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Crystal structure and conduction of BICUTIVOX. / Buyanova, E. S.; Petrova, S. A.; Emel’yanova, Yu. V. et al.
In: Russian Journal of Inorganic Chemistry, Vol. 54, No. 6, 01.06.2009, p. 864-872.

Research output: Contribution to journalArticlepeer-review

Harvard

Buyanova, ES, Petrova, SA, Emel’yanova, YV, Borodina, NA, Zakharov, RG & Zhukovskii, VM 2009, 'Crystal structure and conduction of BICUTIVOX', Russian Journal of Inorganic Chemistry, vol. 54, no. 6, pp. 864-872. https://doi.org/10.1134/S0036023609060084

APA

Vancouver

Buyanova ES, Petrova SA, Emel’yanova YV, Borodina NA, Zakharov RG, Zhukovskii VM. Crystal structure and conduction of BICUTIVOX. Russian Journal of Inorganic Chemistry. 2009 Jun 1;54(6):864-872. doi: 10.1134/S0036023609060084

Author

Buyanova, E. S. ; Petrova, S. A. ; Emel’yanova, Yu. V. et al. / Crystal structure and conduction of BICUTIVOX. In: Russian Journal of Inorganic Chemistry. 2009 ; Vol. 54, No. 6. pp. 864-872.

BibTeX

@article{ea3a5dd4220f494da179c8643780ac3b,
title = "Crystal structure and conduction of BICUTIVOX",
abstract = "Existence boundaries, structure, and transport parameters were studied for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) solid solutions. Doping levels within x = 0.025-0.15 distort the C2/m crystal lattice (this lattice is characteristic of individual the Bi4V2O11 phase) and lowers its symmetry to triclinic. The solid solutions with 0.25 a parts per thousand currency sign x a parts per thousand currency sign 0.30 crystallize in tetragonal space group I4/mmm. High-temperature X-ray diffraction and dilatometry measurements for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) (x a parts per thousand currency sign 0.35) solid solutions verified the existence of three structural varieties within 298-1023 K. Electrical conductivity of BICUTIVOX was studied by impedance spectroscopy as a function of temperature, composition, and oxygen partial pressure. Equivalent circuits of cells were analyzed. Features of electrical conductivity versus temperature for the structural varieties are noted. Above 873 K, the solid solutions samples with x = 0.05 have the highest conductivity. At lower temperatures, higher conductivities are in the solid solutions that retain the gamma phase in the low-temperature region. The dominant oxygen-ion conduction mechanism was discovered in the solid solutions.",
author = "Buyanova, {E. S.} and Petrova, {S. A.} and Emel{\textquoteright}yanova, {Yu. V.} and Borodina, {N. A.} and Zakharov, {R. G.} and Zhukovskii, {V. M.}",
note = "This work was supported by the Russian Foundation for Basic Research (project no. 06-03-32378).",
year = "2009",
month = jun,
day = "1",
doi = "10.1134/S0036023609060084",
language = "English",
volume = "54",
pages = "864--872",
journal = "Russian Journal of Inorganic Chemistry",
issn = "0036-0236",
publisher = "Pleiades Publishing",
number = "6",

}

RIS

TY - JOUR

T1 - Crystal structure and conduction of BICUTIVOX

AU - Buyanova, E. S.

AU - Petrova, S. A.

AU - Emel’yanova, Yu. V.

AU - Borodina, N. A.

AU - Zakharov, R. G.

AU - Zhukovskii, V. M.

N1 - This work was supported by the Russian Foundation for Basic Research (project no. 06-03-32378).

PY - 2009/6/1

Y1 - 2009/6/1

N2 - Existence boundaries, structure, and transport parameters were studied for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) solid solutions. Doping levels within x = 0.025-0.15 distort the C2/m crystal lattice (this lattice is characteristic of individual the Bi4V2O11 phase) and lowers its symmetry to triclinic. The solid solutions with 0.25 a parts per thousand currency sign x a parts per thousand currency sign 0.30 crystallize in tetragonal space group I4/mmm. High-temperature X-ray diffraction and dilatometry measurements for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) (x a parts per thousand currency sign 0.35) solid solutions verified the existence of three structural varieties within 298-1023 K. Electrical conductivity of BICUTIVOX was studied by impedance spectroscopy as a function of temperature, composition, and oxygen partial pressure. Equivalent circuits of cells were analyzed. Features of electrical conductivity versus temperature for the structural varieties are noted. Above 873 K, the solid solutions samples with x = 0.05 have the highest conductivity. At lower temperatures, higher conductivities are in the solid solutions that retain the gamma phase in the low-temperature region. The dominant oxygen-ion conduction mechanism was discovered in the solid solutions.

AB - Existence boundaries, structure, and transport parameters were studied for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) solid solutions. Doping levels within x = 0.025-0.15 distort the C2/m crystal lattice (this lattice is characteristic of individual the Bi4V2O11 phase) and lowers its symmetry to triclinic. The solid solutions with 0.25 a parts per thousand currency sign x a parts per thousand currency sign 0.30 crystallize in tetragonal space group I4/mmm. High-temperature X-ray diffraction and dilatometry measurements for Bi4V2 - x Cu Ti-x/2 O-x/2(11 - x) (x a parts per thousand currency sign 0.35) solid solutions verified the existence of three structural varieties within 298-1023 K. Electrical conductivity of BICUTIVOX was studied by impedance spectroscopy as a function of temperature, composition, and oxygen partial pressure. Equivalent circuits of cells were analyzed. Features of electrical conductivity versus temperature for the structural varieties are noted. Above 873 K, the solid solutions samples with x = 0.05 have the highest conductivity. At lower temperatures, higher conductivities are in the solid solutions that retain the gamma phase in the low-temperature region. The dominant oxygen-ion conduction mechanism was discovered in the solid solutions.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000267298300008

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U2 - 10.1134/S0036023609060084

DO - 10.1134/S0036023609060084

M3 - Article

VL - 54

SP - 864

EP - 872

JO - Russian Journal of Inorganic Chemistry

JF - Russian Journal of Inorganic Chemistry

SN - 0036-0236

IS - 6

ER -

ID: 38603483