Cargando…

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

Many photoactivated processes involve a change in oxidation state during the reaction pathway and formation of highly reactive photoactivated species. Isolating these reactive species and studying their early-stage femtosecond to nanosecond (fs–ns) photodynamics can be challenging. Here we introduce...

Descripción completa

Detalles Bibliográficos
Autores principales: Goia, Sofia, Turner, Matthew A. P., Woolley, Jack M., Horbury, Michael D., Borrill, Alexandra J., Tully, Joshua J., Cobb, Samuel J., Staniforth, Michael, Hine, Nicholas D. M., Burriss, Adam, Macpherson, Julie V., Robinson, Ben R., Stavros, Vasilios G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730129/
https://www.ncbi.nlm.nih.gov/pubmed/35126981
http://dx.doi.org/10.1039/d1sc04993c
_version_ 1784627071241158656
author Goia, Sofia
Turner, Matthew A. P.
Woolley, Jack M.
Horbury, Michael D.
Borrill, Alexandra J.
Tully, Joshua J.
Cobb, Samuel J.
Staniforth, Michael
Hine, Nicholas D. M.
Burriss, Adam
Macpherson, Julie V.
Robinson, Ben R.
Stavros, Vasilios G.
author_facet Goia, Sofia
Turner, Matthew A. P.
Woolley, Jack M.
Horbury, Michael D.
Borrill, Alexandra J.
Tully, Joshua J.
Cobb, Samuel J.
Staniforth, Michael
Hine, Nicholas D. M.
Burriss, Adam
Macpherson, Julie V.
Robinson, Ben R.
Stavros, Vasilios G.
author_sort Goia, Sofia
collection PubMed
description Many photoactivated processes involve a change in oxidation state during the reaction pathway and formation of highly reactive photoactivated species. Isolating these reactive species and studying their early-stage femtosecond to nanosecond (fs–ns) photodynamics can be challenging. Here we introduce a combined ultrafast transient absorption-spectroelectrochemistry (TA-SEC) approach using freestanding boron doped diamond (BDD) mesh electrodes, which also extends the time domain of conventional spectrochemical measurements. The BDD electrodes offer a wide solvent window, low background currents, and a tuneable mesh size which minimises light scattering from the electrode itself. Importantly, reactive intermediates are generated electrochemically, via oxidation/reduction of the starting stable species, enabling their dynamic interrogation using ultrafast TA-SEC, through which the early stages of the photoinduced relaxation mechanisms are elucidated. As a model system, we investigate the ultrafast spectroscopy of both anthraquinone-2-sulfonate (AQS) and its less stable counterpart, anthrahydroquinone-2-sulfonate (AH(2)QS). This is achieved by generating AH(2)QS in situ from AQS via electrochemical means, whilst simultaneously probing the associated early-stage photoinduced dynamical processes. Using this approach we unravel the relaxation mechanisms occurring in the first 2.5 ns, following absorption of ultraviolet radiation; for AQS as an extension to previous studies, and for the first time for AH(2)QS. AQS relaxation occurs via formation of triplet states, with some of these states interacting with the buffered solution to form a transient species within approximately 600 ps. In contrast, all AH(2)QS undergoes excited-state single proton transfer with the buffered solution, resulting in formation of ground state AHQS(−) within approximately 150 ps.
format Online
Article
Text
id pubmed-8730129
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-87301292022-02-04 Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple Goia, Sofia Turner, Matthew A. P. Woolley, Jack M. Horbury, Michael D. Borrill, Alexandra J. Tully, Joshua J. Cobb, Samuel J. Staniforth, Michael Hine, Nicholas D. M. Burriss, Adam Macpherson, Julie V. Robinson, Ben R. Stavros, Vasilios G. Chem Sci Chemistry Many photoactivated processes involve a change in oxidation state during the reaction pathway and formation of highly reactive photoactivated species. Isolating these reactive species and studying their early-stage femtosecond to nanosecond (fs–ns) photodynamics can be challenging. Here we introduce a combined ultrafast transient absorption-spectroelectrochemistry (TA-SEC) approach using freestanding boron doped diamond (BDD) mesh electrodes, which also extends the time domain of conventional spectrochemical measurements. The BDD electrodes offer a wide solvent window, low background currents, and a tuneable mesh size which minimises light scattering from the electrode itself. Importantly, reactive intermediates are generated electrochemically, via oxidation/reduction of the starting stable species, enabling their dynamic interrogation using ultrafast TA-SEC, through which the early stages of the photoinduced relaxation mechanisms are elucidated. As a model system, we investigate the ultrafast spectroscopy of both anthraquinone-2-sulfonate (AQS) and its less stable counterpart, anthrahydroquinone-2-sulfonate (AH(2)QS). This is achieved by generating AH(2)QS in situ from AQS via electrochemical means, whilst simultaneously probing the associated early-stage photoinduced dynamical processes. Using this approach we unravel the relaxation mechanisms occurring in the first 2.5 ns, following absorption of ultraviolet radiation; for AQS as an extension to previous studies, and for the first time for AH(2)QS. AQS relaxation occurs via formation of triplet states, with some of these states interacting with the buffered solution to form a transient species within approximately 600 ps. In contrast, all AH(2)QS undergoes excited-state single proton transfer with the buffered solution, resulting in formation of ground state AHQS(−) within approximately 150 ps. The Royal Society of Chemistry 2021-12-17 /pmc/articles/PMC8730129/ /pubmed/35126981 http://dx.doi.org/10.1039/d1sc04993c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Goia, Sofia
Turner, Matthew A. P.
Woolley, Jack M.
Horbury, Michael D.
Borrill, Alexandra J.
Tully, Joshua J.
Cobb, Samuel J.
Staniforth, Michael
Hine, Nicholas D. M.
Burriss, Adam
Macpherson, Julie V.
Robinson, Ben R.
Stavros, Vasilios G.
Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title_full Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title_fullStr Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title_full_unstemmed Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title_short Ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
title_sort ultrafast transient absorption spectroelectrochemistry: femtosecond to nanosecond excited-state relaxation dynamics of the individual components of an anthraquinone redox couple
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730129/
https://www.ncbi.nlm.nih.gov/pubmed/35126981
http://dx.doi.org/10.1039/d1sc04993c
work_keys_str_mv AT goiasofia ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT turnermatthewap ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT woolleyjackm ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT horburymichaeld ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT borrillalexandraj ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT tullyjoshuaj ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT cobbsamuelj ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT staniforthmichael ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT hinenicholasdm ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT burrissadam ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT macphersonjuliev ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT robinsonbenr ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple
AT stavrosvasiliosg ultrafasttransientabsorptionspectroelectrochemistryfemtosecondtonanosecondexcitedstaterelaxationdynamicsoftheindividualcomponentsofananthraquinoneredoxcouple