Standard

Stabilization of high-temperature Ag2Se phase at room temperature during the crystallization of an amorphous film. / Tveryanovich, Yury S. ; Razumtcev, Aleksandr A. ; Fazletdinov, Timur R. ; Krzhizhanovskaya, Mariya G. ; Borisov, Evgenii N. .

In: Thin Solid Films, Vol. 709, 138187, 01.09.2020.

Research output: Contribution to journalArticlepeer-review

Harvard

APA

Vancouver

Author

BibTeX

@article{302d4cc8c907432aa6928202048f46f3,
title = "Stabilization of high-temperature Ag2Se phase at room temperature during the crystallization of an amorphous film",
abstract = "Amorphous films of Ag2Se were prepared by laser ablation. After being heated up to 270 °C, the films form oriented crystalline structure of orthorhombic β-modification upon further cooling at temperatures of 110 – 90 °С. The films undergo reversible β↔α phase transitions during the following temperature cycling, while the oriented crystalline structure stays the same. X-ray analysis showed no impurities reflections, excluding the one with very low intensity attributed to an elemental silver. The silver nanocrystals apparently form due to the selenium evaporation from the film surface during heating. The temperature dependence of the film's conductivity coincides with the one for bulk stoichiometric Ag2Se samples.It was shown that a considerable amount of α-Ag2Se is preserved in the film at room temperature even at low cooling rate. This phase is subjected to a significant mechanical stress caused by a density difference between α and β modifications. This circumstance points to the possibility of stabilization of high-temperature superionic modification of Ag2Se at room temperature in a nanolayered structure, in which some alternating layers create a similar stress on the Ag2Se layers.",
keywords = "Laser ablation, Silver selenide, Solid electrolytes, Surfaces, Thin films",
author = "Tveryanovich, {Yury S.} and Razumtcev, {Aleksandr A.} and Fazletdinov, {Timur R.} and Krzhizhanovskaya, {Mariya G.} and Borisov, {Evgenii N.}",
note = "Funding Information: This work was supported by the Russian Foundation for Basic Research ; project A-20-03-00185 . Scientific research was performed at the Research Center (RC) for X-ray Diffraction Studies of SPbSU, SPbSU Interdisciplinary resource center “Nanotechnology”, RC “Center for diagnosis of functional materials in medicine, pharmacology and nanoelectronics”, “Center for optical and laser materials research”.",
year = "2020",
month = sep,
day = "1",
doi = "10.1016/j.tsf.2020.138187",
language = "English",
volume = "709",
journal = "Thin Solid Films",
issn = "0040-6090",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Stabilization of high-temperature Ag2Se phase at room temperature during the crystallization of an amorphous film

AU - Tveryanovich, Yury S.

AU - Razumtcev, Aleksandr A.

AU - Fazletdinov, Timur R.

AU - Krzhizhanovskaya, Mariya G.

AU - Borisov, Evgenii N.

N1 - Funding Information: This work was supported by the Russian Foundation for Basic Research ; project A-20-03-00185 . Scientific research was performed at the Research Center (RC) for X-ray Diffraction Studies of SPbSU, SPbSU Interdisciplinary resource center “Nanotechnology”, RC “Center for diagnosis of functional materials in medicine, pharmacology and nanoelectronics”, “Center for optical and laser materials research”.

PY - 2020/9/1

Y1 - 2020/9/1

N2 - Amorphous films of Ag2Se were prepared by laser ablation. After being heated up to 270 °C, the films form oriented crystalline structure of orthorhombic β-modification upon further cooling at temperatures of 110 – 90 °С. The films undergo reversible β↔α phase transitions during the following temperature cycling, while the oriented crystalline structure stays the same. X-ray analysis showed no impurities reflections, excluding the one with very low intensity attributed to an elemental silver. The silver nanocrystals apparently form due to the selenium evaporation from the film surface during heating. The temperature dependence of the film's conductivity coincides with the one for bulk stoichiometric Ag2Se samples.It was shown that a considerable amount of α-Ag2Se is preserved in the film at room temperature even at low cooling rate. This phase is subjected to a significant mechanical stress caused by a density difference between α and β modifications. This circumstance points to the possibility of stabilization of high-temperature superionic modification of Ag2Se at room temperature in a nanolayered structure, in which some alternating layers create a similar stress on the Ag2Se layers.

AB - Amorphous films of Ag2Se were prepared by laser ablation. After being heated up to 270 °C, the films form oriented crystalline structure of orthorhombic β-modification upon further cooling at temperatures of 110 – 90 °С. The films undergo reversible β↔α phase transitions during the following temperature cycling, while the oriented crystalline structure stays the same. X-ray analysis showed no impurities reflections, excluding the one with very low intensity attributed to an elemental silver. The silver nanocrystals apparently form due to the selenium evaporation from the film surface during heating. The temperature dependence of the film's conductivity coincides with the one for bulk stoichiometric Ag2Se samples.It was shown that a considerable amount of α-Ag2Se is preserved in the film at room temperature even at low cooling rate. This phase is subjected to a significant mechanical stress caused by a density difference between α and β modifications. This circumstance points to the possibility of stabilization of high-temperature superionic modification of Ag2Se at room temperature in a nanolayered structure, in which some alternating layers create a similar stress on the Ag2Se layers.

KW - Laser ablation

KW - Silver selenide

KW - Solid electrolytes

KW - Surfaces

KW - Thin films

UR - http://www.scopus.com/inward/record.url?scp=85086630569&partnerID=8YFLogxK

U2 - 10.1016/j.tsf.2020.138187

DO - 10.1016/j.tsf.2020.138187

M3 - Article

VL - 709

JO - Thin Solid Films

JF - Thin Solid Films

SN - 0040-6090

M1 - 138187

ER -

ID: 61803850