2011
DOI: 10.1002/zaac.201100268
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Crystal Structure of [Li8(H2O)29]­[Sn10O4S20]·2H2O

Abstract: Li 8 (H 2 O) 29 ][Sn 10 O 4 S 20 ]·2H 2 O (1), which was obtained by an unusual synthesis pathway, represents the Li + salt of the supertetrahedral cluster anion [Sn 10 O 4 S 20 ] 8-. Due to the distinct hydration tendency of Li + , the crystal structure differs notably from that of a corresponding Cs + salt. Compound 1 extends the still very fragmentary

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

4
21
0

Year Published

2011
2011
2021
2021

Publication Types

Select...
7

Relationship

5
2

Authors

Journals

citations
Cited by 17 publications
(26 citation statements)
references
References 25 publications
4
21
0
Order By: Relevance
“…18,19 While the lighter homologous ternary systems Li 4 SiS 4 and Li 4−x Si 1−x P x S 4 have been synthesized and show similar conductivities to the corresponding germanates, 13,20 the influence of replacing germanium with the heavier homologue tin has not been investigated so far. On the thiostannate side, the only known compounds are the salt of the dinuclear anion, Li 4 Sn 2 S 6 ·8en, 21 and the salt of a super-tetrahedral cluster, [Li 8 22 In contrast to a variety of heavier homologues, 23 the ortho-thiostannate salt of the lightest alkali metal ion, Li 4 SnS 4 , has not been published to date neither in solvent-free form nor as any solvate. Motivated by the promising developments in inorganic Li + ion conductors, we intended to fill this gap by generating the so far missing, smallest unit and to determine its Li + ion conductivity.…”
Section: S·cmmentioning
confidence: 99%
“…18,19 While the lighter homologous ternary systems Li 4 SiS 4 and Li 4−x Si 1−x P x S 4 have been synthesized and show similar conductivities to the corresponding germanates, 13,20 the influence of replacing germanium with the heavier homologue tin has not been investigated so far. On the thiostannate side, the only known compounds are the salt of the dinuclear anion, Li 4 Sn 2 S 6 ·8en, 21 and the salt of a super-tetrahedral cluster, [Li 8 22 In contrast to a variety of heavier homologues, 23 the ortho-thiostannate salt of the lightest alkali metal ion, Li 4 SnS 4 , has not been published to date neither in solvent-free form nor as any solvate. Motivated by the promising developments in inorganic Li + ion conductors, we intended to fill this gap by generating the so far missing, smallest unit and to determine its Li + ion conductivity.…”
Section: S·cmmentioning
confidence: 99%
“…Before 1985, only lithium metal and lithium alloys were used as anode materials. Especially silicon has shown to be very attractive, due to a very high theoretical capacity of approximately 4000 mAh/g, with a maximum uptake of 4.4 equivalents of Li per Si atom in Li 22 Si 5 . Graphite, with a theoretical capacity of 372 mAh/g, has so far been the standard anode material in commercial lithium batteries.…”
Section: Introductionmentioning
confidence: 99%
“…[2][3][4] A variety of materials-mostly tin or silicon compounds-belong to the most interesting candidates. Especially silicon has shown to be very attractive, due to a very high theoretical capacity of approximately 4000 mAh/g, with a maximum uptake of 4.4 equivalents of Li per Si atom in Li 22 Si 5 . The main challenge for the implementation of these composite anodes is the large volume change during lithium insertion and extraction.…”
Section: Introductionmentioning
confidence: 99%
“…It has an idealized T d symmetry and can be described as a supertetrahedral cluster (denoted as T3) formed by ten corner‐linked SnS 4 polyhedra. Four empty sites are occupied by O 2– anions expanding the coordination number of Sn from four to five or six , , . All Sn‐O‐S compounds contain isolated [Sn 10 S 20 O 4 ] 8– anionic clusters with inorganic cations compensating the negative charges like in [Cs 8 (H 2 O) 13 ][Sn 10 S 20 O 4 ] and [Li 8 (H 2 O) 29 ][Sn 10 S 20 O 4 ] · 2H 2 O, and only in {[Ni(1,2‐dach) 2 (ma)] 4 [Sn 10 S 20 O 4 ]} (1,2‐dach = 1,2‐diaminocyclohexane; ma = methylamine) the cluster is expanded via sulfur atoms to Ni 2+ centered complexes.…”
Section: Introductionmentioning
confidence: 99%
“…Four empty sites are occupied by O 2anions expanding the coordination number of Sn from four to five or six. [24,25,29] [24] and only in {[Ni(1,2-dach) 2 (ma)] 4 [Sn 10 S 20 O 4 ]} (1,2-dach = 1,2-diaminocyclohexane; ma = methylamine) [30] the cluster is expanded via sulfur atoms to Ni 2+ centered complexes.…”
Section: Introductionmentioning
confidence: 99%