Efficient chemical fixation of CO2 from direct air under environment-friendly co-catalyst and solvent-free ambient conditions

被引:70
|
作者
Das, Rajesh [1 ]
Ezhil, Thirumavalavan [1 ]
Palakkal, Athulya S. [2 ]
Muthukumar, D. [2 ]
Pillai, Renjith S. [2 ,3 ]
Nagaraja, C. M. [1 ]
机构
[1] Indian Inst Technol Ropar, Dept Chem, Rupnagar 140001, Punjab, India
[2] SRM Inst Sci & Technol, Fac Engn & Technol, Dept Chem, Chennai 603203, Tamil Nadu, India
[3] Christ Univ, Dept Chem, Bangalore 560023, Karnataka, India
关键词
METAL-ORGANIC FRAMEWORK; CARBON-DIOXIDE; CYCLIC CARBONATES; RATIONAL DESIGN; FLUE-GAS; CAPTURE; CONVERSION; MOF; CYCLOADDITION; TRANSFORMATION;
D O I
10.1039/d1ta05138e
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
The capture and conversion of CO2 from direct air into value-added products under mild conditions represents a promising step towards environmental remediation and energy sustainability. Consequently, herein, we report the first example of a Mg(ii)-based MOF exhibiting highly efficient fixation of CO2 from direct air into value-added cyclic carbonates under eco-friendly co-catalyst and solvent-free mild conditions. The bifunctional MOF catalyst was rationally constructed by utilizing an eco-friendly Lewis acidic metal ion, Mg(ii), and a nitrogen-rich tripodal linker, TATAB. The MOF possesses a high BET surface area of 2606.13 m(2) g(-1) and highly polar 1D channels decorated with a high density of CO2-philic sites which promote a remarkably high CO2 uptake of 50.2 wt% at 273 K with a high heat of adsorption value of 55.13 kJ mol(-1). The high CO2-affinity combined with the presence of a high density of nucleophilic and Lewis acidic sites conferred efficient catalytic properties to the Mg-MOF for chemical fixation of CO2 from direct air under environment-friendly mild conditions. The remarkable performance of the Mg-MOF for the fixation of CO2 from direct air was further supported by in-depth theoretical calculations. Moreover, the computational studies provided an insight into the mechanistic details of the catalytic process in the absence of any co-catalyst and solvent. Overall, this work represents a rare demonstration of carbon capture and utilization (CCU) from direct air under eco-friendly mild conditions.
引用
收藏
页码:23127 / 23139
页数:13
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