Pan Jingwen, Wang Dongbo, Wu Donghai, Cao Jiamu, Fang Xuan, Zhao Chenchen, Zeng Zhi, Zhang Bingke, Liu Donghao, Liu Sihang, Liu Gang, Jiao Shujie, Xu Zhikun, Zhao Liancheng, Wang Jinzhong
School of Materials Science and Engineering, Harbin Institute of Technology, Harbin, 150001, China.
Henan Key Laboratory of Nanocomposites and Applications, Huanghe Science and Technology College, Institute of Nanostructured Functional Materials, Zhengzhou, 450006, China.
Adv Sci (Weinh). 2024 Apr;11(13):e2309293. doi: 10.1002/advs.202309293. Epub 2024 Jan 23.
The efficiency of photocatalytic hydrogen evolution is currently limited by poor light adsorption, rapid recombination of photogenerated carriers, and ineffective surface reaction rate. Although heterojunctions with innovative morphologies and structures can strengthen built-in electric fields and maximize the separation of photogenerated charges. However, how to rational design of novel multidimensional structures to simultaneously improve the above three bottleneck problems is still a research imperative. Herein, a unique CuO─S@graphene oxide (GO)@ZnCdS Three dimensional (3D) hollow heterostructure is designed and synthesized, which greatly extends the carrier lifetime and effectively promotes the separation of photogenerated charges. The H production rate reached 48.5 mmol g h under visible light after loading Ni on the heterojunction surface, which is 97 times higher than that of pure ZnCdS nanospheres. Furthermore, the H production rate can reach 77.3 mmol g h without cooling, verifying the effectiveness of the photothermal effect. Meanwhile, in situ characterization and density flooding theory calculations reveal the efficient charge transfer at the p-n 3D hollow heterojunction interface. This study not only reveals the detailed mechanism of photocatalytic hydrogen evolution in depth but also rationalizes the construction of superior 3D hollow heterojunctions, thus providing a universal strategy for the materials-by-design of high-performance heterojunctions.
目前,光催化析氢效率受到光吸收差、光生载流子快速复合以及表面反应速率低的限制。尽管具有创新形态和结构的异质结可以增强内建电场并使光生电荷的分离最大化。然而,如何合理设计新型多维结构以同时改善上述三个瓶颈问题仍是一项研究要务。在此,设计并合成了一种独特的CuO─S@氧化石墨烯(GO)@ZnCdS三维(3D)中空异质结构,其大大延长了载流子寿命并有效促进了光生电荷的分离。在异质结表面负载Ni后,可见光下的产氢速率达到48.5 mmol g h,比纯ZnCdS纳米球高97倍。此外,不进行冷却时产氢速率可达到77.3 mmol g h,证实了光热效应的有效性。同时,原位表征和密度泛函理论计算揭示了p-n 3D中空异质结界面处的高效电荷转移。这项研究不仅深入揭示了光催化析氢的详细机制,还合理化了优异3D中空异质结的构建,从而为高性能异质结的材料设计提供了一种通用策略。