光催化
石墨氮化碳
异质结
贵金属
材料科学
分解水
化学工程
金属
氮化碳
催化作用
氧化还原
载流子
纳米技术
氮化物
可见光谱
化学
光电子学
有机化学
冶金
工程类
图层(电子)
作者
Hui Zhao,Zhifeng Jiang,Kemeng Xiao,Hongli Sun,Ho Shing Chan,Tsz Ho Tsang,Shijian Yang,Po Keung Wong
标识
DOI:10.1016/j.apcatb.2020.119456
摘要
The dual cocatalysts photocatalytic heterostructures are beneficial for water splitting. Here we report a simple photo-assisted synthesis of novel g-C3N4/Co3O4/MoS2 heterojunction with low-cost Co3O4 (oxidation) and MoS2 (reduction) cocatalyst separately deposited onto g-C3N4 nanosheets. Driven by the synergy between Co3O4 and MoS2, the photocatalytic H2 evolution (PHE) activity of g-C3N4/Co3O4-1.9/MoS2-0.9 under visible light irradiation is about 885, 25.6 and 18.2 times better than those for g-C3N4, g-C3N4/Co3O4-1.9 and g-C3N4/MoS2-0.9, respectively, and is also higher than those of g-C3N4 based heterojunctions decorated by MoS2, dual MoS2- and other metal sulfides-based cocatalysts. The g-C3N4/Co3O4-1.9/MoS2-0.9 exhibits stable PHE in the recycle experiment and in various real water matrices. Detail characterization reveals that rapid electron-hole separation and charge species transferring through both Z-scheme and Type-I routes contribute to the improved PHE. With this synthetic strategy, the reduction cocatalyst can be extended to NiS (CoS), and the acquired g-C3N4/Co3O4-1.9/NiS (CoS) also possesses synergistically efficient PHE.
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