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We have evidenced for polycarbonate:M2 film at excitation with wavelengths of 335, 350, 385 and 400 nm a strong emission band situated between 400 and 500 nm with two maxima centred at 420 and 450 nm which became at excitation with a wavelength longer than 400 nm a single maximum emission band centred at 500 nm.
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Fluorescence spectroscopy showed that the fluorescence of HSA can be quenched remarkably by 3d under physiological condition with a slight shift of maximum fluorescence emission bands from 360 nm to 363 nm.
The relative fluorescence intensities of the samples were approximately evaluated via comparing the values obtained by dividing the fluorescence intensity at the maximum of BSA emission band by the optical density at the maximum of BSA absorption band at λ = 280 nm.
The maximum of the emission band located around 930 nm is because of the presence of dominant small PbS nanoparticles (3-5 nm) [28].
The maximum of the second emission band is at about 13 meV.
As assessed by changes of the integrated fluorescence intensity and the full width at half maximum of the 0 0 emission band with temperature, chain mobility decreases with increasing crosslinking density.
In the case of single fluorophoric system, such as koenigine (A), koenidine (B), girinimbine (C), and mahanimbine (D) along with quercetin and the NP sets synthesized by them, the respective emission band maxima were found to be comparatively sharper [Figs. S7 and S8 of the Electronic Supplementary Material (page S14)].
The maximum absorption and emission bands showed gradual red-shift with the increase in electron donating strength of the 3,6-substituent.
The PL from these regions was measured using a microscopic portable device, and it is found that PL spectra consist of only one emission band with maxima at ~720 nm (or 1.72 eV).
Eosin exhibits an emission band with a maximum at 564 nm.
The strong green emission band with a maximum at 544 nm corresponds to the 5D4 → 7F5 transition.
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