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Atomic resolution observation of conversion-type anode RuO2 during the first electrochemical lithiation

机译:第一次电化学锂化过程中转化型阳极RuO2的原子分辨率观察

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Transition metal oxides have attracted great interest as alternative anode materials for rechargeable lithium-ion batteries. Among them, ruthenium dioxide is considered to be a prototype material that reacts with the Li ions in the conversion type. In situ transmission electron microscopy reveals a two-step process during the initial lithiation of the RuO2 nanowire anode at atomic resolution. The first step is characterized by the formation of the intermediate phase LixRuO2 due to the Li-ion intercalation. The following step is manifested by the solid-state amorphization reaction driven by advancing the reaction front. The crystalline/amorphous interface is consisted of {011} atomic terraces, revealing the orientation-dependent mobility. In the crystalline matrix, lattice disturbance and dislocation are identified to be two major stress-induced distortions. The latter can be effective diffusion channels, facilitating transportation of the Li ions inside the bulk RuO2 crystal and further resulting in non-uniform Li-ion distribution. It is expected that the local enrichment of the Li ions may account for the homogeneous nucleation of dislocations in the bulk RuO2 crystal and the special island-like structures. These results elucidate the structural evolution and the phase transformation during electrochemical cycling, which sheds light on engineering RuO2 anode materials.
机译:过渡金属氧化物作为可再充电锂离子电池的替代阳极材料引起了极大的兴趣。其中,二氧化钌被认为是与转化型锂离子反应的原型材料。原位透射电子显微镜揭示了在RuO2纳米线阳极的初始锂化过程中以原子分辨率进行的两步过程。第一步的特征是由于锂离子的嵌入而形成了中间相LixRuO2。通过前进反应前沿而驱动的固态非晶化反应表明了以下步骤。晶体/非晶界面由{011}原子阶组成,揭示了取向依赖性迁移率。在晶体基质中,晶格扰动和位错被确定为两个主要的应力诱导形变。后者可以是有效的扩散通道,促进锂离子在块状RuO2晶体内部的运输,并进一步导致锂离子分布不均匀。预期锂离子的局部富集可解释块状RuO2晶体和特殊的岛状结构中位错的均匀成核。这些结果阐明了电化学循环过程中的结构演变和相变,这为工程RuO2阳极材料提供了启示。

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