Rational design of thermally stable polymorphic layered cathode materials for next generation lithium rechargeable batteries. (December 2022)

• Record Type: Journal Article
• Authors: Li, Xiao; Gu, Qingwen; Qiu, Bao; Yin, Chong; Wei, Zhining; Wen, Wen; Zhang, Yibin; Zhou, Yuhuan; Gao, Han; Liang, Haoyan; He, Zhilong; Zhang, Minghao; Meng, Ying Shirley; Liu, Zhaoping
• Is Part Of: Materials today. Volume 61(2022)
• Page Start: 91
• Page End: 103
• Publication Date: 2022-12
• Subjects: Li-ion batteries -- Li-rich layered cathode -- Thermal stability -- Local structure modulation -- Polymorphic composition design; Materials science -- Periodicals; Metallurgy -- Periodicals; Metal-work -- Periodicals; Biomedical and Dental Materials -- Periodicals; Manufactured Materials -- Periodicals; Metals -- Periodicals; 620.11
• DOI: 10.1016/j.mattod.2022.09.013
• Languages: English
• ISSNs: 1369-7021

Abstract

Graphic abstract: Abstract: Classical layered transition metal oxides have remained the preferred cathode materials for commercial lithium-ion batteries. Variation in the transition metal composition and local ordering can greatly affect the structure stability. In classical layered cathodes, high concentrations of electrochemically inert Mn elements usually act as a pillar to stabilize the structure. When excess amount of Li and Mn are present in the layered structure, the capacity of the Li-rich layered oxide (molar ratio of lithium over transition metal is larger than one by design) can exceed that expected from transition metal redox. However, the over lithiation in the classical layered structure results in safety issues, which remains challenging for the commercialization of Li-rich layered oxides. To characterize the safety performance of a series of Li-rich layered cathodes, we utilize differential scanning calorimeter and thermal gravimetric analysis; this is coupled with local structural changes using in situ temperature dependent synchrotron X-ray diffraction and X-ray adsorption spectroscopy. These methods demonstrate that the gradual decrease of the Mn–M (M = Ni, Co, Mn and Li) coordination number directly reduces structural stability and accelerates oxygen release. For safety characterization tests in practice, we evaluate the thermal runaway process through accelerating rate calorimeter in 1.0 Ah pouch cells to confirm this trend. Using the insights obtained in this work, we design a polymorphic composition to improve the thermal stability of Li-rich layered cathode material, which outperforms Ni-rich layered oxides in terms of both electrochemical and safety performances.