Lewis Acid Sites Assisted PtCu/CeO<sub>2</sub>‐C Enabling High‐Performance for Oxygen Reduction

Improvement in the durable and active low-Pt nanocatalysts for oxygen reduction reaction (ORR) is the essential target for clean energy. Herein, an efficient CeO<sub>2</sub> supported PtCu alloy catalyst (PtCu/CeO<sub>2</sub>-C) for ORR in acid media is developed. The CeO<sub>2</sub> support can effectively anchor the PtCu particles and inhibit their migration during the long-life cycling, which is beneficial to the catalytic performance. According to the electrochemical experiments, the specific and mass activities of PtCu/CeO<sub>2</sub>-C are 1.09 mA cm<sup>-2</sup> and 0.49 A mg<sub>Pt</sub> <sup>-1</sup> at 0.9 V, which are 9.9 and 6.1 times as large as that of Pt/C, demonstrating its outstanding ORR activities in acid media. Moreover, the theoretical studies confirm that oxygen vacancies (V<sub>O</sub>) as Lewis acid sites can facilitate the adsorption and dissociation of O<sub>2</sub>, regulate the electronic structure of Pt, and thus endow PtCu/CeO<sub>2</sub>-C with an efficient 4-electron ORR pathway. The results suggest that the rational design of supported Pt-based catalysts is of great significance for efficient ORR reaction.

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Publication Details

Journal
Small
Published
2024-12-10
DOI
https://doi.org/10.1002/smll.202408391
Citations
3
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.31

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article

Lewis Acid Sites Assisted PtCu/CeO2‐C Enabling High‐Performance for Oxygen Reduction

Xiaojing Yang, Guichao Zhang, Zunming Lu, Beibei Li et al.
3 citations
Small
Electrocatalysts for Energy Conversion
0.31
article

Lewis Acid Sites Assisted PtCu/CeO2‐C Enabling High‐Performance for Oxygen Reduction

Xiaojing Yang, Guichao Zhang, Zunming Lu, Beibei Li, Lanlan Li, Xinghua Zhang, Yangyang Ren, Xiaofei Yu
article en
3 citations

Abstract

Improvement in the durable and active low-Pt nanocatalysts for oxygen reduction reaction (ORR) is the essential target for clean energy. Herein, an efficient CeO<sub>2</sub> supported PtCu alloy catalyst (PtCu/CeO<sub>2</sub>-C) for ORR in acid media is developed. The CeO<sub>2</sub> support can effectively anchor the PtCu particles and inhibit their migration during the long-life cycling, which is beneficial to the catalytic performance. According to the electrochemical experiments, the specific and mass activities of PtCu/CeO<sub>2</sub>-C are 1.09 mA cm<sup>-2</sup> and 0.49 A mg<sub>Pt</sub> <sup>-1</sup> at 0.9 V, which are 9.9 and 6.1 times as large as that of Pt/C, demonstrating its outstanding ORR activities in acid media. Moreover, the theoretical studies confirm that oxygen vacancies (V<sub>O</sub>) as Lewis acid sites can facilitate the adsorption and dissociation of O<sub>2</sub>, regulate the electronic structure of Pt, and thus endow PtCu/CeO<sub>2</sub>-C with an efficient 4-electron ORR pathway. The results suggest that the rational design of supported Pt-based catalysts is of great significance for efficient ORR reaction.

SmallVol. 21(5)
Hebei University of Technology (CN)
National Natural Science Foundation of China
Industry, innovation and infrastructure
Openalex Percentile: Top 51%
Electrocatalysts for Energy Conversion
0.31
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