| Literature DB >> 27632252 |
Jing Li1,2, Kai He1, Qingping Meng1, Xin Li3, Yizhou Zhu4, Sooyeon Hwang1, Ke Sun1, Hong Gan1, Yimei Zhu1, Yifei Mo4, Eric A Stach1, Dong Su1.
Abstract
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.Entities:
Keywords: Co3O4 nanoparticles; in situ TEM; lithium-ion battery
Year: 2016 PMID: 27632252 DOI: 10.1021/acsnano.6b04958
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881