光催化
兴奋剂
异质结
光致发光
纳米复合材料
材料科学
载流子
热液循环
制氢
分解水
肖特基势垒
金属
纳米技术
催化作用
氢
化学工程
化学
光电子学
冶金
有机化学
二极管
生物化学
工程类
作者
Shiwen Du,Shengqi Lin,Kuankuan Ren,Chunhe Li,Fuxiang Zhang
标识
DOI:10.1016/j.apcatb.2023.122503
摘要
Having an insight into the optimizations of intrinsic properties of cocatalysts via doping foreign atoms to promote solar-driven water splitting into hydrogen (H2) energy conversion is increasingly important, but it remains a challenging scheme. Herein, zero-dimensional/one-dimensional (0D/1D) structured TMCoSe/CdS0.95Se0.05 was successfully synthesized through a two-pot hydrothermal treatment. Experimental results show that the FeCoSe/CdS0.95Se0.05 photocatalyst exhibits the most excellent photocatalytic H2 evolution performance (513.76 μmol h−1), which is 36.6 times and 2.0 times higher than that of CdS0.95Se0.05 and the optimal CoSe/CdS0.95Se0.05, respectively. In addition, photochemical and photoluminescence results reveal that the FeCoSe/CdS0.95Se0.05 sample shows the most rapid carrier dynamics among all samples. Theoretical calculations demonstrate that the excellent activity of FeCoSe/CdS0.95Se0.05 nanocomposite can be attributed to the formation of Schottky-type heterojunction between semi-metallic FeCoSe cocatalyst and CdS0.95Se0.05, which can enhance the efficiency of charge carrier separation and utilization, thus promoting the H2-generation performance.
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