Polyphenol-Gated Composite Electrolytes with Enhanced Cross-Phase Lithium-Ion Transport for Solid-State Lithium Batteries

Published in Chemistry and Materials

Polyphenol-Gated Composite Electrolytes with Enhanced Cross-Phase Lithium-Ion Transport for Solid-State Lithium Batteries
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Springer Nature Singapore
Springer Nature Singapore Springer Nature Singapore

Polyphenol-Gated Composite Electrolytes with Enhanced Cross-Phase Lithium-Ion Transport for Solid-State Lithium Batteries - Nano-Micro Letters

Highlights A biomimetic polyphenol-gated strategy is proposed to promote interfacial Li+ - selective transport in composite solid electrolytes by chemically bonding the polymer matrix and ceramic nanofibers. The polyphenol interlayers serve as the chemical gates with –OH and –NH groups to immobilize lithium salt anions and carbonyl groups to coordinate Li+, thus lowering the energy barrier and promoting rapid Li+ transport at interface. The assembled Li||LiFePO4 batteries exhibits an impressive capacity of 151.6 mAh g−1 and long lifespan over 600 cycles. Abstract Solid-state lithium (Li) batteries offer high-energy density and operational safety but face sluggish Li+ transport in polymer/ceramic composite solid-state electrolytes. Herein, we propose a bioinspired polyphenol-gated interfacial engineering that mimics ion-selective protein channels to enhance Li+-selective transport across the polymer–ceramic interface. Polyphenols such as polydopamine, poly-tannic acid, and poly-gallic acid chemically couple La0.56Li0.33TiO3 ceramic nanofibers and glycidyl polyether matrix. Within this interface, carbonyl groups selectively coordinate Li⁺ and facilitate directional migration. On the other hand, hydroxyl and amino groups immobilize anions via hydrogen bonding. This chemical gating nearly doubles interfacial Li+ concentration and boosts transference number to 0.68. The corresponding Li||LiFePO4 battery exhibits stable cycling over 600 cycles with 85.5% capacity retention at 1 C, while the pouch cell delivers reliable operation under mechanical stress caused by bending and puncturing. This work demonstrates that polyphenol-gated interfaces are essential for promoting selective and efficient cross-phase Li⁺ transport for high-performance solid-state lithium-metal batteries.

As the demand for high-performance solid-state lithium batteries continues to grow, conventional polymer-ceramic composite electrolytes face critical limitations in interfacial Li+ transport and low Li+ transference numbers. Now, researchers from Donghua University, led by Professor Yue-E Miao, Professor Hui Zhang, and Professor Feili Lai, have presented a breakthrough polyphenol-gated composite electrolyte that bridges the gap between polymer flexibility and ceramic ionic conductivity.

Why This Electrolyte Matters

Traditional composite solid-state electrolytes suffer from sluggish Li⁺ transport across polymer-ceramic interfaces due to incompatible conduction mechanisms and space-charge layer effects, resulting in low Li⁺ transference numbers (often <0.4). The novel polyphenol-gated strategy overcomes this limitation by mimicking biological ion-selective channels—enabling fast, selective Li⁺ transport while immobilizing anions through hydrogen bonding, achieving an exceptional Li⁺ transference number of 0.68.

Innovative Design and Mechanism

The material employs bioinspired polyphenol interlayers (polydopamine, poly-tannic acid, or poly-gallic acid) that chemically bridge La0.56Li0.33TiO3 ceramic nanofibers and glycidyl polyether matrix. Within this interface, carbonyl groups selectively coordinate Li+ to lower energy barriers, while hydroxyl and amino groups immobilize TFSI- anions. This "ion-gating" effect nearly doubles interfacial Li+ concentration and creates a three-dimensional percolation network for rapid cross-phase ion migration.

Outstanding Performance

PDA2@LLTO/GE delivers a high ionic conductivity of 3.01×10-4 S cm-1 at 60°C—more than four times higher than unmodified systems. The assembled Li||LiFePO4 battery exhibits an impressive capacity of 151.6 mAh g-1 and stable cycling over 600 cycles with 85.5% capacity retention. Remarkably, the pouch cell maintains 82.9% capacity after 400 cycles and operates reliably under mechanical stress including folding, cutting, and puncturing.

Applications and Future Outlook

This work establishes a universal design principle for selective ion conduction across polymer-ceramic interfaces, opening promising avenues for next-generation solid-state lithium-metal batteries combining high safety, fast charging, and long cycling stability.

Stay tuned for more groundbreaking research from this collaborative team at Donghua University, Shanghai Jiao Tong University, and international partners!

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Batteries
Physical Sciences > Materials Science > Materials for Energy and Catalysis > Batteries
Electrochemistry
Physical Sciences > Chemistry > Physical Chemistry > Electrochemistry
Surfaces, Interfaces and Thin Film
Physical Sciences > Materials Science > Surfaces, Interfaces and Thin Film
Nanoscale Design, Synthesis and Processing
Physical Sciences > Materials Science > Nanotechnology > Nanoscale Design, Synthesis and Processing
Composites
Physical Sciences > Chemistry > Materials Chemistry > Composites
  • Nano-Micro Letters Nano-Micro Letters

    Nano-Micro Letters is a peer-reviewed, international, interdisciplinary and open-access journal that focus on science, experiments, engineering, technologies and applications of nano- or microscale structure and system in physics, chemistry, biology, material science, and pharmacy.