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

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作者
Lixia Guo
Joseph Hurd
Meng He
Wanpeng Lu
Jiangnan Li
Danielle Crawshaw
Mengtian Fan
Sergei Sapchenko
Yinlin Chen
Xiangdi Zeng
Meredydd Kippax-Jones
Wenyuan Huang
Zhaodong Zhu
Pascal Manuel
Mark D. Frogley
Daniel Lee
Martin Schröder
Sihai Yang
机构
[1] University of Manchester,Department of Chemistry
[2] University of Manchester,Department of Chemical Engineering
[3] Harwell Science and Innovation Campus,Diamond Light Source
[4] ISIS Facility,undefined
[5] STFC Rutherford Appleton Laboratory,undefined
[6] Chilton,undefined
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摘要
The development of stable sorbent materials to deliver reversible adsorption of ammonia (NH3) is a challenging task. Here, we report the efficient capture and storage of NH3 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 NH3 of 4.8 and 12.8 mmol g−1 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 NH3 molecules in MIL-160, with H/D site-exchange between the host and guest and an unusual distortion of the local structure of [AlO6] moieties being observed. Dynamic breakthrough experiments confirm the excellent ability of MIL-160 to capture of NH3 with a dynamic uptake of 4.2 mmol g−1 at 1000 ppm. The combination of high porosity, pore aperture size and multiple binding sites promotes the significant binding affinity and capacity for NH3, which makes it a promising candidate for practical applications.
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