离子液体
化学吸附
离子键合
碳纤维
化学
金属
离子
水溶液中的金属离子
胺气处理
化学工程
纳米技术
无机化学
材料科学
有机化学
催化作用
复合数
工程类
复合材料
作者
Xian Suo,Zhenzhen Yang,Yuqing Fu,Chi‐Linh Do‐Thanh,Dmitry S. Maltsev,Huimin Luo,Shannon M. Mahurin,De‐en Jiang,Huabin Xing,Sheng Dai
出处
期刊:Chemsuschem
[Wiley]
日期:2021-12-18
卷期号:15 (2)
被引量:8
标识
DOI:10.1002/cssc.202102136
摘要
Development of efficient carbon capture-and-release technologies with minimal energy input is a long-term challenge in mitigating CO2 emissions, especially via CO2 chemisorption driven by engineered chemical bond construction. Herein, taking advantage of the structural diversity of ionic liquids (ILs) in tuning their physical and chemical properties, precise reaction energy regulation of CO2 chemisorption was demonstrated deploying metal-ion-amino-based ionic liquids (MAILs) as absorbents. The coordination ability of different metal sites (Cu, Zn, Co, Ni, and Mg) to amines was harnessed to achieve fine-tuning on stability constants of the metal ion-amine complexes, acting as the corresponding cations in the construction of diverse ILs coupled with CO2 -philic anions. The as-afforded MAILs exhibited efficient and controllable CO2 release behavior with great reduction in energy input and minimal sacrifice on CO2 uptake capacity. This coordination-regulated approach offers new prospects for the development of ILs-based systems and beyond towards energy-efficient carbon capture technologies.
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