TY - JOUR
T1 - High-Performance P2-Na 0.70 Mn 0.80 Co 0.15 Zr 0.05 O 2 Cathode for Sodium-Ion Batteries
AU - Wang, Yongqing
AU - Zhao, Fengyue
AU - Qian, Yumin
AU - Ji, Hongbing
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/12/12
Y1 - 2018/12/12
N2 - Roomerature sodium-ion batteries (NIBs) using a manganese-based layered cathode have been considered promising candidates for grid-scale energy storage applications. However, manganese-based materials suffer from serious Jahn-Teller distortion, phase transition, and unstable interface, resulting in severe structure degradation, sluggish sodium diffusion kinetics, and poor cycle, respectively. Herein, we demonstrate a Zr-doped Na 0.70 Mn 0.80 Co 0.15 Zr 0.05 O 2 material with much improved specific capacity and rate capability compared with Zr-free Na 0.70 Mn 0.85 Co 0.15 O 2 when used as cathode materials for NIBs. The material delivers a reversible capacity of 173 mA h g -1 at 0.1 C rate, corresponding to approximately 72% of the theoretical capacity (239 mA h g -1 ) based on a single-electron redox process, and a capacity retention of 88% after 50 cycles was obtained. Additionally, a homogenous solid-state interphase (SEI) film was revealed directly by high-resolution transmission electron microscopy in Zr-doped material after battery cycling. Electrochemical impedance spectroscopy proves that the formation of SEI films provides the Zr-doped material with special chemical/electrochemical stability. These results here give clear evidence of the utility of Zr-doping to improve the surface and environmental stability, sodium diffusion kinetics, and electrochemical performance of P2-type layered structure, promising advanced sodium-ion batteries with higher energy density, higher surface stability, and longer cycle life compared with the commonly used magnesiumdoping method in electrode materials.
AB - Roomerature sodium-ion batteries (NIBs) using a manganese-based layered cathode have been considered promising candidates for grid-scale energy storage applications. However, manganese-based materials suffer from serious Jahn-Teller distortion, phase transition, and unstable interface, resulting in severe structure degradation, sluggish sodium diffusion kinetics, and poor cycle, respectively. Herein, we demonstrate a Zr-doped Na 0.70 Mn 0.80 Co 0.15 Zr 0.05 O 2 material with much improved specific capacity and rate capability compared with Zr-free Na 0.70 Mn 0.85 Co 0.15 O 2 when used as cathode materials for NIBs. The material delivers a reversible capacity of 173 mA h g -1 at 0.1 C rate, corresponding to approximately 72% of the theoretical capacity (239 mA h g -1 ) based on a single-electron redox process, and a capacity retention of 88% after 50 cycles was obtained. Additionally, a homogenous solid-state interphase (SEI) film was revealed directly by high-resolution transmission electron microscopy in Zr-doped material after battery cycling. Electrochemical impedance spectroscopy proves that the formation of SEI films provides the Zr-doped material with special chemical/electrochemical stability. These results here give clear evidence of the utility of Zr-doping to improve the surface and environmental stability, sodium diffusion kinetics, and electrochemical performance of P2-type layered structure, promising advanced sodium-ion batteries with higher energy density, higher surface stability, and longer cycle life compared with the commonly used magnesiumdoping method in electrode materials.
KW - P2
KW - cathode
KW - doping
KW - sodium-ion batteries
KW - solid-state interface
UR - http://www.scopus.com/inward/record.url?scp=85058306863&partnerID=8YFLogxK
U2 - 10.1021/acsami.8b15693
DO - 10.1021/acsami.8b15693
M3 - Article
C2 - 30461267
AN - SCOPUS:85058306863
SN - 1944-8244
VL - 10
SP - 42380
EP - 42386
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 49
ER -