Zhao Chen-Zi, Zhao Qing, Liu Xiaotun, Zheng Jingxu, Stalin Sanjuna, Zhang Qiang, Archer Lynden A
Robert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY, 14853, USA.
Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Adv Mater. 2020 Mar;32(12):e1905629. doi: 10.1002/adma.201905629. Epub 2020 Feb 13.
Solid-state batteries enabled by solid-state polymer electrolytes (SPEs) are under active consideration for their promise as cost-effective platforms that simultaneously support high-energy and safe electrochemical energy storage. The limited oxidative stability and poor interfacial charge transport in conventional polymer electrolytes are well known, but difficult challenges must be addressed if high-voltage intercalating cathodes are to be used in such batteries. Here, ether-based electrolytes are in situ polymerized by a ring-opening reaction in the presence of aluminum fluoride (AlF ) to create SPEs inside LiNi Co Mn O (NCM) || Li batteries that are able to overcome both challenges. AlF plays a dual role as a Lewis acid catalyst and for the building of fluoridized cathode-electrolyte interphases, protecting both the electrolyte and aluminum current collector from degradation reactions. The solid-state NCM || Li metal batteries exhibit enhanced specific capacity of 153 mAh g under high areal capacity of 3.0 mAh cm . This work offers an important pathway toward solid-state polymer electrolytes for high-voltage solid-state batteries.
由固态聚合物电解质(SPE)实现的固态电池正受到积极关注,因其有望成为具有成本效益的平台,同时支持高能量和安全的电化学储能。传统聚合物电解质中有限的氧化稳定性和较差的界面电荷传输是众所周知的,但如果要在这类电池中使用高压插层阴极,就必须应对一些艰巨的挑战。在此,醚基电解质在氟化铝(AlF)存在下通过开环反应原位聚合,在LiNiCoMnO(NCM)||Li电池内部生成能够克服这两个挑战的SPE。AlF作为路易斯酸催化剂以及用于构建氟化阴极-电解质界面,起到双重作用,保护电解质和铝集流体免受降解反应的影响。固态NCM||Li金属电池在3.0 mAh cm的高面积容量下表现出153 mAh g的增强比容量。这项工作为高压固态电池的固态聚合物电解质提供了一条重要途径。