A synergetic promotion of surface stability for high-voltage LiCoO 2 by multi-element surface doping: a first-principles study

• Published in: Physical chemistry chemical physics : PCCP 2024-01, Vol.26 (5), p.4174-4183
• Main Authors: Lin, Hongbin, Kang, Xiumei, Xu, Guigui, Chen, Yue, Zhong, Kehua, Zhang, Jian-Min, Huang, Zhigao
• Format: Article
• Language: English
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/d3cp04130a

The utilization of high-voltage LiCoO is an effective approach to break through the bottleneck of practical energy density in lithium ion batteries. However, the structural and interfacial degradations at the deeply delithiated state as well as the associated safety concerns impede the application of high-voltage LiCoO . Herein, we present a synergetic strategy for promoting the surface stability of LiCoO at high voltage by Ti-Mg-Al co-doping and systematically study the effects of the dopants on the surface stability, electronic structure and Li diffusion properties of the LiCoO (104) surface using first-principles calculations. It is found that Ti, Mg and Al dopants can be facilely introduced into the Co sites of the LiCoO (104) surface. Furthermore, the co-doping could significantly stabilize the surface oxygen of LiCoO at a high delithiation state. Particularly, by aggregating Ti-Mg-Al co-dopant distribution in the surface layer, surface oxygen loss is dramatically suppressed. In addition, analysis of the electronic structure indicates that Ti-Mg-Al co-doping can enhance the electronic conductivity of the LiCoO (104) surface and greatly inhibit the charge deficiency of the superficial lattice O atoms at a highly delithiated state. In spite of a negligible improvement in the surface Li diffusion kinetics, the Ti-Mg-Al surface-modified LiCoO is expected to exhibit improved electrochemical performance at high voltage due to its superior surface stability. Our results suggest that aggregating Ti, Mg and Al co-dopant distribution in the surface layer is a promising modulation strategy to synergistically promote the surface oxygen stability of LiCoO at high voltages.