| Texto completo | |
| Autor(es): Mostrar menos - |
Galdino, C. W.
[1]
;
Freitas, D. C.
[2]
;
Medrano, C. P. C.
[2]
;
Sanchez, D. R.
[2]
;
Tartaglia, R.
[1]
;
Rabello, L. P.
[2]
;
Mendonca, A. A.
[3]
;
Ghivelder, L.
[3]
;
Continentino, M. A.
[4]
;
Zapata, M. J. M.
[5]
;
Pinheiro, C. B.
[5]
;
Azevedo, G. M.
[6]
;
Rodriguez-Velamazan, J. A.
[7]
;
Garbarino, G.
[8]
;
Nunez-Regueiro, M.
[9]
;
Granado, E.
[1]
Número total de Autores: 16
|
| Afiliação do(s) autor(es): | [1] Univ Estadual Campinas, Gleb Wataghin Inst Phys, UNICAMP, BR-13083859 Campinas, SP - Brazil
[2] Univ Fed Fluminense, Inst Fis, Campus Praia Vennelha, BR-24210346 Niteroi, RJ - Brazil
[3] Univ Fed Rio de Janeiro, Inst Fis, Caixa Postal 68528, BR-21941972 Rio De Janeiro, RJ - Brazil
[4] Ctr Brasileiro Pesquisas Fis, Rua Dr Xavier Sigaud 150, BR-22290180 Rio De Janeiro, RJ - Brazil
[5] Univ Fed Minas Gerais, Dept Fis, BR-31270901 Belo Horizonte, MG - Brazil
[6] Univ Fed Rio Grande Sul UFRGS, Inst Fis, BR-90040060 Porto Alegre, RS - Brazil
[7] Inst Laue Langevin, F-38042 Grenoble - France
[8] European Synchrotron Radiat Facil, F-38043 Grenoble - France
[9] UJF, CNRS, Inst Neel, F-38042 Grenoble - France
Número total de Afiliações: 9
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Physical Review B; v. 104, n. 19 NOV 29 2021. |
| Citações Web of Science: | 0 |
| Resumo | |
Charge ordering is prone to occur in crystalline materials with mixed-valence ions. It is presumably accompanied by a structural phase transition, with possible exceptions in compounds that already present more than one inequivalent site for the mixed-valence ions in the charge-disordered phase. In this work, we investigate the representative case of the homometallic Co ludwigite Co2+2Co3+O2BO3 (Pbam space group) with four distinct Co crystallographic sites {[}M1-M 4] surrounded by oxygen octahedra. The mixed-valent character of the Co ions up to at least T = 873 K is verified through x-ray absorption near-edge structure (XANES) experiments. Single crystal x-ray diffraction (XRD) and neutron powder diffraction (NPD) confirm that the Co ions at the M4 site are much smaller than the others at low temperatures, consistent with a Co3+ oxidation state at M4 and Co2+ at the remaining sites. The size difference between the Co ions in the M4 and M2 sites is continuously reduced upon warming above approximate to 370 K, indicating a gradual charge redistribution within the M4-M2-M 4 (424) ladder in the average structure. Minor structural anomalies with no space group modification are observed near 475 and 495 K, where sharp phase transitions were previously revealed by calorimetry and electrical resistivity data. An increasing structural disorder, beyond a conventional thermal effect, is noted above approximate to 370 K, manifested by an anomalous increment of XRD Debye-Waller factors and broadened vibrational modes observed by Raman scattering. The local Co-O distance distribution, revealed by Co K-edge extended x-ray absorption fine structure (EXAFS) data and analyzed with an evolutionary algorithm method, is similar to that inferred from the XRD crystal structure below approximate to 370 K. At higher temperatures, the local Co-O distance distribution remains similar to that found at low temperatures, at variance with the average crystal structure obtained with XRD. We conclude that the oxidation states Co2+ and Co3+ are instantaneously well defined in a local atomic level at all temperatures, however the thermal energy promotes local defects in the charge-ordered configuration of the 424 ladders upon warming. These defects coalesce into a phase-segregated state within a narrow temperature interval (475 < T < 495 K). Finally, a transition at approximate to 500 K revealed by differential scanning calorimetry (DSC) in the iron ludwigite Fe3O2BO3 is discussed. (AU) | |
| Processo FAPESP: | 18/20142-8 - Dinâmica vibracional, ondas de spin e excitações orbitais em óxidos de metais de transição |
| Beneficiário: | Eduardo Granado Monteiro da Silva |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |