Vinylene-linked donor-acceptor covalent organic polymers with low exciton binding energy for enhanced photocatalytic oxidation of sulfides

被引:1
|
作者
Liu, Wenhao [1 ]
Li, Yujie [1 ]
Duan, Fang [1 ]
Liu, Haiping [1 ]
Ren, Yanyan [1 ]
Yan, Shengrong [1 ]
Lu, Shuanglong [1 ]
Du, Mingliang [1 ]
Chen, Xin [1 ]
Wang, Jun [2 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Dept Packaging Engn, Jiangsu Key Lab Adv Food Mfg Equipment & Technol, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
FRAMEWORKS;
D O I
10.1039/d4ta06162d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic organic synthesis is a promising technology for green and sustainable organic conversion. Covalent organic polymers (COPs) as an emerging class of porous organic polymers have attracted more and more attention in photocatalytic organic synthesis. However, the relatively high exciton binding energy (Eb) of COPs significantly restricts the exciton dissociation and charge separation in the photocatalytic process, resulting in low photocatalytic efficiency. In this work, a vinylene-linked conjugated COP (Btt-Bdd) with a donor-acceptor (D-A) structure has been prepared through the Knoevenagel condensation reaction. The introduction of a planar pi-skeleton donor and vinylene linkage extends the planar pi-conjugation of COPs and significantly reduces the Eb to 39.2 meV and improves the charge separation efficiency. Therefore, fully conjugated Btt-Bdd shows excellent photocatalytic performance towards sulfide oxidation with a high conversion and selectivity. The synergistic effect between the D-A structure and vinylene linkage is proved to be an effective way for reducing Eb and thus improving the photocatalytic performance, which provides a good strategy for designing efficient photocatalysts with low Eb for organic synthesis.
引用
收藏
页码:786 / 794
页数:9
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