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通过双卟啉异质结构构建界面电场促进光催化析氢

Construction of Interfacial Electric Field via Dual-Porphyrin Heterostructure Boosting Photocatalytic Hydrogen Evolution.

作者信息

Jing Jianfang, Yang Jun, Li Wenlu, Wu Zhaohui, Zhu Yongfa

机构信息

Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.

Hunan Key Laboratory of Applied Environmental Photocatalysis, Changsha University, Changsha, Hunan Province, 410022, P. R. China.

出版信息

Adv Mater. 2022 Jan;34(3):e2106807. doi: 10.1002/adma.202106807. Epub 2021 Nov 17.

Abstract

A dual-porphyrin heterostructure is successfully constructed by coupling tetrakis (4-carboxyphenyl) zinc porphyrin (ZnTCPP) with tetrakis (4-hydroxyphenyl) porphyrin (THPP). The high photocatalytic H evolution rate of 41.4 mmol h g is obtained for ZnTCPP/THPP under full spectrum, which is ≈5.1 and ≈17.0 times higher than that of pure ZnTCPP and THPP, respectively. The significantly enhanced activity is mainly attributed to the giant interfacial electric field formed between dual porphyrins, which greatly facilitates efficient charge separation and transfer. Meanwhile, similar conjugated structures of dual porphyrins also provide proper interface match and decrease interface defects, thus inhibiting the recombination of photoproduced carriers. By rationally combining the appropriate band structures and high-quality interfacial contact of dual porphyrins, this work provides a fresh insight into the interfacial electric field construction to improve the photocatalytic performance.

摘要

通过将四(4-羧基苯基)锌卟啉(ZnTCPP)与四(4-羟基苯基)卟啉(THPP)耦合,成功构建了一种双卟啉异质结构。在全光谱下,ZnTCPP/THPP的光催化析氢速率高达41.4 mmol h g,分别比纯ZnTCPP和THPP高约5.1倍和约17.0倍。活性显著增强主要归因于双卟啉之间形成的巨大界面电场,这极大地促进了电荷的有效分离和转移。同时,双卟啉相似的共轭结构也提供了合适的界面匹配并减少了界面缺陷,从而抑制了光生载流子的复合。通过合理结合双卟啉合适的能带结构和高质量的界面接触,这项工作为通过构建界面电场来提高光催化性能提供了新的见解。

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