TY - JOUR
T1 - A Dual-Functional Synergetic Strategy Enhances the Interfacial and Structural Stability of LiCoO2 at High Voltage
AU - Sun, Weiyu
AU - Yang, Jilin
AU - Shi, Weichen
AU - Zheng, Hong
AU - Cheng, Yonghong
AU - Xu, Xin
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/8/12
Y1 - 2024/8/12
N2 - With the advent of the 5G era, the widespread application of various smart devices and cutting-edge technologies has imposed stringent requirements on the battery lifespan and durability. This study proposes a synergistic modification strategy combining Mg2+ and Y3+ dual doping with Li3PO4 coating. Herein, Mg2+ exhibits a gradient distribution near the surface and a uniform distribution inside, enhancing electronic conductivity while facilitating the penetration of the Y element into the particle interior. What is more, the addition of Y3+ significantly widens the Li+ transmission channels, greatly enhancing the rapid charge-discharge performance. The synergistic interaction of Mg2+ and Y3+ stabilizes the internal structure, while the Li3PO4 coating serves to effectively block a direct interaction between the electrolyte and the cathode surface, stabilizing the surface structure and improving the long-term cycling performance. The findings indicate that the synergistic approach adjusts the Co 3d and O 2p energy bands, effectively suppressing the hybridization phenomenon of Co and O orbitals. Remarkably, the proposed strategy maintains a superb capacity retention rate of nearly 80% after 300 cycles at 4.6 V, and it exhibits an excellent reversible capacity of 109.6 mAh·g-1 even at 10 C, thus demonstrating the superior overall performance and vast application potential of this approach.
AB - With the advent of the 5G era, the widespread application of various smart devices and cutting-edge technologies has imposed stringent requirements on the battery lifespan and durability. This study proposes a synergistic modification strategy combining Mg2+ and Y3+ dual doping with Li3PO4 coating. Herein, Mg2+ exhibits a gradient distribution near the surface and a uniform distribution inside, enhancing electronic conductivity while facilitating the penetration of the Y element into the particle interior. What is more, the addition of Y3+ significantly widens the Li+ transmission channels, greatly enhancing the rapid charge-discharge performance. The synergistic interaction of Mg2+ and Y3+ stabilizes the internal structure, while the Li3PO4 coating serves to effectively block a direct interaction between the electrolyte and the cathode surface, stabilizing the surface structure and improving the long-term cycling performance. The findings indicate that the synergistic approach adjusts the Co 3d and O 2p energy bands, effectively suppressing the hybridization phenomenon of Co and O orbitals. Remarkably, the proposed strategy maintains a superb capacity retention rate of nearly 80% after 300 cycles at 4.6 V, and it exhibits an excellent reversible capacity of 109.6 mAh·g-1 even at 10 C, thus demonstrating the superior overall performance and vast application potential of this approach.
KW - high-voltage LiCoO
KW - interface stability
KW - LiPO coating
KW - Mg and Y codoping
KW - structural reversibility
UR - https://www.scopus.com/pages/publications/85199534859
U2 - 10.1021/acsaem.4c01228
DO - 10.1021/acsaem.4c01228
M3 - 文章
AN - SCOPUS:85199534859
SN - 2574-0962
VL - 7
SP - 6585
EP - 6597
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 15
ER -