Spatial Identification of Mott–Schottky Effect at Electrocatalytic Pd/Metal Oxide Interfaces for the Oxygen Reduction Reaction

To elucidate the microstructure and charge transfer behavior at the interface of Pd/metal oxide semiconductor (MOS) catalysts and systematically explore the crucial role of the Mott-Schottky effect in the oxygen reduction reaction (ORR) electrocatalysis process, this study established a testing system for spatially identifying Mott-Schottky effects and electronic properties at Pd/MOS interfaces, leveraging highly sensitive Kelvin probe force microscopy (KPFM). This system enabled visualization and quantification of the surface potential difference and Mott-Schottky barrier height (Φ<sub>SBH</sub>) at the Pd/MOS heterojunction interfaces. Furthermore, a series of Pd/MOS Mott-Schottky catalysts were constructed based on differences in work functions between Pd and n-type MOS. The abundant oxygen vacancies in these catalysts facilitated the adsorption and activation of oxygen molecules. Notably, the intensity of the built-in electric field in the Pd/MOS Mott-Schottky catalysts was calculated through surface potential and zeta potential analysis, systematically correlating the Mott-Schottky effect at the heterojunction interface of Pd/MOS with ORR activity and kinetics. By comprehensively exploring the correlation between the Mott-Schottky effect and ORR performance in Pd/MOS catalysts using the KPFM testing system, this study provides necessary tools and approaches for a deep understanding of heterogeneous interface charge transfer mechanisms, as well as for optimizing catalyst design and enhancing ORR performance.

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Publication Details

Journal
ACS Nano
Published
2024-08-20
DOI
https://doi.org/10.1021/acsnano.4c06049
Citations
30
Primary Topic
Electrochemical Analysis and Applications
Type
article
Field-Weighted Citation Impact
5.17

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article

Spatial Identification of Mott–Schottky Effect at Electrocatalytic Pd/Metal Oxide Interfaces for the Oxygen Reduction Reaction

Qinggang He, Shiyuan Chen, Miao Wang, Jing He et al.
30 citations
ACS Nano
Electrochemical Analysis and Applications
5.17
article

Spatial Identification of Mott–Schottky Effect at Electrocatalytic Pd/Metal Oxide Interfaces for the Oxygen Reduction Reaction

Qinggang He, Shiyuan Chen, Miao Wang, Jing He, Zhuang Ma
article en
30 citations

Abstract

To elucidate the microstructure and charge transfer behavior at the interface of Pd/metal oxide semiconductor (MOS) catalysts and systematically explore the crucial role of the Mott-Schottky effect in the oxygen reduction reaction (ORR) electrocatalysis process, this study established a testing system for spatially identifying Mott-Schottky effects and electronic properties at Pd/MOS interfaces, leveraging highly sensitive Kelvin probe force microscopy (KPFM). This system enabled visualization and quantification of the surface potential difference and Mott-Schottky barrier height (Φ<sub>SBH</sub>) at the Pd/MOS heterojunction interfaces. Furthermore, a series of Pd/MOS Mott-Schottky catalysts were constructed based on differences in work functions between Pd and n-type MOS. The abundant oxygen vacancies in these catalysts facilitated the adsorption and activation of oxygen molecules. Notably, the intensity of the built-in electric field in the Pd/MOS Mott-Schottky catalysts was calculated through surface potential and zeta potential analysis, systematically correlating the Mott-Schottky effect at the heterojunction interface of Pd/MOS with ORR activity and kinetics. By comprehensively exploring the correlation between the Mott-Schottky effect and ORR performance in Pd/MOS catalysts using the KPFM testing system, this study provides necessary tools and approaches for a deep understanding of heterogeneous interface charge transfer mechanisms, as well as for optimizing catalyst design and enhancing ORR performance.

ACS NanoVol. 18(35)
Zhejiang University of Technology (CN), Zhejiang University (CN)
National Natural Science Foundation of China, China Southern Power Grid
Openalex Percentile: Top 2%
Electrochemical Analysis and Applications
5.17
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