共轭体系
X射线光电子能谱
光催化
异质结
材料科学
聚合物
光化学
开尔文探针力显微镜
密度泛函理论
化学工程
接受者
光电子学
纳米技术
化学
计算化学
有机化学
催化作用
复合材料
物理
工程类
原子力显微镜
凝聚态物理
作者
Yaqi Li,Sijie Wan,Weichen Liang,Bei Cheng,Wang Wang,Yao Xiang,Jiaguo Yu,Shaowen Cao
出处
期刊:Small
[Wiley]
日期:2024-03-05
卷期号:20 (31)
被引量:12
标识
DOI:10.1002/smll.202312104
摘要
Abstract Owing to the improved charge separation and maximized redox capability of the system, Step‐scheme (S‐scheme) heterojunctions have garnered significant research attention for efficient photocatalysis of H 2 evolution. In this work, an innovative linear donor–acceptor (D–A) conjugated polymer fluorene‐alt‐(benzo‐thiophene‐dione) (PFBTD) is coupled with the CdS nanosheets, forming the organic–inorganic S‐scheme heterojunction. The CdS/PFBTD (CP) composite exhibits an impressed hydrogen production rate of 7.62 mmol g −1 h −1 without any co‐catalysts, which is ≈14 times higher than pristine CdS. It is revealed that the outstanding photocatalytic performance is attributed to the formation of rapid electron transfer channels through the interfacial Cd─O bonding as evidenced by the density functional theory (DFT) calculations and in situ X‐ray photoelectron spectroscopy (XPS) analysis. The charge transfer mechanism involved in S‐scheme heterojunctions is further investigated through the photo‐irradiated Kelvin probe force microscopy (KPFM) analysis. This work provides a new point of view on the mechanism of interfacial charge transfer and points out the direction of designing superior organic–inorganic S‐scheme heterojunction photocatalysts.
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