Li2TMSiO4 (TM = Mn, Fe, Co, etc.) is regarded as a new class of cathode materials for next generation Li-ion batteries because of the theoretical possibility of reversible deintercalation of two Li ions from the structure (ca. 330 mA hg−1). Nevertheless, the silicate cathode still suffers from low electronic conductivity, slow Li ion diffusion and structural instability upon deep cycling. To solve these problems, for the first time, we propose a rational design of mesocrystalline Li2FeSiO4 hollow discoids with an ordered single-crystal-like structure and highly exposed (001) facets. The Li2FeSiO4 mesocrystals display a near theoretical discharge capacity, superior rate capability and good cycling stability. The enhanced Li storage performance is ascribed to the unique structural features with a large surface area generated from the hollow mesocrystal structure and a shortened Li+ diffusion path along (001) exposed facets. This new facile, elegant synthesis method that enables the manipulation of crystal growth and subsequent improvements in the electronic and ionic kinetics and structural integrity should have a positive impact on the research and development of silicate materials as promising cathodes for next generation Li-ion batteries.
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