Source abstract
Abstract
Polyanion compounds have relatively low energy density compared to plain oxides as cathode materials. We for the first time report on a Li-rich fluorophosphate compound, Li5V2PO4F8, that can have high energy density originating from both the multielectron reaction of vanadium and high voltage induced by a fluorine. The developed material has a new crystal structure that has a robust three-dimensional framework of corner-sharing octahedra VO2F4 with tetrahedra PO4 and three-dimensional lithium ion diffusion pathways, which can facilitate the (de)intercalation of lithium ions. Its theoretical capacity is 285 mAh/g when two electrons are exploited. Practically, it shows the highest redox voltage, ∼4.4 V (vs Li/Li+), among V3+/V4+ redox reactions, with 111 mAh/g of reversible capacity. Only in the first charge does it show an active redox reaction of the V4+/V5+ at ∼4.9 V (vs Li/Li+) with 228 mAh/g of charge capacity. Moreover, the vanadium-deficient phase shows stable capacity retention and good rate capability at both charging and discharging rates up to the 2C rate. The discovery of the lithium- and fluorine-rich phosphate compounds reported here introduces a new family of cathode materials, and further exploration and optimization can be expected to unlock the full potential of this family.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea
Energy Storage and Distributed Resources Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States
Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, New South Wales 2234, Australia
School of Chemistry, The University of Sydney, Sydney 2006, Australia
Funding
Ministry of Education · National Research Foundation of Korea