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Three-dimensional atomic-scale observation of structural evolution of cathode material in a working all-solid-state battery

机译:全固态工作电池中正极材料结构演变的三维原子尺度观察

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摘要

Most technologically important electrode materials for lithium-ion batteries are essentially lithium ions plus a transition-metal oxide framework. However, their atomic and electronic structure evolution during electrochemical cycling remains poorly understood. Here we report the in situ observation of the three-dimensional structural evolution of the transition-metal oxide framework in an all-solid-state battery. The in situ studies LiNi0.5Mn1.5O4 from various zone axes reveal the evolution of both atomic and electronic structures during delithiation, which is found due to the migration of oxygen and transition-metal ions. Ordered to disordered structural transition proceeds along the <100>, <110>, <111> directions and inhomogeneous structural evolution along the <112> direction. Uneven extraction of lithium ions leads to localized migration of transition-metal ions and formation of antiphase boundaries. Dislocations facilitate transition-metal ions migration as well. Theoretical calculations suggest that doping of lower valence-state cations effectively stabilize the structure during delithiation and inhibit the formation of boundaries.
机译:锂离子电池最重要的技术电极材料基本上是锂离子加过渡金属氧化物骨架。但是,它们在电化学循环过程中原子和电子结构的演变仍知之甚少。在这里,我们报告在全固态电池中过渡金属氧化物骨架的三维结构演变的原位观察。从不同区域轴进行的原位研究LiNi0.5Mn1.5O4揭示了在脱锂过程中原子结构和电子结构的演变,这是由于氧和过渡金属离子的迁移所致。有序至无序的结构过渡沿<100>,<110>,<111>方向进行,并沿<112>方向进行不均匀的结构演化。锂离子的不均匀萃取会导致过渡金属离子的局部迁移并形成反相边界。位错也促进过渡金属离子的迁移。理论计算表明,低价态阳离子的掺杂有效地稳定了脱锂过程中的结构并抑制了边界的形成。

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