纳米孔
吸附
碳酸氢盐
化学
吸附剂
水解
化学工程
碳酸盐
分子
水蒸气
水分
离子
纳米尺度
湿度
纳米技术
材料科学
吸附
有机化学
热力学
工程类
物理
作者
Xiaoyang Shi,Hang Xiao,Klaus S. Lackner,Xi Chen
标识
DOI:10.1002/anie.201507846
摘要
Abstract 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 CO 3 2− to HCO 3 − and OH − . This phenomenon led to a nano‐structured CO 2 sorbent that binds CO 2 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 CO 3 2− hydrolysis in nanopores reduces with a decrease of water availability. This promotes the formation of OH − , which has a high affinity to CO 2 . 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.
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