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

Author:

Goia Sofia12ORCID,Turner Matthew A. P.123,Woolley Jack M.1ORCID,Horbury Michael D.14ORCID,Borrill Alexandra J.15ORCID,Tully Joshua J.15ORCID,Cobb Samuel J.156ORCID,Staniforth Michael1,Hine Nicholas D. M.3ORCID,Burriss Adam7,Macpherson Julie V.1ORCID,Robinson Ben R.7,Stavros Vasilios G.1ORCID

Affiliation:

1. Department of Chemistry, University of Warwick, Coventry, CV4 7AL, UK

2. Molecular Analytical Science CDT, Senate House, University of Warwick, Coventry, CV4 7AL, UK

3. Department of Physics, University of Warwick, Coventry, CV4 7AL, UK

4. School of Electronic and Electrical Engineering, University of Leeds, LS2 9JT, UK

5. Diamond Science and Technology CDT, University of Warwick, Coventry, CV4 7AL, UK

6. Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, UK

7. Syngenta, Warfield, Bracknell, RG42 6EY, UK

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.

Funder

Royal Society

Engineering and Physical Sciences Research Council

Leverhulme Trust

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

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