Wednesday, 4 October 2017
Prince George's Exhibit Hall D/E (Gaylord National Resort and Convention Center)
Owing to the increasing demand for the electrochemical energy storage devices with sufficient capacity, high reliability and low cost, rechargeable sodium-ion batteries (SIBs) have recently regarded as alternative candidates to lithium-ion batteries (LIBs) because of their benefits on material abundance, cost-effectiveness and electrochemical similarities. However, the energy density delivered from the current SIBs is still not comparable with that of the LIBs, which was ascribed to the lower cell voltage. Therefore, developing the cathode materials with higher redox potentials is eagerly anticipated. As one of the most promising cathode materials, carbon-coated sodium vanadium fluorophosphates (Na3V2(PO4)2F3/C) nanocomposites have been extensively investigated due to the merits of their sodium superionic conductor (NASICON) structures for facile ionic transportations, high voltage and high capacity. In this study, the Na3V2(PO4)2F3/C nanoparticles were synthesized using a wet-chemistry route, followed by calcination in an argon atmosphere. The resulting powders were characterized by powder X-ray diffractometer, electron microscopes and thermogravimetric analyzer to confirm their crystalline structure, morphologies and amount of carbon loading, respectively. Benefiting from the nanostructures and continuous carbon coatings, the outstanding reversible capacity (128 mAhemail@example.com A/g), rate capability (106 mAhfirstname.lastname@example.org A/g) and capacity retention (98.2 %@100 email@example.com A/g) were achieved as demonstrated by galvanostatic testing. Given the improved electrochemical properties, the NASICON-type Na3V2(PO4)2F3/C nanoparticles synthesized in the present study were anticipated to function as efficient cathode materials for SIBs.
Acknowledgement: We gratefully acknowledge financial support from the Bureau of Energy (BOE), Ministry of Economy Affair (MOEA), Taiwan.