异质结
氧化还原
压电
催化作用
材料科学
降级(电信)
激进的
亚甲蓝
化学
光化学
纳米技术
光电子学
无机化学
光催化
有机化学
复合材料
电气工程
工程类
作者
Jianyong Yue,Rong Wu,Yù Zhang,Ning Zhang,Haitong Jing,Shunhang Wei,Fangping Ouyang
标识
DOI:10.1016/j.apsusc.2023.157033
摘要
In recent years, odd-layer 2H-MoS2 nanosheets have proved to be promising piezoelectric catalysts to solve environmental pollution problems. To further improve the 2H-MoS2 piezoelectric performance, 1T@2H-MoS2/Bi2S3 heterostructures were prepared using Bi2WO6 as a precursor. Compared with 1T@2H-MoS2, 1T@2H-MoS2/Bi2S3 piezoelectric degradation of methylene blue is significantly improved under dark and ultrasonic conditions. It is attributed to the free carrier separation being facilitated through the type-II heterojunction, and the electron transport paths are optimized by high conductivity 1T-MoS2. In the radical scavenging experiment and ESR measurement, the hydroxyl radicals produced by 1T@2H-MoS2/Bi2S3 are more than those produced by 1T@2H-MoS2 in the piezoelectric catalysis process. It indicates that the piezoelectric field can realize the free carrier rearrangement by adjusting the band structure. Thus, free carriers in the 1T@2H-MoS2/Bi2S3 heterojunction have the opportunity to shift to the position with high redox potential to unlock the higher redox capability compared with the lower redox potential of the original 1T@2H-MoS2 and Bi2S3. In conclusion, this study shows that the piezoelectric field can regulate the free carrier rearrangement in the type-II heterojunction, allowing the type-II heterojunction can not only efficiently separate free carriers but also maintain a high redox potential.
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