光催化
罗丹明B
异质结
材料科学
可见光谱
二硫化钼
热液循环
光化学
降级(电信)
化学工程
催化作用
光电子学
化学
复合材料
工程类
电信
生物化学
计算机科学
作者
Kun Li,Xuede Qi,Xuede Qi,Jingwen Liu,Xiang Qi,Xiaoyi Huang,Xueqiang Qi,Xueqiang Qi,Qiaoyun Qin
标识
DOI:10.1002/slct.202501046
摘要
Abstract Due to the relatively large band gap and the rapid recombination of photogenerated electron‐hole pairs (e − ‐h + ) of pristine TiO 2 , its photocatalytic activity is severely limited. Molybdenum disulfide (MoS 2 ) features a large specific surface area and abundant active sites, thereby serving as a favorable support for enhancing the photocatalytic activity of TiO 2 . In this study, a ball‐flower TiO 2 /MoS 2 ‐80 heterojunction photocatalyst was prepared with a facile hydrothermal method. This heterojunction structure improves photocatalytic activity by enhancing visible light absorption, active site expansion, photogenerated charge separation, and transfer. Under visible light irradiation, the photocatalytic activity of TiO 2 /MoS 2 ‐80 heterojunction composites was evaluated for photocatalytic degradation of Rhodamine B (RhB). The results showed that TiO 2 /MoS 2 ‐80 heterojunction photocatalyst achieved a photocatalytic degradation efficiency of 90.1% for RhB in 1.5 h. The TiO 2 /MoS 2 ‐80 also exhibited the fastest degradation, with the highest kinetic rate of 2.48 × 10 −2 min −1 , which is 8.3 and 4.5 times higher than that of pristine MoS 2 and TiO 2 . The free radical trapping experiments indicate that the primary active species in the photocatalytic process are h + .
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