High-performance transition metal–doped Pt 3 Ni octahedra for oxygen reduction reaction

Author:

Huang Xiaoqing12,Zhao Zipeng12,Cao Liang3,Chen Yu12,Zhu Enbo12,Lin Zhaoyang4,Li Mufan4,Yan Aiming567,Zettl Alex567,Wang Y. Morris8,Duan Xiangfeng24,Mueller Tim9,Huang Yu12

Affiliation:

1. Department of Materials Science and Engineering, University of California, Los Angeles, CA 90095, USA.

2. California NanoSystems Institute (CNSI), University of California, Los Angeles, CA 90095, USA.

3. Department of Physics and Astronomy, Johns Hopkins University, Baltimore, MD 21218, USA.

4. Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.

5. Department of Physics and Center of Integrated Nanomechanical Systems, University of California, Berkeley, CA 94720, USA.

6. Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

7. Kavli Energy NanoSciences Institute at the University of California, Berkeley, and the Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

8. Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory (LLNL), Livermore, CA 94550, USA.

9. Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Abstract

Molybdenum doping drives high activity Platinum (Pt) is an effective catalyst of the oxygen reduction reaction in fuel cells but is scarce. One approach to extend Pt availability is to alloy it with more abundant metals such as nickel (Ni). Although these catalysts can be highly active, they are often not durable because of Ni loss. Huang et al. show that doping the surface of octahedral Pt 3 Ni nanocrystals with molybdenum not only leads to high activity (∼80 times that of a commercial catalyst) but enhances their stability. Science , this issue p. 1230

Funder

National Science Foundation

NSF

Office of Naval Research

Extreme Science and Engineering Development Environment

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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