Molybdenum-functionalized metal–organic framework crystals interconnected by carbon nanotubes as negative electrodes for supercapacitors

IF 3.3 Q3 ENERGY & FUELS
Yu-Hsiu Chen, Chengliang Shen, Tzu-En Chang, Yi‐Ching Wang, You-Liang Chen, Chung‐Wei Kung
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引用次数: 1

Abstract

Abstract As the pseudocapacitive material operated in the negative potential window in an aqueous electrolyte, the molybdenum-functionalized MOF-808-CNT nanocomposite can obviously outperform both the molybdenum-functionalized MOF-808 and molybdenum-functionalized CNT . Crystals of a water-stable Zr-based metal–organic framework (MOF), MOF-808, are directly grown on the surface of carboxylic acid-functionalized carbon nanotubes (CNT) to synthesize the nanocomposites with tunable MOF-to-CNT ratios. The crystallinity, morphology, porosity, and electrical conductivity of all nanocomposites are characterized. To install the electrochemically active sites within the highly porous MOF framework, the obtained MOF-808-CNT nanocomposites are further subjected to the functionalization of spatially dispersed Mo(VI) sites by a self-limiting process followed by the electrochemical reduction to generate the molybdenum nanoparticles confined within the MOF pore. Thin films of these Mo-functionalized materials are served as the pseudocapacitive materials in aqueous electrolytes and operated in a negative potential window. By utilizing the electrochemically active molybdenum confined within the highly porous MOF and the electronic conduction between MOF crystals facilitated by CNT, the optimal Mo-functionalized nanocomposite can significantly outperform both the Mo-functionalized MOF and Mo-functionalized CNT. Discussion MOFs are highly porous materials, which should be attractive candidates for electrochemical energy storage, but their poor chemical stability and low electrical conductivity hinder the practical use of MOFs in supercapacitors. Even though several MOFs have been directly applied for supercapacitors in aqueous electrolytes, most of these reported MOFs are not stable in water (or the alkaline electrolytes tested), which would generate MOF-derived materials. Reported examples of MOF-based materials for supercapacitors that are chemically robust in the tested electrolytes are relatively rare. Pseudocapacitive materials show higher specific capacitances than the double-layer-type materials, but most pseudocapacitive materials can only be operated in the positive potential window. Thus, asymmetric supercapacitors are usually fabricated by serving the double-layer-type material as the negative electrode. Molybdenum-based pseudocapacitive materials can be operated in the negative potential window, which makes it feasible to design the supercapacitors based on all pseudocapacitive materials. Graphical abstract
用碳纳米管连接的钼功能化金属有机框架晶体作为超级电容器的负极
摘要钼功能化的MOF-808-CNT纳米复合材料作为一种在水性电解质负电位窗口中工作的赝电容材料,其性能明显优于钼功能化MOF-808和钼功能化CNT。在羧酸官能化碳纳米管(CNT)表面直接生长水稳定的Zr基金属-有机框架(MOF)MOF-808晶体,以合成具有可调MOF/CNT比例的纳米复合材料。对所有纳米复合材料的结晶度、形态、孔隙率和电导率进行了表征。为了将电化学活性位点安装在高度多孔的MOF框架内,通过自限制过程进一步对所获得的MOF-808-CNT纳米复合材料进行空间分散的Mo(VI)位点的功能化,然后进行电化学还原以产生限制在MOF孔内的钼纳米颗粒。这些Mo功能化材料的薄膜在水性电解质中用作赝电容材料,并在负电位窗口中操作。通过利用限制在高度多孔MOF内的电化学活性钼和CNT促进的MOF晶体之间的电子传导,最佳的Mo官能化纳米复合材料可以显著优于Mo官能化MOF和Mo官能化CNT。讨论MOFs是一种高度多孔的材料,应该是电化学储能的有吸引力的候选者,但其较差的化学稳定性和较低的电导率阻碍了MOFs在超级电容器中的实际应用。尽管有几种MOF已直接应用于水性电解质中的超级电容器,但大多数报道的MOF在水中(或测试的碱性电解质)不稳定,这将产生MOF衍生材料。在测试的电解质中具有化学稳定性的用于超级电容器的MOF基材料的报道实例相对罕见。伪电容材料比双层型材料表现出更高的比电容,但大多数伪电容材料只能在正电位窗口中工作。因此,不对称超级电容器通常通过使用双层型材料作为负电极来制造。钼基赝电容材料可以在负电位窗口中工作,这使得设计基于所有赝电容物质的超级电容器是可行的。图形摘要
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来源期刊
MRS Energy & Sustainability
MRS Energy & Sustainability ENERGY & FUELS-
CiteScore
6.40
自引率
2.30%
发文量
36
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