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It is a complex mixture of organic and inorganic compounds that protects the anode, facilitates lithium-ion conduction, and contributes to battery stability by minimizing capacity loss.
The interface can be controlled by a metal interlayer on the electrolyte to form a Li alloy buffer that facilitates stable Li plating/stripping, thereby mitigating the loss of physical contact and preventing short circuits.
The optimized catholyte buffer layer enabled thermal and electrochemical stability at interface level, delivering comparable cycling stability of garnet-based all solid-state lithium battery, i.e., capacity retention of 98.5% after 100 cycles at 60 °C, and 89.6% after 50 cycles at 80 °C.
Since Sony introduced lithium-ion batteries (LIBs) to the market in 1991, they have become prevalent in the consumer electronics industry and are rapidly gaining traction in the growing electric vehicle (EV) sector. The EV industry demands batteries with high energy density and exceptional longevity.
The buffer layer shows a remarkable ion conductivity of 3.21 × 10 −4 S cm −1 at 25 °C originating from the exceptional Li + -H + ion exchange capability of HMO.
The first layer is the inner inorganic layer toward the electrode/SEI interface, composed of, for example, Li 2 CO 3, Li 2 O, LiF, or stated, one sublayer of carbonate and another sublayer of fluoride, an oxide-type compound. This layer facilitates the conduction of lithium ions.
During cycling, the accumulation of dead lithium exacerbates non-uniform Li deposition, causing the formation and growth of dendritic lithium, which leads to the failure of cell [52, 53]. In contrast, the cycling performance of the cell with PDMS membrane exhibits high stability and it ran for 15th cycle without short-circuiting.
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