溶解
材料科学
多孔性
吸附
溶解度
溶剂
化学工程
制作
离子液体
多孔介质
离子键合
金属
选择性
多孔硅
纳米技术
可见光谱
荧光
光化学
作者
Han‐Yan Jin,Yang Liu,Zhiwei Xing,Yuxia Li,Lin‐Bing Sun
出处
期刊:Small
[Wiley]
日期:2026-02-18
卷期号:: e13827-e13827
标识
DOI:10.1002/smll.202513827
摘要
Photoresponsive porous liquids (PPLs) have garnered increasing attention due to their ability to controllably modulate gas uptake upon light irradiation. Currently, the modulation on gas uptake of reported PPLs is based on configuration transformation of photoresponsive motifs, while their permanent pores remain unchanged. Here we report for the first time the fabrication of type II PPLs with adsorption capacities tunable by light-controlled exposure/blockage of permanent cavities. The charged metal-organic cage (MOC-SO3Na) is modified by 3-phenylazopyridine ligands on metal open sites, producing a new photoresponsive porous host MOC-SO3Na-Azo (MSA). A phosphorus-containing bulky ionic liquid, [P6,6,6,14][Cl], provides electrostatic interactions that enable the dissolution of MSA with high solubility (70 mg mL-1). The obtained type II PPL, PPL-MSA, shows CO2 uptake (9.9 cm3 g-1 at 25°C, 1 bar) much superior to all reported type II porous liquids (0.2-3.0 cm3 g-1). Under different light conditions, PPL-MSA demonstrates 49.3% change in CO2 uptake, which is obviously higher than the porous host (7.6%) and solvent (0.3%). This photoresponsive efficiency is attributed to exposure/blockage of permanent cavities within PPL-MSA.
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