4.8 Article

In Situ Constructing Robust and Highly Conductive Solid Electrolyte with Tailored Interfacial Chemistry for Durable Li Metal Batteries

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SMALL
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WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202307942

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in situ polymerization; interfacial stability; ion regulation; lithium metal battery; nanofiber framework; solid electrolyte

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This research presents a stable nanofiber framework for in situ polymerized solid-state lithium metal batteries (SSLMBs), which has built-in lithium ion transport channels and high interfacial lithium ion flux. By applying a molecular reinforcement protocol, the distribution of lithium ions on the lithium metal surface and the nucleation of lithium dendrites can be controlled, leading to improved cycling performance of the batteries.
Employing nanofiber framework for in situ polymerized solid-state lithium metal batteries (SSLMBs) is impeded by the insufficient Li+ transport properties and severe dendritic Li growth. Both critical issues originate from the shortage of Li+ conduction highways and nonuniform Li+ flux, as randomly-scattered nanofiber backbone is highly prone to slippage during battery assembly. Herein, a robust fabric of Li0.33La0.56Ce0.06Ti0.94O3-delta/polyacrylonitrile framework (p-LLCTO/PAN) with inbuilt Li+ transport channels and high interfacial Li+ flux is reported to manipulate the critical current density of SSLMBs. Upon the merits of defective LLCTO fillers, TFSI- confinement and linear alignment of Li+ conduction pathways are realized inside 1D p-LLCTO/PAN tunnels, enabling remarkable ionic conductivity of 1.21 mS cm-1 (26 degrees C) and tLi+ of 0.93 for in situ polymerized polyvinylene carbonate (PVC) electrolyte. Specifically, molecular reinforcement protocol on PAN framework further rearranges the Li+ highway distribution on Li metal and alters Li dendrite nucleation pattern, boosting a homogeneous Li deposition behavior with favorable SEI interface chemistry. Accordingly, excellent capacity retention of 76.7% over 1000 cycles at 2 C for Li||LiFePO4 battery and 76.2% over 500 cycles at 1 C for Li||LiNi0.5Co0.2Mn0.3O2 battery are delivered by p-LLCTO/PAN/PVC electrolyte, presenting feasible route in overcoming the bottleneck of dendrite penetration in in situ polymerized SSLMBs. A novel nanofiber architecture as the 3D skeleton is developed for in situ polymerized PVC electrolyte to facilitate rapid Li+ transport kinetics and inhibit dendrites penetration, endowing solid lithium metal batteries with ultra-stable cycling performances.image

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