Interfacial Assembly and Jamming of Soft Nanoparticle Surfactants into Colloidosomes and Structured Liquids

被引:14
|
作者
Wang, Beibei [1 ]
Yin, Bangqi [1 ]
Yu, Hao [1 ]
Zhang, Zhao [1 ]
Wang, Guan [1 ]
Shi, Shaowei [1 ]
Gu, Xinggui [1 ,5 ]
Yang, Wantai [1 ]
Tang, Ben Zhong [2 ]
Russell, Thomas P. [3 ,4 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
[2] Chinese Univ Hong Kong Shenzhen, Shenzhen Inst Aggregate Sci & Technol, Sch Sci & Engn, Shenzhen 518172, Peoples R China
[3] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[4] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[5] Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
liquid-liquid interfaces; self-assembly; colloidosomes; structured liquids; aggregation-induced emission; AGGREGATION-INDUCED EMISSION; PARTICLES;
D O I
10.1021/acsami.2c13414
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanoparticle surfactant (NPS) offers a powerful strategy to generate all-liquid constructs that integrate the inherent properties of the NPs into 3D architectures. Here, using the co-assembly of fluorescent polymeric nanoparticles and amine-functionalized polyhedral oligomeric silsesquioxane, the assembly and jamming behavior of a new type of NPS at the oil-water interface is uncovered. Unlike "solid" inorganic nanoparticles, "soft" polymeric nanoparticles can reorganize when jammed, leading to a relaxation and deformation of the interfacial assemblies, for example, the 3D printed sugar-coated haw stick-like liquid tubules. With NPS serving as emulsifiers, stable Pickering emulsions are prepared that can be converted into robust colloidosomes with pH responsiveness, showing numerous potential applications for encapsulation and controlled release.
引用
收藏
页码:54287 / 54292
页数:6
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