Affiliation:
1. NorthEast Center for Chemical Energy Storage Binghamton University Binghamton NY 139020‐6000 USA
2. Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge MA 02139 USA
3. Department of Physics Applied Physics and Astronomy and NorthEast Center for Chemical Energy Storage Binghamton University Binghamton NY USA
4. X‐ray Science Division Advanced Photon Source Argonne National Laboratory Argonne IL 60439 USA
5. Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK
6. Department of NanoEngineering University of California San Diego 9500 GilmanDrive #0448 La Jolla CA 92093 USA
7. Department of Chemistry Stony Brook University Stony Brook New York NY 11974 USA
Abstract
AbstractVanadyl phosphates comprise a class of multielectron cathode materials capable of cycling two Li+, about 1.66 Na+, and some K+ ions per redox center. In this review, structures, thermodynamic stabilities, and ion diffusion kinetics of various AxVOPO4 (A = Li, Na, K, NH4) polymorphs are discussed. Both the experimental data and first‐principle calculations indicate kinetic limitations for alkali metal ions cycling, especially between for 0 ≤ x ≤ 1, and metastability of phases with x > 1. This creates challenges for multiple‐ion cycling, as the slow kinetics call for nanosized particles, which being metastable and reactive with organic electrolytes are prone to side reactions. Thus, various synthesis approaches, surface coating, and transition metal ion substitution strategies are discussed here as possible ways to stabilize AxVOPO4 structures and improve alkali metal ion diffusion. The role of advanced characterization techniques, such as X‐ray absorption spectroscopy, diffraction, pair distribution function analysis and 7Li and 31P NMR, in understanding the reaction mechanism from both structural and electronic points of view is emphasized.
Funder
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Argonne National Laboratory
Cited by
33 articles.
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