光催化
材料科学
过氧化氢
制氢
分解水
纳米结构
光化学
纳米技术
电子顺磁共振
化学工程
氢
光催化分解水
纳米-
催化作用
化学
有机化学
复合材料
核磁共振
工程类
物理
作者
Sen Lin,Qi Wang,Hongwei Huang,Yihe Zhang
出处
期刊:Small
[Wiley]
日期:2022-04-11
卷期号:18 (19)
被引量:69
标识
DOI:10.1002/smll.202200914
摘要
Hydrogen peroxide (H2 O2 ) as a useful chemical has a wide range of applications, and the development of efficient semiconducting materials for H2 O2 production is deemed as a promising strategy to realize the energy conversion. In this paper, Cdx Zn1-x S (x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, 1) nano-branches are fabricated and the piezocatalytic and photocatalytic H2 O2 evolution performance are studied. Under ultrasound condition, the H2 O2 yield of as-synthesized solid solutions is all higher than those of pristine ZnS and CdS, and optimal evolution rate achieves 21.9 µmol g-1 h-1 for Cd0.5 Zn0.5 S without any sacrificial agent, while it is increased to 151.6 µmol g-1 h-1 under visible light irradiation. The piezo/photoelectrochemical tests, piezoresponse force microscopy (PFM), and computational simulation reveal that the nano-branch structure benefits the mechanical energy conversion more, favoring the H2 O2 evolution for Cd0.5 Zn0.5 S, and a higher concentration of charge carriers is generated in photocatalysis. The active radical trapping and in situ electron spin resonance (ESR) experiments demonstrate that both of the H2 O2 generation pathways are originated from oxygen reduction by the sequential two-step single-electron reaction. This work opens a door for promoting the H2 O2 production from nanostructure and solid solution design.
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