Capture CO2 from Ambient Air Using Nanoconfined Ion Hydration

被引:91
|
作者
Shi, Xiaoyang [1 ]
Xiao, Hang [1 ]
Lackner, Klaus S. [2 ]
Chen, Xi [1 ]
机构
[1] Columbia Univ, Dept Earth & Environm Engn, 905E Mudd,500 West 120th St, New York, NY 10027 USA
[2] Arizona State Univ, Sch Sustainable Engn & Built Environm, Tempe, AZ 85287 USA
关键词
air-water interfaces; CO2; capture; free energy; ion hydration; molecular dynamics; CARBON-DIOXIDE CAPTURE; HYDROPHILIC SURFACES; AIR/WATER INTERFACE; SODIUM-CARBONATE; WATER; SIMULATION; SOLVATION; DYNAMICS; ENERGY; SALTS;
D O I
10.1002/anie.201507846
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Water confined in nanoscopic pores is essential in determining the energetics of many physical and chemical systems. Herein, we report a recently discovered unconventional, reversible chemical reaction driven by water quantities in nanopores. The reduction of the number of water molecules present in the pore space promotes the hydrolysis of CO32- to HCO3- and OH-. This phenomenon led to a nano-structured CO2 sorbent that binds CO2 spontaneously in ambient air when the surrounding is dry, while releasing it when exposed to moisture. The underlying mechanism is elucidated theoretically by computational modeling and verified by experiments. The free energy of CO32- hydrolysis in nanopores reduces with a decrease of water availability. This promotes the formation of OH-, which has a high affinity to CO2. The effect is not limited to carbonate/bicarbonate, but is extendable to a series of ions. Humidity-driven sorption opens a new approach to gas separation technology.
引用
收藏
页码:4026 / 4029
页数:4
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