Jeremy P. Lowen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jeremy P. Lowen has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Beatriceveena Tharigopala Vincent
School of Chemistry, University of Birmingham, Edgbaston, B15 2TT, UK
2 shared publications - Bo Dong
School of Chemistry
2 shared publications - Clare P. Grey
Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK
2 shared publications - Emma Kendrick
School of Metallurgy and Materials, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK
2 shared publications - Joshua W. Makepeace
School of Chemistry, University of Birmingham, Edgbaston, B15 2TT, UK
2 shared publications - Mark P. Stockham
School of Metallurgy and Materials, University of Birmingham, Pritchatts Road, Birmingham, UK
2 shared publications
Latest Publications
- Open Access
- 9 June 2025
- Published by Royal Society of Chemistry (RSC) in EES Batteries
- Vol. 1 (3) , 527-540
Probing the electrochemical behaviour of lithium imide as an electrolyte for solid-state batteries
Lithium imide is an underexplored candidate for an all-solid-state battery electrolyte. Here it is shown to possess many desirable properties and unusual electrochemical behaviour, alongside its first operation in two lithium metal batteries.
- 9 June 2025
- Published by Royal Society of Chemistry (RSC) in EES Batteries
- Vol. 1 (3) , 527-540
Open AccessProbing the electrochemical behaviour of lithium imide as an electrolyte for solid-state batteries
Lithium imide is an underexplored candidate for an all-solid-state battery electrolyte. Here it is shown to possess many desirable properties and unusual electrochemical behaviour, alongside its first operation in two lithium metal batteries.
- Open Access
- 6 September 2024
- Published by American Chemical Society (ACS) in ChemRxiv
Quasi-liquid grain boundary conductivity in solid electrolyte candidate lithium imide
All-solid-state batteries utilising a Li-metal anode have long promised to be the next-generation of high-performance energy storage device, with a step-change in energy density, cycling stability and cell safety touted as potential advantages compared to conventional Li-ion battery cells. A key to enabling this technology is the development of solid-state electrolytes with the elusive combination of high ionic conductivity, wide electrochemical stability and the ability to form a conductive and stable interface with Li metal. Presently, oxide and sulfide-based materials, particularly garnet and argyrodite-type structures, have proved most promising for this application. However, these still suffer from a number of challenges, including resistive lithium metal interfaces, poor lithium dendrite suppression (at high current density) and low voltage stability. Here we report the first application of lithium imide, an antifluorite-structured material, as a solid electrolyte in a Li-metal battery. Low-temperature synthesis of lithium imide produces promising Li-ion conductivity, reaching > 1 mS cm-1 at 30 ˚C using a modest post-synthetic mechanochemical treatment, as well as displaying at least 5 V stability vs Li+/Li. In situ electrochemical operation of lithium imide with Li-metal electrodes reveals a 1000-fold increase in its measured ionic conductivity, whilst appearing to remain an electronic insulator. It is postulated that stoichiometry variation at the grain boundary leads to a highly disordered quasi-liquid state, facilitating this conductivity improvement. Furthermore, the material is shown to possess impressive stability under high current density conditions (70 mA cm-2) as well as the ability to operate in Li-metal battery cells. These results not only highlight the promising performance of lithium imide, but also its potential to be the basis for a new family of antifluorite based solid electrolytes.
- 6 September 2024
- Published by American Chemical Society (ACS) in ChemRxiv
Open AccessQuasi-liquid grain boundary conductivity in solid electrolyte candidate lithium imide
All-solid-state batteries utilising a Li-metal anode have long promised to be the next-generation of high-performance energy storage device, with a step-change in energy density, cycling stability and cell safety touted as potential advantages compared to conventional Li-ion battery cells. A key to enabling this technology is the development of solid-state electrolytes with the elusive combination of high ionic conductivity, wide electrochemical stability and the ability to form a conductive and stable interface with Li metal. Presently, oxide and sulfide-based materials, particularly garnet and argyrodite-type structures, have proved most promising for this application. However, these still suffer from a number of challenges, including resistive lithium metal interfaces, poor lithium dendrite suppression (at high current density) and low voltage stability. Here we report the first application of lithium imide, an antifluorite-structured material, as a solid electrolyte in a Li-metal battery. Low-temperature synthesis of lithium imide produces promising Li-ion conductivity, reaching > 1 mS cm-1 at 30 ˚C using a modest post-synthetic mechanochemical treatment, as well as displaying at least 5 V stability vs Li+/Li. In situ electrochemical operation of lithium imide with Li-metal electrodes reveals a 1000-fold increase in its measured ionic conductivity, whilst appearing to remain an electronic insulator. It is postulated that stoichiometry variation at the grain boundary leads to a highly disordered quasi-liquid state, facilitating this conductivity improvement. Furthermore, the material is shown to possess impressive stability under high current density conditions (70 mA cm-2) as well as the ability to operate in Li-metal battery cells. These results not only highlight the promising performance of lithium imide, but also its potential to be the basis for a new family of antifluorite based solid electrolytes.