Zhang Qi, Xiao Yingbo, Li Qi, Wang Jia, Guo Sijia, Li Xin, Ouyang Yuan, Zeng Qinghan, He Wenchao, Huang Shaoming
Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage Devices, School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510006, China and Synergy Innovation Institute of GDUT, Heyuan, 517000, China.
Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage Devices, School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510006, China.
Dalton Trans. 2021 Mar 2;50(8):2928-2935. doi: 10.1039/d0dt03336g.
Metal-organic frameworks (MOFs) have recently emerged as promising solid electrolytes (SEs) for solid-state batteries (SSBs). Developing MOFs with high-density functional groups may improve the spatial density of hopping sites and facilitate ion transport. Herein we synthesized a new series of ion conductive MOFs, Zr-MA-M (M = Li+, Na+, K+, Zn2+), with high density -SH groups functionalized in small pores and metal ions adsorbed on the thiol groups. Taking advantage of the interaction between S and metal ions, such ion conductors show high ionic conductivity, low interfacial resistance, high lithium ion (Li+) transference number (0.63) and wide electrochemical window up (4.6 V). Moreover, the SSBs assembled with Zr-MA-Li+ based SE exhibit excellent rate performance (106 mA h g-1 at 2C) and remarkable cyclic stability (low decay rate of 0.21‰ per cycle for 700 cycles at 2C). Thus, this study provides a new route for developing high-performance MOF-based SEs via the application of host-guest interaction.
金属有机框架材料(MOFs)最近已成为固态电池(SSBs)中很有前景的固体电解质(SEs)。开发具有高密度官能团的MOFs可能会提高跳跃位点的空间密度并促进离子传输。在此,我们合成了一系列新的离子导电MOFs,即Zr-MA-M(M = Li+、Na+、K+、Zn2+),其在小孔中具有高密度的-SH基团官能化,且金属离子吸附在硫醇基团上。利用S与金属离子之间的相互作用,这类离子导体表现出高离子电导率、低界面电阻、高锂离子(Li+)迁移数(0.63)以及宽电化学窗口(高达4.6 V)。此外,用基于Zr-MA-Li+的SE组装的SSBs表现出优异的倍率性能(在2C时为106 mA h g-1)和显著的循环稳定性(在2C下700次循环,每循环的低衰减率为0.21‰)。因此,本研究通过主客体相互作用的应用为开发高性能的基于MOF的SEs提供了一条新途径。