The discovery of cation-disordered rocksalts and their percolation rules unlocked an unprecedented chemical space for the exploration of high-capacity lithium-ion cathodes which do not contain Co and have high capacity[1]. The facile Li diffusion in these materials is enabled through a network of Li-rich environments (so-called 0-TM channels) created by excess Li. Following this insight, many new high-energy-density cathode materials that involve mostly earth-abundant elements have been developed, such as Li1.2Mn0.4Ti0.4O2[2], Li1.2Ni1/3Ti1/3Mo2/15O2[3], as well as their fluorinated variants[4, 5].
A prevailing assumption when studying disordered rocksalt cathodes is that all the cation species are randomly distributed. However, we will demonstrate that even minor deviations from randomness, not detectable by typical X-ray diffraction (XRD), can have profound influence on performance. We employ a combination of thorough experimental characterization and multi-scale computer simulations to reveal that cation short-range order is ubiquitous in these long-range disordered materials. More importantly, the short-range order controls Li transport by altering the distribution of local environments and the connectivity between them. By considering a variety of different chemistries, we explain the microscopic origin of short-range order and identify general guidelines for local-structure manipulation for the benefit of Li transport. This breakthrough in the fundamental understanding of structure-property relationship in disordered Li-ion cathodes sets an exciting new direction for future optimization.
[1] J. Lee, et al, Science 343 (2014) 519-522.
[2] N. Yabuuchi, et al, Nature communications 7 (2016) 13814.
[3] J. Lee, et al, Energy & Environmental Science 8 (2015) 3255-3265.
[4] R. Chen, et al, Advanced Energy Materials 5 (2015).
[5] J. Lee, et al, Nature communications 8 (2017) 981.