ترغب بنشر مسار تعليمي؟ اضغط هنا

Understanding blue shift of the longitudinal surface plasmon resonance during growth of gold nanorods

69   0   0.0 ( 0 )
 نشر من قبل Aditya Kumar Sahu
 تاريخ النشر 2021
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We have investigated in detail the growth dynamics of gold nanorods with various aspect ratios in different surrounding environments. Surprisingly, a blue shift in the temporal evolution of colloidal gold nanorods in aqueous medium has been observed during the growth of nanorods by UV visible absorption spectroscopy. The longitudinal surface plasmon resonance peak evolves as soon as the nanorods start to grow from spheres, and the system undergoes a blue shift in the absorption spectra. Although a red-shift is expected as a natural phenomenon during the growth process of all nanosystems, our blue shift observation is regarded as a consequence of competition between the parameters of growth solution and actual growth of nanorods. The growth of nanorods contributes to the red-shift which is hidden under the dominating contribution of the growth solution responsible for the observed massive blue shift.



قيم البحث

اقرأ أيضاً

The dependence of the surface plasmons resonance (SPR) frequency on the size of gold nanoparticles (GNPs) is experimentally studied. The measured data for the SPR frequency by UV-Vis spectroscopy and GNPs diameter by Dynamic Light Scattering (DLS), T ransmission Electron Microscopy (TEM) and Atomic Force Microscopy (AFM) are collected in the course of classical citrate GNPs synthesis. The relationship between the GNPs size and the blue shift of the light absorption is presented. They are fitted by an equation with a single free parameter, the dielectric permittivity of the surrounding media. Thus, the refractive index of the surrounding media is determined, which characterizes the GNPs surface shell.
We report the effects of variation in length on the electronic structure of CdSe nanorods derived from atomic clusters and passivated by fictitious hydrogen atoms. These nanorods are augmented by attaching gold clusters at both the ends to form a nan odumbbell. The goal is to assess the changes at nanolevel after formation of contacts with gold clusters serving as electrodes and compare the results with experimental observations [PRL, 95, 056805 (2005)]. Calculations involving nanorods of length 4.6 Angstrom to 116.6 Angstrom are performed using density functional theory implemented within plane-wave basis set. The binding energy per atom saturates for nanorod of length 116.6 Angstrom. It is interesting to note that upon attaching gold clusters, the nanorods shorter than 27 Angstrom develop metallicity by means of metal induced gap states (MIGS). Longer nanorods exhibit a nanoscale Schottky barrier emerging at the center. For these nanorods, interfacial region closest to the gold electrodes shows a finite density of states in the gap due to MIGS, which gradually decreases towards the center of the nanorod opening up a finite gap. Bader charge analysis indicates localized charge transfer from metal to semiconductor.
We present theoretical calculations for the absorption properties of protein-coated gold nanoparticles on graphene and graphite substrates. As the substrate is far away from nanoparticles, numerical results show that the number of protein bovine seru m molecules molecules aggregating on gold surfaces can be quantitatively determined for gold nanoparticles with arbitrary size by means of the Mie theory and the absorption spectra. The presence of graphitic substrate near protein-conjugated gold nanoparticles substantially enhances the red shift of the surface plasmon resonances of the nanoparticles. Our findings show that graphene and graphite provide the same absorption band when the distance between the nanoparticles and the substrate is large. However at shorter distances, the resonant wavelength peak of graphene-particle system differs from that of graphite-particle system. Furthermore, the influence of the chemical potential of graphene on the optical spectra is also investigated.
The programmable assembly of DNA strands is a promising tool for building tailored bottom-up nanostructures. Here, we present a plasmonic nanosystem obtained by the base-pairing mediated aggregation of gold nanoparticles (NPs) which are separately fu nctionalized with two different single-stranded DNA chains. Their controlled assembly is mediated by a complementary DNA bridge sequence. We monitor the formation of DNA assembled NP aggregates in solution, and we study their Surface Enhanced Raman Scattering (SERS) response by comparison with the single NP constituents. We interpret the revealed SERS signatures in terms of the molecular and NP organization at the nanoscale, demonstrating that the action of the DNA bridge molecule yields regular NP aggregates with controlled interparticle distance and reproducible SERS response. This demonstrates the potential of the present system as a stable, biocompatible, and recyclable SERS sensor.
In this letter, we study how coupling between AuNPs and ZnO thin films affects their emission properties. The emission intensity of ZnO thin films changes when Al2O3 spacer layer of different thickness are included in ZnO/Au films, consistent with th eoretical predictions. The emission properties are also controlled using the polarization of the excitation source. Emission properties depended on the polarization of the excitation source because of the surface plasmon resonance of AuNPs. The photoluminescence anisotropy of these systems shows that enhanced photoluminescence can be achieved through coupling of the emission from ZnO with the surface plasmon resonance of AuNPs.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا