Dequan Bao, Yi Tao, Yihong Zhong, Wei Zhao, Mingfa Peng, Hao Zhang, Xuhui Sun
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引用次数: 1
Abstract
Succinonitrile (SN)‐based plastic crystal electrolytes (PCE) show great promise for solid‐state lithium‐metal batteries (LMBs) because of their outstanding electrochemical properties. However, limited by the low mechanical strength of SN, SN‐based PCEs are difficult to act as an independent self‐supporting electrolyte films, which seriously restricts their practical application. In this study, a SN‐regulated poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVDF‐HFP) porous host is proposed via a facile phase separation method as a promising strategy for addressing this issue, which enables a high‐performance dual‐salt SN‐based PCE (named as DPCE). The as‐prepared host simultaneously provides homogeneous porous network and robust mechanical support, which is convenient to accommodate DPCE evenly and increases the strength of DPCE to restrict dendrites growth. As a result, with this efficient host, the Li symmetric cell assembled with DPCE shows superior long‐term stability for >1200 h at a current density of 0.1 mA cm−2. Moreover, the assembled Li|LiFePO4 cell delivers a high‐capacity retention of 99.3% after 700 cycles under 2 C at room temperature, demonstrating the promising potential for developing high‐performance solid‐state LMBs.
丁二腈(SN)基塑料晶体电解质(PCE)因其优异的电化学性能在固态锂金属电池(lmb)中具有广阔的应用前景。然而,受SN机械强度低的限制,SN基pce难以作为独立的自支撑电解质膜,严重制约了其实际应用。在本研究中,通过易相分离方法提出了一种sn调控的聚偏氟乙烯-共六氟丙烯(PVDF-HFP)多孔主体,作为解决这一问题的一种有希望的策略,该策略使高性能双盐sn基PCE(称为DPCE)成为可能。制备的基质同时提供了均匀的多孔网络和坚固的机械支撑,便于均匀地容纳DPCE,提高了DPCE的强度,限制了枝晶的生长。结果表明,有了这种高效的宿主,用DPCE组装的锂对称电池在0.1 mA cm−2的电流密度下表现出优越的1200小时的长期稳定性。此外,组装的Li|LiFePO4电池在室温下2℃下循环700次后可提供99.3%的高容量保持率,显示出开发高性能固态lmb的巨大潜力。
期刊介绍:
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