Flexible engineering of circular dichroism enabled by chiral surface lattice resonances

被引:7
作者
Qiao, Shuqi [1 ]
Liang, Qinghua [2 ,3 ]
Zhang, Xiaochen [2 ,3 ]
Liu, Xing [2 ,3 ]
Feng, Shuai [1 ]
Ji, Chang-Yin [2 ,3 ]
Guo, Honglian [1 ]
Li, Jiafang [2 ,3 ,4 ]
机构
[1] Minzu Univ China, Sch Sci, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Minist Educ, Key Lab Adv Optoelect Quantum Architecture & Measu, Beijing Key Lab Nanophoton & Ultrafine Optoelect S, Beijing 100081, Peoples R China
[3] Beijing Inst Technol, Sch Phys, Beijing 100081, Peoples R China
[4] Beijing Inst Technol, Yangtze Delta Reg Acad, Jiaxing 314019, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
40;
D O I
10.1063/5.0118263
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Engineering the chiroptical responses of artificial nanostructures is vital for realizing applications in the fields of optical devices, enantioselective separation, and bio-sensing. Here, by utilizing the nano-kirigami based meta-molecule arrays, the flexible engineering of circular dichroism (CD) is achieved in the near-infrared wavelength region by the excitation of chiral surface lattice resonances (SLRs). It is found that the chiral SLRs can be flexibly tailored by a tiny structural perturbation. As a result, the wavelength, intensity, and sign of CD peak/dip can be abruptly engineered. Specifically, a CD peak with the value of +0.44 is evolved into a CD dip with an intensity of -0.66 when the etching silt length of the meta-molecules is simply decreased by 190 nm. Importantly, such CD reversal is experimentally demonstrated with the nano-kirigami method without requiring the inversion of geometric chirality. Moreover, it is found that the asymmetric dielectric environment around the meta-molecules can significantly suppress the chiral SLRs, providing an insightful understanding of the chiral SLR. Such flexible tailoring of the CD with chiral SLRs paves a versatile way toward the manipulation of chiral light-matter interactions and chiroptical functional devices. (C) 2022 Author(s).
引用
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页数:9
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