TY - JOUR
T1 - Enhancing chemomechanical stability and high-rate performance of nickel-rich cathodes for lithium-ion batteries through three-in-one modification
AU - Li, Cong
AU - Liu, Jinzhong
AU - Su, Yuefeng
AU - Dong, Jinyang
AU - Zhang, Hongyun
AU - Wang, Meng
AU - Guan, Yibiao
AU - Yan, Kang
AU - Liu, Na
AU - Lu, Yun
AU - Li, Ning
AU - Su, Yu
AU - Wu, Feng
AU - Chen, Lai
N1 - Publisher Copyright:
© 2024
PY - 2025/1
Y1 - 2025/1
N2 - Ni-rich cathode, recognized for high specific capacities and cost-effectiveness, are deemed promising candidates for high-energy Li-ion batteries. However, these cathodes display notable structural instability and experience severe strain propagation during rapid charging and extended cycling under high voltage, hindering their widespread commercialization. To tackle this chemo-mechanical instability without compromising energy and power density, we propose an efficient modification strategy involving hexavalent metal cation-induced three-in-one modification to reconstruct the nanoscale surface phase. This strategy includes uniform W-doping, integration of cation-mixed phases, and Li2WO4 nanolayers on the surface of Ni-rich cathode microspheres. W-doping strengthen the bond to oxygen, thereby enhancing structural stability and suppressing oxygen loss linked to a layered-to-rock salt phase transition during deep delithiation process. Additionally, establishing a cation-mixing domain with an optimal thickness on the cathode surface enhances Li⁺ diffusivity and alleviates particle structural degradation. Moreover, Li2WO4 nanolayers reduce electrolyte side reactions and act as a damping medium against cycling stresses. Importantly, detailed investigations into structural changes before and after modification at varying current rates were conducted to better comprehend the rate-dependent degradation mechanism. These findings yield valuable mechanistic insights into the high-rate utilization of a viable Ni-rich cathode, ensuring prolonged service life in electric vehicles.
AB - Ni-rich cathode, recognized for high specific capacities and cost-effectiveness, are deemed promising candidates for high-energy Li-ion batteries. However, these cathodes display notable structural instability and experience severe strain propagation during rapid charging and extended cycling under high voltage, hindering their widespread commercialization. To tackle this chemo-mechanical instability without compromising energy and power density, we propose an efficient modification strategy involving hexavalent metal cation-induced three-in-one modification to reconstruct the nanoscale surface phase. This strategy includes uniform W-doping, integration of cation-mixed phases, and Li2WO4 nanolayers on the surface of Ni-rich cathode microspheres. W-doping strengthen the bond to oxygen, thereby enhancing structural stability and suppressing oxygen loss linked to a layered-to-rock salt phase transition during deep delithiation process. Additionally, establishing a cation-mixing domain with an optimal thickness on the cathode surface enhances Li⁺ diffusivity and alleviates particle structural degradation. Moreover, Li2WO4 nanolayers reduce electrolyte side reactions and act as a damping medium against cycling stresses. Importantly, detailed investigations into structural changes before and after modification at varying current rates were conducted to better comprehend the rate-dependent degradation mechanism. These findings yield valuable mechanistic insights into the high-rate utilization of a viable Ni-rich cathode, ensuring prolonged service life in electric vehicles.
KW - Cation-mixing domain
KW - LiWO coating
KW - Ni-rich materials
KW - Rate-dependent degradation
KW - W doping
UR - http://www.scopus.com/inward/record.url?scp=85208719005&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2024.103893
DO - 10.1016/j.ensm.2024.103893
M3 - Article
AN - SCOPUS:85208719005
SN - 2405-8297
VL - 74
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 103893
ER -