光催化
异质结
材料科学
硝酸盐
化学工程
催化作用
选择性
化学
无机化学
光电子学
生物化学
工程类
有机化学
作者
Xiao Li,Mingyi Zhang,Jing Feng,Chengying Bai,Yueming Ren
标识
DOI:10.1016/j.jcis.2021.09.069
摘要
Photocatalytic NO3- reduction in water has been regarded as a promising route due to its high efficiency and green feature. Several limiting factors, such as lack of catalytic sites, insufficient light collection, and spatial charge separation capacity photocatalytic denitrification, still need to be overcome for the practical applications. Herein, an innovative LiNbO3/ZnS heterojunction with a unilateral opening core-shell structure was constructed. ZnS was tightly anchored on the surface of LiNbO3 by modified electrostatic self-assembly method. High nitrate removal rate (98.84%) and N2 selectivity (98.92%) were achieved with a molar ratio of LiNbO3 and ZnS of 1:5 (1:5L-ZS) using formic acid as a hole scavenge. The LiNbO3/ZnS degradation kinetics of NO3- was corresponding to the first-order kinetics equation. The nitrate removal rate and N2 selectivity remained stable after three cycles in such photocatalytic NO3- reduction. The outstanding photocatalyst performance can be ascribed to the improved surface active sites, the well-matched band structure, and the unique core-shell structure. It provides an effective strategy for controllable fabrication of core-shell photocatalyst with strong light-harvesting ability and charge separation efficiency to enhance the removal rate of nitrate in water.
科研通智能强力驱动
Strongly Powered by AbleSci AI