Time-resolved Fourier transform infrared spectroscopy of optically pumped carbon monoxide

被引:48
|
作者
Plönjes, E [1 ]
Palm, P [1 ]
Chernukho, AP [1 ]
Adamovich, IV [1 ]
Rich, JW [1 ]
机构
[1] Ohio State Univ, Dept Engn Mech, Columbus, OH 43220 USA
关键词
D O I
10.1016/S0301-0104(00)00096-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The paper discusses measurements of vibration-to-vibration (V-V) energy transfer rates for GO-CO using time-resolved step-scan Fourier transform infrared spectroscopy of optically pumped carbon monoxide. In the experiments, time evolution of all vibrational states of carbon monoxide excited by a CO laser and populated by V-V processes (up to nu similar to 40) is monitored simultaneously. The V-V rates are inferred from these data using a kinetic model that incorporates spatial power distribution of the focused laser beam, transport processes, and multi-quantum V-V processes. Although the model predictions agree well with the time-dependent step-scan relaxation data, there is variance between the model predictions and the up-pumping data, however. Comparison of calculations using two different sets of V-V rates with experimental spectra showed that the use of the semi-empirical V-V rates of DeLeon and Rich provides better agreement with experiment. It is also shown that the multi-quantum V-V rates among high vibrational quantum numbers, calculated by Cacciatore and Billing, are substantially overpredicted. The results provide some new insight into nonequilibrium vibrational kinetics, and also demonstrate the capabilities of the step-scan Fourier transform spectroscopy for time-resolved studies of molecular energy transfer processes and validation of theoretical rate models. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:315 / 331
页数:17
相关论文
共 50 条
  • [21] PRACTICAL ASPECTS OF RAPID SCANNING FOURIER-TRANSFORM TIME-RESOLVED INFRARED-SPECTROSCOPY
    GARRISON, AA
    CROCOMBE, RA
    MAMANTOV, G
    DEHASETH, JA
    APPLIED SPECTROSCOPY, 1980, 34 (04) : 399 - 404
  • [22] Time-resolved Fourier-transform infrared and visible luminescence spectroscopy of photoexcited porous silicon
    Wang, JP
    Song, L
    Zou, BS
    El-Sayed, MA
    PHYSICAL REVIEW B, 1999, 59 (07): : 5026 - 5031
  • [23] Time-resolved Fourier transform infrared spectroscopy of the gas phase during atomic layer deposition
    Sperling, Brent A.
    Kimes, William A.
    Maslar, James E.
    Chu, Pamela M.
    JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A, 2010, 28 (04): : 613 - 621
  • [24] Nematic director reorientation dynamics studied by time-resolved Fourier-transform infrared spectroscopy
    Toriumi, H
    Akahane, T
    JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 1998, 37 (02): : 608 - 612
  • [25] Photochemical Reaction of Benzoin Caged Compound: Time-Resolved Fourier Transform Infrared Spectroscopy Study
    Dai, Xiao-juan
    Yu, You-qing
    Liu, Kun-hui
    Su, Hong-mei
    CHINESE JOURNAL OF CHEMICAL PHYSICS, 2016, 29 (01) : 91 - 98
  • [26] TIME-RESOLVED FOURIER SPECTROSCOPY
    MURPHY, RE
    COOK, FH
    SAKAI, H
    JOURNAL OF THE OPTICAL SOCIETY OF AMERICA, 1975, 65 (05) : 600 - 604
  • [27] TIME-RESOLVED FOURIER SPECTROSCOPY
    MURPHY, RE
    COOK, F
    SAKAI, H
    JOURNAL OF THE OPTICAL SOCIETY OF AMERICA, 1974, 64 (10) : 1364 - 1364
  • [28] Vibrational spectroscopy of a transient species through time-resolved Fourier transform infrared emission spectroscopy: The vinyl radical
    Letendre, L
    Liu, DK
    Pibel, CD
    Halpern, JB
    Dai, HL
    JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (21): : 9209 - 9212
  • [29] Frequency-resolved, phase-resolved and time-resolved step-scan Fourier transform infrared photoacoustic spectroscopy
    Jiang, EY
    Drapcho, DL
    McCarthy, WJ
    Crocombe, RA
    FOURIER TRANSFORM SPECTROSCOPY, 1998, (430): : 381 - 384
  • [30] Real-time pursuit of crystal growth by millisecond time-resolved multichannel Fourier transform infrared spectroscopy
    Hashimoto, M
    Hamaguchi, HO
    APPLIED SPECTROSCOPY, 1998, 52 (02) : 222 - 225