Mapping the magnetic state as a function of antisite disorder in Sm2NiMnO6 double perovskite thin films

The predictability of any characteristic functional aspect in a double perovskite system has always been compromised by its strong dependence on the inevitably present antisite disorders (ASD). Here, we aim to precisely map the quantitative and qualitative nature of ASD with the corresponding modifications in observables describing the magnetic and electronic state in epitaxial Sm2NiMnO6 (SNMO) double perovskite thin films. The concentration and distribution patterns of ASD are effectively controlled by optimizing growth conditions and estimated on both local and global scales utilizing extended x-ray absorption fine structure and bulk magnetometry. Depending upon the defect densities, the nature of disorder distribution can vary from homogeneous to partially segregated patches. Primarily, the effect of varying B-site cationic arrangement in SNMO is reflected as the competition of long-range ferromagnetic (FM) and short-scale antiferromagnetic (AFM) interactions originated from ordered Ni-O-Mn and disordered Ni-O-Ni or Mn-O-Mn bonds, respectively, which leads to a systematic shift in magnetic transition temperature and a drastic drop in saturation magnetization. In addition, we have observed that the gradual increment in the density of ASD leads to a significant deviation from the uniaxial anisotropy character, reduction in anisotropy energy, and enhancement of moment pinning efficiency. However, the observed signatures of Ni2+ + Mn4+ -> Ni3+ + Mn3+ charge disproportionation is found to be independent of cation disorder densities. This work serves as a basic route map to tune the characteristic magnetic anisotropy, magnetic phase transitions, and magnetization reversal mechanism by controlling ASD in a general double perovskite system.

Automated summary

This article investigates the influence of antisite disorders on the magnetic and electronic states in double perovskite materials, and explores how to tune the magnetic anisotropy, magnetic phase transitions, and magnetization reversal mechanism by controlling these disorders.