4.5 Article

An In Situ Synchrotron X-Ray Diffraction Study on the Influence of Hydrogen on the Crystallization of Ge-Rich Ge 2 Sb 2 Te 5

Journal

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/pssr.202100658

Keywords

chalcogenides; crystallization; data storage; in situ synchrotron X-ray diffraction; phase-change materials

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This study investigates the effects of hydrogen treatment on the crystallization behavior of N-doped, Ge-rich Ge2Sb2Te5 phase-change materials for memory applications. The results show that hydrogen treatment lowers the crystallization temperature of Ge2Sb2Te5 cubic phase and promotes the formation of the trigonal phase in thin films.
To passivate Si - SiO 2 dangling bonds, metal-oxide-semiconductor field-effect transistor devices are usually treated with hydrogen. Herein, the effects of such a treatment on the crystallization behavior on N-doped, Ge-rich Ge 2 Sb 2 Te 5 phase-change materials for memory applications are investigated using synchrotron X-ray diffraction (XRD) in situ during heat treatment. Uniform thin films, and laterally confined, metallized ones (simulating devices of different complexity) of initially amorphous N-doped GGST are investigated. The specimens are heated up to 450-500 degrees C at a rate of 2 degrees C/min. Some of the specimens are treated with H/D; the equivalent untreated specimen is investigated for each of them. Crystallization onsets are estimated by quantification of the crystallized quantity during material transformation from the XRD patterns. In thin films, the hydrogen treatment results in lowered crystallization temperatures of the emerging cubic, metastable Ge 2 Sb 2 Te 5 phase. Its trigonal, thermodynamically stable polymorph always forms, but its crystallization temperature is unchanged. Patterned and metallized samples show less differences, are strongly textured, and no trigonal phase is observed. It is shown that certain questions might only be answered at large-scale facilities where high energy photons are available at high flux, allowing data acquisition during the annealing process with a temperature resolution sufficient for a fine description of the sample transformation.

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