Large low-field cryogenic magnetocaloric effect in ferromagnetic NaNd1-xEuxO2 (x=0, 0.05 and 0.1) compounds

IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS
Yingwei Wu , Naikun Sun , Meiling Li , Xinguo Zhao , Juan Cheng , Jiaohong Huang
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引用次数: 0

Abstract

Heavy rare-earth (RE)-based oxides possessing large magnetocaloric effect (MCE) have great application prospects in ultra-low-temperature magnetocaloric cooling. However, their large MCE based on the antiferromagnetic (AFM) ordering of heavy RE ions were generally obtained under high magnetic field changes. In this work, light RE-based tetragonal NaNd1-xEuxO2 (x = 0, 0.05, 0.1) compounds (I41/amd space group) were prepared by a facile ball-milling assisted sintering method. These oxides exhibit a second-order ferromagnetic (FM) to paramagnetic transition (PM) transition at the Curie temperature (TC) of 2.4 K to below 2 K, which is accompanied by an excellent low-field magnetocaloric cooling performance. In 0–1 T, a large magnetic entropy change ΔSM of 7.7, 7.6 and 7 J kg−1 K−1 was obtained at 2.5 K in NaNd1-xEuxO2 for x = 0, 0.05 and 0.1, respectively. These values are approximately twice as much as that for the commercial gallium gadolinium garnet (GGG) material (3.9 J kg−1 K−1, at 2 K). More favorably, these compounds show negligible coercivity and hysteretic loss, indicating reversibility of the large MCE. Eu3+ doping leads to a decrease of both the lattice constants and lengths of the Nd-O and Na-O bonds, accompanied by a lowering of TC and a decrease of effective magnetic moments of the RE3+. The excellent low-field MCE in the light RE-based FM oxides provides a novel insight for exploring suitable cryogenic magnetic refrigeration materials.
铁磁性 NaNd1-xEuxO2(x=0、0.05 和 0.1)化合物中的大型低磁场低温磁致效应
重稀土基氧化物具有较大的磁热效应,在超低温磁热冷却方面具有广阔的应用前景。然而,它们基于重稀土离子的反铁磁(AFM)有序的大MCE通常是在高磁场变化下获得的。本文采用球磨辅助烧结的方法制备了轻稀土基四边形NaNd1-xEuxO2 (x = 0,0.05, 0.1)化合物(I41/amd空间基团)。这些氧化物在居里温度(TC)为2.4 K至2 K以下时表现出二级铁磁(FM)到顺磁(PM)的转变,并具有优异的低场磁热冷却性能。在0 - 1 T下,在2.5 K下,当x = 0、0.05和0.1时,NaNd1-xEuxO2的磁熵变化ΔSM分别为7.7、7.6和7 J kg−1 K−1。这些值大约是商业镓钆石榴石(GGG)材料(3.9 J kg−1 K−1,2k)的两倍。更有利的是,这些化合物的矫顽力和滞后损失可以忽略不计,表明大MCE的可逆性。Eu3+的掺杂导致了Nd-O键和Na-O键的晶格常数和长度的减小,同时降低了RE3+的TC和有效磁矩。轻稀土基FM氧化物中优异的低场MCE为探索合适的低温磁致冷材料提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ceramics International
Ceramics International 工程技术-材料科学:硅酸盐
CiteScore
9.40
自引率
15.40%
发文量
4558
审稿时长
25 days
期刊介绍: Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties. Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour. Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.
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