过电位
海水
电解质
析氧
无机化学
磷酸盐
吸附
催化作用
分解水
选择性
材料科学
磷化物
化学工程
化学
电极
电化学
海洋学
地质学
有机化学
工程类
物理化学
光催化
作者
Tianshui Li,Zhao Xiu-ping,Marshet Getaye Sendeku,Xingheng Zhang,Ling Xu,Zhaolei Wang,Shiyuan Wang,Xinxuan Duan,Hai Liu,Wei Liu,Daojin Zhou,Haijun Xu,Yun Kuang,Xiaoming Sun
标识
DOI:10.1016/j.cej.2023.141413
摘要
Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV@10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte.
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