Covalency-reinforced oxygen evolution reaction catalyst

Shunsuke Yagi(Osaka Prefecture University), Ikuya Yamada(Osaka Prefecture University), Hirofumi Tsukasaki(Osaka Prefecture University), Akihiro Seno(Osaka Prefecture University), Makoto Murakami(Osaka Prefecture University), Hiroshi Fujii(Osaka Prefecture University), Hungru Chen(National Institute for Materials Science), Naoto Umezawa(National Institute for Materials Science), Hideki Abe(National Institute for Materials Science), Norimasa Nishiyama(Deutsches Elektronen-Synchrotron DESY), Shigeo Mori(Osaka Prefecture University)
Nature Communications
September 10, 2015
Cited by 535Open Access
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Abstract

The oxygen evolution reaction that occurs during water oxidation is of considerable importance as an essential energy conversion reaction for rechargeable metal-air batteries and direct solar water splitting. Cost-efficient ABO3 perovskites have been studied extensively because of their high activity for the oxygen evolution reaction; however, they lack stability, and an effective solution to this problem has not yet been demonstrated. Here we report that the Fe(4+)-based quadruple perovskite CaCu3Fe4O12 has high activity, which is comparable to or exceeding those of state-of-the-art catalysts such as Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-δ) and the gold standard RuO2. The covalent bonding network incorporating multiple Cu(2+) and Fe(4+) transition metal ions significantly enhances the structural stability of CaCu3Fe4O12, which is key to achieving highly active long-life catalysts.


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