Key design considerations for synthesis of mesoporous α-Li3V2(PO4)3/C for high power lithium batteries
Creators
- 1. Department of Mechanical Engineering, National University of Singapore, 117575 (Singapore)
Description
Highlight• Reports facile and scalable one-pot soft-template synthesis for α-Li3V2(PO4)3/C. • Mesoporous α-Li3V2(PO4)3/C particles are formed by 20-30nm grains & 3-25nm pores. • Densely packed α-Li3V2(PO4)3/C shows high discharge capacity of 178mAh/g at 0.1C. • α-Li3V2(PO4)3/C exhibits impressive rate performance with 90mAh/g at 30C. In this article, we propose key design criteria to synthesis carbon coated α-Li3V2(PO4)3 positive electrode material for high power lithium batteries. A facile and scalable one-pot soft template method is adopted to synthesize α-Li3V2(PO4)3/C (LVP/C), which exhibits unique morphology of micron-size mesoporous secondary particles comprising interconnected primary nanoparticles showing good storage and rate performances with long cycle life. This cathode material displays high discharge capacities of 178, 90 and 59 mAh.g−1 at 0.1C, 30C and 80C, respectively. The mesoporous LVP/C with a 3D lithium diffusion network exhibits better rate performance (90 mAh.g−1 at 30C) as compared to the known phosphate, silicate or oxide cathode materials for lithium-ion batteries (LIBs). In addition, LVP/C electrode material retains 80% (at 1C) and 100% (at 20C) of its initial capacity after 1,000 cycles. The phase transitions during delitiation/litiation are discussed at different cutoff voltages, corresponding to the number of moles of lithium involved in the redox reactions. The reversibility of electrochemical extraction/insertion processes are confirmed using operando XRD measurements. Observed storage performances can be attributed not only to high crystallinity of LVP/C calcined at 800°C for 6 h; also to the unique mesoporous architecture of this carbon coated cathode material forming high packing density during the soft template synthesis. Obtained dense packed mesoporous architecture of LVP/C allows favourable (i) electrolyte wettability for lithium-incorporation from the electrolyte and (ii) long electronic wiring by the well-connected carbon coating towards the current collector.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2021.137831Additional details
Additional titles
- Augmented title (English)
- Lithium storage;Lithium vanadium phosphate;Cathode material;Mesoporous morphology;High rate;Electron diffusion length
Identifiers
- DOI
- 10.1016/j.electacta.2021.137831;
- PII
- S0013468621001201;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 372
- Journal Page Range
- vp.
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54120908
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- CAPACITORS; CAPACITY; CATHODES; ELECTROCHEMISTRY; LITHIUM ION BATTERIES; NANOPARTICLES; NANOSTRUCTURES; OXIDES; PACKINGS; PHASE TRANSFORMATIONS; REDOX REACTIONS; STOWING; SYNTHESIS; X-RAY DIFFRACTION
- Descriptors DEC
- CHALCOGENIDES; CHEMICAL REACTIONS; CHEMISTRY; COHERENT SCATTERING; DIFFRACTION; ELECTRIC BATTERIES; ELECTRICAL EQUIPMENT; ELECTROCHEMICAL CELLS; ELECTRODES; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; EQUIPMENT; OXYGEN COMPOUNDS; PARTICLES; SCATTERING
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier Ltd. All rights reserved.