Liang Guojin, Tang Zijie, Han Bing, Zhu Jiaxiong, Chen Ao, Li Qing, Chen Ze, Huang Zhaodong, Li Xinliang, Yang Qi, Zhi Chunyi
Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, 999077, P. R. China.
Songshan Lake Materials Laboratory, Dongguan, Guangdong, 523808, P. R. China.
Adv Mater. 2023 May;35(20):e2210051. doi: 10.1002/adma.202210051. Epub 2023 Mar 30.
The introduction of inorganic crystallites into a solid-electrolyte interphase (SEI) is an effective strategy for improving the reversibility of the Zn metal anode (ZMA). However, the structure-performance relationship of the SEI is not fully understood because the existing forms of its inorganic and organic components in their pristine states are not resolved. Here, a highly effective SEI is constructed for ZMA using a bisolvent electrolyte and resolved its composition/structure by cryogenic transmission electron microscopy. This highly fluorinated SEI with amorphous inorganic ZnF uniformly distributed in the organic matrix is largely different from the common mosaic and multilayer SEIs with crystalline inorganics. It features improved structural integrity, mechanical toughness, and Zn ion conductivity. Consequently, the ZMA exhibits excellent reversibility with an enhanced plating/stripping Coulombic efficiency of 99.8%. The ZMA-based full cell achieves a high Zn utilization ratio of 54% at a practical areal capacity of 3.2 mAh cm and stable cycling over 1800 h during which the accumulated capacity reached 5600 mAh cm . This research highlights the detailed structure and composition of amorphous SEIs for highly reversible metal anodes.
将无机微晶引入固体电解质界面(SEI)是提高锌金属阳极(ZMA)可逆性的有效策略。然而,由于SEI的无机和有机成分在其原始状态下的存在形式尚未得到解决,其结构-性能关系尚未完全理解。在此,使用双溶剂电解质为ZMA构建了一种高效的SEI,并通过低温透射电子显微镜解析了其组成/结构。这种高度氟化的SEI中,非晶态无机ZnF均匀分布在有机基质中,与具有结晶无机物的常见镶嵌和多层SEI有很大不同。它具有改善的结构完整性、机械韧性和锌离子传导性。因此,ZMA表现出优异的可逆性,电镀/剥离库仑效率提高到99.8%。基于ZMA的全电池在实际面积容量为3.2 mAh cm时实现了54%的高锌利用率,并在1800 h内稳定循环,在此期间累积容量达到5600 mAh cm 。这项研究突出了用于高可逆金属阳极的非晶态SEI的详细结构和组成。