过电位
镍
分解水
吸附
催化作用
制氢
材料科学
化学工程
磷化物
无定形固体
电化学
双功能
氢
歧化
化学
冶金
物理化学
电极
结晶学
工程类
光催化
有机化学
生物化学
作者
Xinyu Wei,Changwu Wan,Yi Zhang,Qin Zhong,Hongxia Qu
标识
DOI:10.1016/j.ijhydene.2023.06.039
摘要
Through a simple redox reaction, the precursor of Ni (OH)2 mixed with SnO2 was in situ transformed into a core-shell structure with elemental Ni blend SnO2 as the core and nickel metaborate as the shell. The metaborate shell is an excellent adsorption site for water molecules, which paves the way for subsequent hydride adsorption. When a small amount of SnO2 is mixed with elemental Ni, the electronic structure is optimized, and the electron enrichment of Ni is realized, making the hydrogen adsorption performance better. This core-shell synergy promotes the Vomer step in HER, thereby enhancing HER performance. In addition, Ni–Sn@NiBO/NF possesses larger electrochemical surface area and smaller charge transfer resistance. Only an overpotential of 22 mV is needed to drive a current density of 10 mA cm−2, indicating the excellent HER performance of the Ni–Sn@NiBO/NF catalyst. At high current density of 50 mA cm−2, the overpotential is only 79 mV. When Ni–Sn@NiBO/NF is used as the bifunctional catalyst for coupling HER and OER, the voltage is only 1.595 V at 10 mA cm−2. It shows that the catalyst has great application potential in electrocatalytic water decomposition to produce hydrogen.
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