IEEE.org| IEEE Xplore Digital Library| IEEE Standards| IEEE Spectrum| More Sites

Cart (Loading....) | Create Account | 

Close category search window
Author Searchbeta |  Advanced Search  |  Preferences |  Search Tips  |  More Search Options  
 
Browse Journals & Magazines > Review of Scientific Instrume ...> Volume:76 Issue:2 Help

High resolution kinetic energy by long time-delayed core-sampling photofragment translational spectroscopy

Full Text Sign-In or Purchase

Sign In

Cookies must be enabled to login.After enabling cookies , please use refresh or reload or ctrl+f5 on the browser for the login options.

Formats Non-Member Member
$31 $31
Learn how you can qualify for the best price for this item!
Become an IEEE Member or Subscribe to
IEEE Xplore for exclusive pricing! close button
puzzle piece

IEEE membership options for an individual and IEEE Xplore subscriptions for an organization offer the most affordable access to essential journal articles, conference papers, standards, eBooks, and eLearning courses.

Learn more about:

IEEE membership

IEEE Xplore subscriptions

3 Author(s)
Li, Guosheng ; Department of Chemistry, University of Southern California, Los Angeles, California 90089 ; Hwang, Hyun Jin ; Jung, Hyun Chai

Your organization might have access to this article on the publisher's site. To check, click on this link:http://dx.doi.org/+10.1063/1.1844412 

A pulsed core-sampling photofragment translational spectroscopy (PTS) method with a long time-delay, which allows an extremely high kinetic energy resolution, is presented in this article. More commonly applying a short time delay between laser and pulsed acceleration electric field leads to a low kinetic energy resolution for the pulsed core-sampling method. This low kinetic energy resolution problem was overcome by applying a longer time delay. An absolute recoil velocity resolution of Δv=8 m/s and a relative kinetic energy resolution of ΔE/E=3.6% were obtained in this experiment, by applying a time-delay of 8 μs between the laser and the acceleration electric field. The vibrational distributions of the CH3 radical for the I* and I channel of CH3I photodissociation at 266 nm were directly resolved for first time to presented an improvement of the kinetic energy resolution.

Published in:
Review of Scientific Instruments  (Volume:76 ,  Issue: 2 )

Date of Publication: Feb 2005

Page(s):
023105 - 023105-7
ISSN :
0034-6748
Digital Object Identifier :
10.1063/1.1844412
Product Type:
Journals & Magazines
Date of Current Version :
18 June 2009
Issue Date :
Feb 2005

IEEE Account

Purchase Details

Profile Information

Need Help?


IEEE Advancing Technology for Humanity About IEEE Xplore | Contact | Help | Terms of Use | Nondiscrimination Policy | Site Map | Privacy & Opting Out of Cookies

A not-for-profit organization, IEEE is the world's largest professional association for the advancement of technology.
© Copyright 2013 IEEE - All rights reserved. Use of this web site signifies your agreement to the terms and conditions.