Bai Jie, Zhou Tianning, Gao Yihao, Zhang Meilin, Jing Xiaofei, Gong Yaqiong
School of Chemical Engineering and Technology, North University of China, Taiyuan, Shanxi, 030051, China.
Key Lab Polyoxometalate Sci, Minist Educ, Northeast Normal University, Changchun, 130024, China.
Dalton Trans. 2022 Mar 22;51(12):4853-4861. doi: 10.1039/d1dt04224f.
Due to the slow reaction kinetics of the oxygen evolution reaction (OER), the electrolysis rate of water is greatly limited. Therefore, it is of great significance to study stable and efficient non-noble metal based electrocatalysts. In this paper, three-dimensional (3D) spherical V-NiFe LDH@NiS was developed by exquisitely decorating ultra-thin V-doped NiFe layered dihydroxide (NiFe-LDH) on NiS nanosheets supported by nickel foam (NF). It is worth mentioning that V-NiFe LDH@NiS exhibits an excellent electrocatalytic performance and only 178 mV overpotential is required in 1 M KOH to achieve a current density of 10 mA cm. Long-term chronoamperometry manifests its superior electrochemical stability. The combination of NiFe LDH and conductive substrate coupling can drastically afford abundant active sites and accelerate charge transfer, and V doping can markedly regulate the electronic structure. Therefore, the activity and durability of the electrocatalysts are greatly improved. This study may provide a new strategy for the preparation of efficient OER electrocatalysts.
由于析氧反应(OER)的反应动力学缓慢,水的电解速率受到极大限制。因此,研究稳定高效的非贵金属基电催化剂具有重要意义。本文通过在泡沫镍(NF)负载的NiS纳米片上精细修饰超薄V掺杂的NiFe层状双氢氧化物(NiFe-LDH),制备了三维(3D)球形V-NiFe LDH@NiS。值得一提的是,V-NiFe LDH@NiS表现出优异的电催化性能,在1 M KOH中仅需178 mV的过电位即可实现10 mA cm的电流密度。长期计时电流法表明其具有优异的电化学稳定性。NiFe LDH与导电基底的耦合能够大幅提供丰富的活性位点并加速电荷转移,而V掺杂能够显著调节电子结构。因此,电催化剂的活性和耐久性得到了极大提高。本研究可能为制备高效OER电催化剂提供一种新策略。