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@ARTICLE{Alahmari:859588,
author = {Alahmari, Fatimah and Davaasuren, Bambar and Emwas,
Abdul-Hamid and Rothenberger, Alexander},
title = {{T}hioaluminogermanate {M}({A}l{S}2)({G}e{S}2)4 ({M} =
{N}a, {A}g, {C}u): {S}ynthesis, {C}rystal {S}tructures,
{C}haracterization, {I}on-{E}xchange and {S}olid-{S}tate
27{A}l and 23{N}a {NMR} {S}pectroscopy},
journal = {Inorganic chemistry},
volume = {57},
number = {7},
issn = {1520-510X},
address = {Washington, DC},
publisher = {American Chemical Society},
reportid = {FZJ-2019-00437},
pages = {3713 - 3719},
year = {2018},
abstract = {The new thioaluminogermanate Na(AlS2)(GeS2)4 (1) was
successfully synthesized by a direct combination reaction.
The compound crystallizes in the monoclinic space group
P21/n (no. 14) with unit cell parameters a = 6.803(3) Å, b
= 38.207(2) Å, c = 6.947(4) Å, and β = 119.17(3)°. The
crystal structure is composed of a [(AlS2)(GeS2)4]− 3D
polyanionic network, in which Al and Ge atoms share the
atomic positions and Na cations occupy the channels and
voids formed by the connection of (Ge/Al)S4 tetrahedra. The
title compound shows a cation-exchange property with
monovalent Ag+ and Cu+ ions at room temperature in solvent
media, resulting in the formation of the isostructural
compounds Ag(AlS2)(GeS2)4 (2) and Cu(AlS2)(GeS2)4 (3),
respectively. The ion-exchange products Ag(AlS2)(GeS2)4 (2)
and Cu(AlS2)(GeS2)4 (3) show higher air stability and
narrower bandgap energies compared to those of the parent
compound Na(AlS2)(GeS2)4 (1).},
cin = {IEK-1},
ddc = {540},
cid = {I:(DE-Juel1)IEK-1-20101013},
pnm = {131 - Electrochemical Storage (POF3-131)},
pid = {G:(DE-HGF)POF3-131},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:29537828},
UT = {WOS:000429283200028},
doi = {10.1021/acs.inorgchem.7b02980},
url = {https://juser.fz-juelich.de/record/859588},
}