Hollow sp2-conjugated covalent organic framework encapsulating thiophene-based photosensitizer for enhanced visible-light-driven hydrogen evolution

Chen Yang, Huawei Hu, Cheng Qian, Yaozu Liao
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Abstract

Vinylene-linked covalent organic frameworks (COFs) have gained increasing attention for photocatalytic hydrogen evolution. However, the photocatalytic activity of vinylene-linked COFs has been restricted due to low exciton dissociation efficiency and wide band gap. Herein, we fabricated a novel p-n type Z-scheme heterostructure, g2T-T@HCOFs, through the hybridization of vinylene-linked COFs with a hollow structure and thiophene-based photosensitizer (g2T-T) using a template method and post-encapsulating modification. The hollow-structured HCOFs enable uniform encapsulation of the g2T-T both within their channels and on their surfaces, which facilitates the formation of a firm and stable interface between n-type HCOF and p-type g2T-T. Therefore, the encapsulation of g2T-T enables the realization of a Z-scheme pathway for efficient charge separation and transfer, leading to enhanced electron accumulation within the HCOFs during water splitting. Consequently, the obtained p-n type Z-scheme heterostructure g2T-T@HCOFs exhibit a remarkable 5.5-fold enhancement in visi-ble-light-induced hydrogen evolution activity compared to the pristine COF.
中空sp2共轭共价有机骨架包封噻吩基光敏剂,增强可见光驱动析氢
乙烯链共价有机框架(COFs)在光催化析氢方面受到越来越多的关注。然而,由于激子解离效率低和带隙宽,乙烯链COFs的光催化活性受到限制。本文中,我们通过模板法和后包封修饰,将具有中空结构的乙烯链COFs与噻吩基光敏剂(g2T-T)杂化,制备了一种新的p-n型Z-scheme异质结构g2T-T@HCOFs。空心结构的HCOFs可以使g2T-T在通道内和表面均匀封装,从而促进n型HCOF和p型g2T-T之间形成牢固稳定的界面。因此,g2T-T的封装可以实现有效电荷分离和转移的Z-scheme途径,从而在水分裂过程中增强HCOFs内的电子积累。因此,得到的p-n型z型异质结构g2T-T@HCOFs在可见光诱导下的析氢活性比原始COF提高了5.5倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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