TY - JOUR
T1 - Mg-doped Li 1.133 Ni 0.2 Co 0.2 Mn 0.467 O 2 in Li site as high-performance cathode material for Li-ion batteries
AU - Jin, Yanling
AU - Xu, Youlong
AU - Ren, Fang
AU - Ren, Penggang
N1 - Publisher Copyright:
© 2019
PY - 2019/8
Y1 - 2019/8
N2 - Li- and Mn-rich layered oxides as cathode materials attract considerable attention owing to the superior capacity. However, their practical applications are still hindered by the inherent drawbacks such as the poor rate capability. Based on the structure characteristics that Li diffuses through two-dimensional lithium ion diffusion tunnel during intercalation/extraction, enlarging Li layer spacing is an effective strategy to increase Li + diffusion coefficient and enhance rate capability. In this work, Mg-doping in Li site is employed to enhance the electrochemical performance of Li 1.133 Ni 0.2 Co 0.2 Mn 0.467 O 2 . With the ionic radius similar to that of Li + , Mg 2+ is more suitable to occupy Li site and enlarge lattice parameter c which is critical to Li layer spacing and lithium ion diffusion coefficient. Consequently, Li 1.123 Mg 0.010 Ni 0.2 Co 0.2 Mn 0.467 O 2 exhibits high initial capacity of 308 mAh g −1 at 25 mA g −1 and better rate capability as high as 166.1 mAh g −1 at 625 mA g −1 under 2.0–4.8 V vs. Li/Li + . Its ionic conductivity at 4.1 V during charge and 3.7 V during discharge is 4.1 ∗ 10 −12 cm 2 ·s −1 and 9.2 ∗ 10 −13 cm 2 ·s −1 , 6.10 times and 6.07 times higher than that of pristine sample, indicating that magnesium doping facilitates the migration and diffusion of Li + due to the enlargement of lithium ion diffusion channel.
AB - Li- and Mn-rich layered oxides as cathode materials attract considerable attention owing to the superior capacity. However, their practical applications are still hindered by the inherent drawbacks such as the poor rate capability. Based on the structure characteristics that Li diffuses through two-dimensional lithium ion diffusion tunnel during intercalation/extraction, enlarging Li layer spacing is an effective strategy to increase Li + diffusion coefficient and enhance rate capability. In this work, Mg-doping in Li site is employed to enhance the electrochemical performance of Li 1.133 Ni 0.2 Co 0.2 Mn 0.467 O 2 . With the ionic radius similar to that of Li + , Mg 2+ is more suitable to occupy Li site and enlarge lattice parameter c which is critical to Li layer spacing and lithium ion diffusion coefficient. Consequently, Li 1.123 Mg 0.010 Ni 0.2 Co 0.2 Mn 0.467 O 2 exhibits high initial capacity of 308 mAh g −1 at 25 mA g −1 and better rate capability as high as 166.1 mAh g −1 at 625 mA g −1 under 2.0–4.8 V vs. Li/Li + . Its ionic conductivity at 4.1 V during charge and 3.7 V during discharge is 4.1 ∗ 10 −12 cm 2 ·s −1 and 9.2 ∗ 10 −13 cm 2 ·s −1 , 6.10 times and 6.07 times higher than that of pristine sample, indicating that magnesium doping facilitates the migration and diffusion of Li + due to the enlargement of lithium ion diffusion channel.
KW - Electrochemical performance
KW - Li- and Mn-rich layered oxides
KW - Lithium ion diffusion coefficient
KW - Mg-doping in Li site
UR - https://www.scopus.com/pages/publications/85063448526
U2 - 10.1016/j.ssi.2019.03.020
DO - 10.1016/j.ssi.2019.03.020
M3 - 文章
AN - SCOPUS:85063448526
SN - 0167-2738
VL - 336
SP - 87
EP - 94
JO - Solid State Ionics
JF - Solid State Ionics
ER -