{"title":"Transformation of Plasmonic MoO3–x Nanoparticles into Dielectric MoS2 Nanoparticles","authors":"Ruoqi Ai, Ka Kit Chui, Yilin Chen, Jianfang Wang","doi":"10.1021/acs.jpcc.4c08803","DOIUrl":null,"url":null,"abstract":"Transformation from plasmonic to dielectric properties allows for control over light–matter interactions, enabling the development of nanoparticles that can dynamically adjust their optical characteristics and enhance their functionalities. The exploration of the transformation aligns with the demand for applications in adaptive optics and responsive photonic devices. The transformation of metal plasmonic nanoparticles to dielectric nanoparticles typically requires a complex structure design while ensuring the preservation of their original morphology. Herein, we report on the transformation of plasmonic MoO<sub>3–<i>x</i></sub> nanoparticles into dielectric MoS<sub>2</sub> nanoparticles. The plasmonic properties of MoO<sub>3–<i>x</i></sub> nanoparticles, prepared by aerosol spray, were investigated at the single-particle level. A comprehensive analysis of the size-dependent electromagnetic resonances of the product nanoparticles was conducted from both experimental and simulation perspectives. The transformation process was carried out in a tube furnace under a sulfur atmosphere, allowing for a complete change in optical response from plasmonic MoO<sub>3–<i>x</i></sub> nanoparticles to dielectric MoS<sub>2</sub> nanoparticles. The degree of transformation can be controlled by varying the sulfurization time with the formation of (MoO<sub>3–<i>x</i></sub> core)@(MoS<sub>2</sub> shell) nanostructures. Our results demonstrate a potential strategy for transforming plasmonic nanoparticles into dielectric nanoparticles.","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"24 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcc.4c08803","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Transformation from plasmonic to dielectric properties allows for control over light–matter interactions, enabling the development of nanoparticles that can dynamically adjust their optical characteristics and enhance their functionalities. The exploration of the transformation aligns with the demand for applications in adaptive optics and responsive photonic devices. The transformation of metal plasmonic nanoparticles to dielectric nanoparticles typically requires a complex structure design while ensuring the preservation of their original morphology. Herein, we report on the transformation of plasmonic MoO3–x nanoparticles into dielectric MoS2 nanoparticles. The plasmonic properties of MoO3–x nanoparticles, prepared by aerosol spray, were investigated at the single-particle level. A comprehensive analysis of the size-dependent electromagnetic resonances of the product nanoparticles was conducted from both experimental and simulation perspectives. The transformation process was carried out in a tube furnace under a sulfur atmosphere, allowing for a complete change in optical response from plasmonic MoO3–x nanoparticles to dielectric MoS2 nanoparticles. The degree of transformation can be controlled by varying the sulfurization time with the formation of (MoO3–x core)@(MoS2 shell) nanostructures. Our results demonstrate a potential strategy for transforming plasmonic nanoparticles into dielectric nanoparticles.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.