Loading…

Magnetic Phase Separation in Double Perovskite Sr2TiMnO5.87

The double perovskite Sr 2 TiMnO 5.87 was synthesized via the solution combustion precursor method using Sr(NO 3 ) 2 , MnO 2 , i-Ti(OC 3 H 7 ) 4 , and disubstituted ammonium citrate as a complexing agent. The crystal structure and unit cell parameters are refined by the Rietveld method using powder...

Full description

Saved in:
Bibliographic Details
Published in:Applied magnetic resonance 2023-05, Vol.54 (4-5), p.561-580
Main Authors: Popov, D. V., Yatsyk, I. V., Batulin, R. G., Cherosov, M. A., Vakhitov, I. R., Faizrakhmanov, I. A., Yusupov, R. V., Chupakhina, T. I., Deeva, Yu. A., Fazlizhanov, I. I., Maiti, T., Eremina, R. M.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The double perovskite Sr 2 TiMnO 5.87 was synthesized via the solution combustion precursor method using Sr(NO 3 ) 2 , MnO 2 , i-Ti(OC 3 H 7 ) 4 , and disubstituted ammonium citrate as a complexing agent. The crystal structure and unit cell parameters are refined by the Rietveld method using powder X-ray diffraction. The magnetic properties of double perovskites Sr 2 TiMnO 5.87 were studied using the ESR spectroscopy, specific heat measurements in the temperature range ~ 5–300 K, and magnetometry under cooling in zero- (ZFC) and nonzero-fields (FC). The four ESR line were observed in ESR spectra, three ESR lines with g ~ 2 and fourth ESR at B res  = 50 mT in both X-and Q-bands measurements in the temperature range 37.5–42 K in Sr 2 TiMnO 5.87 . The peaks obtained in real and imaginary parts of AC magnetization measurements confirm phase separation at the same temperatures. The antiferromagnetic ordering was found out below the temperature T N ≈ 12 K. The fitting Debye and Einstein temperatures, obtained from the specific heat measurements, are equal to θ D  = 217 K, θ E1  = 275 K, θ E2  = 615 K, and θ E3  = 2000 K.
ISSN:0937-9347
1613-7507
DOI:10.1007/s00723-023-01541-y