An optimised cell for in situ XAS of gas diffusion electrocatalyst electrodes
An optimised cell for in situ XAS of gas diffusion electrocatalyst electrodes
The quality of in situ XAS of electrochemical systems is highly sensitive to electrode disturbances, such as gas evolution and gas consumption at an electrolyte / catalyst interface. A novel in situ spectro-electrochemical X-ray absorption spectroscopy (SPEC-XAS)
cell is presented as a new tool for the characterisation of gas evolving and consuming electrocatalysts at high overpotentials. By utilising a thin, porous membrane with efficient electrolyte and gas circulating loops, an improved three phase interface is established that enabled efficient gas supply and minimised the interference from bubble formation. X-ray absorption spectroscopy (XAS) measurements were conducted in fluorescence mode with three experiments selected to demonstrate the cell’s performance. The first two reactions; an in-situ study of a highly active amorphous iridium oxide catalyst during the oxygen evolution reaction (OER) and an in-situ study of copper oxide during the carbon dioxide reduction reaction (CO2RR) are used to exemplify the XAS data quality achieved under operational conditions. Thirdly, a detailed XAS investigation of a highly dispersed platinum catalyst during the oxygen reduction reaction (ORR) is presented, along with comparative data in nitrogen. These measurements show the retention of oxygen on the surface of the platinum metal particles down to 0.48 V (vs. RHE), well below the platinum oxide reduction peak.
CO RR, Electrochemistry, OER, ORR, in situ XAS
Sherwin, Connor Matthew
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Celorrio, Verónica
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Podbevšek, Urša
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Rigg, Katie
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Hodges, Toby
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Ibraliu, Armando
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Telfer, Abbey J.
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McLeod, Lucy
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Difilippo, Alessandro
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Corbos, Elena C.
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Russell, Andrea E.
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7 October 2024
Sherwin, Connor Matthew
b4e01340-ac4d-46a3-8904-ec306c903761
Celorrio, Verónica
7a8ccfa9-5d90-4502-8008-5e1bb15035c5
Podbevšek, Urša
ffcc80dc-5dd8-4c8a-81e1-80da87a6b128
Rigg, Katie
2051cc16-6c45-4808-be02-be4281f29f17
Hodges, Toby
a60b0292-f3b7-4e31-9d17-05b8f0bb00ff
Ibraliu, Armando
5fe3aa2c-a711-47bd-abd4-9ae0f01f4d92
Telfer, Abbey J.
5344ad64-a232-495e-ba45-a8b6092420b3
McLeod, Lucy
98043bf9-f919-46e2-a04c-4ca8c736dbb9
Difilippo, Alessandro
ef10b49e-2945-4927-8dd5-0ee64bb2ef0f
Corbos, Elena C.
fb2d9cfb-e361-471f-8d05-f07ba67aa669
Russell, Andrea E.
b6b7c748-efc1-4d5d-8a7a-8e4b69396169
Sherwin, Connor Matthew, Celorrio, Verónica, Podbevšek, Urša, Rigg, Katie, Hodges, Toby, Ibraliu, Armando, Telfer, Abbey J., McLeod, Lucy, Difilippo, Alessandro, Corbos, Elena C. and Russell, Andrea E.
(2024)
An optimised cell for in situ XAS of gas diffusion electrocatalyst electrodes.
ChemCatChem, 16 (19), [e202400221].
(doi:10.1002/cctc.202400221).
Abstract
The quality of in situ XAS of electrochemical systems is highly sensitive to electrode disturbances, such as gas evolution and gas consumption at an electrolyte / catalyst interface. A novel in situ spectro-electrochemical X-ray absorption spectroscopy (SPEC-XAS)
cell is presented as a new tool for the characterisation of gas evolving and consuming electrocatalysts at high overpotentials. By utilising a thin, porous membrane with efficient electrolyte and gas circulating loops, an improved three phase interface is established that enabled efficient gas supply and minimised the interference from bubble formation. X-ray absorption spectroscopy (XAS) measurements were conducted in fluorescence mode with three experiments selected to demonstrate the cell’s performance. The first two reactions; an in-situ study of a highly active amorphous iridium oxide catalyst during the oxygen evolution reaction (OER) and an in-situ study of copper oxide during the carbon dioxide reduction reaction (CO2RR) are used to exemplify the XAS data quality achieved under operational conditions. Thirdly, a detailed XAS investigation of a highly dispersed platinum catalyst during the oxygen reduction reaction (ORR) is presented, along with comparative data in nitrogen. These measurements show the retention of oxygen on the surface of the platinum metal particles down to 0.48 V (vs. RHE), well below the platinum oxide reduction peak.
Text
AcceptedArticle_Sherwin_etal
- Accepted Manuscript
More information
Accepted/In Press date: 11 June 2024
Published date: 7 October 2024
Additional Information:
Publisher Copyright:
© 2024 The Authors. ChemCatChem published by Wiley-VCH GmbH.
Keywords:
CO RR, Electrochemistry, OER, ORR, in situ XAS
Identifiers
Local EPrints ID: 501647
URI: http://eprints.soton.ac.uk/id/eprint/501647
ISSN: 1867-3880
PURE UUID: 6ca0b5ae-a7bf-4763-9fe9-1acbcda3475e
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Date deposited: 04 Jun 2025 17:12
Last modified: 05 Jun 2025 02:02
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Contributors
Author:
Connor Matthew Sherwin
Author:
Verónica Celorrio
Author:
Urša Podbevšek
Author:
Katie Rigg
Author:
Toby Hodges
Author:
Armando Ibraliu
Author:
Abbey J. Telfer
Author:
Lucy McLeod
Author:
Alessandro Difilippo
Author:
Elena C. Corbos
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