Grafting Block Copolymer Nanoparticles to a Surface via Aqueous Photoinduced Polymerization-induced Self-Assembly at Room Temperature

被引:2
|
作者
Niu, Bing [1 ]
Huang, Honggao [1 ]
Zhang, Li [1 ,2 ]
Tan, Jianbo [1 ,2 ]
机构
[1] Guangdong Univ Technol, Sch Mat & Energy, Dept Polymer Mat & Engn, Guangzhou 510006, Peoples R China
[2] Guangdong Prov Key Lab Funct Soft Condensed Matter, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
POWER CONVERSION EFFICIENCY; DISPERSION POLYMERIZATION; MOLECULAR-WEIGHT; HIGH-RESOLUTION; NANO-OBJECTS; SOLAR-CELLS; LARGE-SCALE; PARTICLES; BRUSHES; CRYSTALLIZATION;
D O I
10.1021/acsmacrolett.4c00098
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The creation of well-defined surface nanostructures is important for a diverse set of applications such as cell adhesion, superhydrophobic coating, and lithography. In this study, we describe a robust bottom-up method for surface functionalization that involves surface-initiated reversible deactivation radical polymerization (RDRP) and the grafting of block copolymer nanoparticles to material surfaces via aqueous photoinduced polymerization-induced self-assembly (photo-PISA) at room temperature. Using silica nanoparticles as a model substrate, colloidal mesoscale hybrid assemblies with various morphologies were successfully prepared. The morphologies can be easily tuned by changing the lengths of macromolecular chain transfer agents and parameters of the silica nanoparticles. The surface-initiated photo-PISA approach can also be employed for other large-scale substrates such as silicon wafer. Taking advantage of mild reaction conditions of this method (room temperature, aqueous medium, and visible light), enzymatic deoxygenation was introduced to develop oxygen-tolerant surface-initiated photo-PISA that can fabricate well-defined nanostructures on large-scale substrates under open-to-air conditions.
引用
收藏
页码:577 / 585
页数:9
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