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钴基、镍基、铜基和锌基水稳定柱撑金属有机框架的合成

Synthesis of cobalt-, nickel-, copper-, and zinc-based, water-stable, pillared metal-organic frameworks.

作者信息

Jasuja Himanshu, Jiao Yang, Burtch Nicholas C, Huang You-gui, Walton Krista S

机构信息

School of Chemical and Biomolecular Engineering, Georgia Institute of Technology , 311 Ferst Drive Northwest, Atlanta, Georgia 30332, United States.

出版信息

Langmuir. 2014 Dec 2;30(47):14300-7. doi: 10.1021/la503269f. Epub 2014 Nov 17.

Abstract

The performance of metal-organic frameworks (MOFs) in humid or aqueous environments is a topic of great significance for a variety of applications ranging from adsorption separations to gas storage. While a number of water-stable MOFs have emerged recently in the literature, the majority of MOFs are known to have poor water stability compared to zeolites and activated carbons, and there is therefore a critical need to perform systematic water-stability studies and characterize MOFs comprehensively after water exposure. Using these studies we can isolate the specific factors governing the structural stability of MOFs and direct the future synthesis efforts toward the construction of new, water-stable MOFs. In this work, we have extended our previous work on the systematic water-stability studies of MOFs and synthesized new, cobalt-, nickel-, copper-, and zinc-based, water-stable, pillared MOFs by incorporating structural factors such as ligand sterics and catenation into the framework. Stability is assessed by using water vapor adsorption isotherms along with powder X-ray diffraction patterns and results from BET modeling of N2 adsorption isotherms before and after water exposure. As expected, our study demonstrates that unlike the parent DMOF structures (based on Co, Ni, Cu, and Zn metals), which all collapse under 60% relative humidity (RH), their corresponding tetramethyl-functionalized variations (DMOF-TM) are remarkably stable, even when adsorbing more than 20 mmol of H2O/g of MOF at 80% RH. This behavior is due to steric factors provided by the methyl groups grafted on the BDC (benzenedicarboxylic acid) ligand, as shown previously for the Zn-based DMOF-TM. Moreover, 4,4',4″,4‴-benzene-1,2,4,5-tetrayltetrabenzoic acid based, pillared MOFs (based on Co and Zn metals) are also found to be stable after 90% RH exposure, even when the basicity of the bipyridyl-based pillar ligand is low. This is due to the presence of catenation in their frameworks, similar to MOF-508 (Zn-BDC-BPY), which has also been reported to be stable after exposure to 90% RH.

摘要

金属有机框架材料(MOFs)在潮湿或水环境中的性能对于从吸附分离到气体存储等各种应用而言是一个具有重大意义的课题。尽管近期文献中出现了一些水稳定的MOFs,但与沸石和活性炭相比,大多数MOFs的水稳定性较差,因此迫切需要进行系统的水稳定性研究,并在水暴露后对MOFs进行全面表征。通过这些研究,我们可以找出影响MOFs结构稳定性的具体因素,并指导未来的合成工作,以构建新型的水稳定MOFs。在这项工作中,我们扩展了之前关于MOFs系统水稳定性研究的工作,并通过将配体空间位阻和连锁等结构因素纳入框架,合成了新型的钴基、镍基、铜基和锌基水稳定柱状MOFs。通过使用水蒸气吸附等温线以及粉末X射线衍射图谱,并结合水暴露前后N2吸附等温线的BET模型结果来评估稳定性。正如预期的那样,我们的研究表明,与母体DMOF结构(基于钴、镍、铜和锌金属)不同,它们在相对湿度(RH)为60%时都会坍塌,而其相应的四甲基官能化变体(DMOF-TM)却非常稳定,即使在80%RH下吸附超过20 mmol H2O/g的MOF时也是如此。这种行为归因于接枝在BDC(苯二甲酸)配体上的甲基提供的空间位阻因素,正如之前基于锌的DMOF-TM所显示的那样。此外,基于4,4',4″,4‴-苯-1,2,4,5-四羧酸的柱状MOFs(基于钴和锌金属)在暴露于90%RH后也被发现是稳定的,即使基于联吡啶的柱状配体的碱性较低。这是由于其框架中存在连锁,类似于MOF-508(Zn-BDC-BPY),据报道它在暴露于90%RH后也很稳定。

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