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Published on: November 11, 2013
Dual Interlocked Mediators Enable Single-Ion-Conducting Quasi-Solid-State Electrolytes for Ultrafast-Charging
Yuan Zhang1, Long Pan2, Cheong Wa Leong1
1State Key Laboratory of Engineering Materials for Major Infrastructure, School of Materials Science and Engineering, Southeast University, Nanjing, 211189, People's Republic of China.
Abstract:
Quasi-solid-state electrolytes (QSEs) are critical for ultrafast-charging yet high-safety sodium metal batteries (SMBs), yet their implementation is hindered by sluggish Na+ transport in bulk and at interfaces. Here, we propose dual interlocked mediator engineering that transcends conventional independent approaches by coupling cationic Sn2+ salt with anionic difluoro(oxalato)borate (DFOB⁻) salts to simultaneously regulating bulk ion transport and bilateral interface chemistry. During QSE preparation, Sn2+ initiates in situ cationic polymerization, while DFOB⁻ acts as a retarding agent to suppress runaway polymerization. The first interlocking effect in the Sn-FB QSE bulk builds a uniform network, enabling near-unity Na+ transference number (0.94) and robust puncture strength (8.5 kPa). During cell operation, Sn2+ is reduced to form a hybrid NaSn alloy-based solid-electrolyte interphase, while DFOB⁻ oxidizes to generate a robust yet thin cathode-electrolyte interphase, respectively. This second interlocking effect creates adaptable bilateral interphases that facilitate Na+ diffusion and mitigate interfacial degradation. As a result, the symmetric cells exhibit 6000 h stability, and full cells retain 80.1 mAh g-1 at an ultrafast-charging rate of 15C and retain 90% capacity at 3C over 2000 cycles. Furthermore, high-mass-loading full cells and pressure-free pouch cells are demonstrated, underscoring the potential of dual interlocked mediator engineering for practical SMBs.
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