Actually, different concentrations of DPPH reagent were used by researchers in antioxidant activity assay. However, that is important is the change in concentration of DPPH before and after the addition of extract. Of course all the other experiment factors should be fixed during the assay.
I propose to you a review concerning all the parameters affecting the procedure of DPPH mehod.
Because it is the range where you can have good precision for the spectrophotometer including the decay of the absorbance expected during a DPPH assay (remember that the absorbance A = log (1/Transmitance) with transmittance in % light. When A is high there is actually very littile light reaching the detector so you should aways operate a spectrophotometer below 0.8 absorbance).