Evidence of structural and two magnetic phase transitions in Cu doped La2FeMnO6 double perovskites

被引:15
作者
Mohanty, Sipun [1 ]
Sharma, Rishi [2 ]
Rout, Sanjeeb Kumar [2 ]
Mukherjee, Samrat [1 ]
机构
[1] Natl Inst Technol, Dept Phys, Patna 800005, Bihar, India
[2] Birla Inst Technol Mesra, Dept Appl Phys, Ranchi 835215, Jharkhand, India
关键词
Double perovskites; Structural transitions; Raman spectroscopy; XPS study; Magnetic transitions;
D O I
10.1016/j.jallcom.2022.165694
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
In this report, we have addressed a comprehensive study on the structural phase transitions with the help of a combination of high temperature x-ray diffraction and temperature dependence Raman spectroscopy. We also report the magnetic ground state of all the samples at room temperature and 5 K. The combined high temperature x-ray diffraction and temperature dependence Raman study suggests that the samples undergo structural phase transitions from orthorhombic to tetragonal to cubic dominated mixed phase. With the help of x-ray photoelectron spectroscopy, we confirmed the presence of multi-oxidation states of Fe and Mn ions. The temperature evolution of magnetization data has been recorded at a field of 100 Oe and temperature range between 2 K and 300 K, and reveals the presence of two magnetic phase transitions for pristine, 10% and 20% doping of Cu in the composition La2FeMn1-xCuxO6. The magnetic study of all the samples reveal that the magnetic ground state of all the samples shows paramagnetic nature at room temperature, whereas at lower temperature all the samples are ferromagnetic except the highest doped sample which is purely paramagnetic. The law of approach to saturation method is imposed in the saturation region of M-H curve observed at 5 K. The transition temperature decreases with the amount of Cu doping, due to the substitution of Cu in Mn-site resulting in destroy of the Mn3+-O2-- Mn4+ bridges which is responsible for weakening of double exchange interaction between Mn3+ and Mn4+. (C) 2022 Elsevier B.V. All rights reserved.
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页数:13
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