Tyger H. Salters, James Colagiuri, Andre Koch Liston, Josh Leeman, Tanya Berry, Leslie M. Schoop
{"title":"Synthesis and Stability Phase Diagram of Topological Semimetal Family LnSbxTe2–x–δ","authors":"Tyger H. Salters, James Colagiuri, Andre Koch Liston, Josh Leeman, Tanya Berry, Leslie M. Schoop","doi":"10.1021/acs.chemmater.4c02198","DOIUrl":null,"url":null,"abstract":"The solid solution LnSb<sub><i>x</i></sub>Te<sub>2–<i>x</i>–δ</sub> (Ln = lanthanide) is a family of square-net topological semimetals that exhibit tunable charge density wave (CDW) distortions and band filling dependent on <i>x</i>, offering broad opportunities to examine the interplay of topological electronic states, CDW, and magnetism. While several Ln series have been characterized, gaps in the literature remain, inviting a systematic survey of the remaining composition space that is synthetically accessible. We present our efforts to synthesize LnSb<sub><i>x</i></sub>Te<sub>2–<i>x</i>–δ</sub> across the remaining lanthanides via chemical vapor transport. Compiling our results with the reported literature, we generate a stability phase diagram across the ranges of Ln and <i>x</i>. We find a stability boundary for intermediate <i>x</i> beyond Tb, while <i>x</i> = 1 and <i>x</i> = 0 can be isolated up to Ho and Dy, respectively. SEM and XRD analyses of unsuccessful reactions indicated the formation of several stable binary phases. The presence of structurally related LnTe<sub>3</sub> in samples suggests that stability is limited by the size of Ln, due to increasing compressive strain along the layer stacking axis with decreasing size. Finally, we demonstrate that late Ln can be stabilized in LnSb<sub><i>x</i></sub>Te<sub>2–<i>x</i>–δ</sub> via substitution into larger Ln members, synthesizing La<sub>1–<i>y</i></sub>Ho<sub><i>y</i></sub>Sb<sub><i>x</i></sub>Te<sub>2–<i>x</i>–δ</sub> as a proof of concept.","PeriodicalId":33,"journal":{"name":"Chemistry of Materials","volume":"12 1","pages":""},"PeriodicalIF":7.2000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.chemmater.4c02198","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The solid solution LnSbxTe2–x–δ (Ln = lanthanide) is a family of square-net topological semimetals that exhibit tunable charge density wave (CDW) distortions and band filling dependent on x, offering broad opportunities to examine the interplay of topological electronic states, CDW, and magnetism. While several Ln series have been characterized, gaps in the literature remain, inviting a systematic survey of the remaining composition space that is synthetically accessible. We present our efforts to synthesize LnSbxTe2–x–δ across the remaining lanthanides via chemical vapor transport. Compiling our results with the reported literature, we generate a stability phase diagram across the ranges of Ln and x. We find a stability boundary for intermediate x beyond Tb, while x = 1 and x = 0 can be isolated up to Ho and Dy, respectively. SEM and XRD analyses of unsuccessful reactions indicated the formation of several stable binary phases. The presence of structurally related LnTe3 in samples suggests that stability is limited by the size of Ln, due to increasing compressive strain along the layer stacking axis with decreasing size. Finally, we demonstrate that late Ln can be stabilized in LnSbxTe2–x–δ via substitution into larger Ln members, synthesizing La1–yHoySbxTe2–x–δ as a proof of concept.
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.