Nano core-shell Mn0.5Cd0.5S@ copper phthalocyanine heterojunction structured with high hydrogen production efficiency

异质结 制氢 纳米- 材料科学 芯(光纤) 壳体(结构) 化学 纳米技术 化学工程 光电子学 冶金 复合材料 有机化学 工程类
作者
Jianhai Zhou,Hongdong Zhu,Renjie Ding,Huihua Luo,Lianqing Yu,Yaping Zhang
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:67: 532-539
标识
DOI:10.1016/j.ijhydene.2024.04.165
摘要

The core-shell structure photocatalysts have attracted extensive attention in photocatalysis due to large contact area, multiple reaction sites and high photocatalytic performance. Herein, a series of Mn0.5Cd0.5S@CuPc nano core-shell composites photocatalyst were successfully synthesized by facile solution method. The results showed that the as-prepared Mn0.5Cd0.5S photocatalyst hydrogen evolution was only 0.40 mmol/g·h, while Mn0.5Cd0.5S@CuPc composites show strong light absorption from 600 nm to 800 nm and high catalytic performance compared with pure Mn0.5Cd0.5S. Notably, the hydrogen evolution of Mn0.5Cd0.5S @CuPc-5% reached up to 2.14 mmol/(g·h), representing a remarkable 5.35 times improvement compared to the pure Mn0.5Cd0.5S when the optimal loading capacity of CuPc was set at 5%. The Mn0.5Cd0.5S@CuPc-5% exhibits excellent photocatalytic performance can be attributed to the CuPc forms a uniform molecular film on the surface of Mn0.5Cd0.5S, and the close contact between Mn0.5Cd0.5S and CuPc which can effectively promote the transfer and separation of photo-generated carriers. Moreover, the 5% Mn0.5Cd0.5S@CuPc nano core-shell composites have excellent stability, photocatalyst hydrogen activity reduce was approximately 20.1% after four runs for 12 h. This nano core-shell structure photocatalyst research offers a new strategy for constructing organic-inorganic nanocomposite photocatalysts.
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