Sengupta Debabrata, Bose Saptasree, Wang Xiaoliang, Schweitzer Neil M, Malliakas Christos D, Xie Haomiao, Duncan Joshua, Kirlikovali Kent O, Yildirim Taner, Farha Omar K
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.
Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.
J Am Chem Soc. 2024 Oct 2;146(39):27006-27013. doi: 10.1021/jacs.4c08757. Epub 2024 Sep 20.
Metal-organic frameworks (MOFs) have shown promise in both capturing CO under flue gas conditions and converting it into valuable chemicals. However, the development of a single MOF capable of capturing and selectively converting CO has remained elusive due to a lack of a harmonious combination of selectivity, water stability, and reactivity. For example, Cu(I)-based MOFs are particularly effective for CO conversion, but they do not typically exhibit selective CO adsorption and often suffer from instability in the presence of air and moisture. Developing a Cu(I) MOF that is stable under flue gas conditions while also capturing CO from this mixture would likely afford a material capable of selectively capturing and converting CO in an integrated pathway, which would represent a significant advancement in this field. In this study, we introduce , an ultramicroporous Cu(I) MOF, which exhibits both selectivity for CO adsorption and great stability even in the presence of moisture and air. Comprehensive evaluations involving exposure to air, oxygen, water, and varying temperatures reveal that demonstrates superior stability compared to other known Cu(I) MOFs. Utilizing adsorption isotherms and thermogravimetric analysis coupled with gas chromatography-mass spectrometry (TGA-GCMS), we establish the high selectivity of for CO over common flue gas components, including water, nitrogen, and oxygen. Additionally, under mild reaction conditions (50 °C and H:CO = 3:1), exhibits CO capture and catalytic conversion to formic acid with 100% selectivity. This study marks an important step toward the design of next-generation MOFs capable of integrated carbon capture and utilization (iCCU) under industrial conditions.
金属有机框架材料(MOFs)在烟道气条件下捕获一氧化碳并将其转化为有价值的化学品方面已显示出潜力。然而,由于缺乏选择性、水稳定性和反应活性的和谐结合,开发一种能够捕获并选择性转化一氧化碳的单一MOF仍然难以实现。例如,基于Cu(I)的MOFs对一氧化碳转化特别有效,但它们通常不表现出选择性一氧化碳吸附,并且在空气和水分存在下常常不稳定。开发一种在烟道气条件下稳定同时又能从这种混合物中捕获一氧化碳的Cu(I)MOF,可能会得到一种能够在集成途径中选择性捕获和转化一氧化碳的材料,这将代表该领域的重大进展。在本研究中,我们介绍了一种超微孔Cu(I)MOF,它即使在有水分和空气存在的情况下也表现出对一氧化碳吸附的选择性和很高的稳定性。涉及暴露于空气、氧气、水和不同温度的综合评估表明,与其他已知的Cu(I)MOFs相比,该材料表现出卓越的稳定性。利用吸附等温线、热重分析以及气相色谱 - 质谱联用(TGA - GCMS),我们确定了该材料对一氧化碳相对于常见烟道气成分(包括水、氮气和氧气)具有高选择性。此外,在温和的反应条件下(50°C,氢气与一氧化碳比例为3:1),该材料表现出一氧化碳捕获并催化转化为甲酸,选择性为100%。这项研究标志着朝着设计能够在工业条件下进行集成碳捕获与利用(iCCU)的下一代MOFs迈出了重要一步。