COLLISIONAL DEACTIVATION OF HIGHLY VIBRATIONALLY EXCITED NO2 MONITORED BY TIME-RESOLVED FOURIER-TRANSFORM INFRARED-EMISSION SPECTROSCOPY

被引：55

作者：

HARTLAND, GV

QIN, D

DAI, HL

机构：

[1] Department of Chemistry, University of Pennsylvania, Philadelphia

来源：

JOURNAL OF CHEMICAL PHYSICS | 1994年 / 100卷 / 10期

关键词：

D O I：

10.1063/1.466827

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：

Infrared emission from highly vibrationally excited NO2, prepared by collision induced internal conversion, can be detected with 1 cm(-1) spectral and 0.5 mu s time resolution over the 800-10 000 cm(-1) range by time-resolved Fourier transform emission spectroscopy. The energy distribution of vibrationally excited NO2 during collisional deactivation can be extracted from the emission spectra and shows that the energy loss per collision increases dramatically from <50 cm(-1) below 13 000 cm(-1) energy to 1300 cm(-1) at 20 000 cm(-1) energy.

引用

页码：7832 / 7835

页数：4

共 28 条

[1]

ALDERGOLDEN SM, 1989, J PHYS CHEM-US, V93, P684

[2] INFRARED-EMISSION STUDIES OF THE VIBRATIONAL DEACTIVATION OF BENZENE-DERIVATIVES [J].