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Research Article

Direct observation of metastable face-centered cubic Sb2Te3 crystal

Yonghui Zheng1,§Mengjiao Xia2,§Yan Cheng1( )Feng Rao1( )Keyuan Ding1Weili Liu1Yu Jia2Zhitang Song1( )Songlin Feng1
State Key Laboratory of Functional Materials for InformaticsShanghai Institute of Micro-system and Information TechnologyChinese Academy of SciencesShanghai200050China
International Laboratory of Quantum Functional Materials of HenanSchool of Physics and EngineeringZhengzhou UniversityZhengzhou450001China

§These authors contributed equally to this work.

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Abstract

Although phase change memory technology has developed drastically in the past two decades, the cognition of the key switching materials still ignores an important member, the face-centered cubic Sb2Te3. Apart from the well-known equilibrium hexagonal Sb2Te3 crystal, we prove the metastable face-centered cubic Sb2Te3 phase does exist. Such a metastable crystal contains a large concentration of vacancies randomly occupying the cationic lattice sites. The face-centered cubic to hexagonal phase transformation of Sb2Te3, accompanied by vacancy aggregation, occurs at a quite lower temperature compared to that of Ge2Sb2Te5 alloy. We prove that the covalent-like bonds prevail in the metastable Sb2Te3 crystal, deviating from the ideal resonant features. If a proper doping technique is adopted, the metastable Sb2Te3 phase could be promising for realizing reversibly swift and low-energy phase change memory applications. Our study may offer a new insight into commercialized Ge–Sb–Te systems and help in the design of novel phase change materials to boost the performances of the phase change memory device.

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Nano Research
Pages 3453-3462

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Cite this article:
Zheng Y, Xia M, Cheng Y, et al. Direct observation of metastable face-centered cubic Sb2Te3 crystal. Nano Research, 2016, 9(11): 3453-3462. https://doi.org/10.1007/s12274-016-1221-8

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Received: 08 April 2016
Revised: 12 July 2016
Accepted: 15 July 2016
Published: 31 August 2016
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016