纳米片
分解水
析氧
阳极
催化作用
阴极
化学
材料科学
无机化学
热液循环
镍
电化学
纳米技术
化学工程
光催化
物理化学
电极
冶金
生物化学
工程类
作者
Chenyi Zhang,Xiaoqiang Du,Xiaoshuang Zhang,Yanhong Wang
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2022-12-14
卷期号:52 (3): 763-773
被引量:10
摘要
Here, we synthesized a series of Ni3S2/MxSy-NiCo LDH materials (M = Cu, Fe, V, Ce, and Bi) by a two-step hydrothermal method for the first time, which display excellent oxygen evolution reaction (OER) and urea oxidation reaction (UOR) properties. M (M = Cu, Fe, V, Ce, and Bi) ions were firstly doped into NiCo LDH to change the original electronic structure and enhance the activity of the LDH. Then, Ni3S2 and MxSy were introduced by sulfurization of the Ni support and doping cations, and the combination of Ni3S2, MxSy and NiCo-LDH improved the electron transfer rate and activity of the original material. With Ni3S2/Bi2S3-NiCo LDH/NF as anode and Ni3S2/CuS-NiCo LDH as cathode, an electrolytic cell can reach 10 mA cm-2 at 1.622 V with outstanding durability for overall water splitting. In addition, with Ni3S2/Bi2S3-NiCo LDH/NF as both electrodes, it can reach 10 mA cm-2 at 1.56 V with outstanding durability for overall urea splitting, which is better than that of the overall water splitting. Density functional theory (DFT) calculation shows that the superior electrocatalytic activity can be explained by the water adsorption energy being optimized and enhanced conductivity. This study provides a new idea for improving the catalytic activity and stability of non-noble metals instead of noble metals.
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