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Boosting High‐Rate Li–S Batteries by an MOF‐Derived Catalytic Electrode with a Layer‐by‐Layer Structure

机译:通过MOF衍生的具有分层结构的催化电极助推高速率Li-S电池

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摘要

Rechargeable high‐energy lithium–sulfur batteries suffer from rapid capacity decay and poor rate capability due to intrinsically intermediate polysulfides' shuttle effect and sluggish redox kinetics. To tackle these problems simultaneously, a layer‐by‐layer electrode structure is designed, each layer of which consists of ultrafine CoS2‐nanoparticle‐embedded porous carbon evenly grown on both sides of reduced graphene oxide (rGO). The CoS2 nanoparticles derived from metal–organic frameworks (MOFs) have an average size of ≈10 nm and can facilitate the conversion between Li2S6 and Li2S2/Li2S in the liquid electrolyte by a catalytic effect, leading to improved polysulfide redox kinetics. In addition, the interconnected conductive frameworks with hierarchical pore structure afford fast ion and electron transport and provide sufficient space to confine polysulfides. As a result, the layer‐by‐layer electrodes exhibit good rate capabilities with 1180.7 and 700 mAh g−1 at 1.0 and 5.0 C, respectively, and maintain an impressive cycling stability with a low capacity decay of 0.033% per cycle within ultralong 1000 cycles at 5.0 C. Even with a high sulfur loading of 3.0 mg cm−2, the electrodes still show high rate performance and stable cycling stability over 300 cycles.
机译:可充电的高能锂硫电池由于固有的中间多硫化物的穿梭效应和缓慢的氧化还原动力学而遭受快速容量衰减和差的倍率能力的困扰。为了同时解决这些问题,设计了一个逐层电极结构,该结构的每一层均由均匀地生长在还原氧化石墨烯(rGO)两侧的超细CoS2纳米粒子嵌入多孔碳组成。源自金属-有机骨架(MOF)的CoS2纳米粒子的平均尺寸约为10 nm,并且可以通过催化作用促进液体电解质中Li2S6和Li2S2 / Li2S之间的转化,从而改善了多硫化物的氧化还原动力学。另外,具有分层孔结构的互连导电框架提供了快速的离子和电子传输,并提供了足够的空间限制多硫化物。结果,层电极在1.0和5.0 C时分别具有1180.7和700 mAh g -1 的良好倍率能力,并保持了令人印象深刻的循环稳定性以及低的容量衰减。在5.0 C的超长1000次循环中,每循环0.033%。即使在3.0 mg cm -2 的高硫负荷下,电极在300次循环中仍显示出高倍率性能和稳定的循环稳定性。

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