Dual synergistic effects between Co and Mo2C in Co/Mo2C heterostructure for electrocatalytic overall water splitting

对偶(语法数字) 分解水 催化作用 化学 异质结 材料科学 化学工程 环境科学 光催化 有机化学 光电子学 文学类 工程类 艺术
作者
Shisheng Yuan,Maosheng Xia,Zhipeng Liu,Kaiwen Wang,Lijuan Xiang,Guoqing Huang,Junyu Zhang,Nan Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:430: 132697-132697 被引量:177
标识
DOI:10.1016/j.cej.2021.132697
摘要

Molybdenum carbide (Mo2C) has emerged as a promising electrocatalyst for water splitting because of its Pt-like electronic structure. However, unsatisfactory Hydrogen evolution reaction (HER) activity and poor Oxygen evolution reaction (OER) stability are obstacles to its practical application. Herein, we designed a strategy to improve the electrocatalytic performance of Mo2C by constructing a Co and Mo2C heterostructure supported on carbon (Co/Mo2[email protected]). Experimental and theoretical calculations showed the significant improvements caused by the synergistic effects between Co and Mo2C. Electrons from Co could transfer to Mo2C and accumulate on Mo. This promoted the adsorption of H2O and desorption of H, which improved the HER. In contrast, the Co could inhibit the oxidation and dissolution of Mo2C through a “self-sacrifice” effect, which significantly improved the OER stability of Mo2C. Owing to the synergetic effects between Co and Mo2C, the as-synthesized catalyst exhibited superior electrocatalytic performances in an alkaline electrolyte, and afforded low overpotentials of 98 and 254 mV at 10 mA cm−2 for catalyzing the HER and OER, respectively. Moreover, Co/Mo2[email protected] enabled overall water splitting at a cell voltage of 1.59 V, to achieve a current density of 10 mA cm−2 with an exceptional electrochemical stability that outperformed noble-metal catalysts.
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