Boosting Bifunctional Catalysis by Integrating Active Faceted Intermetallic Nanocrystals and Strained Pt–Ir Functional Shells

Author:

Zhu Shiyu1,Liu Yun2,Gong Yue3,Sun Yuting1,Chen Kang1,Liu Yuan1,Liu Weidi4,Xia Tianyu1,Zheng Qiang3,Gao Han1ORCID,Guo Haizhong15ORCID,Wang Rongming6

Affiliation:

1. Key Laboratory of Materials Physics Ministry of Education School of Physics and Microelectronics Zhengzhou University Zhengzhou 450052 China

2. Zhongyuan Critical Metals Laboratory School of Chemical Engineering Zhengzhou University Zhengzhou 450052 China

3. CAS Key Laboratory of Standardization and Measurement for Nanotechnology CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology Beijing 100190 China

4. Australian Institute for Bioengineering and Nanotechnology the University of Queensland ST Lucia QLD 4072 Australia

5. Institute of Quantum Materials and Physics Henan Academy of Sciences Zhengzhou 450046 China

6. Beijing Advanced Innovation Center for Materials Genome Engineering Beijing Key Laboratory for Magneto‐Photoelectrical Composite and Interface Science School of Mathematics and Physics University of Science and Technology Beijing Beijing 100083 China

Abstract

AbstractPtIr‐based nanostructures are fascinating materials for application in bifunctional oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) catalysis. However, the fabrication of PtIr nanocatalysts with clear geometric features and structural configurations, which are crucial for enhancing the bifunctionality, remains challenging. Herein, PtCo@PtIr nanoparticles are precisely designed and fabricated with a quasi‐octahedral PtCo nanocrystal as a highly atomically ordered core and an ultrathin PtIr atomic layer as a compressively strained shell. Owing to their geometric and core–shell features, the PtCo@PtIr nanoparticles deliver approximately six and eight times higher mass and specific activities, respectively, as an ORR catalyst than a commercial Pt/C catalyst. The half‐wave potential of PtCo@PtIr exhibits a negligible decrease by 9 mV after 10 000 cycles, indicating extraordinary ORR durability because of the ordered arrangement of Pt and Co atoms. When evaluated using the ORR–OER dual reaction upon the introduction of Ir, PtCo@PtIr exhibits a small ORR–OER overpotential gap of 679 mV, demonstrating its great potential as a bifunctional electrocatalyst for fabricating fuel cells. The findings pave the way for designing precise intermetallic core–shell nanocrystals as highly functional catalysts.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Natural Science Foundation of Beijing Municipality

Natural Science Foundation of Henan Province

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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