光催化
接受者
光化学
载流子
氮化碳
材料科学
可见光谱
石墨氮化碳
共轭体系
密度泛函理论
噻吩
氢
化学
催化作用
聚合物
计算化学
光电子学
有机化学
复合材料
物理
凝聚态物理
作者
Runlu Liu,Siyuan Liu,Jingyi Lin,Yao Li,Shunwei Chen,Peikui Wang,Shenmin Zhu,Xiujun Han,John Wang
出处
期刊:Carbon
[Elsevier]
日期:2022-09-01
卷期号:197: 378-388
被引量:12
标识
DOI:10.1016/j.carbon.2022.06.060
摘要
Polymeric carbon nitride (PCN) is a promising candidate for photocatalytic hydrogen evolution reaction (HER). However, the fast recombination of photogenerated charge carriers often gives an overall poor photocatalytic activity. Herein, we report anchoring of a donor-acceptor structure into the C–N skeleton, made in one-pot synthesis, where thiophene and cyano groups are introduced as the donor and acceptor, respectively, to modulate the electronic structure of pristine PCN. The separation and migration of the photogenerated charge-carriers in the PCN with donor-acceptor structure (CN-Cy-Th) were significantly promoted due to the enlarged π-conjugated system and much strengthened electron-redistribution effect, as confirmed by a series of experimental characterizations and density functional theory calculations. As such, the CN-Cy-Th exhibited a remarkable visible-light photocatalytic hydrogen evolution rate of 2.448 mmol g−1h−1, which was 9.0-fold rise as compared with that of pristine PCN (Bulk CN). This work provides a facile and effective new pathway for accelerating the transfer of photogenerated charge carriers in semiconducting materials and constructing high performance photocatalysts.
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