Highly Crystalline Multimetallic Nanoframes with Three-Dimensional Electrocatalytic Surfaces

Author:

Chen Chen123,Kang Yijin4,Huo Ziyang12,Zhu Zhongwei12,Huang Wenyu12,Xin Huolin L.2,Snyder Joshua D.4,Li Dongguo4,Herron Jeffrey A.5,Mavrikakis Manos5,Chi Miaofang6,More Karren L.6,Li Yadong3,Markovic Nenad M.4,Somorjai Gabor A.12,Yang Peidong1278,Stamenkovic Vojislav R.4

Affiliation:

1. Department of Chemistry, University of California, Berkeley, CA 94720, USA.

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

3. Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China.

4. Materials Science Division, Argonne National Laboratory, Argonne, IL 60439, USA.

5. Department of Chemical and Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.

6. Division of Materials Science and Technology, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.

7. Department of Chemistry, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia.

8. Kavli Energy NanoSciences Institute at the University of California, Berkeley, and Lawrence Berkeley National Laboratory, Berkeley, CA 94704, USA.

Abstract

Giving Electrocatalysts an Edge Platinum (Pt) is an excellent catalyst for the oxygen-reduction reaction (ORR) in fuel cells and electrolyzers, but it is too expensive and scarce for widespread deployment, even when dispersed as Pt nanoparticles on carbon electrode supports (Pt/C). Alternatively, Chen et al. (p. 1339 , published online 27 February; see the Perspective by Greer ) made highly active ORR catalysts by dissolving away the interior of rhombic dodecahedral PtNi 3 nanocrystals to leave Pt-rich Pt 3 Ni edges. These nanoframe catalysts are durable—remaining active after 10,000 rounds of voltage cycling—and are far more active than Pt/C.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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