Abstract
As a result of the redox reaction of lattice oxygen occurring at 4.5 V, the Li-rich manganese cathode material with an O3 configuration has a theoretically high discharge capacity (>250 mA h/g). However, it also suffers a structural transition from layered structure to spinel structure in the cycling process, leading to severe voltage decay and capacity fading. On contrary, the O6 type material obtained via ion exchange of P2 type material can effectively inhibit the phase transition and stabilize the layered structure. Hence, in this work, we design an O6/O3 multi-phase composite material after ion exchange of the P2/O3 nanocrystalline composite. Compared with the O3 type cathode, the as-obtained cathode composite exhibits a higher initial discharge capacity (≈265 mA h/g at 20 mA/g) and an excellent capacity retention (≈87% after 100 cycles). Moreover, the first cycle Coulombic efficiency increases by nearly 10%, and voltage attenuation is effectively inhibited. Our findings demonstrate that modulating the O6/O3 configuration is a practical and simple methodology to promote the electrochemical performance of lithium-rich layered materials.
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