“…This typically involves monitoring the current-time (I-t) transients associated with the stochastic collision of NPs from a (dilute) colloidal solution with a collector electrode, with the detected current arising from either: (i) a heterogeneous electron-transfer reaction taking place at the NP surface (e.g., electrocatalytic amplification [3][4][5][6] ); or (ii) the electro-dissolution of the NP itself. 7,8 In this contribution, we introduce a third approach to investigate the dynamic interaction between metal NPs and a collector electrode, in which the detected current arises from NP surface oxidation, as is shown schematically in Figure 1a for the case of an Au NP. This measurement is much more challenging than the (volumetric) anodic oxidation of metal NPs 7,8 , due to the smaller charges involved and much faster timescale of the process, but opens up new prospects for detecting noble metals and analyzing the formation of surface oxides, which can greatly influence (retard or accelerate) electrocatalysis.…”