期刊
NANOSCALE
卷 9, 期 42, 页码 16467-16475出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nr06254k
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资金
- National Natural Science Foundation of China [51371106, 51671115, 51671123]
- Young Tip-top Talent Support Project (Organization Department of the Central Committee of the CPC)
- Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning [TP2014042]
It is a great challenge to design highly active, stable and low-cost catalysts for electrochemically splitting water to realize the clean energy generation and renewable energy storage. Herein, a facile one-step dealloying strategy was proposed to synthesize mesoporous CoFe-based oxides and layered double hydroxides (LDHs). Benefitting from the fast mass transfer and more active sites caused by the open mesoporous structure, the CoFe-based materials exhibit excellent electrocatalytic activities and stability towards the oxygen evolution reaction (OER) in an alkaline electrolyte (1 M KOH). The CoFe-LDH catalyst only needs an overpotential of 0.286 V to achieve 10 mA cm(-2), and a small Tafel slope of 45 mV dec(-1) for the OER. Moreover, an alkaline electrolyzer was constructed with the CoFe-LDH as both the anode and cathode. The electrolyzer delivers a current density of 10 mA cm (2) at a voltage of 1.69 V toward overall water splitting in the 1 M KOH solution.
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