Angulakshmi N, Zhou Yingke, Suriyakumar Shruti, Dhanalakshmi R Baby, Satishrajan M, Alwarappan Subbiah, Alkordi Mohamed H, Stephan A Manuel
The State Key Laboratory of Refractories and Metallurgy, Institute of Advanced Materials and Nanotechnology, College of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan 430 081, P.R.China.
Electrochemical Power Sources Division, CSIR - Central Electrochemical Research Institute, Karaikudi 630 006, India.
ACS Omega. 2020 Apr 1;5(14):7885-7894. doi: 10.1021/acsomega.9b04133. eCollection 2020 Apr 14.
Poly(ethylene oxide) (PEO)-based composite polymer electrolytes (CPEs) containing the amine-functionalized, zirconium-based metal-organic framework @silica (UiO-66-NH@SiO) and lithium, LiN(CFSO) salt (LiTFSI) are prepared using a simple hot press method. The electrochemical properties such as compatibility of the electrolyte with the Li metal anode, Li transference number, and ionic conductivity are investigated for the different systems containing different relative concentrations of the additives. The incorporation of UiO-66-NH@SiO in the PEO-LiTFSI matrix not only enhanced ionic conductivity by one order of magnitude but also offered better compatibility and suppressed the formation of lithium dendrites appreciably. X-ray photoelectron spectroscopy studies on post-cycled materials revealed the formation of lithium alkoxide (RO-Li) on the cathode and LiO on the anode. The coin cell (2032-type) consisting of LiFePO/CPE/Li with UiO-66-NH@SiO as filler provided a discharge capacity of 151 mA h g at 0.1 C-rate at 60 °C, measurably higher than control experiments utilizing SiO and UiO-66-NH. The notable enhancement of electrochemical properties when incorporating the UiO-66-NH@SiO at the CPE was attributed to formation of more uniform ion conduction pockets and channels within the PEO matrix, facilitated by the presence of the microporous UiO-66-NH@SiO. The enhanced distribution of microporous channels, where Li ions are assumed to percolate through within the matrix, is assumed to desirably reduce formation of Li dendrites by increasing diffusion channels and therefore reducing crystallization and growth of dendrites at the electrode surface.
采用简单的热压法制备了含有胺功能化的锆基金属有机骨架@二氧化硅(UiO-66-NH@SiO)和锂盐LiN(CFSO)(LiTFSI)的聚环氧乙烷(PEO)基复合聚合物电解质(CPE)。针对含有不同相对浓度添加剂的不同体系,研究了电解质与锂金属阳极的相容性、锂迁移数和离子电导率等电化学性能。将UiO-66-NH@SiO掺入PEO-LiTFSI基体中,不仅使离子电导率提高了一个数量级,还提供了更好的相容性,并显著抑制了锂枝晶的形成。对循环后的材料进行的X射线光电子能谱研究表明,在阴极上形成了锂醇盐(RO-Li),在阳极上形成了LiO。以UiO-66-NH@SiO为填料的LiFePO/CPE/Li型纽扣电池(2032型)在60℃、0.1 C倍率下的放电容量为151 mA h g,明显高于使用SiO和UiO-66-NH的对照实验。在CPE中掺入UiO-66-NH@SiO时电化学性能的显著提高归因于在微孔UiO-66-NH@SiO的存在下,PEO基体内形成了更均匀的离子传导口袋和通道。假定锂离子在基体内渗透通过的微孔通道分布的增强,有望通过增加扩散通道来减少锂枝晶的形成,从而减少电极表面枝晶的结晶和生长。