摘要
In order to solve the problem of environmental pollution caused by fossil fuel emissions, electrocatalytic overall water splitting is a very promising energy conversion device. In the field of large-scale overall water splitting, it is particularly important to develop new non-precious metal electrocatalysts. In this paper, we successfully prepared CoFe@Co 2 C@Co/NF by hydrothermal synthesis of CoFe-LDH as the precursor and small molecule amine ethylenediamine as the C source. CoFe@Co 2 [email protected] /NF shows excellent electrocatalytic performance in alkaline environment. CoFe@Co 2 [email protected] /NF can provide low overpotential of 53 mV and 246 mV to reach 10 mA cm −2 current density in hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. In addition, CoFe@Co 2 [email protected] /NF was used as the anode and cathode of the electrolytic cell system for overall water splitting, and the current density of 10 mA cm −2 can be reached with a voltage of only 1.57 V, which is superior to the commercial electrolytic cell system composed of Pt/C and RuO 2 . The material exhibits a good coupling effect of soft and hard magnetic exchange. This provides new insights into the development of transition metal carbides as high-performance electrocatalysts.
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