Zhang Hualei, Wang Xinlei, Zhou Jie, Tang Weihua
College of Materials, Xiamen University, Xiamen 361005, China.
School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
Molecules. 2023 Nov 8;28(22):7479. doi: 10.3390/molecules28227479.
The design of well-defined hierarchical free-standing electrodes for robust high-performance energy storage is challenging. We report herein that azo-linkage redox metal-organic frameworks (MOFs) incorporate single-walled carbon nanotubes (CNTs) as flexible electrodes. The in situ-guided growth, crystallinity and morphology of UiO-66-NO MOFs were finely controlled in the presence of CNTs. The MOFs' covalent anchoring to CNTs and solvothermal grafting anthraquinone (AQ) pendants endow the hybrid (denoted as CNT@UiO-66-AQ) with greatly improved conductivity, charge storage pathways and electrochemical dynamics. The flexible CNT@UiO-66-AQ displays a highest areal specific capacitance of 302.3 mF cm (at 1 mA cm) in -0.4~0.9 V potential window, together with 100% capacitance retention over 5000 cycles at 5 mA cm. Its assembled symmetrical supercapacitor (SSC) achieves a maximum energy density of 0.037 mWh cm and a maximum power density of 10.4 mW cm, outperforming many MOFs-hybrids-based SSCs in the literature. Our work may open a new avenue for preparing azo-coupled redox MOFs hybrids with carbaneous substrates for high-performance robust aqueous energy storage.
设计用于高性能稳健储能的结构明确的分级独立电极具有挑战性。我们在此报告,偶氮键合氧化还原金属有机框架(MOF)将单壁碳纳米管(CNT)纳入其中作为柔性电极。在CNT存在的情况下,对UiO-66-NO MOF的原位引导生长、结晶度和形态进行了精细控制。MOF与CNT的共价锚定以及溶剂热接枝蒽醌(AQ)侧链赋予了该杂化物(表示为CNT@UiO-66-AQ)大大提高的导电性、电荷存储途径和电化学动力学。柔性的CNT@UiO-66-AQ在-0.4~0.9 V的电位窗口中显示出最高面积比电容为302.3 mF cm²(在1 mA cm²时),在5 mA cm²下5000次循环中电容保持率为100%。其组装的对称超级电容器(SSC)实现了最大能量密度为0.037 mWh cm²和最大功率密度为10.4 mW cm²,优于文献中许多基于MOF杂化物的SSC。我们的工作可能为制备具有含碳基底的偶氮偶联氧化还原MOF杂化物以实现高性能稳健水系储能开辟一条新途径。