Loading…

Tunable optical activities in chiral transition metal oxide nanoparticles

Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs), i.e. , Mo...

Full description

Saved in:
Bibliographic Details
Published in:Nanoscale 2022-10, Vol.14 (41), p.15414-15421
Main Authors: Xiao, Shuyu, Liang, Jiechun, Li, Junzi, Cheng, Jiaji, Zhu, Xi, He, Tingchao
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Chiral transition metal oxides (TMOs) are widely used in various optoelectronic devices. However, the currently poor understanding of how the optical activities of TMOs can be regulated considerably hinders their applications. We have synthesized a series of chiral TMO nanoparticles (NPs), i.e. , MoO x ( x = 2, 2.4 and 2.5) and Co 3 O 4 . Compared with TMO NPs with l -/ d -cysteine molecules as the capping ligand, l -/ d -histidine-capped TMO NPs possess larger anisotropic factors ( g abs ), which are as high as ∼0.01 and ∼0.02 for l -/ d -histidine-capped MoO 2.5 and Co 3 O 4 NPs, respectively. A nondegenerate coupled oscillator (NDCO) theoretical calculation confirms that l -/ d -histidine molecules can generate a smaller electric dipole moment and thus induce higher optical activity than l -/ d -cysteine molecules. Impressively, the chiral NPs exhibit broadband second harmonic generation. This work indicates that chiral TMO NPs have potential for application in nonlinear optical devices. The optical activities of chiral transition metal oxide nanoparticles are regulated, achieving a maximum anisotropic factor of approximately 0.02. Impressively, the chiral nanoparticles demonstrate broadband second harmonic generation.
ISSN:2040-3364
2040-3372
DOI:10.1039/d2nr02555h