Cation and anion Co-doping synergy to improve structural stability of Li- and Mn-rich layered cathode materials for lithium-ion batteries. (March 2019)

• Record Type: Journal Article
• Authors: Chen, Guorong; An, Juan; Meng, Yiming; Yuan, Changzhou; Matthews, Bryan; Dou, Fei; Shi, Liyi; Zhou, Yongfeng; Song, Pingan; Wu, Gang; Zhang, Dengsong
• Is Part Of: Nano energy. Volume 57(2019)
• Page Start: 157
• Page End: 165
• Publication Date: 2019-03
• Subjects: Layered cathode materials -- Doping -- Li and Mn rich -- Inactive frame -- Lithium ion battery; Nanoscience -- Periodicals; Nanotechnology -- Periodicals; Nanostructured materials -- Periodicals; Power resources -- Technological innovations -- Periodicals; Nanoscience; Nanostructured materials; Nanotechnology; Power resources -- Technological innovations; Periodicals; 621.042
• DOI: 10.1016/j.nanoen.2018.12.049
• Languages: English
• ISSNs: 2211-2855

Abstract

Abstract: Cobalt-free Li and Mn-rich layered cathode materials are promising for next generation lithium ion batteries due to their high specific capacity and low cost. However, these materials are facing serious issues, such as structural collapse due to volume shrinkage during Ni 2+ oxidation to Ni 4+ and oxygen vacancy generation over 4.5V. In this work, we report a strategy to address the issue of volume shrinkage caused by structural deformation via constructing a large-size rigid frame by simultaneously doping inactive and large radius atoms of Cd and S. This strategy significantly reduces the volume shrinkage when fully delithiated relative to the pristine material. The Cd- and S-doped cathode materials present a highly reversible structure, which were determined by using HAADF-STEM and in-situ XRD characterization. The doped Cd and S atoms act as supporting atoms and synergistically enlarge the layer spacing of crystalline from 0.455 to 0.483 nm. The in-situ XRD monitors the structural changes in real time during charging and discharging processes, further verifying structural stability during cycling. Due to the unique structural properites, an initial capacity of 268.5 mAh g −1 at 0.1 C along with a good rate capacity of 153.8 mAh g −1 at 5 C were achieved. Also, a capacity of 243.4 mAh g-1 at 0.1 C over 80 cycles indicate good cyclic stability of the co-doped Li- and Mn-rich layered cathode. Graphical abstract: fx1 Highlights: Li and Mn-rich layered cathode material is co-doped with large radius inactive cation and anion. A large layer spacing of 4.83 nm is obtained and retained stable after 100 cycles. Mechanisms of structural stability during cycles has been elucidated by using HAADF-STEM and in-situ XRD. A capacity of 153 mAh g −1 at 5 C is obtained with a retention of 84.4% after 200 cycles at 1 C.