Xiao Ye, Xu Rui, Yan Chong, Liang Yeru, Ding Jun-Fan, Huang Jia-Qi
School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China.
College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China.
Sci Bull (Beijing). 2020 Jun 15;65(11):909-916. doi: 10.1016/j.scib.2020.02.022. Epub 2020 Feb 26.
Lithium (Li) metal is considered as the ultimate anode choice for developing next-generation high-energy batteries. However, the poor tolerance against moist air and the unstable solid electrolyte interphases (SEI) induced by the intrinsic high reactivity of lithium bring series of obstacles such as the rigorous operating condition, the poor electrochemical performance, and safety anxiety of the cell, which to a large extent hinder the commercial utilization of Li metal anode. Here, an effective encapsulation strategy was reported via a facile drop-casting and a following heat-assisted cross-linking process. Benefiting from the inherent hydrophobicity and the compact micro-structure of the cross-linked poly(vinylidene-co-hexafluoropropylene) (PVDF-HFP), the as-encapsulated Li metal exhibited prominent stability toward moisture, as well corroborated by the evaluations both under the humid air at 25 °C with 30% relative humidity (RH) and pure water. Moreover, the encapsulated Li metal anode exhibits a decent electrochemical performance without substantially increasing the cell polarization due to the uniform and unblocked ion channels, which originally comes from the superior affinity of the PVDF-HFP polymer toward non-aqueous electrolyte. This work demonstrates a novel and valid encapsulation strategy for humidity-sensitive alkali metal electrodes, aiming to pave the way for the large-scale and low-cost deployment of the alkali metal-based high-energy-density batteries.
锂(Li)金属被认为是开发下一代高能电池的最终阳极选择。然而,锂对潮湿空气的耐受性较差,以及其固有的高反应活性所导致的不稳定固体电解质界面(SEI),带来了一系列障碍,如苛刻的操作条件、较差的电化学性能以及电池的安全隐患,这在很大程度上阻碍了锂金属阳极的商业应用。在此,通过简便的滴铸法和随后的热辅助交联过程报道了一种有效的封装策略。受益于交联聚偏氟乙烯-六氟丙烯(PVDF-HFP)固有的疏水性和致密的微观结构,封装后的锂金属对水分表现出显著的稳定性,在25℃、相对湿度(RH)为30%的潮湿空气中以及纯水中的评估均证实了这一点。此外,由于PVDF-HFP聚合物对非水电解质具有优异的亲和力,从而形成均匀且畅通的离子通道,封装后的锂金属阳极表现出良好的电化学性能,且不会大幅增加电池极化。这项工作展示了一种针对湿度敏感型碱金属电极的新颖且有效的封装策略,旨在为碱金属基高能量密度电池的大规模低成本部署铺平道路。