Zhang Wenxuan, Wang Jiangpeng, Hu Yingmo, Yu Xuelian, An Xiaoqiang
Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing), 100083, Beijing, China.
Center for Water and Ecology, State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, 100084, Beijing, China.
ChemSusChem. 2025 Mar 3;18(5):e202401929. doi: 10.1002/cssc.202401929. Epub 2024 Nov 17.
Homostructure construction has been proven to be an effective method for boosting the photocatalytic activity of polymeric carbon nitride. However, the contribution of the intrinsic activity of molecular fragments in the catalytic performance of homostructured carbon nitride is yet to be explored. In this paper, a facile hydrogen-assisted strategy was used to synthesize triazine/heptazine intermolecular homojunctions (g-CN(MU-H)) with an ultrathin and defective structure, via the co-pyrolysis of melamine and urea precursors. Experimental characterizations and theoretical calculations indicated the copolymerization of triazine- and heptazine-based carbon nitride generated a homostructured interface with a large build-in electric field for efficient separation of photogenerated carriers. Owing to the synergestic effect between the homostructured interface and nitrogen vacancies, as-synethesized g-CN(MU-H) exhibited an outstanding activity for photocatalytic CO reduction, with 14.45 μmol h CO yield, which was 23.5 and 3.64 times higher than those of bulk g-CN and g-CN(M-H) synthesized from a single precursor, respectively. In this study, We provided a novel route for optimizing the charge separation efficiency of CO photoreduction catalysts by constructing intramolecular homojunction.
同质结构构建已被证明是提高聚合氮化碳光催化活性的有效方法。然而,分子片段的本征活性在同质结构氮化碳催化性能中的贡献尚待探索。本文采用一种简便的氢辅助策略,通过三聚氰胺和尿素前驱体的共热解,合成了具有超薄和缺陷结构的三嗪/七嗪分子间同质结(g-CN(MU-H))。实验表征和理论计算表明,基于三嗪和七嗪的氮化碳的共聚产生了一个具有大内置电场的同质结构界面,用于光生载流子的有效分离。由于同质结构界面和氮空位之间的协同效应,合成的g-CN(MU-H)对光催化CO还原表现出优异的活性,CO产率为14.45 μmol h,分别是由单一前驱体制备的块状g-CN和g-CN(M-H)的23.5倍和3.64倍。在本研究中,我们通过构建分子内同质结为优化CO光还原催化剂的电荷分离效率提供了一条新途径。