Dealloying-directed synthesis of efficient mesoporous CoFe-based catalysts towards the oxygen evolution reaction and overall water splitting. Issue 42 (24th October 2017)

• Record Type: Journal Article
• Authors: Han, Lulu; Dong, Chaoqun; Zhang, Chi; Gao, Yulai; Zhang, Jie; Gao, Hui; Wang, Ying; Zhang, Zhonghua
• Is Part Of: Nanoscale. Volume 9:Issue 42(2017)
• Page Start: 16467
• Page End: 16475
• Publication Date: 2017-10-24
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c7nr06254k
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : We propose a facile one-step dealloying strategy to synthesize mesoporous CoFe-based nanomaterials as efficient water splitting electrocatalysts. Abstract : 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.