纳米片
析氧
材料科学
塔菲尔方程
石墨烯
过电位
电催化剂
氢氧化物
氧化物
化学工程
分解水
电解质
无机化学
纳米技术
层状双氢氧化物
电化学
电极
催化作用
化学
冶金
有机化学
物理化学
工程类
光催化
作者
Yin Xiong,Yani Hua,Zhan Gao
标识
DOI:10.1016/j.est.2023.109102
摘要
The application of NiFe-layered double hydroxide (NiFe-LDH) as electrocatalysts for oxygen evolution reaction (OER) is seriously limited owing to low conductivity, insufficient active sites and self-aggregation. The construction of anion-doped NiFe-LDH nanoarray structures with ideal electrochemical activity is an effective strategy. Herein, we report a facile solvothermal approach for the synthesis of S-doped NiFe-LDH nanosheets loaded in situ on porous reduced graphene oxide (rGO) to form a composite with nanosheet array structure (S-NiFe-LDH/rGO) for OER. The S-NiFe-LDH/rGO nanosheet array ensures a large specific surface area, abundant accessible active sites and high stability. The moderate S doping in NiFe-LDH can tune the local electronic structures of Ni and Fe to optimize the binding of metal sites with reaction intermediates, thus enhancing the OER activity. The S-NiFe-LDH/rGO electrocatalyst shows the small OER overpotential of 264 mV at 10 mA cm−2 and the low Tafel slope of 55 mV dec−1. Moreover, S-NiFe-LDH/rGO displays good durability and structural stability due to the strong anchoring effect. The assembled two-electrode S-NiFe-LDH/rGO||Pt electrolytic cell exhibits a low cell voltage of 1.53 V at 10 mA cm−2, which is superior to the RuO2||Pt benchmark cell (1.60 V), indicating the practical feasibility for water electrolysis. This design strategy provides a promising insight into the fabrication of advanced OER non-noble metal electrocatalysts.
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