Mass-selected ion–molecule cluster beam apparatus for ultrafast photofragmentation studies

Author:

Wang Xiaojun1ORCID,Hasan Mahmudul1ORCID,Fan Lin1ORCID,Wang Yibo1ORCID,Li Hui2ORCID,Slaughter Daniel S.3ORCID,Centurion Martin1ORCID

Affiliation:

1. Department of Physics and Astronomy, University of Nebraska-Lincoln 1 , Lincoln, Nebraska 68588, USA

2. Department of Chemistry, Nebraska Center for Materials and Nanoscience, and Center for Integrated Biomolecular Communication, University of Nebraska-Lincoln 2 , Lincoln, Nebraska 68588, USA

3. Chemical Sciences Division, Lawrence Berkeley National Laboratory 3 , 1 Cyclotron Rd., Berkeley, California 94720, USA

Abstract

We describe an apparatus for investigating the excited-state dissociation dynamics of mass-selected ion–molecule clusters by mass-resolving and detecting photofragment-ions and neutrals, in coincidence, using an ultrafast laser operating at high repetition rates. The apparatus comprises a source that generates ion–molecule clusters, a time-of-flight spectrometer, and a mass filter that selects the desired anions, and a linear-plus-quadratic reflectron mass spectrometer that discriminates the fragment anions after the femtosecond laser excites the clusters. The fragment neutrals and anions are then captured by two channeltron detectors. The apparatus performance is tested by measuring the photofragments: I−, CF3I−, and neutrals from photoexcitation of the ion–molecule cluster CF3I·I− using femtosecond UV laser pulses with a wavelength of 266 nm. The experimental results are compared with our ground state and excited state electronic structure calculations as well as the existing results and calculations, with particular attention to the generation mechanism of the anion fragments and dissociation channels of the ion–molecule cluster CF3I·I− in the charge-transfer excited state.

Funder

Chemical Sciences, Geosciences, and Biosciences Division

Publisher

AIP Publishing

Subject

Instrumentation

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