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Add a Pinch of Tetrel: The Transformation of a Centrosymmetric Metal into a Nonsymmorphic and Chiral Semiconductor.
Lee, Shannon J; Viswanathan, Gayatri; Carnahan, Scott L; Harmer, Colin P; Akopov, Georgiy; Rossini, Aaron J; Miller, Gordon J; Kovnir, Kirill.
Afiliação
  • Lee SJ; Department of Chemistry, Iowa State University, 50011, Ames, IA, USA.
  • Viswanathan G; Ames Laboratory, US DOE, 50011, Ames, IA, USA.
  • Carnahan SL; Department of Chemistry, Iowa State University, 50011, Ames, IA, USA.
  • Harmer CP; Ames Laboratory, US DOE, 50011, Ames, IA, USA.
  • Akopov G; Department of Chemistry, Iowa State University, 50011, Ames, IA, USA.
  • Rossini AJ; Ames Laboratory, US DOE, 50011, Ames, IA, USA.
  • Miller GJ; Department of Chemistry, Iowa State University, 50011, Ames, IA, USA.
  • Kovnir K; Ames Laboratory, US DOE, 50011, Ames, IA, USA.
Chemistry ; 28(9): e202104319, 2022 Feb 16.
Article em En | MEDLINE | ID: mdl-34882857
Centrosymmetric skutterudite RhP3 was converted to a nonsymmorphic and chiral compound RhSi0.3 P2.7 (space group P21 21 21 ) by means of partial replacement of Si for P. The structure, determined by a combination of X-ray crystallography and solid state 31 P NMR, exhibits branched polyanionic P/Si chains that are unique among metal phosphides. A driving force to stabilize the locally noncentrosymmetric cis-RhSi2 P4 and fac-RhSi3 P3 fragments is π-electron back-donation between the Rh t2g -type orbitals and the unoccupied antibonding Si/P orbitals, which is more effective for Si than for P. In situ studies and total energy calculations revealed the metastable nature of RhSi0.3 P2.7 . Electronic structure calculations predicted centrosymmetric cubic RhP3 to be metallic which was confirmed by transport properties measurements. In contrast, the electronic structure for chiral orthorhombic RhSi0.3 P2.7 contained a bandgap, and this compound was shown to be a narrow gap semiconductor.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article