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氧化锌纳米线的氮化

The nitridation of ZnO nanowires.

作者信息

Zervos Matthew, Karipi Chrystalla, Othonos Andreas

机构信息

Nanostructured Materials and Devices Laboratory, Department of Mechanical Engineering, Materials Science Group, University of Cyprus, P,O, Box 20537, Nicosia, 1678, Cyprus.

出版信息

Nanoscale Res Lett. 2012 Mar 8;7(1):175. doi: 10.1186/1556-276X-7-175.

Abstract

ZnO nanowires (NWs) with diameters of 50 to 250 nm and lengths of several micrometres have been grown by reactive vapour transport via the reaction of Zn with oxygen on 1 nm Au/Si(001) at 550°C under an inert flow of Ar. These exhibited clear peaks in the X-ray diffraction corresponding to the hexagonal wurtzite crystal structure of ZnO and a photoluminescence spectrum with a peak at 3.3 eV corresponding to band edge emission close to 3.2 eV determined from the abrupt onset in the absorption-transmission through ZnO NWs grown on 0.5 nm Au/quartz. We find that the post growth nitridation of ZnO NWs under a steady flow of NH3 at temperatures ≤600°C promotes the formation of a ZnO/Zn3N2 core-shell structure as suggested by the suppression of the peaks related to ZnO and the emergence of new ones corresponding to the cubic crystal structure of Zn3N2 while maintaining their integrity. Higher temperatures lead to the complete elimination of the ZnO NWs. We discuss the effect of nitridation time, flow of NH3, ramp rate and hydrogen on the conversion and propose a mechanism for the nitridation.

摘要

通过在550°C的氩气惰性气流下,使锌与氧气反应,利用反应气相传输法在1纳米厚的金/硅(001)衬底上生长出了直径为50至250纳米、长度为几微米的氧化锌纳米线(NWs)。这些纳米线在X射线衍射中呈现出清晰的峰,对应于氧化锌的六方纤锌矿晶体结构,并且在光致发光光谱中,有一个峰值在3.3电子伏特处,这对应于在0.5纳米厚的金/石英上生长的氧化锌纳米线的吸收-透射突然起始所确定的接近3.2电子伏特的带边发射。我们发现,在温度≤600°C的稳定氨气流下对氧化锌纳米线进行生长后氮化处理,会促进形成氧化锌/氮化锌核壳结构,这一点由与氧化锌相关的峰的抑制以及对应于氮化锌立方晶体结构的新峰的出现所表明,同时保持了它们的完整性。更高的温度会导致氧化锌纳米线完全消失。我们讨论了氮化时间、氨气流、升温速率和氢气对转化的影响,并提出了氮化的机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad2/3329639/cb8ef596d292/1556-276X-7-175-1.jpg

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