Abstract

The electrochemical quartz-crystal nanobalance has been used in electrochemistry research for over three decades. It provides an atomic/molecular level insight into the nature of interfacial electrochemical phenomena by measuring in situ mass changes on the nanogram scale. The sensitivity of this technique remains unknown because there have been no attempts to determine its limits of detection (LOD) or quantification (LOQ). We propose an experimental approach for determining the values of LOD and LOQ for Pt electrodes in aqueous H2SO4 solutions that employs cyclic voltammetry and frequency variation measurements. However, this methodology is also appropriate to other electrode materials and electrolytes. The LOD and LOQ values depend on the electrolyte concentration and decrease (i.e., the sensitivity increases) as the concentration decreases. Knowledge of the LOD and LOQ values determines the applicability of this technique in research on the oxidation and degradation of Pt catalysts employed in fuel cells.

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