锌
吸附
枝晶(数学)
阳极
水溶液
材料科学
电解质
电偶阳极
化学工程
电镀(地质)
电化学
肺表面活性物质
无机化学
离子
电池(电)
化学
有机化学
阴极保护
电极
冶金
几何学
物理化学
工程类
功率(物理)
地质学
物理
量子力学
数学
地球物理学
作者
Weili Xie,Kaiyue Zhu,Weikang Jiang,Hanmiao Yang,Manxia Ma,Lingli Zhao,Weishen Yang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-08-02
卷期号:18 (32): 21184-21197
被引量:74
标识
DOI:10.1021/acsnano.4c04181
摘要
Rechargeable aqueous zinc-ion batteries (AZIBs) are gaining recognition as promising next-generation energy storage solution, due to their intrinsic safety and low cost. Nevertheless, the advancement of AZIBs is greatly limited by the abnormal growth of zinc dendrites during cycling. Electrolyte additives are effective at suppressing zinc dendrites, but there is currently no effective additive screening criterion. Herein, we propose employing the interfacial electrostatic adsorption strength of zinc ions for the initial screening of additives. Subsequently, dendrite-free plating is achieved by employing the anionic surfactant sodium dodecyl benzenesulfonate (SDBS) to enhance electrostatic adsorption. The cycled zinc anode exhibited a dense plating morphology and a high (002) orientation (I002/I101 = 22). The Zn||MnO2 full cell with SDBS exhibited a capacity retention of 85% after 1000 cycles at 1 A g-1. Furthermore, an instantaneous nucleation model and continuous nucleation model (CNM) are constructed to reveal the microscale plating/stripping dynamics under the scenarios of weak adsorption and strong adsorption. The CNM accurately explains the self-optimizing reconstruction of electrodes resulting from enhanced electrostatic adsorption. Our exploration was extended to other anionic surfactants (sodium dodecyl sulfate and disodium laureiminodipropionate), confirming the effectiveness of strong electrostatic adsorption in the screening of electrolyte additives.
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