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Proton conductivity, structural and thermal properties of (1–x) CsH2PO4−xBa(H2PO4)2. / Ponomareva, V. G.; Bagryantseva, I. N.

In: Physics of the Solid State, Vol. 59, No. 9, 01.09.2017, p. 1829-1835.

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Ponomareva VG, Bagryantseva IN. Proton conductivity, structural and thermal properties of (1–x) CsH2PO4−xBa(H2PO4)2. Physics of the Solid State. 2017 Sept 1;59(9):1829-1835. doi: 10.1134/S1063783417090244

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Ponomareva, V. G. ; Bagryantseva, I. N. / Proton conductivity, structural and thermal properties of (1–x) CsH2PO4−xBa(H2PO4)2. In: Physics of the Solid State. 2017 ; Vol. 59, No. 9. pp. 1829-1835.

BibTeX

@article{e4ea6823eca142a19cccc2bcbac0ee0e,
title = "Proton conductivity, structural and thermal properties of (1–x) CsH2PO4−xBa(H2PO4)2",
abstract = "The structural, electrotransport, and thermodynamic properties of the (1–x)CsH2PO4−xBa(H2PO4)2 system in a wide range of compositions (x = 0.1–0.4) were firstly studied to develop the highly conductive proton electrolytes within the medium-temperature range. At x = 0—0.1, formation of disordered substitutional solid solutions, isostructural to CsH2PO4 (P21/m), with a decrease of the unit cell parameters and considerable increase of proton conductivity as a result of formation of vacancies in the cesium sublattice and weakening of the system of hydrogen bonds, was observed. At x = 0.15–0.4, the heterophase highly conductive systems demonstrating high values of proton conductivity ~10–2 S/cm at x = 0.15—0.2, stable under the long-term isothermal exposures and low humidity (T ~ 200—210°C, RH ~ 15%), are formed. The phase transition disappears, the energy of activation of conductivity decreases from 0.9 to 0.55 eV at x = 0.2. The conductivity of high-temperature phase does not vary with Ba(H2PO4)2 fraction increase to x = 0.2. The mechanisms of transfer of protons were discussed. It has been shown that when x > 0.10 the contribution to proton conductivity of molecules of the water adsorbed on the phase boundary of the composite systems increases.",
keywords = "FUEL-CELLS, SUPERPROTONIC CONDUCTIVITY, CSH2PO4, COMPOSITES, CONDUCTORS, CRYSTALS, INTERCALATION, CS1-XRBXH2PO4, BEHAVIOR",
author = "Ponomareva, {V. G.} and Bagryantseva, {I. N.}",
year = "2017",
month = sep,
day = "1",
doi = "10.1134/S1063783417090244",
language = "English",
volume = "59",
pages = "1829--1835",
journal = "Physics of the Solid State",
issn = "1063-7834",
publisher = "PLEIADES PUBLISHING INC",
number = "9",

}

RIS

TY - JOUR

T1 - Proton conductivity, structural and thermal properties of (1–x) CsH2PO4−xBa(H2PO4)2

AU - Ponomareva, V. G.

AU - Bagryantseva, I. N.

PY - 2017/9/1

Y1 - 2017/9/1

N2 - The structural, electrotransport, and thermodynamic properties of the (1–x)CsH2PO4−xBa(H2PO4)2 system in a wide range of compositions (x = 0.1–0.4) were firstly studied to develop the highly conductive proton electrolytes within the medium-temperature range. At x = 0—0.1, formation of disordered substitutional solid solutions, isostructural to CsH2PO4 (P21/m), with a decrease of the unit cell parameters and considerable increase of proton conductivity as a result of formation of vacancies in the cesium sublattice and weakening of the system of hydrogen bonds, was observed. At x = 0.15–0.4, the heterophase highly conductive systems demonstrating high values of proton conductivity ~10–2 S/cm at x = 0.15—0.2, stable under the long-term isothermal exposures and low humidity (T ~ 200—210°C, RH ~ 15%), are formed. The phase transition disappears, the energy of activation of conductivity decreases from 0.9 to 0.55 eV at x = 0.2. The conductivity of high-temperature phase does not vary with Ba(H2PO4)2 fraction increase to x = 0.2. The mechanisms of transfer of protons were discussed. It has been shown that when x > 0.10 the contribution to proton conductivity of molecules of the water adsorbed on the phase boundary of the composite systems increases.

AB - The structural, electrotransport, and thermodynamic properties of the (1–x)CsH2PO4−xBa(H2PO4)2 system in a wide range of compositions (x = 0.1–0.4) were firstly studied to develop the highly conductive proton electrolytes within the medium-temperature range. At x = 0—0.1, formation of disordered substitutional solid solutions, isostructural to CsH2PO4 (P21/m), with a decrease of the unit cell parameters and considerable increase of proton conductivity as a result of formation of vacancies in the cesium sublattice and weakening of the system of hydrogen bonds, was observed. At x = 0.15–0.4, the heterophase highly conductive systems demonstrating high values of proton conductivity ~10–2 S/cm at x = 0.15—0.2, stable under the long-term isothermal exposures and low humidity (T ~ 200—210°C, RH ~ 15%), are formed. The phase transition disappears, the energy of activation of conductivity decreases from 0.9 to 0.55 eV at x = 0.2. The conductivity of high-temperature phase does not vary with Ba(H2PO4)2 fraction increase to x = 0.2. The mechanisms of transfer of protons were discussed. It has been shown that when x > 0.10 the contribution to proton conductivity of molecules of the water adsorbed on the phase boundary of the composite systems increases.

KW - FUEL-CELLS

KW - SUPERPROTONIC CONDUCTIVITY

KW - CSH2PO4

KW - COMPOSITES

KW - CONDUCTORS

KW - CRYSTALS

KW - INTERCALATION

KW - CS1-XRBXH2PO4

KW - BEHAVIOR

UR - http://www.scopus.com/inward/record.url?scp=85029636126&partnerID=8YFLogxK

U2 - 10.1134/S1063783417090244

DO - 10.1134/S1063783417090244

M3 - Article

AN - SCOPUS:85029636126

VL - 59

SP - 1829

EP - 1835

JO - Physics of the Solid State

JF - Physics of the Solid State

SN - 1063-7834

IS - 9

ER -

ID: 9908757