Published November 2019 | Version v1
Journal article

Oxygen-vacancy and charge hopping related dielectric relaxation of CuMoO4 ceramic

  • 1. Anhui Key Laboratory of Advanced Building Material, School of Materials Science and Chemical Engineering, Anhui Jianzhu University, Hefei, Anhui 230026 (China)
  • 2. Laboratory of Advanced Functional Materials and Devices, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230022 (China)

Description

Highlights: • The transition process from γ phase to α phase for CuMoO4 is observed by dielectric means for the first time. • The dielectric relaxation mechanisms of CuMoO4 related to oxygen vacancies and polarons are first proposed. • All research results open a new path for research methods and defect transmission mechanisms of related materials. -- Abstract: Single-phase CuMoO4 samples were prepared by a modified sol-gel method, and the functional relationship between dielectric properties of the samples and temperature (−130 °C–150 °C) or frequency (1 Hz–10 MHz) was investigated by measuring the dielectric spectrum. The temperature dependence of ε ́ and tan δ can determine the first-order phase transition (γ→α) in the CuMoO4 material. Three thermally activated relaxations were observed in the frequency dependence of tan δ and M ́ ́. The results show that relaxation 1 is related to the hopping motion of partial charge carriers between Cu2+ and Cu+, so this relaxation of the low-temperature segments is attributed to polarization relaxation. Relaxation 2 and relaxation 3 are dominated by the oxygen vacancy motion, where relaxation 2 is due to a movement of singly ionized oxygen vacancies and relaxation 3 is the result of an ordered movement of doubly ionized oxygen vacancies.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.physb.2019.08.029

Additional details

Identifiers

DOI
10.1016/j.physb.2019.08.029;
PII
S092145261930537X;

Publishing Information

Journal Title
Physica. B, Condensed Matter
Journal Volume
573
Journal Page Range
p. 62-66
ISSN
0921-4526
CODEN
PHYBE3

Optional Information

Copyright
Copyright (c) 2019 Elsevier B.V. All rights reserved.