Ding Haojia, Bao Linping, Su Yao, Li Yuqin, Xu Guodong, Dai Chunhui, Zeng Chao
Institute of Advanced Materials, College of Chemistry and Chemical Engineering, Key Laboratory of Functional Small Molecules for Ministry of Education, Jiangxi Normal University, Nanchang, Jiangxi Province, 330022, PR China.
Institute of Advanced Scientific Research (iASR), Analysis and Testing Center, Jiangxi Normal University, Nanchang, Jiangxi Province, 330022, PR China.
J Environ Manage. 2022 Jul 1;313:115008. doi: 10.1016/j.jenvman.2022.115008. Epub 2022 Apr 6.
Constructing direct Z-scheme system is a promising strategy to boost the photocatalytic performance for pollution waters restoration, but it is of great challenge because of the requirement of appropriately staggered energy band alignment and intimate interfacial interaction between semiconductors. Herein, a class of core-shell structured AgS-AgIO Z-scheme heterostructure photocatalysts are designed and developed. AgS is generated by the in-situ ion exchange reaction and anchored on the surface of AgIO, so the intimate interface between AgIO and AgS is realized. Integration of AgIO and AgS extends the ultraviolet absorption of AgIO to Vis-NIR region, and also promote the charge separation and migration efficiency, contributing to the enhanced photocatalysis activity for composite catalysts. The optimal AgS-AgIO-4 catalyst exhibits a MO photo-degradation rate constant of 0.298 h, which reaches 5.77 and 11.4-folds higher than that of AgIO (0.044 h) and AgS (0.024 h). The as-obtained composite catalyst exhibits universally photocatalytic activity in disintegrating diverse industrial pollutants and pharmaceuticals. Particularly, driven by natural sunlight, the AgS-AgIO-4 can effectively decompose MO. A plausible Z-scheme photocatalytic mechanism and reaction pathways of MO degradation over composite catalyst are systemically investigated and proposed.
构建直接Z型体系是提高光催化性能用于污染水体修复的一种有前景的策略,但由于需要半导体之间适当的交错能带排列和紧密的界面相互作用,这极具挑战性。在此,设计并开发了一类核壳结构的AgS-AgIO Z型异质结构光催化剂。AgS通过原位离子交换反应生成并锚定在AgIO表面,从而实现了AgIO与AgS之间紧密的界面。AgIO和AgS的结合将AgIO的紫外吸收扩展到可见-近红外区域,还提高了电荷分离和迁移效率,有助于提高复合催化剂的光催化活性。最佳的AgS-AgIO-4催化剂表现出的亚甲基蓝光降解速率常数为0.298 h⁻¹,分别比AgIO(0.044 h⁻¹)和AgS(0.024 h⁻¹)高5.77倍和11.4倍。所制备的复合催化剂在分解各种工业污染物和药物方面表现出普遍的光催化活性。特别是,在自然阳光驱动下,AgS-AgIO-4能有效分解亚甲基蓝。系统地研究并提出了复合催化剂上亚甲基蓝光降解的合理Z型光催化机理和反应途径。