异质结
材料科学
纤锌矿晶体结构
同质结
肖特基势垒
三元运算
光催化
载流子
相(物质)
电子转移
纳米技术
化学工程
光电子学
催化作用
物理化学
锌
化学
二极管
生物化学
有机化学
计算机科学
工程类
冶金
程序设计语言
作者
Qiqi Zhang,Zhen Wang,Yuhang Song,Jun Fan,Tao Sun,Enzhou Liu
标识
DOI:10.1016/j.jmst.2023.05.066
摘要
Effective bulk phase and surface charge separation is critical for charge utilization during the photocatalytic energy conversion process. In this work, the ternary Ni2P-NiS/twinned Mn0.5Cd0.5S (T-MCS) nanohybrids were successfully constructed via combining Ni2P-NiS with T-MCS solid solution for visible light photocatalytic H2 evolution. T-MCS is composed of zinc blende Mn0.5Cd0.5S (ZB-MCS) and wurtzite Mn0.5Cd0.5S (WZ-MCS) and those two alternatively arranged crystal phases endow T-MCS with excellent bulk phase charge separation performance for the slight energy level difference between ZB-MCS and WZ-MCS. S-scheme carriers transfer route between NiS and T-MCS can accelerate the interfacial charge separation and retain the active electrons and holes, meanwhile, co-catalyst Ni2P as electron receiver and proton reduction center can further optimize the H2 evolution reaction kinetics based on the surface Schottky barrier effect. The above-formed homo-heterojunctions can establish multiple charge transfer channels in the bulk phase of T-MCS and interface of T-MCS and Ni2P-NiS. Under the synergistic effect of twinned homojunction, S-scheme heterojunction, and Schottky barrier, the ternary Ni2P-NiS/T-MCS composite manifested an H2 production rate of 122.5 mmol h–1 g–1, which was 1.33, 1.24, and 2.58 times higher than those of the NiS/T-MCS (92.4 mmol h–1 g–1), Ni2P/T-MCS (98.4 mmol h–1 g–1), and T-MCS (47.5 mmol h–1 g–1), respectively. This work demonstrates a promising strategy to develop efficient sulfides photocatalyst toward targeted solar-driven H2 evolution through homo-heterojunction engineering.
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