Leveraging the most recent success in expanding the electrochemical stability window of aqueous electrolytes, in this work we create a unique Li-ion/sulfur chemistry of both high energy density and safety. We show that in the superconcentrated aqueous electrolyte, lithiation of sulfur experiences phase change from a high-order polysulfide to low-order polysulfides through solid–liquid two-phase reaction pathway, where the liquid polysulfide phase in the sulfide electrode is thermodynamically phase-separated from the superconcentrated aqueous electrolyte. The sulfur with solid–liquid two-phase exhibits a reversible capacity of 1,327 mAh/(g of S), along with fast reaction kinetics and negligible polysulfide dissolution. By coupling a sulfur anode with different Li-ion cathode materials, the aqueous Li-ion/sulfur full cell delivers record-high energy densities up to 200 Wh/(kg of total electrode mass) for >1,000 cycles at ∼100% coulombic efficiency. These performances already approach that of commercial lithium-ion batteries (LIBs) using a nonaqueous electrolyte, along with intrinsic safety not possessed by the latter. The excellent performance of this aqueous battery chemistry significantly promotes the practical possibility of aqueous LIBs in large-format applications.
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机译:利用最近在扩大水性电解质的电化学稳定性窗口方面取得的成功,在这项工作中,我们创建了具有高能量密度和安全性的独特锂离子/硫化学。我们表明,在超浓缩水电解质中,硫的锂化经历了通过固液两相反应路径从高阶多硫化物到低阶多硫化物的相变,其中硫化物电极中的液态多硫化物相被热力学相分离。来自超浓缩的水性电解质。固液两相硫的可逆容量为1,327 mAh /(g的S),具有快速的反应动力学和可忽略不计的多硫化物溶解。通过将硫磺阳极与不同的锂离子阴极材料耦合,锂离子/硫磺全电池在〜100%的库仑效率下可进行> 1,000次循环,提供高达200 Wh /(kg的总电极质量)的创纪录高能量密度。 。这些性能已经接近使用非水电解质的商用锂离子电池(LIB)的性能,以及后者所不具备的本质安全性。这种水性电池化学性能的卓越性能极大地提高了水性LIB在大幅面应用中的实际可能性。
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