飞秒
超快激光光谱学
异质结
光谱学
吸收(声学)
载流子
光催化
吸收光谱法
材料科学
光化学
硫化镉
化学
光电子学
光学
物理
激光器
无机化学
有机化学
催化作用
复合材料
量子力学
作者
Chang Cheng,Jianjun Zhang,Bicheng Zhu,Guijie Liang,Liuyang Zhang,Jiaguo Yu
标识
DOI:10.1002/ange.202218688
摘要
Abstract The S‐scheme heterojunction is flourishing in photocatalysis because it concurrently realizes separated charge carriers and sufficient redox ability. Steady‐state charge transfer has been confirmed by other methods. However, an essential part, the transfer dynamics in S‐scheme heterojunctions, is still missing. To compensate, a series of cadmium sulfide/pyrene‐ alt ‐difluorinated benzothiadiazole heterojunctions were constructed and the photophysical processes were investigated with femtosecond transient absorption spectroscopy. Encouragingly, an interfacial charge‐transfer signal was detected in the spectra of the heterojunction, which provides solid evidence for S‐scheme charge transfer to complement the results from well‐established methods. Furthermore, the lifetime for interfacial charge transfer was calculated to be ca. 78.6 ps. Moreover, the S‐scheme heterojunction photocatalysts exhibit higher photocatalytic conversion of 1,2‐diols and H 2 production rates than bare cadmium sulfide.
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