Isovalent substitution modulates average and short-range structure in disordered rocksalt oxides

被引:0
|
作者
Langhout, John D. [1 ]
Gager, Elizabeth [1 ]
Ulloa, Talianna [2 ]
Shepard, Shane [1 ]
Nino, Juan C. [1 ]
Butala, Megan M. [1 ]
机构
[1] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Elect & Comp Engn, Gainesville, FL 32611 USA
关键词
TRANSITION-METAL OXIDES; ELECTRODE MATERIALS; DISTORTIONS; CHALLENGES; CRYSTAL; ENTROPY;
D O I
10.1039/d4ta05971a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Li-excess disordered rocksalt oxides are promising candidate materials for high-energy density Li-ion battery cathodes. Their disordered cation sublattice provides opportunity to design compositions that balance performance and sustainability, especially enabling the use of abundant and inexpensive elements. However, relationships between composition, short-range cation ordering, and their effects on performance are not well-understood. Here, we use a compositional series of the form Li1.2Mn0.4Ti0.4-xZrxO2, in which Ti4+ is gradually replaced with Zr4+, to study the effect of Zr content on average- and short-range structure using synchrotron X-ray diffraction and pair distribution function analysis. We report the coexistence of multiple modes of short-range order, which have a major impact on battery capacity. However, the effects of Zr on degree of short-range ordering, lattice parameter, and chemical segregation also influence battery capacity, reflecting the complex dependencies of composition on structure across length scales in these disordered materials.
引用
收藏
页码:32140 / 32153
页数:14
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