Li Chao, Wang Kuaibing, Li Jingze, Zhang Qichun
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, P. R. China.
Nanoscale. 2020 Apr 14;12(14):7870-7874. doi: 10.1039/d0nr00964d. Epub 2020 Mar 30.
Finding new organic materials to address several issues (e.g. capacity, stability, and cycle life) in organic potassium-ion batteries (OPIBs) is very important and highly desirable. Here, to directly investigate the redox reaction of organic pyridine dicarboxylate in OPIBs and to avoid the interference from the redox-active metal ions, a non-redox-metal potassium metal-organic framework (K-MOF), [CHKNO], based on pyridine-2,6-dicarboxylic acid (HPDA), has been successfully synthesized and applied as a promising organic anode for long-cycle life PIBs. The crystal structure of [CHKNO] was confirmed by single-crystal X-ray diffraction analysis and FT-IR spectra. Moreover, the potassium-storage mechanism of organic pyridine dicarboxylate ligand was revealed by ex situ FT-IR/XRD characterization and theoretical calculations. The as-synthesized K-MOF resulted in a unique and reversible three-step redox reaction, exhibited superior electrochemical performance with the aid of N-K/O-K coordination bonds, and showed a high average specific capacity of 115 mA h g at 100 mA g for 300 cycles with the capacity retention of 92%.
寻找新型有机材料以解决有机钾离子电池(OPIBs)中的若干问题(如容量、稳定性和循环寿命)非常重要且十分必要。在此,为了直接研究OPIBs中有机吡啶二羧酸的氧化还原反应并避免氧化还原活性金属离子的干扰,基于吡啶 - 2,6 - 二羧酸(HPDA)成功合成了一种非氧化还原金属钾金属有机框架(K - MOF)[CHKNO],并将其用作长循环寿命PIBs的有前景的有机阳极。通过单晶X射线衍射分析和傅里叶变换红外光谱(FT - IR)确认了[CHKNO]的晶体结构。此外,通过非原位FT - IR/XRD表征和理论计算揭示了有机吡啶二羧酸配体的储钾机制。所合成的K - MOF导致独特且可逆的三步氧化还原反应,借助N - K/O - K配位键展现出优异的电化学性能,在100 mA g下300次循环时平均比容量高达115 mA h g,容量保持率为92%。