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Yoshimi Kubo

Publications and source records attributed to Yoshimi Kubo.

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Interplay of Inhomogeneous Electrochemical Reactions with Mechanical Responses in Silicon-Graphite Anode and its Impacts on Degradation

Enhanced EV market penetration requires durability of the battery with high energy throughput. For long-term cycle stability of silicon-graphite anode capable of high energy density, the reversible redox reactions are crucial. Here, we unveil intriguing electrochemical phenomena such as crosstalk of lithium ion ($Li^{+}$) between silicon and graphite, $Li^{+}$ accumulation in silicon, and capacity depression of graphite under high pressure, which engender the irreversible redox reactions. Active material properties, i.e. the size of silicon and the hardness of graphite, silicon-graphite anode, are modified based on the unveiled results to enhance the reaction homogeneity and reduce subsequent degradation. Owing to the property change of the anode active materials, silicon-graphite anode paired with high nickel cathode allows the prismatic cell with 8.7 Ah to reach cycling performance over 750 cycles with volumetric energy density of 665 $Whl^{-1}$, which is corresponding to 800 $Whl^{-1}$ in the prismatic cell with 87 Ah. Finally, the cycling performance can be tailored by the design of electrode regulating $Li^{+}$ crosstalk. Our findings provide electrochemical insights into degradation mechanisms and a promising direction on the progressive improvement of materials and the design of electrodes in silicon-graphite anode.

cond-mat.mtrl-sci

Revealing evolving affinity between Coulombic reversibility and hysteretic Li-Si phase transformations

Nano-structured silicon anodes are attractive alternatives to graphite in Li-ion batteries. Despite recent remarkable progresses in numerous Si-C composites, the commercialisation with significance is still limited. One of the most critical issues remained to understand is fundamentals on Li-Si Coulombic efficiency, namely, CE. Particularly, it is key to quantitatively and qualitatively resolve CE alterations and evolutions by the various Li-Si structural changes over longer cycling. However, such work is surprisingly scarce. Here, we provide new findings that iterating the hysteretic amorphous-crystalline Li-Si phase transformations accumulatively governs CE evolutions, the manner of which is numerically distinguished from incremental amorphous Li-Si volume changes. The iterations, usually featured as capacity degradation factors, can form the most efficient CE profiles over hundreds of cycles, i.e. minimising accumulative irreversible Li consumption, among the given Li-Si reaction sequences. Combined with atomistic probing methodologies, we show that the iteration drastically alters electrochemical and structural characteristics, which is synchronised with the CE behaviours.

cond-mat.mtrl-sci