College of Chemistry, Fuzhou University, Fuzhou 350108, China.
CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, and State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China.
Molecules. 2023 May 18;28(10):4177. doi: 10.3390/molecules28104177.
Aqueous zinc-ion batteries (AZIBs) show enormous potential as a large-scale energy storage technique. However, the growth of Zn dendrites and serious side reactions occurring at the Zn anode hinder the practical application of AZIBs. For the first time, we reported a fluorine-containing surfactant, i.e., potassium perfluoro-1-butanesulfonate (PPFBS), as an additive to the 2 M ZnSO electrolyte. Benefitting from its hydrophilic sulfonate anion and hydrophobic long fluorocarbon chain, PPFBS can promote the uniform distribution of Zn flux at the anode/electrolyte interface, allowing the Zn/Zn cell to cycle for 2200 h. Furthermore, PPFBS could inhibit side reactions due to the existence of the perfluorobutyl sulfonate (CFSO) adsorption layer and the presence of CFSO in the solvation structure of Zn. The former can reduce the amount of HO molecules and SO in contact with the Zn anode and CFSO entering the Zn-solvation structure by replacing SO. The Zn/Cu cell exhibits a superior average CE of 99.47% over 500 cycles. When coupled with the VO cathode, the full cell shows impressive cycle stability. This work provides a simple, effective, and economical solution to the common issues of the Zn anode.
水系锌离子电池(AZIBs)作为一种大规模储能技术具有巨大的潜力。然而,锌枝晶的生长和锌阳极处发生的严重副反应阻碍了 AZIBs 的实际应用。我们首次报道了一种含氟表面活性剂,即双(三氟甲烷磺酰)亚胺钾(PPFBS),作为 2 M ZnSO4电解质的添加剂。得益于其亲水性磺酸盐阴离子和疏水性长氟碳链,PPFBS 可以促进锌流在阳极/电解质界面的均匀分布,使 Zn/Zn 电池循环 2200 小时。此外,由于存在全氟丁基磺酸盐(CFSO)吸附层和 CFSO 存在于 Zn 的溶剂化结构中,PPFBS 可以抑制副反应。前者可以通过取代 SO 来减少与 Zn 阳极接触的 HO 分子和 SO 的数量,以及 CFSO 进入 Zn 溶剂化结构的数量。Zn/Cu 电池在 500 次循环中表现出超过 99.47%的平均 CE。当与 VO 阴极耦合时,全电池表现出令人印象深刻的循环稳定性。这项工作为锌阳极的常见问题提供了一种简单、有效和经济的解决方案。