Issue 7, 2023

Magnetotransport and magnetic properties of Cr-modified Mn2Sb epitaxial thin films

Abstract

High-quality Mn2−xCrxSb (x = 0.01, 0.04, and 0.1) epitaxial thin films were grown on SrTiO3 (STO) (001) single-crystal substrates using molecular beam epitaxy. Magnetotransport and magnetic measurements reveal that the x = 0.01 sample undergoes a quasi-ferrimagnetic (I) [Q-FIM(I)]-to-ferrimagnetic (II) [FIM(II)] spin reorientation (SR) transition and a giant magnetoresistance (MR) associated first-order ferrimagnetic(II)-to-antiferromagnetic (AFM) phase transition upon cooling, resulting in the AFM ground state with a weak in-plane net moment. Upon increasing the doping level from x = 0.01 to 0.1, both the SR transition and the first-order magnetic transition are suppressed. For x = 0.1, the former transition is suppressed, leaving only the Q-FIM(I)-to-AFM transition within the whole temperature region. TAFM−FIM shows almost similar changes upon the application of either in-plane or out-of-plane magnetic fields. TAFM−FIM values of the x = 0.01 and 0.04 samples are much higher than those of the Mn2–xCrxSb bulk with similar doping levels, which can be understood by the clamping effect from STO substrates. For each thin-film sample, the MR effect is observed near TAFM−FIM and disappears in the high temperature Q-FIM(I) phase and low temperature AFM phase, indicating that MR is related to the spin-dependent electron scattering during the first-order magnetic phase transition. Based on the magnetotransport and magnetic data, a magnetic phase diagram is established for the Mn2–xCrxSb films in the low doping level region.

Graphical abstract: Magnetotransport and magnetic properties of Cr-modified Mn2Sb epitaxial thin films

Associated articles

Article information

Article type
Paper
Submitted
21 Nov 2022
Accepted
19 Jan 2023
First published
20 Jan 2023

Phys. Chem. Chem. Phys., 2023,25, 5785-5794

Magnetotransport and magnetic properties of Cr-modified Mn2Sb epitaxial thin films

T. Chen, S. Li, F. Tang, J. Ying, Y. Zhang, Z. Wang, S. Zhang, F. Luo, L. Chen, Y. Fang and R. Zheng, Phys. Chem. Chem. Phys., 2023, 25, 5785 DOI: 10.1039/D2CP05442F

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