Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells

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作者
Ying Wang
Yao Yang
Shuangfeng Jia
Xiaoming Wang
Kangjie Lyu
Yanqiu Peng
He Zheng
Xing Wei
Huan Ren
Li Xiao
Jianbo Wang
David A. Muller
Héctor D. Abruña
Bing Joe Hwang
Juntao Lu
Lin Zhuang
机构
[1] Wuhan University,College of Chemistry and Molecular Sciences, Hubei Key Lab of Electrochemical Power Sources
[2] Wuhan University,The Institute for Advanced Studies
[3] Cornell University,Department of Chemistry and Chemical Biology, Baker Lab
[4] Ithaca,School of Physics and Technology, Center for Electron Microscopy, MOE Key Laboratory of Artificial Studies
[5] Wuhan University,Department of Chemical Engineering
[6] National Taiwan University of Science and Technology,School of Applied and Engineering Physics
[7] Cornell University,undefined
[8] Ithaca,undefined
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摘要
Alkaline polymer electrolyte fuel cells are a class of fuel cells that enable the use of non-precious metal catalysts, particularly for the oxygen reduction reaction at the cathode. While there have been alternative materials exhibiting Pt-comparable activity in alkaline solutions, to the best of our knowledge none have outperformed Pt in fuel-cell tests. Here we report a Mn-Co spinel cathode that can deliver greater power, at high current densities, than a Pt cathode. The power density of the cell employing the Mn-Co cathode reaches 1.1 W cm−2 at 2.5 A cm−2 at 60 oC. Moreover, this catalyst outperforms Pt at low humidity. In-depth characterization reveals that the remarkable performance originates from synergistic effects where the Mn sites bind O2 and the Co sites activate H2O, so as to facilitate the proton-coupled electron transfer processes. Such an electrocatalytic synergy is pivotal to the high-rate oxygen reduction, particularly under water depletion/low humidity conditions.
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