A multi-plate velocity-map imaging design for high-resolution photoelectron spectroscopy

被引:15
作者
Kregel, Steven J. [1 ]
Thurston, Glen K. [1 ]
Zhou, Jia [1 ]
Garand, Etienne [1 ]
机构
[1] Univ Wisconsin Madison, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-OXYGEN; CLUSTER ANIONS; METAL-CLUSTERS; NEGATIVE-IONS; DYNAMICS; PHOTODISSOCIATION; CS2; CO2; PHOTOIONIZATION; ACETALDEHYDE;
D O I
10.1063/1.4996011
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
A velocity map imaging (VMI) setup consisting of multiple electrodes with three adjustable voltage parameters, designed for slow electron velocity map imaging applications, is presented. The motivations for this design are discussed in terms of parameters that influence the VMI resolution and functionality. Particularly, this VMI has two tunable potentials used to adjust for optimal focus, yielding good VMI focus across a relatively large energy range. It also allows for larger interaction volumes without significant sacrifice to the resolution via a smaller electric gradient at the interaction region. All the electrodes in this VMI have the same dimensions for practicality and flexibility, allowing for relatively easy modifications to suit different experimental needs. We have coupled this VMI to a cryogenic ion trap mass spectrometer that has a flexible source design. The performance is demonstrated with the photoelectron spectra of S- and CS2-. The latter has a long vibrational progression in the ground state, and the temperature dependence of the vibronic features is probed by changing the temperature of the ion trap. Published by AIP Publishing.
引用
收藏
页数:7
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