A velocity map imaging mass spectrometer for photofragments of fast ion beams

被引:25
|
作者
Johnston, M. David [1 ]
Pearson, Wright L., III [1 ,2 ]
Wang, Greg [1 ]
Metz, Ricardo B. [1 ]
机构
[1] Univ Massachusetts Amherst, Dept Chem, Amherst, MA 01003 USA
[2] Kansas State Univ, Dept Phys, JR Macdonald Lab, Manhattan, KS 66506 USA
来源
REVIEW OF SCIENTIFIC INSTRUMENTS | 2018年 / 89卷 / 01期
基金
美国国家科学基金会;
关键词
COLLISION-INDUCED DISSOCIATION; PHOTODISSOCIATION DYNAMICS; NEGATIVE-IONS; SPECTROSCOPY; CATION; SPECTRUM; N2O+; PHOTOELECTRON; IONIZATION; ENERGIES;
D O I
10.1063/1.5012896
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
We present the details of a fast ion velocity map imaging mass spectrometer that is capable of imaging the photofragments of trap-cooled (>= 7 K) ions produced in a versatile ion source. The new instrument has been used to study the predissociation of N2O+ produced by electric discharge and the direct dissociation of Al-2(+) formed by laser ablation. The instrument's resolution is currently limited by the diameter of the collimating iris to a value of Delta v/v = 7.6%. Photofragment images of N2O+ show that when the predissociative state is changed from (2)Sigma(+)(200) to (2)Sigma(+)(300) the dominant product channel shifts from a spin-forbidden ground state, N (S-4) + NO+(v = 5), to a spin-allowed pathway, N*(D-2) + NO+. The first photofragment images of Al-2(+) confirm the existence of a directly dissociative parallel transition ((2)Sigma(+)(u) -> (2)Sigma(+)(g)) that yields products with a large amount of kinetic energy. D-0 of ground state Al-2(+) ((2)Sigma(+)(g)) measured from these images is 138 +/- 5 kJ/mol, which is consistent with the published literature. Published by AIP Publishing.
引用
收藏
页数:8
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