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Vibrational sum-frequency generation spectroscopy of electrode surfaces: studying the mechanisms of sustainable fuel generation and utilisation.
Gardner, Adrian M; Saeed, Khezar H; Cowan, Alexander J.
Afiliação
  • Gardner AM; Stephenson Institute for Renewable Energy and the Department of Chemistry, University of Liverpool, Liverpool, L69 7ZD, UK. acowan@liverpool.ac.uk.
  • Saeed KH; Stephenson Institute for Renewable Energy and the Department of Chemistry, University of Liverpool, Liverpool, L69 7ZD, UK. acowan@liverpool.ac.uk.
  • Cowan AJ; Stephenson Institute for Renewable Energy and the Department of Chemistry, University of Liverpool, Liverpool, L69 7ZD, UK. acowan@liverpool.ac.uk.
Phys Chem Chem Phys ; 21(23): 12067-12086, 2019 Jun 12.
Article em En | MEDLINE | ID: mdl-31143914
ABSTRACT
The electrocatalytic oxidation of water coupled to the reduction of carbon dioxide, to make carbon based products, or the reduction of protons to provide hydrogen, offers a sustainable route to generating useful fuels. However new improved electrocatalysts and electrode materials are needed for these reactions. Similarly fuel cells for fuel utilisation rely on precious metal electrodes and new lower-cost materials are needed. Developing efficient catalysts for sustainable fuel generation can be accelerated with an improved understanding of the underlying mechanisms. Herein, we present a perspective on the use of vibrational sum-frequency generation (VSFG) spectroscopy to study such electrocatalytic mechanisms. We briefly outline the basic principles of VSFG spectroscopy pertinent to the study of electrochemical interfaces. We then review the use of VSFG to study water at charged and electrode interfaces, relevant to the mechanisms of water oxidation, the mechanisms of alcohol oxidation and also molecular electrocatalysts for carbon dioxide reduction.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article