电解质
硫化物
电极
快离子导体
锂(药物)
材料科学
合金
氧化还原
化学工程
离子电导率
无机化学
半电池
化学
锂电池
离子键合
离子
工作电极
冶金
物理化学
医学
内分泌学
有机化学
工程类
作者
Masamitsu Sakuma,Kota Suzuki,Masaaki Hirayama,Ryoji Kanno
标识
DOI:10.1016/j.ssi.2015.07.010
摘要
Reactions at the electrode/electrolyte interface of all-solid-state lithium batteries were studied for combinations of sulfide-based solid electrolytes with various Li4 -xGe1 -xPxS4 and Liy-M (M = Sn, Si) alloys as the negative electrodes, using ac impedance, X-ray diffraction and energy-dispersive X-ray spectroscopy. The solid electrolyte at the interfacial region was found to decompose with the application of a current through the cells, resulting in the formation of a solid electrolyte interphase (SEI) layer. Resistivity changes at the interface varied depending on the electrolyte composition and the redox potential (vs. Li/Li+) of the negative electrode material. Lower resistances were observed with lower Ge contents in the solid electrolyte and the use of a Li–M alloy with a higher redox potential due to the formation of an electrochemically stable SEI layer during battery operation. In contrast, a combination of higher Ge content and an alloy with a lower redox potential led to a rapid increase in the SEI resistance and increase in its thickness. The presence of a Li–P–S compound with low ionic conductivity in the interfacial region was found to be related with the increase of interfacial resistance, leading to poor cycling characteristics. The formation of a suitable SEI layer is an important factor in the future development of all-solid-state batteries and this study serves to clarify the relationships between the formation of the SEI phase, the redox potential of the electrode and the sulfide-based solid electrolyte composition.
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