Revealing Carbon Capture Chemistry with 17-Oxygen NMR Spectroscopy

29 October 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Carbon dioxide capture is an essential greenhouse mitigation technology to achieve net-zero emissions. A key hurdle to the design of improved carbon capture materials is the lack of adequate tools to characterise how CO2 adsorbs. Solid-state nuclear magnetic resonance (NMR) spectroscopy is emerging as a promising probe of CO2 capture, but it remains challenging to distinguish different adsorption products. Here we perform a comprehensive computational investigation of 22 amine-functionalised metal-organic frameworks and discover that 17O NMR is a powerful probe of CO2 capture chemistry that provides excellent differentiation of ammonium carbamate and carbamic acid species. The computational findings are supported by 17O NMR experiments on a series of CO2-loaded frameworks that clearly identify ammonium carbamate chain formation and provide new evidence for a mixed carbamic acid – ammonium carbamate adsorption mode. The fine sensitivity of 17O NMR to local chemistry also shows that hydrogen bonding schemes proposed in previous ammonium carbamate chain structures may be inaccurate and new structures are proposed. Finally, we discover a new mixed CO2 adsorption mechanism and show that carbamic acid formation is more prevalent in this materials class than previously believed. Our work paves the way for new investigations of carbon capture chemistry that can enable the design of improved materials.

Keywords

carbon capture
metal-organic framework
NMR spectroscopy
adsorption

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