I used to correct the excitation spectra by dividing the raw spectra (usually called S1, or S2, or S1c, or S2c) to the spectra of lamp profile (usually shown by R). This way the excitation spectra is normalized to lamp intensity at each wavelength! By doing this, I am supposing that the software is not correcting the excitation spectra automatically! Is this analysis correct?
Two resulting spectra, S1 or S1/R only show diferences on the band's intensity ratio, and of course the band position and overall spectral shape is the same!