Entropy-driven liquid crystalline self-assembly of inorganic nanorods

被引:0
|
作者
Liu Xiao-duo [1 ]
Xie Yong [1 ]
机构
[1] Beihang Univ, Sch Phys, Beijing 102206, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
entropy effect; gold nanorods; self-assembly; inorganic liquid crystal materials; GOLD NANORODS; QUANTUM DOTS; NANOPARTICLES; NANOCRYSTALS; FLUORESCENCE; SUPERLATTICES; EVAPORATION; CONVERSION; PHASES;
D O I
10.37188/YJYXS20203507.0662
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Owing to the existing issues of poor thermal stability and narrow temperature interval in applications of organic liquid crystal materials, developing novel inorganic liquid crystal is an alternative strategy due to the virtues of electron-rich characteristics and high thermal stability of the well-developed inorganic nanomaterials. Starting from the summarization of the phase transition rules and the regulation mechanisms of liquid crystalline self-assembly, including Onsager theory, DLVO theory, and entropy effects on depletion attraction and steric repulsion, this review demonstrates recent progress in entropy-driven liquid crystalline self-assembly of the inorganic nanomaterials. Taking the ideal building block of gold nanorods as an example, the regulations of the advanced self-assembly methods and the interactions between the nanorods on the diverse assembly structures are discussed, and their potential applications in optoelectronic devices are illustrated. Finally, future developments are prospected aiming at the problems in preparing inorganic liquid crystal materials using the self-assembly technology.
引用
收藏
页码:662 / 674
页数:13
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