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Tuesday, 22 May, 2018

Supertetrahedra Lego for future batteries

New materials

T5/T5-type sodium phosphidosilcate supertetrahedron. Picture: A. Hatz

T5/T5-type sodium phosphidosilcate supertetrahedron. Picture: A. Hatz

New sodium-based all-solid-state batteries could enable future energy storage devices using only the easy-to-access, cheap and earth abundant elements sodium, silicon and phosphorous (Na, Si and P). By shaping them into sodium phosphidosilicates containing large supertetrahedral entities, Prof Dirk Johrendt in collaboration with NIM scientist Prof Bettina Lotsch generated solid electrolytes with very high ionic conductivity.

Solid sodium ion conductors, based on the earth abundant and relatively cheap elements Na, Si and P, can be composed into sodium phosphidosilicates. These provide an intriguing structure composed of phosphidosilicate supertetrahedra surrounded by sodium ions.
LMU scientists Professor Opens external link in new windowDirk Johrendt and Professor Opens external link in new windowBettina Lotsch synthesized and analyzed six new phosphidosilicate structures and could show that with increasing size of the supertetrahedra, the ionic conductivity of the structures also increased. The highest ionic conductivity was detected for the T5/T5-type supertetrahedral cluster. Such material is a potential solid electrolyte candidate in a sodium-based all-solid-state battery. All new structures and their properties were described in Opens external link in new windowAngewandte Chemie.

Lego: Stacking tetrahedral building units into supertetrahedra
A T5/T5 supertetrahedron can be pictured as a large tetrahedron with an edge length of five SiP4 tetrahedral building units. The SiP4 units are linked by vertices and as special feature the T5 supertetrahedron lacks one Si atom in its center to attain charge neutrality in its interior. The described T5 supertetrahedra are interconnected by fusing SiP4 tetrahedra at the corner of neighboring supertetrahedra. Connected in this way, the supertetrahedra form interpenetrating networks of two six-membered rings resembling in a three-dimensional diamond-like network. The sodium cations are distributed between the supertetrahedral networks and only partially occupied.
“Our supertetrahedral structures are the only known sodium conducting SiP-based compounds,” explains Anna-Katharina Hatz, one of the first authors of the publication. ”We are very happy we could show them to be as efficient as other known sodium ion conductors, but generated solely from earth abundant and cheap elements.”

All-solid-state batteries
At the moment, all-solid-state batteries are in focus of research. They potentially offer for example higher safety and faster charging than commercial lithium ion batteries (LIBs). Because of a future shortage and high costs of lithium, sodium ion batteries are an attractive replacement for LIBs.
The scientists could show that the conductivity of the sodium phosphidosilicates clearly increased with their cluster size. This could be explained by the dilution of the sodium cations, as the relative anionic charge density decreased with increasing network size. Hence, with the decreasing sodium density, the number of partially occupied sodium sites increased, which in turn then enhanced the conductivity. Within the supertetrahedral cluster, the sodium cations migrate through ion channels. The pathways connecting these channels and the channels themselves became broader with increasing supertetrahedral size, leading to a fast, almost three-dimensional sodium migration.
“With this background, our aim is to find more, even faster ion conductors in the new class of sodium phosphidosilicates, and to provide a new conductor material for the next generation of energy storage devices.”, tells Hatz.


Publication:

Fast sodium ion conductivity in supertetrahedral phosphidosilicates.
Haffner A*, Hatz A-K*, Moudrakovski I, Lotsch BV, Johrendt D. Angewandte Chemie 2018, 57(21):6155-6160. Opens external link in new windowdoi:10.1002/anie.201801405
*contributed equally

Contact:
Prof Dr Bettina Valeska Lotsch
Chemistry Department
Ludwig-Maximilians-Universität München
Butenandtstr. 5-13, Building D
81377 Munich
Germany

Phone: +49 (0)89 2180 - 77429

Email: Opens window for sending emailbettina.lotsch(at)cup.uni-muenchen.de

Web: Opens external link in new windowwww.cup.uni-muenchen.de/ac/lotsch/research/


Prof Dr Bettina Lotsch
Nanochemistry Department
Max Planck Institute for Solid State Research
Heisenbergstr. 1
70569 Stuttgart
Germany

Phone: +49 (0)711 689 - 1610

Email: Opens window for sending emailb.lotsch(at)fkf.mpg.de

Web: Opens external link in new windowwww.fkf.mpg.de/171964/Prof_Dr_Bettina_V_Lotsch

 

Prof Dr Dirk Johrendt
Inorganic and Magnetic Materials
Chemistry Department
Ludwig-Maximilians-Universität München
Butenandtstr. 5-13, Building D
81377 Munich
Germany

Phone: +49 (0)89 2180 - 77430

Email: bettina.lotsch(at)cup.uni-muenchen.deOpens window for sending emaildirk.johrendt(at)cup.uni-muenchen.de

Web: Opens external link in new windowwww.cup.lmu.de/ac/johrendt/

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