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Synergistic Modulation of Active Sites and Charge Transport: N/S Co-doped C Encapsulated NiCo2O4/NiO Hollow Microrods for Boosting Oxygen Evolution Catalysis

塔菲尔方程 过电位 析氧 化学 电催化剂 非阻塞I/O 化学工程 催化作用 无机化学 纳米技术 电化学 电极 材料科学 物理化学 生物化学 工程类
作者
Yusheng Yuan,Liming Sun,Yinwei Li,Wenwen Zhan,Xiaojun Wang,Xiang Han
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:59 (6): 4080-4089 被引量:19
标识
DOI:10.1021/acs.inorgchem.0c00089
摘要

Developing high-efficiency and cost-effective electrocatalysts for the oxygen evolution reaction (OER) is crucial for various energy conversion systems. Herein, N/S co-doped C encapsulated hollow NiCo2O4/NiO hexagonal rods (HNHR@N/S-C) as the electrocatalysts for OER have been successfully prepared with rational control of structure and composition. Experimental and theoretical results have highlighted that the NiCo2O4/NiO heterojunction in the obtained electrocatalyst can provide abundant active Ni and Co sites for the OER, leading to the highly enhanced OER performance. Moreover, attributed to the hierarchical hollow structure, which can provide a large surface area, and the improved electric conductivity with a coating of the N/S co-doped carbon layer, which can facilitate charge transport during the catalytic processes, a remarkable OER activity over HNHR@N/S-C with a low overpotential (η) of 285 mV (at j = 10 mA cm–2) and a Tafel slope of 53.0 mV decade–1 has been achieved, which is comparable to that of the noble metal catalyst IrO2. Because of the protection of the N/S doped C layer coating, HNHR@N/S-C can also maintain the current density of 10 mA cm–2 for at least 12 h in alkaline media without obvious losses of activity.

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