Al-Au Heterogeneous Dimer-trimer Nanostructure for SERS

2020 ◽  
Vol 10 (1) ◽  
pp. 21-28
Author(s):  
Jyoti Katyal

: Tunability in resonance wavelength and the enhancement of the electromagnetic field intensities around the surface are two unique properties which make metal as a plasmonic material. A theoretical investigation on the LSPR and field enhancement for heterogeneous dimer–trimer metallic nanostructure by constituting Al and Au as two different plamsonic materials has been studied. Since electrons in Al exhibit free behavior for LSPR of Au, therefore, they influence the electric field magnitude generated by Au LSPR. Methods: The electromagnetic simulations reported in this paper were performed using the FDTD Solutions (version 7.5.1), a product of Lumerical Solutions Inc., Vancouver, Canada. We adopted a cubic Yee cell of 1 nm side and a time step Δt= 1.31•10-18 s, bounded by Courant condition. Results: The extinction spectrum shows LSPR peak over UV-visible region for isotropic nanostructure which shifts to NIR region for anisotropic shape nanostructure. The spherical shape hetero dimer nanostructure shows enhancement factor ~ 3.9 X 105 whereas it increases to ~ 6.2 X 106 for anisotropic shape at 610 nm. The field distribution corresponding to the trimer nanostructure reveals a large dipolar field distribution on each of the three nanoparticles, oscillating approximately in-phase. The spherical shape Al-Au-Al shows enhancement factor ~ 8.5 X 106 at 571 nm. The anisotropic shape increase the enhancement factor to ~ 2.4 X 107 at peak wavelength 700 nm i.e. tuning the plasmon wavelength towards NIR region. Conclusion: The tunability in plasmon wavelength and field enhancement factor has been evaluated for heterogeneous nanostructure over wider spectrum range i.e. DUV-Visible-NIR using Au-Al dimer and trimer nanostructure. The isotropic shape Au-Al hetero nanostructure shows larger enhancement in the UV-visible region, whereas the anisotropic shape nanostructure contributes towards the NIR region.

2020 ◽  
Vol 12 ◽  
Author(s):  
Jyoti Katyal ◽  
Shivani Gautam

Background: A relatively narrow LSPR peak and a strong inter band transition ranging around 800 nm makes Al strongly plasmonic active material. Usually, Al nanoparticles are preferred for UV-plasmonic as the SPR of small size Al nanoparticles locates in deep UV-UV region of the optical spectrum. This paper focused on tuning the LSPR of Al nanostructure towards infrared region by coating Au layer. The proposed structure has Au as outer layer which prevent the further oxidation of Al nanostructure. Methods: The Finite Difference Time Domain (FDTD) and Plasmon Hybridization Theory has been used to evaluated the LSPR and field enhancement of single and dimer Al-Al2O3-Au MDM nanostructure. Results: It is observed that the resonance mode show dependence on the thickness of Al2O3 layer and also on the composition of nanostructure. The Au layered MDM nanostructure shows two peak of equal intensities simultaneously in UV and visible region tuned to NIR region. The extinction spectra and electric field distribution profiles of dimer nanoparticles are compared with monomer to reveal the extent of coupling. The dimer configuration shows higher field enhancement ~107 at 1049 nm. By optimizing the thickness of dielectric layer the MDM nanostructure can be used over UV-visible-NIR region. Conclusion: The LSPR peak shows dependence on the thickness of dielectric layer and also on the composition of nanostructure. It has been observed that optimization of size and thickness of dielectric layer can provide two peaks of equal intensities in UV and Visible region which is advantageous for many applications. The electric field distribution profiles of dimer MDM nanostructure enhanced the field by ~107 in visible and NIR region shows its potential towards SERS substrate. The results of this study will provide valuable information for the optimization of LSPR of Al-Al2O3-Au MDM nanostructure to have high field enhancement.


2018 ◽  
Vol 7 (2) ◽  
pp. 83-90 ◽  
Author(s):  
J. Katyal

The localized surface plasmon resonance of homo-dimer nanostructures is studied using FDTD simulations. The calculated LSPR wavelength of Au, Ag and Al nanosphere forming a homo-dimer configuration is compared and the results reveal a larger LSPR shift in Ag and Al homo-dimer than in Au homo-dimer. Taking the sensitivity of LSPR shape to the size and interparticle spacing of nanoparticle along with a surrounding refractive index, parameters like refractive index sensitivity have been determined. The spherical homo-dimer over the whole range of particle size, studied here shows the index sensitivity order as Ag>Al>Au. Hence, the use of plasmonic material towards the refractive index sensing applications is useful in this order.  The average refractive index sensitivities of Ag, Al and Au are 287.09 nm/RIU, 210.21 nm/RIU and 192.47 nm/RIU in DUV-Visible-NIR region. Apart from LSPR shift, the highly confined near-field intensity enhancement of homo-dimer nanostructures for SERS has also been studied. The interacting homo-dimer nanoparticles reveals intensity enhancements in the junction. Comparing the field enhancement for Au, Ag and Al homo-dimer nanostructure 10^8-10^9  have been theoretically predicted in DUV-UV-visible region which can be used to strongly enhance the Raman scattering of molecules.


