Tang Junhao, He Minqiang, Zhang Biyang, Zhong Kang, Yang Zhengrui, Wang Zhaolong, Zhu Xingwang, Li Huaming, Yang Jinman, Xu Hui
School of Chemistry and Chemical Engineering, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, China.
School of Chemistry and Chemical Engineering, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, China.
J Colloid Interface Sci. 2025 Sep 15;694:137711. doi: 10.1016/j.jcis.2025.137711. Epub 2025 Apr 25.
The utilization of heterojunction photocatalysts in photocatalytic CO conversion has attracted significant attention. Nevertheless, the interface structure between the two components in the heterojunction material essentially decides the carrier separation efficiency and the performance of photocatalytic CO reduction. The development of semiconductor heterojunctions with suitable materials and intimate interfacial contact is paramount. In this study, SnInS/CoO heterostructures have been successfully fabricated by a facile hydrothermal synthesis method. The experimental results demonstrated that the established internal electric field effectively suppressed the recombination of photogenerated carriers and accelerated charge transfer kinetics. Meanwhile, the increased specific surface area endows SnInS/CoO heterostructures with an improved CO adsorption ability, ultimately achieving a significant improvement in photocatalytic activity. The highest formation rate of CO and CH reaches 38.20 and 3.60 μmol g h. The design strategy reveals the potential of establishing intimate interfacial contacts as an extremely efficient catalyst for photocatalytic CO reduction, facilitating effective charge separation. This work provides distinctive thoughts for the development of advanced catalytic material design for CO conversion and other photocatalytic applications.
异质结光催化剂在光催化CO转化中的应用已引起广泛关注。然而,异质结材料中两种组分之间的界面结构本质上决定了载流子分离效率和光催化CO还原性能。开发具有合适材料和紧密界面接触的半导体异质结至关重要。在本研究中,通过简便的水热合成方法成功制备了SnInS/CoO异质结构。实验结果表明,所建立的内电场有效地抑制了光生载流子的复合并加速了电荷转移动力学。同时,增加的比表面积赋予SnInS/CoO异质结构更高的CO吸附能力,最终实现了光催化活性的显著提高。CO和CH的最高生成速率分别达到38.20和3.60 μmol g h。该设计策略揭示了建立紧密界面接触作为光催化CO还原的高效催化剂的潜力,促进了有效的电荷分离。这项工作为开发用于CO转化和其他光催化应用的先进催化材料设计提供了独特思路。