Thermal Evolution of ZnS Nanostructures: Effect of Oxidation Phenomena on Structural Features and Photocatalytical Performances

微晶 热液循环 X射线光电子能谱 纳米结构 化学 拉曼光谱 化学工程 光催化 纳米技术 热氧化 吸收(声学) 材料科学 催化作用 结晶学 氧化物 有机化学 光学 复合材料 工程类 物理
作者
Nicola Dengo,Angela Federica De Fazio,Morten Weiß,Roland Marschall,Paolo Dolcet,Mattia Fanetti,Silvia Gross
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:57 (21): 13104-13114 被引量:18
标识
DOI:10.1021/acs.inorgchem.8b01101
摘要

ZnS nanosystems are being extensively studied for their possible use in a wide range of technological applications. Recently, the gradual oxidation of ZnS to ZnO was exploited to tune their structural, electronic, and functional properties. However, the inherent complexity and size dependence of the ZnS oxidation phenomena resulted in a very fragmented description of the process. In this work, different-sized nanosystems were obtained through two different low temperature wet chemistry routes, namely, hydrothermal and inverse miniemulsion approaches. These protocols were used to obtain ZnS samples consisting of 21 and 7 nm crystallites, respectively, to be used as reference material. The obtained samples were then calcinated at different temperatures, ranging from 400 to 800 °C toward the complete oxidation of ZnO, passing through the coexistence of the two phases (ZnS/ZnO). A thorough comparison of the effects of thermal handling on ZnS structural, chemical, and functional evolution was carried out by TEM, XRD, XAS, XPS, Raman, FT-IR, and UV–Vis. Finally, the photocatalytic activity in the H2 evolution reaction was also compared for selected ZnS and ZnS/ZnO samples. A correlation between size and the oxidation process was observed, as the smaller nanosystems showed the formation of ZnO at lower temperature, or in a larger amount in the case of the ZnS and ZnO co-presence. A difference in the underlying mechanism of the reaction was also evidenced. Despite the ZnS/ZnO mixed samples being characterized by an increased light absorption in the visible range, their photocatalytic activity was found to be much lower.
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