–T,R) energy transfer. The fraction of DF(v) molecules relaxing by V–V energy transfer is 1.1±0.1 and 0.72±0.10 for v=2 and v=3, respectively. Essentially all of the vibrational energy transfer in v=2 occurs via the V–V mechanism. The slower relaxation of DF(v=3) compared to DF(v=2), in contrast to simple scaling law predictions, reflects the decreasing influence of the V–V mechanism, even though it is still the primary relaxation pathway for DF(v=3). Comparison with HF self-relaxation qualitatively indicates that V–R energy transfer is important in V–T,R relaxation of DF(v=1).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.458853
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  • 6
    Electronic Resource
    Electronic Resource
    TFTR Thomson scattering system (1985)
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 56 (1985), S. 1015-1017 
    Details
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: The TFTR Thomson scattering system has been operational since January 1984. The diagnostic uses two ruby lasers and two spectrometer-detector systems to provide profiles at two times in a discharge. The two scattering lines consist of 76 spatial channels which span the 200-cm vacuum vessel along a major radius. The detectors are gated, intensified CCD arrays with single photoelectron sensitivity. Te(R) and Ne(R) profiles are presented.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.1138255
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  • 7
    Electronic Resource
    Electronic Resource
    Collisional energy transfer via vibrational predissociation: Relaxation of HF(v=1) by HF dimers (1985)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 83 (1985), S. 1132-1137 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Overtone vibration–laser double resonance measurements determine the vibrational relaxation rate of HF(v=1) by HF dimers. Vibration-to-vibration energy transfer from the excited monomer to the dimer followed by vibrational predissociation of the dimer provides an efficient pathway for vibration-to-translation energy transfer that deexcites the monomer at 40% of the gas kinetic collision rate. Analysis of the pressure dependence of the observed decay constants using a simple kinetic model establishes a rough upper limit of 10 ns on the predissociation lifetime of the collisionally excited dimer.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.449475
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  • 8
    Electronic Resource
    Electronic Resource
    Rates and pathways of vibrational self-relaxation of HF(v=2) between 300 and 700 K (1985)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 780-788 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The temperature dependencies of the total self-relaxation rate constants for the vibrational deactivation of HF(v=2) and HF(v=1) and the state-to-state vibration-to-vibration (V–V) and vibration-to-translation-and-rotation (V-T,R) energy transfer components of the HF(v=2) self-relaxation process are measured using the overtone vibration excitation-laser double resonance technique. The total self-relaxation rate constants vary inversely with temperature. The much weaker temperature dependence of HF(v=2) self-relaxation compared to that of HF(v=1) arises from the significant role of the V–V energy transfer route. Competition between energetics and collision duration results in a weaker inverse variation with temperature for the slightly endothermic V–V route than for the exothermic V-T,R route for HF(v=2). The branching ratio for V–V energy transfer increases slightly with temperature and the data suggest that two quantum relaxation processes constitute no more than 10% of the total self-relaxation of HF(v=2). The available temperature dependence data on self-relaxation of HF(v=1–5) form a consistent picture in which the energetics of the V–V and V-T,R relaxation pathways control their relative contributions to the total energy transfer.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.448503
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  • 9
    Electronic Resource
    Electronic Resource
    Laser-assisted (1+1′)-photon ionization-detected absorption spectrum of the 3pπ 2Π state of HCO and DCO (2002)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 8384-8395 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We re-examine the ionization-detected ultraviolet absorption spectrum of the 3pπ 2Π←X 2A′ transition in HCO and DCO using a high-power visible laser to enhance the observation of first-photon resonant features. This technique, which we term here, assisted REMPI, significantly improves the signal-to-noise ratio of the spectrum, making many weak vibronic sub-bands visible for the first time. A comprehensive fit to the structure evident in a progression of bending levels from (000) to (040) refines the assignment of Song and Cool [X. M. Song and T. A. Cool, J. Chem. Phys. 96, 8664 (1992)] to yield a set of rotational constants that vary with K in relation to v2, together with a higher-order contribution to the Renner–Teller splitting in HCO, which is mirrored in DCO for all levels but (040). The (040) band falls at a frequency that is commensurate with that of CD stretch, and Fermi resonance between 3pπ 2Π(1000)Π and the higher-energy (040) K=1(Π) component gives rise to an added splitting that increases the energy of this (040) component and causes an apparent increase in the Renner parameter. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.1467329
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  • 10
    Electronic Resource
    Electronic Resource
    High power picosecond laser system at 248 nm (1988)
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 59 (1988), S. 2235-2240 
    Details
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: We describe a powerful picosecond KrF* laser system consisting of a synchronously pumped dye oscillator, a three-stage dye amplifier, frequency conversion to 248 nm, and amplification through a series of excimer modules. Characteristics are given at each stage of the system. With the first stage of the system complete, a focused intensity of ∼1016 W/cm2 is obtained. Initial visible spectra obtained by interaction with various targets are presented.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.1139940
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