Solid‐state lithium metal batteries are promising next generation energy storage devices and composite solid electrolytes (CSEs) with high ionic conductivity and mechanical stability have attracted widespread attention. However, the slow ion transport kinetics at the heterogeneous interface between ceramic fillers and polymer matrices severely limits the performance of CSEs. This work reports a facile surface modification using biogenic caffeic acid (CA) to functionalize LLZTO. CA monomers anchor on LLZTO via Lewis acid‐base interactions and react with surface lithium carbonate, during which in‐situ polymerization evolves to form a uniform 5 nm poly(caffeic acid) (PCA) coating. After incorporating PCA@LLZTO into the PEO matrix, hydrogen bonding between PCA polar groups and PEO chains promotes filler dispersion and reduces interfacial resistance. The PCA@LLZTO/PEO CSE exhibits significantly enhanced ionic conductivity of 2.19 × 10−4 S cm−1, a reliable Li+ transference number of 0.64, excellent mechanical robustness and superior Li metal compatibility, along with a stable electrochemical window of 5.1 V and long‐term stable cycling over 3200 h in Li||Li symmetric cells. This superior performance stems from the sequential reactions of PCA that homogenize Li+ distribution, suppress Li dendrites, and stabilize the electrolyte/electrode interface, presenting a green strategy for practical solid‐state lithium metal batteries.
Poly(ethylene oxide) (PEO)-based solid polymer electrolytes suffer from low ionic conductivity and limited Na+ transport capability, which restrict their application in solid-state sodium metal batteries. Herein, a Na+-coordinating filler (Al2O3@KHMF) is prepared by grafting organic chains onto the Al2O3 surface thro...
Shu-Wei Wang, Jing-Qun Wen, Fan-Hao Zeng et al.· ACS Applied Energy Materials· 0 citations
Solid‐state lithium batteries (SSBs) represent a promising next‐generation energy storage technology, yet the practical application of poly(ethylene oxide) (PEO)‐based solid polymer electrolytes (SPEs) is hindered by limited ionic conductivity and poor oxidative stability at high voltages. In this work, we present a...
S. Bakkardouch, S. Abouricha, N. Sabi et al.· ENERGY & ENVIRONMENTAL M...· 0 citations
Developing safe and high-energy solid-state lithium metal batteries (LMBs) remains challenging due to the need to simultaneously achieve ultrathin electrolyte membranes, fast ion transport, and mechanical robustness. Herein, we report a scalable 19 μm composite electrolyte based on a porous PTFE scaffold, a PEO/LiTFSI...
Composite solid electrolytes (CSEs) are promising for high‐energy solid‐state lithium metal batteries, yet weakly coupled ceramic/polymer interfaces often induce filler aggregation, interfacial defects, and discontinuous Li+ transport. Here, we establish a molecular‐bridging strategy using bifunctional PFDTES to couple...
Lithium metal batteries (LMBs) are promising next-generation energy storage systems. However, their practical application remains limited by safety concerns and poor compatibility with high-voltage cathodes, arising from interfacial instability, dendrite growth, and uneven ion transport at the electrode–electrolyte i...
Yi-Xin Wei, Jia-Ying Chen, Yao-Wu Cai et al.· ACS Applied Polymer Material...· 0 citations
Solid polymer electrolytes (SPEs) from electrospinning offer robust mechanical frameworks but often require complex post‐treatments and suffer from low room‐temperature ionic conductivity and sluggish Li
+
transport, hindering the development of solid‐state batteries. Here, we propose a surface‐grown protective f...