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
D. Channei ◽  
B. Inceesungvorn ◽  
N. Wetchakun ◽  
S. Phanichphant

Unloaded CeO2and nominal 0.50, 1.00, 1.50, 2.00, 5.00, and 10.00 mol% Fe-loaded CeO2nanoparticles were synthesized by flame spray pyrolysis (FSP). The samples were characterized to obtain structure-activity relation by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Brunauer, Emmett, and Teller (BET) nitrogen adsorption, X-ray photoelectron spectroscopy (XPS), and UV-visible diffuse reflectance spectrophotometry (UV-vis DRS). XRD results indicated that phase structures of Fe-loaded CeO2nanoparticles were the mixture of CeO2and Fe2O3phases at high iron loading concentrations. HRTEM images showed the significant change in morphology from cubic to almost-spherical shape observed at high iron loading concentration. Increased specific surface area with increasing iron content was also observed. The results from UV-visible reflectance spectra clearly showed the shift of absorption edge towards longer visible region upon loading CeO2with iron. Photocatalytic studies showed that Fe-loaded CeO2sample exhibited higher activity than unloaded CeO2, with optimal 2.00 mol% of iron loading concentration being the most active catalyst. Results from XPS analysis suggested that iron in the Fe3+state might be an active species responsible for enhanced photocatalytic activities observed in this study.


2008 ◽  
Vol 1142 ◽  
Author(s):  
Feng Jin ◽  
Yan Liu ◽  
Scott A Little ◽  
Chris M Day

ABSTRACTWe have created a thermionic cathode structure that consists of a thin tungsten ribbon; carbon nanotubes (CNTs) on the ribbon surface; and a thin layer of low work function barium strontium oxide coating on the CNTs. This oxide coated CNT cathode was designed to combine the benefits from the high field enhancement factor from CNTs and the low work function from the emissive oxide coating. The field emission and thermionic emission properties of the cathode have been characterized. A field enhancement factor of 266 and a work function of 1.9 eV were obtained. At 1221 K, a thermionic emission current density of 1.22A/cm2 in an electric field of 1.1 V/μm was obtained, which is four orders of magnitude greater than the emission current density from the uncoated CNT cathode at the same temperature. The high emission current density at such a modest temperature is among the best ever reported for an oxide cathode.


2005 ◽  
Vol 484 (1-2) ◽  
pp. 379-381 ◽  
Author(s):  
Guang Yuan ◽  
Hang Song ◽  
Yixin Jin ◽  
Hidenori Mimura ◽  
Kuniyoshi Yokoo

2010 ◽  
Vol 21 (35) ◽  
pp. 358001 ◽  
Author(s):  
A I Zhbanov ◽  
Yong-Gu Lee ◽  
E G Pogorelov ◽  
Yia-Chung Chang

2007 ◽  
Vol 124-126 ◽  
pp. 723-726 ◽  
Author(s):  
Makoto Kobayashi ◽  
Koji Tomita ◽  
Valery Petrykin ◽  
Shu Yin ◽  
Tsugio Sato ◽  
...  

Highly crystalline titania nano-particles were synthesized by hydrothermal method using novel stable water-soluble titanium complexes. It was confirmed that single phase anatase, rutile and brookite, which can be rarely synthesized as a single phase, can be obtained by varying the ligand in the complex and pH of the aqueous solution. TEM observations and BET specific surface area measurements had shown that these samples consisted of nanosized particles of 5~200 nm and had high specific surface areas of 25~150 m2/g. According to UV-visible diffuse reflectance spectra, these titania samples absorbed light in the visible region (λ > 400 nm). Photocatalytic activities in NO oxidation reaction exhibited by synthesized titania powders under the irradiation by UV- visible light were higher than the activity of the commercial TiO2 photocatalyst P25 (Degussa). Especially, under illumination by only visible light of above 510 nm wavelength, photocatalytic activity of the obtained specimens exceeded that of P25 more than four times. We also clearly demonstrated that single phase brookite had high photocatalytic activity for NO oxidation.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bao-xin Yan ◽  
Yan-ying Zhu ◽  
Yong Wei ◽  
Huan Pei

AbstractIn this paper, the surface enhanced Raman scattering (SERS) characteristics of Au and Au@Al2O3 nanoparticle dimers were calculated and analyzed by using finite element method (3D-FEM). Firstly, the electric field enhancement factors of Au nanoparticles at the dimer gap were optimized from three aspects: the incident angle of the incident light, the radius of nanoparticle and the distance of the dimer. Then, aluminum oxide is wrapped on the Au dimer. What is different from the previous simulation is that Al2O3 shell and Au core are regarded as a whole and the total radius of Au@Al2O3 dimer is controlled to remain unchanged. By comparing the distance of Au nucleus between Au and Au@Al2O3 dimer, it is found that the electric field enhancement factor of Au@Al2O3 dimer is much greater than that of Au dimer with the increase of Al2O3 thickness. The peak of electric field of Au@Al2O3 dimer moves towards the middle of the resonance peak of the two materials, and it is more concentrated than that of the Au dimer. The maximum electric field enhancement factor 583 is reached at the shell thickness of 1 nm. Our results provide a theoretical reference for the design of SERS substrate and the extension of the research scope.


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