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通过分子束外延制备的同型ZnO/SiC异质结——具有显著能带不连续性的化学惰性界面。

The isotype ZnO/SiC heterojunction prepared by molecular beam epitaxy--A chemical inert interface with significant band discontinuities.

作者信息

Zhang Yufeng, Lin Nanying, Li Yaping, Wang Xiaodan, Wang Huiqiong, Kang Junyong, Wilks Regan, Bär Marcus, Mu Rui

机构信息

College of Physical Science and Technology, Xiamen University (XMU), Xiamen, China.

Renewable Energy, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH (HZB), Berlin, Germany.

出版信息

Sci Rep. 2016 Mar 15;6:23106. doi: 10.1038/srep23106.

DOI:10.1038/srep23106
PMID:26976240
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4791549/
Abstract

ZnO/SiC heterojunctions show great potential for various optoelectronic applications (e.g., ultraviolet light emitting diodes, photodetectors, and solar cells). However, the lack of a detailed understanding of the ZnO/SiC interface prevents an efficient and rapid optimization of these devices. Here, intrinsic (but inherently n-type) ZnO were deposited via molecular beam epitaxy on n-type 6H-SiC single crystalline substrates. The chemical and electronic structure of the ZnO/SiC interfaces were characterized by ultraviolet/x-ray photoelectron spectroscopy and x-ray excited Auger electron spectroscopy. In contrast to the ZnO/SiC interface prepared by radio frequency magnetron sputtering, no willemite-like zinc silicate interface species is present at the MBE-ZnO/SiC interface. Furthermore, the valence band offset at the abrupt ZnO/SiC interface is experimentally determined to be (1.2 ± 0.3) eV, suggesting a conduction band offset of approximately 0.8 eV, thus explaining the reported excellent rectifying characteristics of isotype ZnO/SiC heterojunctions. These insights lead to a better comprehension of the ZnO/SiC interface and show that the choice of deposition route might offer a powerful means to tailor the chemical and electronic structures of the ZnO/SiC interface, which can eventually be utilized to optimize related devices.

摘要

ZnO/SiC异质结在各种光电子应用(如紫外发光二极管、光电探测器和太阳能电池)中显示出巨大潜力。然而,由于对ZnO/SiC界面缺乏详细了解,阻碍了这些器件的高效快速优化。在此,通过分子束外延在n型6H-SiC单晶衬底上沉积本征(但本质上为n型)ZnO。利用紫外/ X射线光电子能谱和X射线激发俄歇电子能谱对ZnO/SiC界面的化学和电子结构进行了表征。与通过射频磁控溅射制备的ZnO/SiC界面不同,在分子束外延生长的ZnO/SiC界面上不存在硅锌矿型硅酸锌界面物种。此外,通过实验确定了突变ZnO/SiC界面处的价带偏移为(1.2±0.3) eV,表明导带偏移约为0.8 eV,从而解释了报道的同型ZnO/SiC异质结优异的整流特性。这些见解有助于更好地理解ZnO/SiC界面,并表明沉积路线的选择可能为调整ZnO/SiC界面的化学和电子结构提供有力手段,最终可用于优化相关器件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/8f3dcd132159/srep23106-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/a4f3dd7ebf07/srep23106-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/0643a978b1d9/srep23106-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/af2f44d31c5d/srep23106-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/8f3dcd132159/srep23106-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/a4f3dd7ebf07/srep23106-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/0643a978b1d9/srep23106-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/af2f44d31c5d/srep23106-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44e/4791549/8f3dcd132159/srep23106-f4.jpg

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本文引用的文献

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