T. Block, Jutta Kösters, Samir F. Matar, Valentin Antoine Chamard, Rainer Pöttgen
{"title":"CaRu2Zn10, SrRu2Zn10 and EuRu2Zn10 – new superstructure variants of ThMn12","authors":"T. Block, Jutta Kösters, Samir F. Matar, Valentin Antoine Chamard, Rainer Pöttgen","doi":"10.1515/zkri-2024-0084","DOIUrl":null,"url":null,"abstract":"\n The zinc-rich intermetallic phases CaRu2Zn10, SrRu2Zn10 and EuRu2Zn10 were synthesized by induction-melting of the elements in sealed tantalum ampoules followed by annealing to increase the crystallinity. The samples were characterized by powder X-ray diffraction and the structures were refined from single crystal X-ray diffractometer data: new type, P42/nnm, a = 894.68(14), c = 518.44(9) pm, wR2 = 0.0830, 432 F\n 2 values, 22 variables for CaRu2Zn10, a = 907.01(10), c = 516.35(6), wR2 = 0.0469, 445 F\n 2 values, 22 variables for SrRu2Zn10 and a = 902.84(9), c = 515.91(5) pm, wR2 = 0.0469, 434 F\n 2 values, 22 variables for EuRu2Zn10. The three structures are new ordering variants of the aristotype ThMn12. They are discussed on the basis of a group-subgroup scheme and compared to the known superstructures CaCr2Al10, ErNi10Si2 and ScFe6Ga6. The calcium atoms within the Ca@Ru4Zn16 polyhedra have flattened tetrahedral ruthenium coordination, reducing the calcium site symmetry to \n \n \n \n \n 4\n ‾\n \n \n \n \n$\\bar{4}$\n\n \n \n 2m (instead of 4/mmm in the aristotype). Electronic structure calculations show a substantial charge transfer from calcium to ruthenium and an almost neutral zinc substructure.","PeriodicalId":23855,"journal":{"name":"Zeitschrift für Kristallographie - Crystalline Materials","volume":"120 20","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Kristallographie - Crystalline Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/zkri-2024-0084","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The zinc-rich intermetallic phases CaRu2Zn10, SrRu2Zn10 and EuRu2Zn10 were synthesized by induction-melting of the elements in sealed tantalum ampoules followed by annealing to increase the crystallinity. The samples were characterized by powder X-ray diffraction and the structures were refined from single crystal X-ray diffractometer data: new type, P42/nnm, a = 894.68(14), c = 518.44(9) pm, wR2 = 0.0830, 432 F
2 values, 22 variables for CaRu2Zn10, a = 907.01(10), c = 516.35(6), wR2 = 0.0469, 445 F
2 values, 22 variables for SrRu2Zn10 and a = 902.84(9), c = 515.91(5) pm, wR2 = 0.0469, 434 F
2 values, 22 variables for EuRu2Zn10. The three structures are new ordering variants of the aristotype ThMn12. They are discussed on the basis of a group-subgroup scheme and compared to the known superstructures CaCr2Al10, ErNi10Si2 and ScFe6Ga6. The calcium atoms within the Ca@Ru4Zn16 polyhedra have flattened tetrahedral ruthenium coordination, reducing the calcium site symmetry to
4
‾
$\bar{4}$
2m (instead of 4/mmm in the aristotype). Electronic structure calculations show a substantial charge transfer from calcium to ruthenium and an almost neutral zinc substructure.