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Durham Research Online
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Ultrafast dynamics of low-energy electron attachment via a non-valence correlation-bound state.

Rogers, Joshua P. and Anstöter, Cate S. and Verlet, Jan R. R. (2018) 'Ultrafast dynamics of low-energy electron attachment via a non-valence correlation-bound state.', Nature chemistry., 10 . pp. 341-346.

Abstract

The primary electron-attachment process in electron-driven chemistry represents one of the most fundamental chemical transformations with wide-ranging importance in science and technology. However, the mechanistic detail of the seemingly simple reaction of an electron and a neutral molecule to form an anion remains poorly understood, particularly at very low electron energies. Here, time-resolved photoelectron imaging was used to probe the electron-attachment process to a non-polar molecule using time-resolved methods. An initially populated diffuse non-valence state of the anion that is bound by correlation forces evolves coherently in ∼30 fs into a valence state of the anion. The extreme efficiency with which the correlation-bound state serves as a doorway state for low-energy electron attachment explains a number of electron-driven processes, such as anion formation in the interstellar medium and electron attachment to fullerenes.

Item Type:Article
Full text:(AM) Accepted Manuscript
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Status:Peer-reviewed
Publisher Web site:https://doi.org/10.1038/nchem.2912
Date accepted:15 November 2017
Date deposited:15 January 2018
Date of first online publication:08 January 2018
Date first made open access:08 July 2019

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