Ethan Lowe, Lewis Giannelli, Claire Wilson, Ursula B. Hansen, David Boldrin
{"title":"Toward an Ideal S = 1/2 Kagome Antiferromagnet and Quantum Spin Liquid Candidate through Selective Mg2+ Doping of Averievite","authors":"Ethan Lowe, Lewis Giannelli, Claire Wilson, Ursula B. Hansen, David Boldrin","doi":"10.1021/acs.chemmater.6c01631","DOIUrl":null,"url":null,"abstract":"<p>Quantum spin liquids (QSLs) are exotic states of matter\r\nwhere geometric\r\nfrustration and quantum fluctuations suppress conventional magnetic\r\norder. S = 1/2 kagome antiferromagnets (KAFMs) are an ideal platform\r\nfor realizing such behavior, and several mineral-inspired Cu<sup>2+</sup>-based kagome systems have emerged as promising candidates. Among\r\nthese, Averievite (Cu<sub>5</sub>V<sub>2</sub>O<sub>10</sub>CsCl)\r\noffers a structurally distinct route to frustrated magnetism through\r\nits copper oxovanadate framework, which hosts alternating kagome and\r\nhoneycomb layers. Prior studies have shown that targeted Zn<sup>2+</sup> substitution on the honeycomb Cu<sub>H</sub> site can suppress magnetic\r\norder and promote QSL-like behavior. Here we investigate Mg<sup>2+</sup> substitution in the Averievite family, motivated by the geometric\r\nflexibility and favorable scattering contrast of Mg<sup>2+</sup> relative\r\nto Zn<sup>2+</sup>, the previously explored diamagnetic dopant. Herein\r\nwe present the novel Mg<sub><em>x</em></sub>Cu<sub>5–<em>x</em></sub>V<sub>2</sub>O<sub>10</sub>CsCl (<em>x</em> = 0, 0.5, 1, 2) family, utilizing X-ray diffraction, single-crystal\r\nelectron diffraction, and SQUID magnetometry to obtain precise structural\r\nparameters, including site occupancies, antisite disorder, and local\r\ncoordination information, and to correlate these with the varied magnetic\r\nbehavior. Increasing Mg<sup>2+</sup> content leads to a pronounced\r\nsuppression of both the structural and long-range magnetic ordering,\r\nalongside an increased mean field antiferromagnetic interaction, signaling\r\nenhanced magnetic frustration. Crucially, electron diffraction data\r\nis indicative of less than 1% Mg<sup>2+</sup> antisite disorder onto\r\nthe kagome lattice in the Mg<sub>2</sub> compound. This contrasts\r\nwith Zn-based analogues, preserving the integrity of the S = 1/2 kagome\r\nnetwork. At <em>x</em> = 2, neither long-range order nor spin\r\nfreezing is observed down to 2K, giving a new S = 1/2 KAFM with early\r\nhallmarks of QSL behavior and establishing Mg-doped Averievite as\r\na clean and highly tunable platform for exploring QSL ground states.</p>","PeriodicalId":33,"journal":{"name":"Chemistry of Materials","volume":"38 19","pages":"10085–10094"},"PeriodicalIF":7.1000,"publicationDate":"2026-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.chemmater.6c01631","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/24 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.
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.