In situ Cobalt–Cobalt Oxide/N-Doped Carbon Hybrids As Superior Bifunctional Electrocatalysts for Hydrogen and Oxygen Evolution

Remarkable hydrogen evolution reaction (HER) or superior oxygen evolution reaction (OER) catalyst has been applied in water splitting, however, utilizing a bifunctional catalyst for simultaneously generating H2 and O2 is still a challenging issue, which is crucial for improving the overall efficienc...

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Veröffentlicht in:Journal of the American Chemical Society 2015-02, Vol.137 (7), p.2688-2694
Hauptverfasser: Jin, Haiyan, Wang, Jing, Su, Diefeng, Wei, Zhongzhe, Pang, Zhenfeng, Wang, Yong
Format: Artikel
Sprache:eng
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Zusammenfassung:Remarkable hydrogen evolution reaction (HER) or superior oxygen evolution reaction (OER) catalyst has been applied in water splitting, however, utilizing a bifunctional catalyst for simultaneously generating H2 and O2 is still a challenging issue, which is crucial for improving the overall efficiency of water electrolysis. Herein, inspired by the superiority of carbon conductivity, the propitious H atom binding energy of metallic cobalt, and better OER activity of cobalt oxide, we synthesized cobalt–cobalt oxide/N-doped carbon hybrids (CoO x @CN) composed of Co0, CoO, Co3O4 applied to HER and OER by simple one-pot thermal treatment method. CoO x @CN exhibited a small onset potential of 85 mV, low charge-transfer resistance (41 Ω), and considerable stability for HER. Electrocatalytic experiments further indicated the better performance of CoO x @CN for HER can be attributed to the high conductivity of carbon, the synergistic effect of metallic cobalt and cobalt oxide, the stability of carbon-encapsulated Co nanoparticles, and the introduction of electron-rich nitrogen. In addition, when used as catalysts of OER, the CoO x @CN hybrids required 0.26 V overpotential for a current density of 10 mA cm–2, which is comparable even superior to many other non-noble metal catalysts. More importantly, an alkaline electrolyzer that approached ∼20 mA cm–2 at a voltage of 1.55 V was fabricated by applying CoO x @CN as cathode and anode electrocatalyst, which opened new possibilities for exploring overall water splitting catalysts.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja5127165