The emerging field of block copolymer self-assembly-directed quantum materials

被引:5
作者
Yu, Fei [1 ,2 ]
Wiesner, Ulrich [1 ]
机构
[1] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
Block copolymer; Self-assembly; Quantum materials; METAL-OXIDES; MESOPOROUS MATERIALS; SINGLE-CRYSTAL; DIRECT ACCESS; SOFT-MATTER; TEMPERATURE; TRANSITION; POLYMERS; SUPERCONDUCTIVITY; MORPHOLOGY;
D O I
10.1016/j.polymer.2023.126063
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 area of functional materials derived from block copolymers (BCPs) as structure-directing agents for various inorganic materials has seen substantial growth as a result of the immense scientific as well as technological promise associated with such hybrid materials. The convergence of BCP self-assembly with the fast-growing field of quantum materials now promises solution-based synthetic approaches to classes of materials that to date are dominated by stringent high-vacuum physical deposition techniques and bulk solid state chemical reactions. Moreover, the ensuing periodic nano-and mesostructures, a characteristic of BCP self-assembly, offer a unique platform for manipulating quantum-level properties, in turn resulting in substantial changes of macroscopic properties. This article will make a case for, review the existing work of, and provide our perspectives on this emerging field of block copolymer self-assembly directed quantum materials.
引用
收藏
页数:13
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