In this paper, we report some new findings obtained by in situ radiotracer and voltammetric studies of the simultaneous adsorption of HSO4-/SO42- ions labeled with 35S, and Cr-containing species labeled with 51Cr on a gold electrode in the course of dichromate reduction in 1 mol dm-3 ClO4- supporting electrolyte at various pH values (pH = 0 and pH = 2.0).Special attention is paid to show a modified version of the in situ radiotracer "foil" method, as well as to present a detection and calculation procedure elaborated for the quant. evaluation of the surface excess of radiolabeled Cr species via measurement of the intensity of low energy x-rays (E = 4.90 keV) emitted by 51Cr.From our exptl. results it can be stated that: (i) the electroreduction of Cr(VI) particles presumably proceeds via a ce (chem.-electron-transfer) mechanism to yield a gold surface covered with intermediate surface adlayer containing Cr(VI) species and added anions (HSO4-/SO42-, ClO4-); (ii) the extent and mechanism of adlayer formation are affected by the solution pH values; (iii) the maximum surface excess of Cr-containing species (ΓpH=0 = 1.2 × 10-9 mol cm-2; ΓpH=2.0 = 1.6 × 10-9 mol cm-2), as well as the molar ratio between the Cr species and HSO4-/SO42- ions (m pH=0 ≈ 6 at E = 0.8 V; m pH=2.0 ≈ 2 at E = 0.05 V) attest that the coverage of the gold surface with intermediate complexes does not exceed one monolayer.