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Microstructure evolution and crystallography of the phase-change material TiSbTe films annealed in situ.

Authors :
Chen, Yong-Jin
Zhang, Bin
Ding, Qing-Qing
Deng, Qing-Song
Chen, Yan
Song, Zhi-Tang
Li, Ji-Xue
Zhang, Ze
Han, Xiao-Dong
Source :
Journal of Alloys & Compounds. Sep2016, Vol. 678, p185-192. 8p.
Publication Year :
2016

Abstract

In this work, the morphology, crystallization process and crystal structure of the phase-change material TiSbTe (TST) alloy have been successfully established, which is essential for applying this alloy in phase-change memory. Specifically, atomic force microscopy (AFM) was employed to characterize the as-deposited and post-annealed thin films, and transmission electron microscopy (TEM) analyses of the films annealed in situ were used in combination with selected-area electron diffraction (SAED) and radial distribution function (RDF) analyses to investigate the structural evolution from the amorphous phase to the polycrystalline phase. Moreover, the presence of structures with medium-range order in amorphous TST, which is beneficial for high-speed crystallization, was indicated by the structure factors S(Q)s . The crystallization temperature was determined to be approximately 170 °C, and the grain size varied from several to dozens of nanometers. As the temperature increased, particularly above 200 °C, the first single peak of the rG(r) curves transformed into double shoulder peaks due to the increasing impact of the Ti Te bonds. In general, the majority of Ti atoms were doped into the SbTe lattice and tended to form structural defects, whereas the remainder of the Ti atoms aggregated, leading to the appearance of TiTe 2 phase separation, as confirmed by the SAED patterns, high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM) images and corresponding energy-dispersive X-ray (EDX) mappings. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
678
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
115412152
Full Text :
https://doi.org/10.1016/j.jallcom.2016.03.231