光催化
碳纤维
异质结
钙钛矿(结构)
纳米晶
载流子
热液循环
材料科学
化学工程
纳米技术
光化学
光电子学
化学
催化作用
工程类
复合数
生物化学
复合材料
作者
Kai‐An Tsai,Yao-Jen Chang,Yu-Chieh Li,Meng‐Wei Zheng,Jui-Cheng Chang,Shou‐Heng Liu,Shih-Wen Tseng,Yan Li,Ying‐Chih Pu
标识
DOI:10.1021/acs.jpclett.4c01128
摘要
Nitrogen-doped carbon dots (NCDs) featuring primary pyrrolic N and pyridinic N dominated configurations were prepared using hydrothermal (H-NCDs) and microwave (M-NCDs) methods, respectively. These H-NCDs and M-NCDs were subsequently applied to decorate CsPbBr3 nanocrystals (CPB NCs) individually, using a ligand-assisted reprecipitation process. Both CPB/M-NCDs and CPB/H-NCDs nanoheterostructures (NHSs) exhibited S-scheme charge transfer behavior, which enhanced their performance in photocatalytic CO2 reduction and selectivity of CO2-to-CH4 conversion, compared to pristine CPB NCs. The presence of pyrrolic N configuration at the heterojunction of CPB/H-NCDs facilitated efficient S-scheme charge transfer, leading to a remarkable 43-fold increase in photoactivity. In contrast, CPB/M-NCDs showed only a modest 3-fold enhancement in photoactivity, which was attributed to electron trapping by pyridinic N at the heterojunction. The study offers crucial insights into charge carrier dynamics within perovskite/carbon NHSs at the molecular level to advance the understanding of solar fuel generation.
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