Stability of the LiMn<sub>2</sub>O<sub>4</sub>surface in a LiPF<sub>6</sub>-based non-aqueous electrolyte studied by in-situ atomic force microscopy

抄録

<jats:title>Abstract</jats:title><jats:p>Investigation of the surface stability of electrode materials in a liquid electrolyte is significantly important for understanding the deterioration of stored Li-ion battery cells. Here, we examined LiMn<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub>surfaces in a LiPF<jats:sub>6</jats:sub>-based non-aqueous electrolyte by in-situ atomic force microscopy. A LiMn<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub>(111) surface sample with a well-defined atomically-flat structure was prepared from a MnO(111) wafer. Although the surfaces of non-exposed or dry-air-exposed samples did not change in a typical electrolyte such as LiPF<jats:sub>6</jats:sub>dissolved in propylene carbonate, the surface morphology of an air-exposed sample greatly changed under the same condition. Transmission electron microscopy observation revealed that the surface roughness is increased by the dissolution of one or two atomic layers of LiMn<jats:sub>2</jats:sub>O<jats:sub>4</jats:sub>-crystal surfaces in the electrolyte. The adsorbed water on the air-exposed surface is the origin of this phenomenon.</jats:p>

収録刊行物

被引用文献 (1)*注記

もっと見る

参考文献 (50)*注記

もっと見る

問題の指摘

ページトップへ