Bao Li, Bo Zhang, Xiang Bai, Jiahui Zhang, Xinyue Chang, Lifeng Hou, Hao Huang, Tiantian Lu, Shi Wang, Zhong Jin, Qian Wang
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引用次数: 0
摘要
含水锌离子电池(azib)有望用于大规模储能,但锌金属阳极面临析氢、枝晶生长和腐蚀等问题。在此,我们通过在Zn表面聚合硫辛酸(TA),开发了一种自愈合的azib粘接聚合物层。由于锌金属表面与聚合物链上的S原子之间具有很强的自发亲和力,因此该保护层可以牢固地动态粘附在锌表面。因此,即使在厚度为1 μ m时,保护层与Zn表面的粘附力也高达10.5 N,而保护层中丰富的羧基可以形成分子内氢键,使其具有较高的自愈性,增强了其强度(杨氏模量达到15.1 GPa)。这种保护层在物理上有效地抑制了枝晶的生长,在化学上调节了Zn2+的迁移和沉积行为。因此,对称电池可以分别在1.0和5.0 mA cm−2的电流密度下循环1000小时以上。含有NH4V4O10的完整电池也可以稳定运行1000个循环,具有高容量保留。这项工作为设计高稳定性和长循环的azib多功能聚合物涂层提供了一种有前途的策略。
A Dynamic Self-Healing Protective Layer Enabling Stable Zinc Ion Batteries through Strong Zn-S Affinity and Intramolecular Hydrogen Bonding
Aqueous Zn-ion batteries (AZIBs) are promising for large-scale energy storage, yet Zn metal anodes face issues like hydrogen evolution, dendrite growth, and corrosion. Herein, we develop a self-healable, adhesive polymer layer for AZIBs by polymerizing thioctic acid (TA) on Zn surfaces. Thanks to the strong and spontaneous affinity between Zn metal surface and S atoms on polymer chains, this protective layer can firmly and dynamically adhere to the Zn surface. Thus, even at a thickness of <1 µm, the protective layer exhibits a strong adhesion force of up to 10.5 N with Zn surface, while the abundant carboxyl groups in the protective layer can form intramolecular hydrogen bonds, endowing its high self-healing property and enhancing its strength (Young's modulus reaches 15.1 GPa). Such a protective layer effectively inhibits the dendrite growth physically and regulates the Zn2+ migration and deposition behavior chemically. Therefore, the symmetric cells can be cycled for more than 1000 h at the current densities of 1.0 and 5.0 mA cm−2, respectively. Full cells with NH4V4O10 also run stably for 1000 cycles with a high capacity retention. This work offers a promising strategy for designing multifunctional polymer coating towards high-stability and long-cycling AZIBs.