Cooperative self-assembly of porphyrins and derivatives

被引:9
|
作者
Wei, Wenbo [1 ,2 ]
Sun, Jiajie [3 ]
Fan, Hongyou [4 ,5 ]
机构
[1] Henan Univ, Sch Mat Sci & Engn, Natl & Local Joint Engn Res Ctr High Efficiency D, Key Lab Special Funct Mat, Kaifeng, Henan, Peoples R China
[2] Henan Univ, Collaborat Innovat Ctr Nano Funct Mat & Applicat, Kaifeng, Henan, Peoples R China
[3] Henan Univ, Dept Phys & Elect, Kaifeng, Henan, Peoples R China
[4] Sandia Natl Labs, Ctr Integrated Nanotechnol, Livermore, CA 94550 USA
[5] Univ New Mexico, Dept Chem & Biol Engn, Albuquerque, NM 87131 USA
基金
中国国家自然科学基金;
关键词
self-assembly; nanoscale; nanostructure; nucleation & growth; energy storage; NANOSTRUCTURES; METALLIZATION; NANOPARTICLES; DENDRIMERS; ARRAYS;
D O I
10.1557/mrs.2019.39
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
There has been widespread recent interest in self-Assembly and synthesis of porphyrin and its derivatives-based ordered arrays aiming to emulate natural light-harvesting processes and energy storage. However, technologies that leverage the structural advantages of individual porphyrins have not been fully realized and have been limited by available synthesis methods. This article provides general perspectives on porphyrin and derivative chemistry, and discussions on surfactant-Assisted cooperative self-Assembly using amphiphilic surfactants and functional porphyrins and derivatives. The cooperative self-Assembly amplifies the intrinsic advantages of individual porphyrins by engineering them into well-defined one-dimensional-Three-dimensional (1D-3D) nanostructures. Surfactant-Assisted self-Assembly of amphiphilic surfactants and porphyrins has been utilized to form well-defined micelle-like nanostructures. Driven by intermolecular interactions, subsequent nucleation and growth confined within these nanostructures lead to the formation of 1D-3D ordered optically and electrically active nanomaterials with structure and function on multiple length scales. Copyright © Materials Research Society 2019 A.
引用
收藏
页码:178 / 182
页数:5
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