Efficient capture and storage of ammonia in robust aluminium-based metal-organic frameworks

The development of stable sorbent materials to deliver reversible adsorption of ammonia (NH ) is a challenging task. Here, we report the efficient capture and storage of NH in a series of robust microporous aluminium-based metal-organic framework materials, namely MIL-160, CAU-10-H, Al-fum, and MIL-...

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Published inCommunications chemistry Vol. 6; no. 1; p. 55
Main Authors Guo, Lixia, Hurd, Joseph, He, Meng, Lu, Wanpeng, Li, Jiangnan, Crawshaw, Danielle, Fan, Mengtian, Sapchenko, Sergei, Chen, Yinlin, Zeng, Xiangdi, Kippax-Jones, Meredydd, Huang, Wenyuan, Zhu, Zhaodong, Manuel, Pascal, Frogley, Mark D, Lee, Daniel, Schröder, Martin, Yang, Sihai
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 24.03.2023
Nature Publishing Group UK
Nature Portfolio
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Summary:The development of stable sorbent materials to deliver reversible adsorption of ammonia (NH ) is a challenging task. Here, we report the efficient capture and storage of NH in a series of robust microporous aluminium-based metal-organic framework materials, namely MIL-160, CAU-10-H, Al-fum, and MIL-53(Al). In particular, MIL-160 shows high uptakes of NH of 4.8 and 12.8 mmol g at both low and high pressure (0.001 and 1.0 bar, respectively) at 298 K. The combination of in situ neutron powder diffraction, synchrotron infrared micro-spectroscopy and solid-state nuclear magnetic resonance spectroscopy reveals the preferred adsorption domains of NH molecules in MIL-160, with H/D site-exchange between the host and guest and an unusual distortion of the local structure of [AlO ] moieties being observed. Dynamic breakthrough experiments confirm the excellent ability of MIL-160 to capture of NH with a dynamic uptake of 4.2 mmol g at 1000 ppm. The combination of high porosity, pore aperture size and multiple binding sites promotes the significant binding affinity and capacity for NH , which makes it a promising candidate for practical applications.
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ISSN:2399-3669
2399-3669
DOI:10.1038/s42004-023-00850-4