Affiliation:
1. National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei 230029 P. R. China
2. Institutes of Physical Science and Information Technology Anhui University Hefei 230601 P. R. China
Abstract
AbstractThe construction and understanding of synergy in well‐defined dual‐atom active sites is an available avenue to promote multistep tandem catalytic reactions. Herein, we construct a dual‐hetero‐atom catalyst that comprises adjacent Cu‐N4and Se‐C3active sites for efficient oxygen reduction reaction (ORR) activity.OperandoX‐ray absorption spectroscopy coupled with theoretical calculations provide in‐depth insights into this dual‐atom synergy mechanism for ORR under realistic device operation conditions. The heteroatom Se modulator can efficiently polarize the charge distribution around symmetrical Cu‐N4moieties, and serve as synergistic site to facilitate the second oxygen reduction step simultaneously, in which the key OOH*‐(Cu1‐N4) transforms to O*‐(Se1‐C2) intermediate on the dual‐atom sites. Therefore, this designed catalyst achieves satisfied alkaline ORR activity with a half‐wave potential of 0.905 V vs. RHE and a maximum power density of 206.5 mW cm−2in Zn‐air battery.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Youth Innovation Promotion Association of the Chinese Academy of Sciences
Fundamental Research Funds for the Central Universities
Subject
General Chemistry,Catalysis
Cited by
45 articles.
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