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Shen et al. [25] suggest that the mass extinction event lasted for ~ 200,000 years with the peak of extinction occurring just before 252.28 ± 0.08 million years ago.
Thus, there seems to be a correlation between the number of originations and the number of extinctions, however, not within one interval but rather with a slight delay in the peak of extinction following the origination.
The pronounced peak of extinction corresponds to the resonant extinction due to the excitation of localized surface plasmon polaritons in the individual bowtie antennas.
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These peak shifts and intensity of extinction spectra for various P3HT/PMMA medium arrays are well described by the finite-difference time-domain (FDTD) simulation results.
Secondly, the broad extinction peak of the Pt NPs is unfavored for the LSP coupling [24].
The extinction peak of Au1Ag4@SiO2 NPs is close to the absorption peak of the FITC solution (454 474 nm) (Fig. 3f).
Actually, from Fig. 4 one can see that the main extinction peak of Ag NPs on SiO2 substrate is located at 530 nm, which is far from the band-gap of ZnMgO (3.47 eV, 357 nm), and a minor peak at 360 nm as quadrupole extinction is a second-order effect [12].
The DPP-DT polymer with a large molecular weight and high persistence length exhibited remarkably high optical absorption with a peak mass extinction coefficient of 81.7 L g−1 cm−1, which is one of the highest value among various photothermal agents reported to date.
It is to be noted that the wavelength of the peak extinction shifts with the variation in the volume fraction of inclusions.
Stability was calculated for each time point by expressing the peak extinction at that time point as a percent of the peak extinction of that sample at t = 0 min. DLS measurements were used to investigate changes in particle size in response to increased temperatures as well as NIR irradiation.
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