可扩展性
芯(光纤)
对偶(语法数字)
材料科学
光电子学
多核处理器
波长
纳米技术
计算机科学
并行计算
复合材料
艺术
文学类
数据库
作者
Jiahao Jiang,Shuai Zhao,Jiaxuan Zhang,Zhao‐Ji Lv,Jian Song,Yanqiu Sun,Liang‐Sheng Liao,Xuedong Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-10-07
标识
DOI:10.1021/acs.nanolett.4c03330
摘要
Organic core/shell heterostructures have undergone rapid progress in materials chemistry owing to the integration of a wide array of unique properties. Nonetheless, the intricate challenge of regulating homogeneous nucleation and phase separation processes in excessively analogous cocrystal structures presents a formidable barrier to expanding the synthesis strategy for organic core/shell heterostructures. Herein, we successfully achieved a phase separation growth process facilitated by the organic alloy interface layer through a dynamic visualization to capture the intricate morphological evolution. By finely regulating the nucleation process, homogeneous self-assembly induced by high chemical and structural compatibility is circumvented, enabling the formation of organic core/shell heterostructures. Notably, this core/shell architecture boasts dual-wavelength emission at 496 and 696 nm, accompanied by an optical loss coefficient of 0.092 dB per micrometer. This methodology shows potential for extending to the scalable design of other conformational cocrystal heterostructure systems, thereby offering valuable insights into the realm of organic photonics.
科研通智能强力驱动
Strongly Powered by AbleSci AI