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A membrane-free lithium/polysulfide semi-liquid battery for large-scale energy storage

机译:无膜锂/多硫化物半液体电池,用于大规模储能

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摘要

Large-scale energy storage represents a key challenge for renewable energy and new systems with low cost, high energy density and long cycle life are desired. In this article, we develop a new lithium/ polysulfide (Li/PS) semi-liquid battery for large-scale energy storage, with lithium polysulfide (Li_2S_8) in ether solvent as a catholyte and metallic lithium as an anode. Unlike previous work on Li/S batteries with discharge products such as solid state Li_2S_2 and Li_2S, the catholyte is designed to cycle only in the range between sulfur and Li_2S_4. Consequently all detrimental effects due to the formation and volume expansion of solid Li_2S_2/Li_2S are avoided. This novel strategy results in excellent cycle life and compatibility with flow battery design. The proof-of-concept Li/PS battery could reach a high energy density of 170 W h kg~(-1) and 190 W h L~(-1) for large scale storage at the solubility limit, while keeping the advantages of hybrid flow batteries. We demonstrated that, with a 5 M Li_2S_8 catholyte, energy densities of 97 W h kg~(-1) and 108 W h L~(-1) can be achieved. As the lithium surface is well passivated by LiNO_3 additive in ether solvent, internal shuttle effect is largely eliminated and thus excellent performance over 2000 cycles is achieved with a constant capacity of 200 mA h g~(-1). This new system can operate without the expensive ion-selective membrane, and it is attractive for large-scale energy storage.
机译:大规模储能是可再生能源的主要挑战,因此需要低成本,高能量密度和长循环寿命的新系统。在本文中,我们开发了一种新型的锂/聚硫化物(Li / PS)半液体电池,用于大规模储能,以醚溶剂中的聚硫化锂(Li_2S_8)为阴极,金属锂为阳极。不同于先前对带有放电产物(例如固态Li_2S_2和Li_2S)的Li / S电池的研究,阴极电解液设计为仅在硫和Li_2S_4之间的范围内循环。因此,避免了由于固体Li_2S_2 / Li_2S的形成和体积膨胀引起的所有有害作用。这种新颖的策略可实现出色的循环寿命,并与液流电池设计兼容。概念验证的Li / PS电池可在溶解度极限下达到170 W h kg〜(-1)和190 W h L〜(-1)的高能量密度以进行大规模存储,同时保持了以下优点:混合液流电池。我们证明,使用5 M Li_2S_8阴极电解液,可以实现97 W h kg〜(-1)和108 W h L〜(-1)的能量密度。由于锂表面被LiNO_3添加剂在醚溶剂中充分钝化,因此内部穿梭效应被大大消除,因此在200个循环的循环中以200 mA h g〜(-1)的恒定容量获得了出色的性能。这种新系统无需昂贵的离子选择膜即可运行,并且对大规模储能具有吸引力。

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  • 来源
    《Energy & environmental science》 |2013年第5期|1552-1558|共7页
  • 作者单位

    Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, USA;

    Department of Chemical Engineering, Stanford University, Stanford, California 94305, USA;

    Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, USA,SLAC National Accelerator Laboratory, Stanford Institute for Materials and Energy Sciences, 2575 Sand Hill Road, Menlo Park, California 94025, USA;

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