Toward an Ideal S = 1/2 Kagome Antiferromagnet and Quantum Spin Liquid Candidate through Selective Mg2+ Doping of Averievite

IF 7.1 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Chemistry of Materials Pub Date : 2026-10-13 Epub Date: 2026-09-24 DOI:10.1021/acs.chemmater.6c01631
Ethan Lowe, Lewis Giannelli, Claire Wilson, Ursula B. Hansen, David Boldrin
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引用次数: 0

Abstract

Quantum spin liquids (QSLs) are exotic states of matter where geometric frustration and quantum fluctuations suppress conventional magnetic order. S = 1/2 kagome antiferromagnets (KAFMs) are an ideal platform for realizing such behavior, and several mineral-inspired Cu2+-based kagome systems have emerged as promising candidates. Among these, Averievite (Cu5V2O10CsCl) offers a structurally distinct route to frustrated magnetism through its copper oxovanadate framework, which hosts alternating kagome and honeycomb layers. Prior studies have shown that targeted Zn2+ substitution on the honeycomb CuH site can suppress magnetic order and promote QSL-like behavior. Here we investigate Mg2+ substitution in the Averievite family, motivated by the geometric flexibility and favorable scattering contrast of Mg2+ relative to Zn2+, the previously explored diamagnetic dopant. Herein we present the novel MgxCu5–xV2O10CsCl (x = 0, 0.5, 1, 2) family, utilizing X-ray diffraction, single-crystal electron diffraction, and SQUID magnetometry to obtain precise structural parameters, including site occupancies, antisite disorder, and local coordination information, and to correlate these with the varied magnetic behavior. Increasing Mg2+ content leads to a pronounced suppression of both the structural and long-range magnetic ordering, alongside an increased mean field antiferromagnetic interaction, signaling enhanced magnetic frustration. Crucially, electron diffraction data is indicative of less than 1% Mg2+ antisite disorder onto the kagome lattice in the Mg2 compound. This contrasts with Zn-based analogues, preserving the integrity of the S = 1/2 kagome network. At x = 2, neither long-range order nor spin freezing is observed down to 2K, giving a new S = 1/2 KAFM with early hallmarks of QSL behavior and establishing Mg-doped Averievite as a clean and highly tunable platform for exploring QSL ground states.

通过选择性掺杂mg2 +制备理想的S = 1/2 Kagome反铁磁体和量子自旋液体
量子自旋液体(QSLs)是一种奇异的物质状态,其中几何挫折和量子涨落抑制了传统的磁秩序。S = 1/2 kagome反铁磁体(kafm)是实现这种行为的理想平台,一些基于Cu2+的矿物启发的kagome系统已经成为有希望的候选系统。其中,Averievite (Cu5V2O10CsCl)通过其氧化钒酸铜框架提供了一种结构独特的途径来抑制磁性,该框架具有交替的kagome和蜂窝层。先前的研究表明,在蜂窝CuH位点上靶向取代Zn2+可以抑制磁序并促进类qsl行为。在这里,我们研究了Mg2+在Averievite家族中的取代,这是由Mg2+相对于Zn2+的几何柔韧性和良好的散射对比所驱动的,Zn2+是之前探索的抗磁性掺杂剂。在这里,我们提出了新的MgxCu5-xV2O10CsCl (x = 0,0.5, 1,2)家族,利用x射线衍射,单晶电子衍射和SQUID磁强计来获得精确的结构参数,包括位占用,反位无序和局部配位信息,并将这些与不同的磁性行为联系起来。Mg2+含量的增加导致结构和远程磁有序的明显抑制,以及平均场反铁磁相互作用的增加,表明磁受挫增强。重要的是,电子衍射数据表明,在Mg2化合物的kagome晶格上,Mg2+的反位无序小于1%。这与基于锌的类似物形成对比,保留了S = 1/2 kagome网络的完整性。在x = 2时,在2K范围内既没有观察到长程阶态,也没有观察到自旋冻结,从而给出了具有QSL行为早期特征的新的S = 1/2 KAFM,并将mg掺杂的Averievite建立为探索QSL基态的干净且高度可调的平台。
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来源期刊
Chemistry of Materials
Chemistry of Materials 工程技术-材料科学:综合
CiteScore
14.10
自引率
5.80%
发文量
929
审稿时长
1.5 months
期刊介绍: The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.
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