材料科学
光催化
共轭微孔聚合物
共轭体系
微型多孔材料
载流子
聚合物
电场
离解(化学)
偶极子
纳米技术
激子
化学物理
光化学
光电子学
催化作用
有机化学
化学
物理
量子力学
复合材料
作者
Zhaozhang Deng,Hongwei Zhao,Xinxiu Cao,Shaohui Xiong,Gen Li,Jiyong Deng,Hai Yang,Weijie Zhang,Qingquan Liu
标识
DOI:10.1021/acsami.2c08747
摘要
The built-in electric field (BEF) has been considered as the key kinetic factor for facilitating efficient photoinduced carrier separation and migration of polymeric photocatalysts. Enhancing the BEF of the polymers could enable a directional migration of the photogenerated carriers to accelerate photogenerated charge separation and thus boost photocatalytic performances. However, achieving this approach remains a formidable challenge, which has never been realized in conjugated microporous polymers (CMPs). Herein, we developed a molecular dipole control strategy to modulate the BEF in CMPs by varying the nature of the core. As a result, a series of CMPs with a tunable BEF were designed and prepared via FeCl3-mediated coupling of bicarbazole with different acceptor cores. The optimized CbzCMP-9 featured the strongest BEF induced by its high molecular dipole, which grants it with a powerful driving force to accelerate exciton dissociation into electron-hole pairs and facilitates charge transfer along the backbone of CMPs to the surface, resulting in a remarkable photocatalytic performance toward thiocyano chromones and C-3 thiocyanation of indoles (up to 95 and 98% yields, respectively) and prominently surpassing many other reported photocatalysts. In brief, the proposed strategy highlights that enhancing the BEF by modulating molecular dipole can lead to a dramatic improvement in photocatalytic performance, which is expected to be employed for constructing other photocatalytic systems with high performance.
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