电催化剂
过电位
材料科学
分解水
析氧
催化作用
多孔性
电子转移
阳极
化学工程
电化学
物理化学
电极
复合材料
光催化
工程类
生物化学
化学
作者
Kai Wan,Jiangshui Luo,Chen Zhou,Ting Zhang,Jordi Arbiol,Xihong Lu,Bing‐Wei Mao,Xuan Zhang,Jan Fransaer
标识
DOI:10.1002/adfm.201900315
摘要
Abstract Electrochemical water splitting is a common way to produce hydrogen gas, but the sluggish kinetics of the oxygen evolution reaction (OER) significantly limits the overall energy conversion efficiency of water splitting. In this work, a highly active and stable, meso–macro hierarchical porous Ni 3 S 4 architecture, enriched in Ni 3+ is designed as an advanced electrocatalyst for OER. The obtained Ni 3 S 4 architectures exhibit a relatively low overpotential of 257 mV at 10 mA cm −2 and 300 mV at 50 mA cm −2 . Additionally, this Ni 3 S 4 catalyst has excellent long‐term stability (no degradation after 300 h at 50 mA cm −2 ). The outstanding OER performance is due to the high concentration of Ni 3+ and the meso–macro hierarchical porous structure. The presence of Ni 3+ enhances the chemisorption of OH − , which facilitates electron transfer to the surface during OER. The hierarchical porosity increases the number of exposed active sites, and facilitates mass transport. A water‐splitting electrolyzer using the prepared Ni 3 S 4 as the anode catalyst and Pt/C as the cathode catalyst achieves a low cell voltage of 1.51 V at 10 mA cm −2 . Therefore, this work provides a new strategy for the rational design of highly active OER electrocatalysts with high valence Ni 3+ and hierarchical porous architectures.
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