Light-driven sequential shape transformation of block copolymer particles through three-dimensional confined self-assembly

被引:19
|
作者
Hu, Dengwen [1 ]
Wang, Yaping [1 ]
Liu, Jintao [1 ]
Mao, Yanya [1 ]
Chang, Xiaohua [1 ]
Zhu, Yutian [1 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
RECENT PROGRESS; INTERFACE; BEHAVIOR;
D O I
10.1039/d2nr01172g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Shape-controlled block copolymer (BCP) particles that respond to light stimulus have drawn great attention due to their promising applications in smart materials, yet polymeric particles with light-triggered controllable sequential shape transformation (SST) are still rarely reported. By confined co-assembly of polystyrene-b-poly(2-vinylpyridine) (PS-b-P2VP) and azo-containing light-responsive additives within emulsions, herein, we fabricated BCP particles with light-controlled SST behavior. Attributed to the quaternization of P2VP chains with bromoalkyl additives and the trans-cis isomerization of an azo group under UV light, the interfacial interactions between the BCPs and the surrounding aqueous phase are significantly varied; therefore, the particles exhibit three distinct phases in sequence: (1) elongation of ellipsoidal particles with increasing domain spacing; (2) shape transformation of elongated ellipsoidal particles into accordion-like particles; and (3) disassembly of polymer particles into small spheres. In addition, these particles with SST behavior can be used in light-controlled drug release at a high spatial-temporal resolution, demonstrating their potential in clinical settings and biomedicine.
引用
收藏
页码:6291 / 6298
页数:8
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