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Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2022Embargo end date: 02 Mar 2022 United Kingdom English Publisher:Royal Society of Chemistry (RSC)Journal:Chemical Science, volume 13, pages 486-496 (issn: 2041-6520, eissn: 2041-6539, Copyright policy )Funded by:UKRI | Excitations in Complex En..., UKRI | Sulis: An EPSRC platform ..., UKRI | EPSRC Centre for Doctoral... +3 projects
Authors: Goia, Sofia; Turner, Matthew AP; Woolley, Jack M; Horbury, Michael D; Borrill, Alexandra J; Tully, Joshua J; Cobb, Samuel J; +6 Authors

doi: 10.1039/d1sc04993c , 10.5281/zenodo.5778925 , 10.5281/zenodo.5778924 , 10.17863/cam.81988 , 10.17863/cam.82367

pmid: 35126981

pmc: PMC8730129

Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple

Abstract

A spectroelectrochemical set-up using a boron doped diamond mesh electrode is presented; from ultrafast photodynamics to steady-state, the photochemistry and photophysics of redox active species and their reactive intermediates can be investigated.

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United Kingdom
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Keywords

Chemistry, 34 Chemical Sciences, Redox-active species, 3406 Physical Chemistry, Transient Electronic Absorption Spectroscopy, QD, Spectroelectrochemistry, QC

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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impulse
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