Ren Wei, Cheng Jiajia, Ou Honghui, Huang Caijin, Titirici Maria-Magdalena, Wang Xinchen
State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350116, P.R. China.
School of Engineering and Materials Science, Queen Mary University of London, London, E1 4NS, UK.
ChemSusChem. 2019 Jul 19;12(14):3257-3262. doi: 10.1002/cssc.201901011. Epub 2019 May 17.
Crystalline carbon nitride (CCN)-based semiconductors have recently attracted widespread attention in solar energy conversion. However, further modifying the photocatalytic ability of CCN always results in a trade-off between high crystallinity and good photocatalytic performance. Herein, a facile defect engineering strategy was demonstrated to modify the CCN photocatalysts. Results confirmed that the obtained D-CCN maintained the high crystallinity; additionally, the hydrogen production rate of D-CCN was approximately 8 times higher than that of CCN. Particularly, it could produce H even if the incident light wavelength extended to 610 nm. The significantly improved photocatalytic activity could be ascribed to the introduction of defects into the CCN polymer network to form the midgap states, which significantly broadened the visible-light absorption range and accelerated the charge separation for photoredox catalysis.
基于晶态氮化碳(CCN)的半导体最近在太阳能转换领域引起了广泛关注。然而,进一步提高CCN的光催化能力往往会在高结晶度和良好的光催化性能之间产生权衡。在此,展示了一种简便的缺陷工程策略来修饰CCN光催化剂。结果证实,所制备的D-CCN保持了高结晶度;此外,D-CCN的产氢速率比CCN高出约8倍。特别地,即使入射光波长延长至610nm,它仍能产生氢气。显著提高的光催化活性可归因于在CCN聚合物网络中引入缺陷以形成带隙中间态,这显著拓宽了可见光吸收范围并加速了光氧化还原催化的电荷分离。