• No results found

Nonlinear Optical Properties, Optical Limiting and Optical Switching of Ag Nanoparticles Prepared by a Green Synthetic Method

N/A
N/A
Protected

Academic year: 2020

Share "Nonlinear Optical Properties, Optical Limiting and Optical Switching of Ag Nanoparticles Prepared by a Green Synthetic Method"

Copied!
12
0
0

Loading.... (view fulltext now)

Full text

Loading

Figure

Figure 1. Absorption spectra of synthesized Ag NPs in water with different heating techniques
Figure 3. Variation of the SPR absorption peak with respect to the time for Ag nanoparticles prepared by boiling method
Figure 4. Open aperture Z-scan signal of Ag nanoparticles of diameter 15 nm at 488 nm and a line is a fit of equation 1 to experimental data
Table 1. Nonlinear absorption, nonlinear refractive index and nonlinear susceptibility values of Ag nanoparticles measured for different wavelengths
+4

References

Related documents

Left ventricular dimensions and LV function (FS and EF) changed significantly as the speed decreased from baseline to 6000 rpm with no further significant changes at either 5000

1 International Research Journal of Commerce and Law http://ijmr.net.in, Email: irjmss@gmail.com Illegal Constructions in Delhi: A Socio-Legal perspective.. Ram

Materials and Methods: In this cross sectional study, glucose level was measured using the glucose oxidase/peroxidase method in blood and unstimulated saliva in 50

The present study was therefore undertaken to compare the bioavailability of rifabutin and d-RBT after two different dosing regimens of rifabutin (150 mg tiw and 150 mg daily)

When the bacterial capacities to induce the production of the proinflammatory cytokines IL-12 and TNF- ␣ , the anti- inflammatory cytokine IL-10, and surface maturation markers in

Thus, the aim of this study is to analyze the mandibu- lar condyle volume, area and morphological index in young adult subjects without TMD dysfunction, evalu- ated with CBCT, in

The accuracy of the proposed methods was checked by recovery study, by addition of standard drug solution to preanalysed sample solution at three different concentration levels (50