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Kinetic Phase Evolution of Spinel Cobalt Oxide during Lithiation

机译:尖晶石钴氧化物在锂化过程中的动力学相演化

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Spinel cobalt oxide has been proposed to undergo a multiple-step reaction during the electrochemical lithiation process. Understanding the kinetics of the lithiation process in this compound is crucial to optimize its performance and cyclability. In this work, we have utilized a low-angle annular dark-field scanning transmission electron microscopy method to visualize the dynamic reaction process in real time and study the reaction kinetics at different rates. We show that the particles undergo a two-step reaction at the single-particle level, which includes an initial intercalation reaction followed by a conversion reaction. At low rates, the conversion reaction starts after the intercalation reaction has fully finished, consistent with the prediction of density functional theoretical calculations. At high rates, the intercalation reaction is overwhelmed by the subsequently nucleated conversion reaction, and the reaction speeds of both the intercalation and conversion reactions are increased. Phase-field simulations show the crucial role of surface diffusion rates of lithium ions in controlling this process. This work provides microscopic insights into the reaction dynamics in non-equilibrium conditions and highlights the effect of lithium diffusion rates on the overall reaction homogeneity as well as the performance.
机译:已经提出尖晶石型氧化钴在电化学锂化过程中经历多步反应。了解该化合物锂化过程的动力学对于优化其性能和可循环性至关重要。在这项工作中,我们利用低角度环形暗场扫描透射电子显微镜方法实时可视化了动态反应过程,并研究了不同速率下的反应动力学。我们表明,颗粒在单颗粒水平上经历两步反应,其中包括初始插入反应和随后的转化反应。在低速率下,转化反应在插层反应完全完成后开始,这与密度泛函理论计算的预测一致。在高速率下,随后的有核转化反应使嵌入反应不堪重负,并且嵌入和转化反应的反应速度均提高了。相场模拟显示了锂离子表面扩散速率在控制此过程中的关键作用。这项工作提供了对非平衡条件下反应动力学的微观见解,并突出了锂扩散速率对整体反应均匀性和性能的影响。

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