异质结
光催化
材料科学
范德瓦尔斯力
分子
光电效应
载流子
化学工程
光化学
光电子学
电子转移
纳米技术
反应速率
半导体
电子能带结构
反应速率常数
动力学
催化作用
作者
Hongjun Dong,Chunhong Qu,Jiaming Li,Deping Wang,Min Zhang,Zuoyi Liu,Liqiu Zhang,Chun Mei Li
标识
DOI:10.1016/j.gee.2025.09.004
摘要
Single-molecular heterojunctions have demonstrated significant application potential in the fields of photocatalysis due to prominent photoelectric properties, while the charge transfer behavior still need to be further discussed. In this work, a fresh single-molecular Van der Waals heterojunction is fabricated through self-assembly of dibromo(1,10-phenanthroline-κN1,κN10)nickel (NiphenBr) molecules on the surface PCN nanosheets, which dramatically boosts the performance of selective photocatalytic CO 2 reduction to CO. This unique assembled architecture effectively regulates electronic band structure and promotes the interfacial transfer and separation of photogenerated carriers owing to the π-π coupling effect between NiphenBr and PCN. Meanwhile, the single-molecular dispersed NiphenBr molecules also prevent their aggregation on PCN under the strong π-π interaction, and further provide abundant single-atom active sites for CO 2 reduction reaction. Therefore, the average rate of photocatalytic reduction of CO 2 to CO for the optimal NiphenBr/PCN-1 sample reaches 5.46 and 2.73 times that of PCN and NiphenBr, respectively. This work opens a new avenue for the single-molecular heterojunction in the application of photocatalytic reactions. A fresh single-molecular Van der Waals heterojunction NiphenBr/PCN is fabricated through self-assembly technology, dramatically boosting the selective photocatalytic CO 2 reduction performance, the CO evolution rate of which reaches 5.46 and 2.73 times that of PCN and NiphenBr, respectively. • A single-molecular VdWs heterojunction is fabricated by self-assembly method • Band structure is adjusted owing to π-π coupling effect between NiphenBr and PCN • The carrier separation efficiency and reaction kinetics are improved • NiphenBr/PCN VdWs heterojunction realizes selective photocatalytic CO 2 reduction to CO
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