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通过“液膜”启动可逆水系锌/硫电池。

Initiating a Reversible Aqueous Zn/Sulfur Battery through a "Liquid Film".

作者信息

Zhao Yuwei, Wang Donghong, Li Xinliang, Yang Qi, Guo Ying, Mo Funian, Li Qing, Peng Chengxin, Li Hongfei, Zhi Chunyi

机构信息

Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong, SAR 999077, China.

School of Materials Science and Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, China.

出版信息

Adv Mater. 2020 Aug;32(32):e2003070. doi: 10.1002/adma.202003070. Epub 2020 Jun 28.

Abstract

Sulfur cathodes have been under intensive study in various systems, such as Li/S, Na/S, Mg/S, and Al/S batteries. However, to date, Zn/S chemistry has never been reported. The first reliable aqueous Zn/polysulfide system activated by a "liquid film" comprising 4-(3-butyl-1-imidazolio)-1-butanesulfoni ionic liquid (IL) encapsulated within PEDOT:PSS. CF SO anions in the IL operating as Zn -transfer channels is reported. Moreover, the PEDOT:PSS network retains the IL, which renders Zn -transfer channels and a polysulfide cathode with enhanced structural stability. The Zn/polysulfide system delivers extraordinary capacity of 1148 mAh g and overwhelming energy density of 724.7 Wh kg at 0.3 Ag . During the discharging phase, S is dominantly reduced by Zn to S (S   →  S ). During the charging phase, these short chains are oxidized to form long-chain Zn Li S . A further optimized high-concentrated salt electrolyte is used to improve the reversibility of the battery, demonstrating an extended lifetime over 1600 cycles at 1 Ag with a capacity retention of 204 mAh g . This facile approach and the superior performance of the developed aqueous Zn/S chemistry provide a new platform for sulfur-based battery and potentially solve the problems of other metal/sulfur batteries.

摘要

硫阴极已在各种体系中得到深入研究,如锂/硫、钠/硫、镁/硫和铝/硫电池。然而,迄今为止,锌/硫化学体系从未被报道过。本文报道了首个可靠的水系锌/多硫化物体系,该体系由包裹在聚(3,4-乙撑二氧噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)中的4-(3-丁基-1-咪唑鎓)-1-丁烷磺酸离子液体(IL)组成的“液膜”激活。IL中的CF₃SO₄⁻阴离子作为锌转移通道。此外,PEDOT:PSS网络保留了IL,这使得锌转移通道和多硫化物阴极具有更高的结构稳定性。该锌/多硫化物体系在0.3 A g⁻¹时具有1148 mAh g⁻¹的超高容量和724.7 Wh kg⁻¹的超高能量密度。在放电阶段,锌主要将S₈还原为S₂⁻(S₈→S₂⁻)。在充电阶段,这些短链被氧化形成长链ZnₓLi₂S₆。进一步优化的高浓度盐电解质用于提高电池的可逆性,在1 A g⁻¹时循环寿命超过1600次,容量保持率为204 mAh g⁻¹。这种简便的方法以及所开发的水系锌/硫化学体系的优异性能为硫基电池提供了一个新平台,并有可能解决其他金属/硫电池的问题。

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