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一种无机/有机S型异质结产氢光催化剂及其电荷转移机制。

An Inorganic/Organic S-Scheme Heterojunction H -Production Photocatalyst and its Charge Transfer Mechanism.

作者信息

Cheng Chang, He Bowen, Fan Jiajie, Cheng Bei, Cao Shaowen, Yu Jiaguo

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, P. R. China.

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou, 450001, P. R. China.

出版信息

Adv Mater. 2021 Jun;33(22):e2100317. doi: 10.1002/adma.202100317. Epub 2021 Apr 26.

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 evolution rate of 9.28 mmol h g with continuous release of H 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.

摘要

受自然光合作用的启发,构建无机/有机异质结被认为是设计高效光催化剂的有效策略。在此,通过将无机半导体原位牢固生长在有机半导体上制备了一种阶梯式(S)型异质结光催化剂。通过典型的铃木-宫浦反应合成了一种新型的芘基共轭聚合物芘-alt-三苯胺(PT),然后将其用作锚定硫化镉纳米晶体的基底。优化后的硫化镉/PT复合材料,即2 wt%的PT与硫化镉耦合,表现出稳健的析氢速率,为9.28 mmol h g,并有氢气气泡持续释放,以及24.3%的高表观量子效率,约为纯硫化镉的8倍。通过光辐照开尔文探针测量和原位辐照X射线光电子能谱分析,系统地证明了PT和硫化镉之间的S型电荷转移机制。这项工作为基于无机/有机耦合制备特定的S型异质结光催化剂提供了一种方案。

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