Self-supported Co/CoO anchored on N-doped carbon composite as bifunctional electrocatalyst for efficient overall water splitting

双功能 电催化剂 分解水 析氧 碳化 化学工程 催化作用 电化学 材料科学 电解 化学 碳纤维 无机化学 复合数 电极 物理化学 电解质 复合材料 有机化学 工程类 光催化 扫描电子显微镜
作者
Kaiqing Dai,Ning Zhang,Lili Zhang,Lin-Xin Yin,Yafei Zhao,Bing Zhang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:414: 128804-128804 被引量:156
标识
DOI:10.1016/j.cej.2021.128804
摘要

Designing a non-noble metal-based bifunctional electrocatalyst for simultaneously boosting both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is highly desirable, which is decisive for enhancing the efficiency of overall water splitting. Herein, inspired by the appropriate H atoms binding energy of Co metal, favorable OER reaction kinetics of cobalt oxides, and more efficient electron transfer of self-supported structure, Co/CoO anchored on N-doped carbon layer coated on carbon cloth (Co/[email protected]@CC) is synthesized by a facile self-assembly-carbonization method. Remarkably, the Co/[email protected]@CC exhibits much increased electrochemical activities toward both OER and HER with low overpotentials of 284 and 152 mV required to deliver the current density of 10 mA cm−2, respectively, which are superior to most of the reported Co-based and CoO-based catalysts. More importantly, the fabricated Co/[email protected]@CC‖ Co/[email protected]@CC electrolyzer only needs a small cell voltage of 1.66 V for driving overall water splitting to achieve the current density of 10 mA cm−2. Moreover, the Co/[email protected]@CC behaves superior stability after 25 h of continuous operation. Excellent features including the synergistic effect between Co and CoO, unique hierarchical porous structure, and self-supported construction jointly impart Co/[email protected]@CC highly elevated bifunctional electrocatalytic activities.
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