TY - JOUR
T1 - Lowering Charge Transfer Barrier of LiMn2O4 via Nickel Surface Doping to Enhance Li+ Intercalation Kinetics at Subzero Temperatures
AU - Zhang, Wei
AU - Sun, Xiaoli
AU - Tang, Yuxin
AU - Xia, Huarong
AU - Zeng, Yi
AU - Qiao, Liang
AU - Zhu, Zhiqiang
AU - Lv, Zhisheng
AU - Zhang, Yanyan
AU - Ge, Xiang
AU - Xi, Shibo
AU - Wang, Zhiguo
AU - Du, Yonghua
AU - Chen, Xiaodong
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/9/11
Y1 - 2019/9/11
N2 - Sluggish interfacial kinetics leading to considerable loss of energy and power capabilities at subzero temperatures is still a big challenge to overcome for Li-ion batteries operating under extreme environmental conditions. Herein, using LiMn2O4 as the model system, we demonstrated that nickel surface doping to construct a new interface owning lower charge transfer energy barrier, could effectively facilitate the interfacial process and inhibit the capacity loss with decreased temperature. Detailed investigations on the charge transfer process via electrochemical impedance spectroscopy and density functional theory calculation, indicate that the interfacial chemistry tuning could effectively lower the activation energy of charge transfer process by nearly 20%, endowing the cells with â75.4% capacity at-30 °C, far surpassing the hardly discharged unmodified counterpart. This control of surface chemistry to tune interfacial dynamics proposes insights and design ideas for batteries to well survive under thermal extremes.
AB - Sluggish interfacial kinetics leading to considerable loss of energy and power capabilities at subzero temperatures is still a big challenge to overcome for Li-ion batteries operating under extreme environmental conditions. Herein, using LiMn2O4 as the model system, we demonstrated that nickel surface doping to construct a new interface owning lower charge transfer energy barrier, could effectively facilitate the interfacial process and inhibit the capacity loss with decreased temperature. Detailed investigations on the charge transfer process via electrochemical impedance spectroscopy and density functional theory calculation, indicate that the interfacial chemistry tuning could effectively lower the activation energy of charge transfer process by nearly 20%, endowing the cells with â75.4% capacity at-30 °C, far surpassing the hardly discharged unmodified counterpart. This control of surface chemistry to tune interfacial dynamics proposes insights and design ideas for batteries to well survive under thermal extremes.
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U2 - 10.1021/jacs.9b05531
DO - 10.1021/jacs.9b05531
M3 - Article
C2 - 31448603
AN - SCOPUS:85072057500
SN - 0002-7863
VL - 141
SP - 14038
EP - 14042
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 36
ER -