TY - JOUR
T1 - Na7TaP4
T2 - A Ternary Sodium Phosphidotantalate Containing [TaP4]7-Tetrahedra
AU - Restle, Tassilo M.F.
AU - Dums, Jasmin V.
AU - Raudaschl-Sieber, Gabriele
AU - Klein, Wilhelm
AU - Fässler, Thomas F.
N1 - Publisher Copyright:
©
PY - 2020/12/21
Y1 - 2020/12/21
N2 - While lithium phosphides have been investigated intensively, very little is known about the corresponding sodium-based phosphides. Here, we report on the first ternary Na-Ta-P compound Na7TaP4, which is easily accessible via ball milling of the elements and subsequent annealing. The single crystal X-ray structure determination [monoclinic symmetry; space group P21/c; and lattice parameters a = 11.5604(4), b = 8.1530(3), c = 11.5450(5) Å, and β = 101.602(3)°] reveals [TaP4]7- tetrahedra, which are surrounded by Na+ counterions. Na7TaP4 crystallizes in a new structure type. The structure can be described as a strongly distorted hexagonal close packing of P atoms, in which the Ta atoms are located in tetrahedral voids, and Na atoms occupy all octahedral voids and additionally 3/8 of the tetrahedral voids. The possibility to increase the ion conductivity by changing the number of charge carriers through aliovalent substitution in compounds containing [SiP4]8- and [AlP4]9- is considered. The 31P and 23Na MAS NMR as well as the Raman spectra are in accordance with the structure model, and band structure calculations predict a direct band gap of 2.9 eV.
AB - While lithium phosphides have been investigated intensively, very little is known about the corresponding sodium-based phosphides. Here, we report on the first ternary Na-Ta-P compound Na7TaP4, which is easily accessible via ball milling of the elements and subsequent annealing. The single crystal X-ray structure determination [monoclinic symmetry; space group P21/c; and lattice parameters a = 11.5604(4), b = 8.1530(3), c = 11.5450(5) Å, and β = 101.602(3)°] reveals [TaP4]7- tetrahedra, which are surrounded by Na+ counterions. Na7TaP4 crystallizes in a new structure type. The structure can be described as a strongly distorted hexagonal close packing of P atoms, in which the Ta atoms are located in tetrahedral voids, and Na atoms occupy all octahedral voids and additionally 3/8 of the tetrahedral voids. The possibility to increase the ion conductivity by changing the number of charge carriers through aliovalent substitution in compounds containing [SiP4]8- and [AlP4]9- is considered. The 31P and 23Na MAS NMR as well as the Raman spectra are in accordance with the structure model, and band structure calculations predict a direct band gap of 2.9 eV.
UR - http://www.scopus.com/inward/record.url?scp=85097846640&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.0c03021
DO - 10.1021/acs.inorgchem.0c03021
M3 - Article
C2 - 33251786
AN - SCOPUS:85097846640
SN - 0020-1669
VL - 59
SP - 18420
EP - 18426
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 24
ER -