Hierarchically engineered nanostructures from compositionally anisotropic molecular building blocks

被引:44
作者
Liang, Ruiqi [1 ]
Xue, Yazhen [1 ]
Fu, Xiaowei [1 ,2 ]
Le, An N. [1 ]
Song, Qingliang [3 ]
Qiang, Yicheng [3 ]
Xie, Qiong [3 ]
Dong, Ruiqi [4 ]
Sun, Zehao [5 ]
Osuji, Chinedum O. [4 ]
Johnson, Jeremiah A. [5 ]
Li, Weihua [3 ]
Zhong, Mingjiang [1 ,6 ]
机构
[1] Yale Univ, Dept Chem & Environm Engn, New Haven, CT USA
[2] Sichuan Univ, State Key Lab Polymer Mat Engn, Polymer Res Inst, Chengdu, Peoples R China
[3] Fudan Univ, Dept MacroMol Sci, State Key Lab Mol Engn Polymers, Shanghai, Peoples R China
[4] Univ Penn, Dept Chem & BioMol Engn, Philadelphia, PA USA
[5] MIT, Dept Chem, Cambridge, MA USA
[6] Yale Univ, Dept Chem, New Haven, CT USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
PHASE; TRANSITION; SIMULATION; POLYMERS;
D O I
10.1038/s41563-022-01393-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Independently tailored nano- and mesoscale features are obtained in hierarchically assembled mixed graft block copolymers with precisely defined side-chain sequences. The inability to synthesize hierarchical structures with independently tailored nanoscale and mesoscale features limits the discovery of next-generation multifunctional materials. Here we present a predictable molecular self-assembly strategy to craft nanostructured materials with a variety of phase-in-phase hierarchical morphologies. The compositionally anisotropic building blocks employed in the assembly process are formed by multicomponent graft block copolymers containing sequence-defined side chains. The judicious design of various structural parameters in the graft block copolymers enables broadly tunable compositions, morphologies and lattice parameters across the nanoscale and mesoscale in the assembled structures. Our strategy introduces advanced design principles for the efficient creation of complex hierarchical structures and provides a facile synthetic platform to access nanomaterials with multiple precisely integrated functionalities.
引用
收藏
页码:1434 / +
页数:10
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