Superionic lithium transport via multiple coordination environments defined by two-anion packing

Author:

Han Guopeng1ORCID,Vasylenko Andrij1ORCID,Daniels Luke M.1ORCID,Collins Chris M.1ORCID,Corti Lucia12ORCID,Chen Ruiyong1ORCID,Niu Hongjun1,Manning Troy D.1ORCID,Antypov Dmytro12ORCID,Dyer Matthew S.12ORCID,Lim Jungwoo13ORCID,Zanella Marco1ORCID,Sonni Manel1ORCID,Bahri Mounib4ORCID,Jo Hongil12ORCID,Dang Yun1ORCID,Robertson Craig M.1,Blanc Frédéric123ORCID,Hardwick Laurence J.123ORCID,Browning Nigel D.45ORCID,Claridge John B.12ORCID,Rosseinsky Matthew J.12ORCID

Affiliation:

1. Department of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, UK.

2. Leverhulme Research Centre for Functional Materials Design, Materials Innovation Factory, 51 Oxford Street, University of Liverpool, Liverpool L7 3NY, UK.

3. Stephenson Institute for Renewable Energy, University of Liverpool, Liverpool L69 7ZF, UK.

4. Albert Crewe Centre, University of Liverpool, Research Technology Building, Elisabeth Street, Pembroke Place, Liverpool L69 3GE, UK.

5. School of Engineering, Department of Mechanical, Materials and Aerospace Engineering, University of Liverpool, Liverpool L69 3GH, UK.

Abstract

Fast cation transport in solids underpins energy storage. Materials design has focused on structures that can define transport pathways with minimal cation coordination change, restricting attention to a small part of chemical space. Motivated by the greater structural diversity of binary intermetallics than that of the metallic elements, we used two anions to build a pathway for three-dimensional superionic lithium ion conductivity that exploits multiple cation coordination environments. Li 7 Si 2 S 7 I is a pure lithium ion conductor created by an ordering of sulphide and iodide that combines elements of hexagonal and cubic close-packing analogously to the structure of NiZr. The resulting diverse network of lithium positions with distinct geometries and anion coordination chemistries affords low barriers to transport, opening a large structural space for high cation conductivity.

Publisher

American Association for the Advancement of Science (AAAS)

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