Abstract
The development of efficient, durable and low cost electrocatalysts is crucial but extremely challenging for the oxygen evolution reaction (OER). Herein, we develop a self-template strategy to synthesize hollow Fe-doped CoP prisms (Fe-CoP) via ion exchange of cobalt acetate hydroxide with [Fe(CN)6]3- and phosphorization-induced transformation of CoFe-PBA (Co/Fe-containing prussian blue analogue) prisms in N2 atmosphere. The obtained Fe-CoP not only inherits the hollow prism-like morphology of CoFe-PBA, but also forms rich mesoporous channel. The Fe-CoP prisms exhibit extraordinary OER performances in 1.0 M KOH, with a low overpotential of 236 mV to deliver a current density of 10 mA cm−2 and a low Tafel slope of 32.9 mV dec–1. Moreover, the presented electrocatalyst shows good long-term operating durability and activity. The XPS and TEM analysis confirm that Fe-CoP has undergone surface reconstruction in the process of electrocatalytic OER, and the in situ formed oxides and oxyhydroxides are the real active species to boost OER. This work provides a promising pathway to the design and synthesis of efficient and robust electrocatalysts with hierarchical hollow structure for boosting OER.
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