Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Department of Materials Science and Engineering, University of California, Berkeley, CA, USA.
Nat Mater. 2023 Mar;22(3):353-361. doi: 10.1038/s41563-022-01467-z. Epub 2023 Jan 26.
Lithium-rich cathodes are promising energy storage materials due to their high energy densities. However, voltage hysteresis, which is generally associated with transition metal migration, limits their energy efficiency and implementation in practical devices. Here we reveal that voltage hysteresis is related to the collective migration of metal ions, and that isolating the migration events from each other by creating partial disorder can create high-capacity reversible cathode materials, even when migrating transition metal ions are present. We demonstrate this on a layered Li-rich chromium manganese oxide that in its fully ordered state displays a substantial voltage hysteresis (>2.5 V) associated with collective transition metal migration into Li layers, but can be made to achieve high capacity (>360 mAh g) and energy density (>1,100 Wh kg) when the collective migration is perturbed by partial disorder. This study demonstrates that partially cation-disordered cathode materials can accommodate a high level of transition metal migration, which broadens our options for redox couples to those of mobile cations.
富锂正极材料由于其高能量密度而成为很有前途的储能材料。然而,通常与过渡金属迁移相关的电压滞后限制了它们的能量效率和在实际设备中的应用。在这里,我们揭示了电压滞后与金属离子的集体迁移有关,并且通过创建部分无序来使迁移事件彼此隔离,可以创造出具有高容量的可逆正极材料,即使存在迁移的过渡金属离子也是如此。我们在层状富锂铬锰氧化物上证明了这一点,在其完全有序的状态下,它显示出与过渡金属集体迁移到 Li 层相关的显著电压滞后(>2.5 V),但当集体迁移受到部分无序的干扰时,它可以实现高容量(>360 mAh g)和能量密度(>1100 Wh kg)。这项研究表明,部分阳离子无序的正极材料可以容纳高水平的过渡金属迁移,这拓宽了我们对氧化还原对的选择,可以选择那些具有迁移性的阳离子。