异质结
结晶度
量子产额
无定形固体
材料科学
氮化物
氮化碳
无定形碳
光催化
化学工程
化学
光电子学
纳米技术
结晶学
复合材料
催化作用
有机化学
光学
物理
图层(电子)
工程类
荧光
作者
Cheng Cheng,Liuhao Mao,Xin Kang,Chung‐Li Dong,Yucheng Huang,Shaohua Shen,Jinwen Shi,Liejin Guo
标识
DOI:10.1016/j.apcatb.2023.122733
摘要
Polymeric carbon nitride suffers terrible recombination of photo-generated carriers and thus usually results in limited photocatalytic activity. Improving crystallinity and creating novel structure can effectively alleviate the aforementioned problem. Herein, a high-cyano groups-content and amorphous-crystalline carbon nitride isotype heterojunction (BCN-NaK) was obtain via a post treatment strategy in eutectic salt. The cyano groups acted as electron acceptors, and the intimate isotype heterojunction constructed by amorphous carbon nitride and crystalline poly-heptazine-imide built interfacial electric field. Both synergistically enabled BCN-NaK more efficient charge transfer than other amorphous and crystalline carbon nitrides. Comprehensive and systematic analysis demonstrated that the promoted charge transfer made the predominant contribution to the ultrahigh photocatalytic H2-production activity of BCN-NaK with an excellent apparent quantum yield of 68.9 % at 405 nm. In addition, BCN-NaK exhibited a good photocatalytic CO2-to-CO conversion rate of 22.8 μmol h−1 gcat−1 without adding sacrificial agent or loading metal under visible light.
科研通智能强力驱动
Strongly Powered by AbleSci AI