纳米颗粒
杂原子
分解水
催化作用
析氧
黄铁矿
电子转移
氧气
氢
化学
化学工程
材料科学
无机化学
电化学
纳米技术
光化学
矿物学
物理化学
光催化
有机化学
电极
工程类
戒指(化学)
作者
Wenpin Wang,Weijie Wang,Yue Xu,Xiaoxuan Ren,Xien Liu,Zhongcheng Li
标识
DOI:10.1016/j.apsusc.2021.149985
摘要
Construction of bi-functional noble metal-free catalysts with low cost and high efficiency is greatly desired for hydrogen and oxygen evolution reactions. It is of vital importance to regulate the surface electron state of pyrite to improve the electrocatalytic performance towards overall water splitting. In this work, we provide a simple one-pot interface-regulated strategy to synthesize Ni3S4/NiS2/FeS2 nanoparticles with exposed interfacial structures between Ni-S and Fe-S, which can then affect the conductivity and activity of pyrite. Notably, Ni3S4/NiS2/FeS2 nanoparticles are highly active in the hydrogen evolution reaction with 197 mV at 10 mA/cm2. Superior oxygen evolution activity is observed for Ni3S4/NiS2/FeS2 nanoparticles with 1.46 V at 10 mA/cm2, outperforming RuO2 with 1.54 V. Impressively, Ni3S4/NiS2/FeS2 nanoparticles could efficiently drive water splitting into hydrogen and oxygen at a voltage of 1.68 V at 10 mA/cm2 in a two-electrode configuration and robust long-term stability was verified by continuous 20 h i-t tests without apparent loss in the current density. The outstanding catalytic activity could be traced back to the presence of interfacial structures between Ni-S and Fe-S. This work highlights that engineering heteroatoms into pyrite that can trigger the generation of interfacial structures, which beneficially accelerates electron transfer during the water splitting process.
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