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Nanostructure-Mediated Phase Evolution in Lithiation/Delithiation of Co3O4

机译:纳米结构介导的CO3O4锂锂化/脱盐的阶段演变

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Nanostructured transition-metal oxides have been under intensive investigation for their tantalizing potential as anodes of next-generation lithium-ion batteries (LIBs). However, the exact mechanism for nanostructures to influence the LIB performance remains largely elusive. In this work, we discover the nanostructure-mediated lithiation mechanism in Co_(3)O_(4) anodes using ex situ transmission electron microscopy (TEM) and X-ray diffractometry: while Co_(3)O_(4) nanosheets exhibit a typical two-step conversion reaction (from Co_(3)O_(4) to CoO and then to Co~(0)), Co_(3)O_(4) nanoarrays can go through a direct conversion from Co_(3)O_(4) to Co~(0) at a high discharge rate. Such nanostructure-dependent lithiation can be rationalized by the slow lithiation kinetics intrinsic to Co_(3)O_(4) nanoarrays, which at a high discharge rate may cause local accumulation of lithium to initiate a one-step Co_(3)O_(4)-to-Co~(0) conversion. Combined with the larger volume change observed in Co_(3)O_(4) nanoarrays, the slow lithiation kinetics can lead to inhomogeneous expansion with large stress developed at the reaction front, which can eventually cause structure failure and irreversible capacity loss, as explicitly observed by in situ TEM as well as galvanostatic discharge–charge measurement. Our observation resolves the nanostructure-dependent lithiation mechanism of Co_(3)O_(4) and provides important insights into the interplay among lithiation kinetics, phase evolution, and lithium-storage performance, which can be translated into electrode design strategies for next-generation LIBs.
机译:纳米结构的过渡金属氧化物作为下一代锂离子电池(LIB)的阳极具有诱人的潜力,因此受到了广泛的研究。然而,纳米结构影响LIB性能的确切机制在很大程度上仍不清楚。在这项工作中,我们利用非原位透射电子显微镜(TEM)和X射线衍射仪发现了Co_3)O_4阳极中纳米结构介导的锂化机制:虽然Co_3)O_4纳米片表现出典型的两步转化反应(从Co_3)O_4到CoO,然后到Co~(0)),Co_3)O_4纳米阵列可以在高放电速率下从Co_3)O_4直接转化为Co~(0)。这种依赖于纳米结构的锂化可以通过Co_3)O_4纳米阵列固有的缓慢锂化动力学合理化,在高放电速率下,这可能会导致锂的局部积累,从而启动一步Co_3)O_4-到Co~(0)的转化。结合在Co_(3)O_(4)纳米阵列中观察到的较大体积变化,缓慢的锂化动力学可导致不均匀膨胀,并在反应前沿产生较大应力,最终可能导致结构破坏和不可逆的容量损失,这是通过原位TEM以及恒流放电-充电测量明确观察到的。我们的观察解决了Co_3)O_4的纳米结构相关的锂化机制,并对锂化动力学、相演化和锂存储性能之间的相互作用提供了重要的见解,这些可以转化为下一代锂离子电池的电极设计策略。

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