文摘
A novel synchronous lithiation route has been successfully used to coat Li+-conductive Li2ZrO3 on the surface of LiNi1/3Co1/3Mn1/3O2 (Li2ZrO3@LNCMO). In this strategy, Li2ZrO3 layer and LiNi1/3Co1/3Mn1/3O2 host simultaneously form from ZrO2@Ni1/3Co1/3Mn1/3C2O4路xH2O precursor. In compared to bare LNCMO, the reversible capacity, cycling performance, thermal stability, rate capability, and polarization of Li2ZrO3@LNCMO have all been greatly improved. At 0.1 and 10 C, the specific capacity of Li2ZrO3@LNCMO is 192 and 106 mAh g鈥?, respectively, while they are 178 and 46 mAh g鈥? for bare LNCMO. At a current density of 5 C, the capacity retention of Li2ZrO3@LNCMO at 25 and 55 掳C after 400 cycles is enhanced to 93.8% and 85.1%, respectively, compared to 69.2% and 37.4% of bare LNCMO. The largely enhanced electrochemical performances of Li2ZrO3@LNCMO cathode can be attributed to the high Li-ion conductivity as well as the proctection of Li2ZrO3 coating. Li+ conductivity of Li2ZrO3@LNCMO is about 20 times higher than that of bare LNCMO. Moreover, the migration of partial Zr4+ to the host LNCMO phase not only benefits Li-ion or electron conductivity but also alleviates the Li鈥揘i cation mixing and improves the structure stability. The cations migration, doping effect, and the reduced cation mixing further contribute to the electrochemical performance enhancement.