posted on 2018-01-31, 00:00authored byJiali Wang, Hailong Wu, Yanhua Cui, Shengzhou Liu, Xiaoqing Tian, Yixiu Cui, Xiaojiang Liu, Yin Yang
Searching for high-performance
cathode materials is a crucial task to develop advanced lithium-ion
batteries (LIBs) with high-energy densities for electrical vehicles
(EVs). As a promising lithium-rich material, Li2MnO3 delivers high capacity over 200 mAh g–1 but suffers from poor structural stability and electronic conductivity.
Replacing Mn4+ ions by relatively larger Sn4+ ions is regarded as a possible strategy to improve structural stability
and thus cycling performance of Li2MnO3 material.
However, large difference in ionic radii of Mn4+ and Sn4+ ions leads to phase separation of Li2MnO3 and Li2SnO3 during high-temperature
synthesis. To prepare solid-solution phase of Li2MnO3–Li2SnO3, a buffer agent of Ru4+, whose ionic radius is in between that of Mn4+ and Sn4+ ions, is introduced to assist the formation
of a single solid-solution phase. The results show that the Li2RuO3–Li2MnO3–Li2SnO3 ternary system evolves from mixed composite
phases into a single solid-solution phase with increasing Ru content.
Meanwhile, discharge capacity of this ternary system shows significantly
increase at the transformation point which is ascribed to the improvement
of Li+/e– transportation kinetics and
anionic redox chemistry for solid-solution phase. The role of Mn/Sn
molar ratio of Li2RuO3–Li2MnO3–Li2SnO3 ternary system
has also been studied. It is revealed that higher Sn content benefits
cycling stability of the system because Sn4+ ions with
larger sizes could partially block the migration of Mn4+ and Ru4+ from transition metal layer to Li layer, thus
suppressing structural transformation of the system from layered-to-spinel
phase. These findings may enable a new route for exploring ternary
or even quaternary lithium-rich cathode materials for LIBs.