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Absence of Long-Range Magnetic Ordering in a Trirutile High-Entropy Oxide (Mn0.2Fe0.2Co0.2Ni0.2Cu0.2)Ta1.92O6-δ

2024/05/24 by Gina Angelo, Liana M. Klivansky, Angelo, Gina +5
Engineering · Materials Science · #Advanced materials and composites #Copper-based nanomaterials and applications #FOS: Physical sciences #Magnetic and transport properties of perovskites and related materials #Materials Science (cond-mat.mtrl-sci)

paper · pdf · doi:10.48550/arxiv.2405.15501

openalex publication_date 2024/05/24 · openalex created_date 2024/05/28 · openalex updated_date 2026/07/30

Abstract

Functionalities of solid-state materials are usually considered to be dependent on their crystal structures. The limited structural types observed in the emerged high-entropy oxides put constraints on exploration of their physical properties and potential applications. Herein, we synthesized the first high-entropy oxide in a trirutile structure, (Mn0.2Fe0.2Co0.2Ni0.2Cu0.2)Ta1.92O6-δ, and investigated its magnetism. The phase purity and high-entropy nature were confirmed by powder X-ray diffraction and energy-dispersive spectroscopy, respectively. X-ray photoelectron spectroscopy indicated divalent Mn, Co, Ni and Cu along with trivalent Fe. Magnetic properties measurements showed antiferromagnetic coupling and potential short-range magnetic ordering below ~ 4 K. The temperature-dependent heat capacity data measured under zero and high magnetic field confirmed the lack of long-range magnetic ordering and a possible low-temperature phonon excitation. The discovery of the first trirutile high-entropy oxide opens a new way for studying the relationship between the highly disordered atomic arrangement and their magnetic interaction. Furthermore, it provides a new direction for exploring functionalities of high-entropy oxides.

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