光催化
异质结
材料科学
光电流
钴
化学工程
制氢
光致发光
介电谱
载流子
电子转移
纳米技术
氢
光化学
电化学
光电子学
电极
化学
催化作用
物理化学
冶金
有机化学
工程类
生物化学
作者
Xuli Li,Yangqin Gao,Ning Li,Lei Ge
标识
DOI:10.1016/j.ijhydene.2022.06.119
摘要
Designing an efficient heterojunction interface is an effective way to promote the electrons' transfer and improve the photocatalytic H2 evolution performance. In this work, a novel hollow hybrid system of [email protected]/CdS has been fabricated and constructed. CdS nanospheres are anchored on the hollow-structured cobalt incorporated nitrogen-doped carbon ([email protected]) through a one-pot in-situ chemical deposition approach, forming an intimate interface and establishing an excellent channel to improve the electrons transfer and charge carriers separation between CdS and [email protected] cocatalyst, which immensely promotes the photocatalytic activity. The rate of photocatalytic H2 evolution over hollow structured [email protected]/CdS heterojunction can be achieved 8.2 mmol g−1 h−1, which is about 45 times of pristine CdS nanospheres. The photocatalytic H2 evolution mechanism has been investigated by the techniques of photoluminescence (PL) spectra, photocurrent-time (i-t) curves, electrochemical impedance spectroscopy (EIS) etc. This work aims to provide a new way in developing of high-performance advanced 3D heterojunction for photocatalytic hydrogen evolution.
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