High-Entropy Perovskites as Multifunctional Metal Oxide Semiconductors: Synthesis and Characterization of (Gd0.2Nd0.2La0.2Sm0.2Y0.2)CoO3

反铁磁性 材料科学 带隙 凝聚态物理 顺磁性 正交晶系 基态 化学 结晶学 晶体结构 原子物理学 光电子学 物理
作者
Paweł A. Krawczyk,M. Jurczyszyn,Jakub Pawlak,Wojciech Salamon,Paweł Baran,Angelika Kmita,Ł. Gondek,Marcin Sikora,Cz. Kapusta,Tomasz Strączek,Jan Wyrwa,Antoni Żywczak
出处
期刊:ACS applied electronic materials [American Chemical Society]
卷期号:2 (10): 3211-3220 被引量:56
标识
DOI:10.1021/acsaelm.0c00559
摘要

Single-phase multicomponent perovskite-type cobalt oxide containing five cations in equiatomic amounts on the A-site, namely, (Gd0.2Nd0.2La0.2Sm0.2Y0.2)CoO3, has been synthesized via the modified coprecipitation hydrothermal method. Using an original approach for heat treatment, which comprises quenching utilizing liquid nitrogen as a cooling medium, a single-phase ceramic with high configuration entropy, crystallizing in an orthorhombic distorted structure was obtained. It reveals the anomalous temperature dependence of the lattice expansion with two weak transitions at approx. 80 and 240 K that are assigned to gradual crossover from the low- via intermediate- to high-spin state of Co3+. The compound exhibits weak ferromagnetism at T ≤ 10 K and signatures of antiferromagnetic correlations in the paramagnetic phase. Ab initio calculations predict a band gap Δ = 1.18 eV in the ground-state electronic structure with the dominant contribution of O_p and Co_d orbitals in the valence and conduction bands, respectively. Electronic transport measurements confirm the negative temperature coefficient of resistivity characteristic to a semiconducting material and reveal a sudden drop in activation energy at T ∼ 240 K from Ea ∼ 1 eV in the low-temperature phase to Ea ∼ 0.3 eV at room temperature. The possibility of fine tuning of the semiconducting band gap via a subtle change in A-site stoichiometry is discussed.
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