TY - JOUR
T1 - Enhanced Sodium Ion Storage Behavior of P2-Type Na2/3Fe1/2Mn1/2O2 Synthesized via a Chelating Agent Assisted Route
AU - Bai, Ying
AU - Zhao, Lixiang
AU - Wu, Chuan
AU - Li, Hui
AU - Li, Yu
AU - Wu, Feng
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/2/3
Y1 - 2016/2/3
N2 - On the basis of resource abundance and low cost, high capacity layered P2-type Na2/3Fe1/2Mn1/2O2 material is regarded as a potential cathode material for sodium-ion batteries but suffers from its unstable structure during cycling. In this work, P2-type Na2/3Fe1/2Mn1/2O2 layered materials were synthesized by a chelating agent assisted sol-gel method with NH3·H2O. With the addition of NH3·H2O and the control of the synthesis conditions, highly active material with a more stable structure and better electrochemical performance was obtained. Furthermore, the influences of structure changes during different voltage ranges (1.5-4.0 V and 1.5-4.3 V vs Na+/Na) on the Na+ storage behaviors were also evaluated and compared. It is confirmed that, when being charged to 4.2 V, an OP4-type phase emerges, which can reduce the damage by the gilding of the MeO2 layers but leads to an unstable crystal structure. For long-term cycling, it is preferred to cut off at 4.0 V rather than at 4.3 V. For the optimized P2-type Na2/3Fe1/2Mn1/2O2 calcined at 900 °C, a discharge capacity of 92 mAh/g remains after 40 cycles in the voltage range of 1.5-4.0 V, and the Coulombic efficiency remains 100%.
AB - On the basis of resource abundance and low cost, high capacity layered P2-type Na2/3Fe1/2Mn1/2O2 material is regarded as a potential cathode material for sodium-ion batteries but suffers from its unstable structure during cycling. In this work, P2-type Na2/3Fe1/2Mn1/2O2 layered materials were synthesized by a chelating agent assisted sol-gel method with NH3·H2O. With the addition of NH3·H2O and the control of the synthesis conditions, highly active material with a more stable structure and better electrochemical performance was obtained. Furthermore, the influences of structure changes during different voltage ranges (1.5-4.0 V and 1.5-4.3 V vs Na+/Na) on the Na+ storage behaviors were also evaluated and compared. It is confirmed that, when being charged to 4.2 V, an OP4-type phase emerges, which can reduce the damage by the gilding of the MeO2 layers but leads to an unstable crystal structure. For long-term cycling, it is preferred to cut off at 4.0 V rather than at 4.3 V. For the optimized P2-type Na2/3Fe1/2Mn1/2O2 calcined at 900 °C, a discharge capacity of 92 mAh/g remains after 40 cycles in the voltage range of 1.5-4.0 V, and the Coulombic efficiency remains 100%.
KW - P2-type NaFeMnO
KW - cathode
KW - chelating agent
KW - phase transition
KW - sodium ion batteries
KW - sodium ion diffusion
UR - http://www.scopus.com/inward/record.url?scp=84957581464&partnerID=8YFLogxK
U2 - 10.1021/acsami.5b11848
DO - 10.1021/acsami.5b11848
M3 - Article
AN - SCOPUS:84957581464
SN - 1944-8244
VL - 8
SP - 2857
EP - 2865
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 4
ER -