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基于痕量 l-半胱氨酸添加剂的长循环寿命高效电解质,实现稳定的锌金属负极。

Long Shelf-Life Efficient Electrolytes Based on Trace l-Cysteine Additives toward Stable Zinc Metal Anodes.

机构信息

College of Materials Science and Engineering, Hunan Province Key Laboratory for Advanced Carbon Materials and Applied Technology, Hunan University, Changsha, 410082, P. R. China.

出版信息

Small. 2022 Sep;18(37):e2203674. doi: 10.1002/smll.202203674. Epub 2022 Aug 8.

DOI:10.1002/smll.202203674
PMID:35941099
Abstract

The unstable anode/electrolyte interface (AEI) triggers the corrosion reaction and dendrite formation during cycling, hindering the practical application of zinc metal batteries. Herein, for the first time, l-cysteine (Cys) is employed to serve as an electrolyte additive for stabilizing the Zn/electrolyte interface. It is revealed that Cys additives tend to initially approach the Zn surface and then decompose into multiple effective components for suppressing parasitic reactions and Zn dendrites. As a consequence, Zn|Zn symmetric cells using trace Cys additives (0.83 mm) exhibit a steady cycle life of 1600 h, outperforming that of prior studies. Additionally, an average Coulombic efficiency of 99.6% for 250 cycles is also obtained under critical test conditions (10 mA cm /5 mAh cm ). Cys additives also enable Zn-V O and Zn-MnO full cells with an enhanced cycle stability at a low N/P ratio. More importantly, Cys/ZnSO electrolytes are demonstrated to be still effective after resting for half year, favoring the practical production.

摘要

不稳定的正极/电解液界面(AEI)在循环过程中引发腐蚀反应和枝晶形成,阻碍了锌金属电池的实际应用。在此,首次将半胱氨酸(Cys)用作电解液添加剂来稳定 Zn/电解液界面。研究表明,Cys 添加剂倾向于首先接近 Zn 表面,然后分解为多种有效成分,以抑制寄生反应和 Zn 枝晶的形成。因此,使用痕量 Cys 添加剂(0.83mm)的 Zn|Zn 对称电池表现出稳定的 1600 小时循环寿命,优于先前的研究。此外,在苛刻的测试条件(10mAcm/5mAhcm)下,经过 250 次循环后还可获得平均库仑效率为 99.6%。Cys 添加剂还可使 Zn-VO 和 Zn-MnO 全电池在低 N/P 比下具有增强的循环稳定性。更重要的是,Cys/ZnSO 电解液在静置半年后仍然有效,有利于实际生产。

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引用本文的文献

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Interface solvation regulation stabilizing the Zn metal anode in aqueous Zn batteries.界面溶剂化调控稳定水系锌电池中的锌金属负极
Chem Sci. 2023 Jul 11;14(30):8076-8083. doi: 10.1039/d3sc01831h. eCollection 2023 Aug 2.