An Ir(IV)Ox center dot nH(2)O nanostructured electrode prepared by electroflocculation is reported; the electrode efficiently catalyzes the electrochemical reduction of hydrogen peroxide (H2O2). Linear sweep voltammograms reveal that the potential onset arising due to the reduction of H2O2 (1 mM) occurs at -0.1 V (vs. Ag/AgCl), which is more anodic than the onset potential occurring on the glassy carbon electrode by 400 mV, thereby substantiating the catalytic utility of Ir(IV)Ox center dot nH(2)O. The number of electrons transferred in the process, estimated via the Koutecky-Levich equation, is 1.89 +/- 0.30. The Tafel slope obtained from polarization measurements is ca. 240.9 mV/dec. Furthermore, the Ir(IV)Ox center dot nH(2)O nanostructured electrode exhibits response with linear relationship against H2O2 concentrations ranging over 0-1 mM (when agitated) and 0-150 mu M (in flow injection analysis); the limit of detection (3 sigma), as determined under flow injection analysis, is 5 mu M. The as-fabricated electrode is insensitive to the oxidation of ascorbic acid (0.1 mM) and acetaminophen (0.1 mM) and exhibits stable amperometric response (over twenty successive trials), albeit a slight drift in the sensor response is observed during the initial six evaluations. Based on the results, the electrocatalytic mechanism involving the following steps is proposed: (1) the reduction of Ir from Ir-IV to Ir-III, (2) catalytic cleavage of the O-O bond to generate OH center dot radicals, and (3) the reduction of the OH center dot radicals to OH- via the reoxidation of Ir-III to Ir-IV. (C) 2015 Elsevier Ltd. All rights reserved.