CORE EXTRACTION FOR MEASURING STATE-TO-STATE DIFFERENTIAL-CROSS SECTIONS OF BIMOLECULAR REACTIONS

被引:114
|
作者
SIMPSON, WR
ORREWING, AJ
RAKITZIS, TP
KANDEL, SA
ZARE, RN
机构
[1] Department of Chemistry, Stanford University, Stanford
[2] School of Chemistry, University of Bristol
来源
JOURNAL OF CHEMICAL PHYSICS | 1995年 / 103卷 / 17期
关键词
D O I
10.1063/1.470304
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
We describe a method we call core extraction for measuring the speed distributions of products from photoinitiated bimolecular reactions for the purpose of determining state-to-state differential cross sections. Core extraction is demonstrated; by determination of the state-to-state differential cross section for the reaction Cl+CH4(upsilon(3)=1)+-->HCl(upsilon=1, J=1)+CH3. The method of core extraction measures three-dimensional projections of the velocity distribution using a time-of-flight mass spectrometer equipped with a mask to reject off-axis scattered products. This three-dimensional projection is then converted to a state-to-state differential cross section via simple transformations. Competition between instrumental resolution and signal in core extraction is discussed, and the behavior of our system is checked with simple velocity distributions that result from photodissociation of Cl-2. Core extraction is compared with other methods for the measurement of state-resolved differential cross sections. (C) 1995 American Institute of Physics.
引用
收藏
页码:7299 / 7312
页数:14
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