Temperature-dependent kinetic studies of the chlorine evolution reaction over RuO2(110) model electrodes

Abstract

\u3cp\u3eUltrathin single-crystalline RuO \u3csub\u3e2\u3c/sub\u3e(110) films supported on Ru(0001) are employed as model electrodes to extract kinetic information about the industrially important chlorine evolution reaction (CER) in a 5M concentrated NaCl solution under well-defined electrochemical conditions and variable temperatures. A combination of chronoamperometry (CA) and online electrochemical mass spectrometry (OLEMS) experiments provides insight into the selectivity issue: At pH = 0.9, the CER dominates over oxygen evolution, whereas at pH = 3.5, oxygen evolution and other parasitic side reactions contribute mostly to the total current density. From temperature-dependent CA data for pH = 0.9, we determine the apparent free activation energy of the CER over RuO \u3csub\u3e2\u3c/sub\u3e(110) to be 0.91 eV, which compares reasonably well with the theoretical value of 0.79 eV derived from first-principles microkinetics. The experimentally determined apparent free activation energy of 0.91 eV is considered as a benchmark for assessing future improved theoretical modeling from first principles. \u3c/p\u3