异质结
光催化
材料科学
X射线光电子能谱
量子点
光化学
紫外线
激进的
可见光谱
吸收(声学)
量子产额
激子
光电子学
产量(工程)
带隙
化学工程
电场
能量转换效率
复合数
量子效率
载流子
反应速率常数
紫外线
能量转换
宽禁带半导体
化学能
吸收光谱法
乙醇
半导体
超快激光光谱学
氧化还原
作者
Jyotirmayee Sahu,Bhagyashree Priyadarshini Mishra,Jayashree Panda,Kulamani Parida
标识
DOI:10.1021/acs.iecr.5c02972
摘要
High Resolution Image Download MS PowerPoint Slide The photocatalytic O 2 reduction reaction to produce H 2 O 2 has received a lot of attention as a potential approach for energy conversion owing to its economical and sustainable pathway. Here, we have synthesized the Zn 0.5 Cd 0.5 Se (ZCSe)/Bi 2 S 3 S-scheme heterojunction by decorating ZCSe QDs over the Bi 2 S 3 nanoflower. The optimized ZCSe/Bi 2 S 3 (ZB100) composite sample yield was 2.54 mmol g –1 h –1 with ethanol as the sacrificial agent under visible light irradiation, and it was stable for up to four cycles and achieved a solar to chemical conversion efficiency of 0.11% in pure water. The S-scheme mechanism facilitated interfacial charge transfer owing to the interfacial electric field between ZCSe QDs and Bi 2 S 3 . The energy band alignment in the ZCSe/Bi 2 S 3 S-scheme heterojunction was determined from X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy, Tauc plot, and Mott–Schottky analysis. The incorporation of Bi 2 S 3 and ZCSe QDs diminished the recombination rate of excitons and enhanced the light absorption capacity. The active radical trapping experiments and NBT test corroborated that superoxide radicals were the dominant intermediate species produced during the H 2 O 2 production reaction following a two-step single-electron pathway.
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