Solvated dielectrons from optical excitation: An effective source of low-energy electrons
Author(s) -
Sebastian Hartweg,
J. V. Barnes,
Bruce L. Yoder,
Gustavo A. García,
Laurent Nahon,
Evangelos Miliordos,
Ruth Signorell
Publication year - 2023
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.adh0184
Subject(s) - solvated electron , photoexcitation , electron , chemical physics , electron transfer , chemistry , excitation , photochemistry , atomic physics , ultraviolet , work (physics) , extreme ultraviolet , materials science , aqueous solution , radiolysis , optoelectronics , excited state , physics , laser , optics , quantum mechanics , thermodynamics
Low-energy electrons dissolved in liquid ammonia or aqueous media are powerful reducing agents that promote challenging reduction reactions but can also cause radiation damage to biological tissue. Knowledge of the underlying mechanistic processes remains incomplete, particularly with respect to the details and energetics of the electron transfer steps. In this work, we show how ultraviolet (UV) photoexcitation of metal-ammonia clusters could be used to generate tunable low-energy electrons in situ. Specifically, we identified UV light-induced generation of spin-paired solvated dielectrons and their subsequent relaxation by an unconventional electron transfer-mediated decay as an efficient, low-energy electron source. The process is robust and straightforward to induce with the prospect of improving our understanding of radiation damage and fostering mechanistic studies of solvated electron reduction reactions.
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