析氧
过电位
材料科学
镍
海水
电催化剂
电解
催化作用
氢氧化物
氯化物
分解水
无机化学
阳极
化学工程
冶金
电化学
化学
电极
海洋学
电解质
地质学
有机化学
工程类
物理化学
光催化
作者
Jin‐Tao Ren,Lei Chen,Wenwen Tian,Xin‐Lian Song,Qing‐Hui Kong,Hao‐Yu Wang,Zhong‐Yong Yuan
出处
期刊:Small
[Wiley]
日期:2023-03-25
卷期号:19 (27)
被引量:41
标识
DOI:10.1002/smll.202300194
摘要
Versatile electrocatalysis at higher current densities for natural seawater splitting to produce hydrogen demands active and robust catalysts to overcome the severe chloride corrosion, competing chlorine evolution, and catalyst poisoning. Hereto, the core-shell-structured heterostructures composed of amorphous NiFe hydroxide layer capped Ni3 S2 nanopyramids which are directly grown on nickel foam skeleton (NiS@LDH/NF) are rationally prepared to regulate cooperatively electronic structure and mass transport for boosting oxygen evolution reaction (OER) performance at larger current densities. The prepared NiS@LDH/NF delivers the anodic current density of 1000 mA cm-2 at the overpotential of 341 mV in 1.0 m KOH seawater. The feasible surface reconstruction of Ni3 S2 -FeNi LDH interfaces improves the chemical stability and corrosion resistance, ensuring the robust electrocatalytic activity in seawater electrolytes for continuous and stable oxygen evolution without any hypochlorite production. Meanwhile, the designed Ni3 S2 nanopyramids coated with FeNi2 P layer (NiS@FeNiP/NF) still exhibit the improved hydrogen evolution reaction (HER) activity in 1.0 m KOH seawater. Furthermore, the NiS@FeNiP/NF||NiS@LDH/NF pair requires cell voltage of 1.636 V to attain 100 mA cm-2 with a 100% Faradaic efficiency, exhibiting tremendous potential for hydrogen production from seawater.
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