离子液体
水溶液
化学工程
聚电解质
材料科学
固化(化学)
相(物质)
化学
高分子化学
有机化学
聚合物
复合材料
催化作用
工程类
作者
Chongrui Zhang,Xufei Liu,Jiang Gong,Qiang Zhao
标识
DOI:10.1038/s41467-023-38236-8
摘要
Abstract Aqueous two-phase systems (ATPS) provide imperative interfaces and compartments in biology, but the sculpture and conversion of liquid structures to functional solids is challenging. Here, inspired by phase evolution of mussel foot proteins ATPS, we tackle this problem by designing poly(ionic liquids) capable of responsive condensation and phase-dependent curing. When mixed with poly(dimethyl diallyl ammonium chloride), the poly(ionic liquids) formed liquid condensates and ATPS, which were tuned into bicontinuous liquid phases under stirring. Selective, rapid curing of the poly(ionic liquids)-rich phase was facilitated under basic conditions (pH 11), leading to the liquid-to-gel conversion and structure sculpture, i.e., the evolution from ATPS to macroporous sponges featuring bead-and-string networks. This mechanism enabled the selective embedment of carbon nanotubes in the poly(ionic liquids)-rich phase, which showed exceptional stability in harsh conditions (10 wt% NaCl, 80 o C, 3 days) and high (2.5 kg/m 2 h) solar thermal desalination of concentrated salty water under 1-sun irradiation.
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