“…Here, the smaller the particle becomes, i.e., the more strongly the exciton experiences spatial restriction, the larger the E ex value and the more clearly defined are the maxima of the exciton series in the absorption spectra of the semiconductor nanoparticles. Resolution of one or more exciton maxima in the absorption spectrum at room temperature is observed during the transition to the regime of quantum restriction in the crystals of such semiconductors as CdS [4, 21, 36, 40, 44, 76-78, 81-85, 89, 95, 103, 107, 114, 116, 123, 125, 138-141, 220, 221], PbS [59,164,166], ZnS [76,83,147,151], HgS [83], CdSe [4, 27, 44, 47, 141, 201, 202, 207, 210, 211, 218, 219, 223-232, 253, 293], CdSe x Te 1-x [231,[238][239][240], ZnSe [249], PbSe [64,122,123,241,242], CuInSe 2x Te 2(1-x) [252], CdTe [44,47,141,253,261,262,[265][266][267][268][269]294], ZnO [178,179,188,295], CuCl [4,278], PbI 2 [282], etc. The position of the exciton maxima in the absorption spectra of semiconductor nanocrystals can be calculated accurately using the second derivative of the spectral curve (Fig.…”