异质结
材料科学
光催化
X射线光电子能谱
基质(水族馆)
半导体
量子效率
化学工程
光化学
三苯胺
芘
光降解
光电子学
纳米技术
催化作用
有机化学
化学
工程类
地质学
海洋学
作者
Chang Cheng,Bowen He,Jiajie Fan,Bei Cheng,Shaowen Cao,Jiaguo Yu
标识
DOI:10.1002/adma.202100317
摘要
Abstract Inspired by natural photosynthesis, constructing inorganic/organic heterojunctions is regarded as an effective strategy to design high‐efficiency photocatalysts. Herein, a step (S)‐scheme heterojunction photocatalyst is prepared by in situ growth of an inorganic semiconductor firmly on an organic semiconductor. A new pyrene‐based conjugated polymer, pyrene‐ alt ‐triphenylamine (PT), is synthesized via the typical Suzuki–Miyaura reactions, and then employed as a substrate to anchor CdS nanocrystals. The optimized CdS/PT composite, coupling 2 wt% PT with CdS, exhibits a robust H 2 evolution rate of 9.28 mmol h −1 g −1 with continuous release of H 2 bubbles, as well as a high apparent quantum efficiency of 24.3%, which is ≈8 times that of pure CdS. The S‐scheme charge transfer mechanism between PT and CdS, is systematically demonstrated by photoirradiated Kelvin probe measurement and in situ irradiated X‐ray photoelectron spectroscopy analyses. This work provides a protocol for preparing specific S‐scheme heterojunction photocatalysts on the basis of inorganic/organic coupling.
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