Issue 34, 2022

Time-resolved photoelectron spectroscopy: the continuing evolution of a mature technique

Abstract

Time-resolved photoelectron spectroscopy (TRPES) has become one of the most widespread techniques for probing nonadiabatic dynamics in the excited electronic states of molecules. Furthermore, the complementary development of ab initio approaches for the simulation of TRPES signals has enabled the interpretation of these transient spectra in terms of underlying coupled electronic–nuclear dynamics. In this perspective, we discuss the current state-of-the-art approaches, including efforts to push femtosecond pulses into vacuum ultraviolet and soft X-ray regimes as well as the utilization of novel polarizations to use time-resolved optical activity as a probe of nonadiabatic dynamics. We close this perspective with a forward-looking prospectus on the new areas of application for this technique.

Graphical abstract: Time-resolved photoelectron spectroscopy: the continuing evolution of a mature technique

Article information

Article type
Perspective
Submitted
23 dek 2021
Accepted
04 mar 2022
First published
07 mar 2022

Phys. Chem. Chem. Phys., 2022,24, 20012-20024

Time-resolved photoelectron spectroscopy: the continuing evolution of a mature technique

M. S. Schuurman and V. Blanchet, Phys. Chem. Chem. Phys., 2022, 24, 20012 DOI: 10.1039/D1CP05885A

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