手性(物理)
量子点
圆二色性
激子
分子
化学物理
半导体
偶极子
密度泛函理论
材料科学
化学
分子物理学
纳米技术
凝聚态物理
结晶学
光电子学
计算化学
物理
量子力学
手征对称性
有机化学
Nambu–Jona Lasinio模型
夸克
作者
Pingping Han,Tingli Du,Xiaowei Yang,Yanyan Zhao,Si Zhou,Jijun Zhao
标识
DOI:10.1021/acs.jpclett.3c03554
摘要
Introduction of chirality to colloidal semiconductor quantum dots (QDs) triggers a chiroptical effect. However, there remains a knowledge gap in the mechanism of chirality transfer and amplification from molecules to QDs. By time-dependent density functional theory calculations combined with a correlated electron–hole picture, we explored the chiroptical activity of CdSe QDs decorated with different chiral monocarboxylic acids from an excitonic perspective. Our calculations showed strong circular dichroism (CD) signals in the visible region for the chiral CdSe QDs. The excitonic states with large CD originate from QDs, while the chiral molecules break the orthogonality between electric and magnetic transition dipoles, which synergistically facilitates the prominent dissymmetric effect. The considered monocarboxylic acid chiral molecules all favor the bidentate adsorption configuration of the carboxyl group on the CdSe surface, endowing an identical CD signature but distinct excitonic characteristics. These findings are crucial for the regulation of chirality and excitons in semiconductor QDs to develop excitonic devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI