共聚物
热致变色
材料科学
智能聚合物
马来酰亚胺
光致变色
氧化铟锡
单体
智能材料
聚合物
纳米技术
介孔材料
倍半硅氧烷
光热治疗
双稳态
纳米材料
光电子学
化学工程
光热效应
低临界溶液温度
相变
模板
高分子化学
铟
兴奋剂
玻璃化转变
相(物质)
热稳定性
光学双稳态
纳米结构
链式转移
作者
Qian Li,Tong Wang,Qu Wang,Kaihao Wang,Li Wang,Wantai Yang
标识
DOI:10.1002/adfm.202522619
摘要
Abstract Engineering advanced thermochromic smart windows capable of simultaneously addressing multifaceted performance, durability, and multifunctionality requirements is crucial for their practical applications. Herein, a mini library of lower critical solution temperature (LCST) copolymers with well‐defined structure and programmed hydrophile‐lipophile balance (HLB) is synthesized by the reversible addition‐fragmentation chain transfer (RAFT) copolymerization of highly hydrophilic N‐vinylpyrrolidone (NVP) and four maleimide derivative (MI) monomers with descending hydrophilicity. MI‐NVP copolymers afford a copolymer composition‐dependent phase transition temperature tunable over an ultra‐wide range of 20–67 °C and efficient UV shielding capability. By ingeniously doping MI‐NVP copolymers into non‐thermoresponsive polyacrylamide hydrogel, smart windows with outstanding thermochromic properties, solar modulation performance, inherent stability (1000 cycles), and fast response rate (14 ± 2 s) are obtained. Further integration with photothermal Cs x WO 3 or electrothermal indium tin oxide (ITO) glass delivers enhanced spectral selectivity or active‐mode regulation. Overall, by meticulously tailoring the multilevel structure of thermochromic hydrogels, this strategy establishes a novel MI‐NVP copolymer platform for thermochromic smart windows that significantly advances energy conservation and occupant comfort.
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