Solid-State Lithium Metal Batteries with Extended Cycling Enabled by Dynamic Adaptive Solid-State Interfaces.
basic_science · Level V
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- Record sourced from PubMed, PMID 33604935.
- Also identified by DOI 10.1002/adma.202008084.
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Abstract
Improving the long-term cycling stability of solid-state lithium (Li)-metal batteries (SSBs) is a severe challenge because of the notorious solid-solid interfacial contact loss originating from the repeated expansion and contraction of the Li anodes. Here, it is reported that high-performance SSBs are enabled by constructing brick-and-mortar electrolytes that can dynamically adapt to the interface changes during cycling. An electrolyte film with a high mechanical strain (250%) is fabricated by filling viscoelastic (600% strain) and piezoelectric block-copolymer electrolytes (mortar) into a mixed conductor Li<sub>0.33</sub> La<sub>0.56</sub> TiO<sub>3-x</sub> nanofiber film (brick). During Li-plating, the electrolytes can homogenize the interfacial electric field and generate piezoelectricity to promote uniform Li-deposition, while the mortar can adhere to the Li-anode without interfacial disintegration in the reversed Li-stripping. As a result, the electrolytes show excellent compatibility with the electrodes, leading to a long electrochemical cyclability at room temperature. The symmetrical Li//Li cells run stably for 1880 h without forming dendrites, and the LiFePO<sub>4</sub> /Li full batteries deliver high coulombic efficiency (>99.5%) and capacity retention (>85%) over 550 cycles. More practically, the pouch cells exhibit excellent flexibility and safety for potential practical applications.