材料科学
聚合物
钙钛矿(结构)
化学工程
铸造
电致发光
光致发光
溶剂
软质材料
纳米复合材料
分子间力
纳米技术
复合材料
光电子学
有机化学
化学
分子
图层(电子)
工程类
作者
Jae‐Man Park,Jinwoo Park,Young‐Hoon Kim,Huanyu Zhou,Young‐Hoon Lee,Seung Hyeon Jo,Jinwoo Ma,Tae‐Woo Lee,Jeong‐Yun Sun
标识
DOI:10.1038/s41467-020-18383-y
摘要
Existing gels are mostly polar, whose nature limits their role in soft devices. The intermolecular interactions of nonpolar polymer-liquid system are typically weak, which makes the gel brittle. Here we report highly soft and transparent nonpolar organogels. Even though their elements are only carbon and hydrogen, their elastic modulus, transparency, and stretchability are comparable to common soft hydrogels. A key strategy is introducing aromatic interaction into the polymer-solvent system, resulting in a high swelling ratio that enables efficient plasticization of the polymer networks. As a proof of applicability, soft perovskite nanocomposites are synthesized, where the nonpolar environment of organogels enables stable formation and preservation of highly concentrated perovskite nanocrystals, showing high photoluminescence efficiency (~99.8%) after water-exposure and environmental stabilities against air, water, acid, base, heat, light, and mechanical deformation. Their superb properties enable the demonstration of soft electroluminescent devices that stably emit bright and pure green light under diverse deformations.
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