Abrupt Negative Thermal Expansion and Magnetic Structure of V3O5

被引:4
|
作者
Aguilar-Maldonado, Cintli [1 ,2 ]
Solana-Madruga, Elena [1 ,3 ]
Ritter, Clemens [4 ]
Mentre, Olivier [1 ]
Arevalo-Lopez, Angel M. [1 ]
机构
[1] Univ Lille, Univ Artois, UCCS Unite Catalyse & Chim Solide, Cent Lille,CNRS,UMR 8181, F-59000 Lille, France
[2] Univ Caen Basse Normandie, ENSICAEN, CRISMAT, UMR CNRS 6508, F-14050 Caen, France
[3] Univ Complutense Madrid, Fac CC Quim, Dept Quim Inorgan, Madrid 28040, Spain
[4] Inst Laue Langevin, F-38042 Grenoble, France
关键词
TEMPERATURE MODIFICATION; INSULATOR-TRANSITION; ORDER;
D O I
10.1021/acs.chemmater.2c01030
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report bulk dilatometry and diffraction data through the TMIT = 427 K metal-insulator transition of the n = 3 member of the VnO2n-1 Magne??li series. Besides VO2, V3O5 is the only other vanadium oxide with a potentially useful MIT transition above room temperature. A narrow (Delta T = 10 K) abrupt negative thermal expansion of aL = -21.4 x 10-6 (dilatometric) and aV = -213 x 10-6 K-1 (crystallographic) is observed. We argue that the combination of the MIT along with the simultaneous vanadium charge ordering is responsible for such large values. The low temperature magnetic properties are also clarified, and neutron diffraction measurements show a k = [1/2 1/2 0] magnetic structure at 1.5 K. DFT calculations of the exchange interactions support the low dimensionality and allow the modeling of the magnetic susceptibility.
引用
收藏
页码:5294 / 5300
页数:7
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