TY - JOUR
T1 - Efficient Capture and Storage of Ammonia in Robust Aluminium-based Metal-Organic Frameworks
AU - Guo, Lixia
AU - Hurd, Joseph
AU - He, Meng
AU - Lu, Wanpeng
AU - Li, Jiangnan
AU - Crawshaw, Danielle
AU - Fan, Mengtian
AU - Sapchenko, Sergei
AU - Chen, Yinlin
AU - Zeng, Xiangdi
AU - Kippax-Jones, Meredydd
AU - Huang, Wenyuan
AU - Zhu, Zhaodong
AU - Manuel, Pascal
AU - Frogley, Mark D
AU - Lee, Daniel
AU - Schröder, Martin
AU - Yang, Sihai
PY - 2023/3/24
Y1 - 2023/3/24
N2 - 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 adsorbed 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 for the 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.
AB - 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 adsorbed 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 for the 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.
U2 - 10.1038/s42004-023-00850-4
DO - 10.1038/s42004-023-00850-4
M3 - Article
SN - 2399-3669
VL - 6
JO - Communications Chemistry
JF - Communications Chemistry
M1 - 55
ER -