Understanding CO2 adsorption mechanisms in porous adsorbents: A solid-state NMR survey

被引:18
作者
Pereira, Daniel [1 ]
Fonseca, Rita [1 ]
Marin-Montesinos, Ildefonso [1 ]
Sardo, Mariana [1 ]
Mafra, Luis [1 ]
机构
[1] Univ Aveiro, CICECO Aveiro Inst Mat, Dept Chem, Campus Univ Santiago, P-3810193 Aveiro, Portugal
基金
欧洲研究理事会;
关键词
CO2; capture; Solid adsorbents; Solid-state NMR; Chemisorp-; tion; Physisorption; METAL-ORGANIC FRAMEWORK; CARBON-DIOXIDE; CHEMISORBED CO2; HIGH-PRESSURE; CAPTURE; DIFFUSION; CHEMISTRY; TECHNOLOGIES; RELAXATION; SIMULATION;
D O I
10.1016/j.cocis.2023.101690
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reaching a historic high of 36.3 gigatonnes in 2021, global CO2 emissions from fossil fuel combustion continue to increase at an alarming rate. CO2 removal technologies are part of the solution to tackle this crucial environmental challenge. Thus, the devel-opment of porous materials for storage and capture of gas mol-ecules (in particular, carbon capture and storage) has attracted great interest both in academic and industrial communities due to its potential in mitigating atmospheric CO2 concentrations. Atomic-scale studies in porous materials are essential to stimulate progress in the design of better CO2-adsorbents by elucidating gas-sorption surface mechanisms. Spectroscopic techniques have the potential to shed light on the structural details of distinct materials' surfaces, including the type of chemical species formed upon CO2 adsorption. Herein, we review the last 5 years of scientific developments wherein solid-state NMR and computational studies have been explored to investigate at the atomic level the structure and molecular dynamics of CO2 species formed at porous surfaces.
引用
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页数:19
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