Ultracompact Electrical Double Layers at TiO<sub>2</sub>(110) Electrified Interfaces

Metal-oxide aqueous interfaces are important in areas as varied as photocatalysis and mineral reforming. Crucial to the chemistry at these interfaces is the structure of the electrical double layer formed when anions or cations compensate for the charge arising from adsorbed H<sup>+</sup> or OH<sup>-</sup>. This has proven extremely challenging to determine at the atomic level. In this work, we use a surface science approach, involving atomic level characterization, to determine the structure of pH-dependent model electrified interfaces of TiO<sub>2</sub>(110) with HCl and NaOH using surface X-ray diffraction (SXRD). A comparison with ab initio molecular dynamics calculations reveals the formation of surprisingly compact double layers. These involve inner-sphere bound Cl and Na ions, with respectively H<sup>+</sup> and O<sup>-</sup>/OH<sup>-</sup> in the contact layer. Their exceptionally high electric fields will play a key role in determining the chemical reactivity.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-11-25
DOI
https://doi.org/10.1021/jacs.4c09911
Citations
4
Primary Topic
Electrochemical Analysis and Applications
Type
article
Field-Weighted Citation Impact
0.69

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article

Ultracompact Electrical Double Layers at TiO2(110) Electrified Interfaces

Matthew O. Blunt, Christopher Penschke, Axel Wilson, X. Torrelles et al.
4 citations
Journal of the American Chemical Society
Electrochemical Analysis and Applications
0.69
article

Ultracompact Electrical Double Layers at TiO2(110) Electrified Interfaces

Matthew O. Blunt, Christopher Penschke, Axel Wilson, X. Torrelles, Ji Chen, Angelos Michaelides, R. Lindsay, Christopher Nicklin, Hadeel Hussain, Immad M. Nadeem, G. Thornton, Grégory Cabailh, J. Zegenhagen, Oier Bikondoa
article en
4 citations

Abstract

Metal-oxide aqueous interfaces are important in areas as varied as photocatalysis and mineral reforming. Crucial to the chemistry at these interfaces is the structure of the electrical double layer formed when anions or cations compensate for the charge arising from adsorbed H<sup>+</sup> or OH<sup>-</sup>. This has proven extremely challenging to determine at the atomic level. In this work, we use a surface science approach, involving atomic level characterization, to determine the structure of pH-dependent model electrified interfaces of TiO<sub>2</sub>(110) with HCl and NaOH using surface X-ray diffraction (SXRD). A comparison with ab initio molecular dynamics calculations reveals the formation of surprisingly compact double layers. These involve inner-sphere bound Cl and Na ions, with respectively H<sup>+</sup> and O<sup>-</sup>/OH<sup>-</sup> in the contact layer. Their exceptionally high electric fields will play a key role in determining the chemical reactivity.

Journal of the American Chemical SocietyVol. 146(49)
Centre National de la Recherche Scientifique (FR), London Centre for Nanotechnology (GB), European Synchrotron Radiation Facility (FR), Diamond Light Source (GB), University of Manchester (GB), University of Warwick (GB), Sorbonne Université (FR), Institut de Ciència de Materials de Barcelona (ES), Institut des NanoSciences de Paris (FR), University College London (GB)
Alexander von Humboldt-Stiftung, Diamond Light Source, Ministerio de Ciencia e Innovación, Engineering and Physical Sciences Research Council, European Research Council
Affordable and clean energy
Openalex Percentile: Top 36%
Electrochemical Analysis and Applications
0.69
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