Localised visualisation of O2 consumption and H2O2 formation by means of SECM for the characterisation of fuel cell catalyst activity

Catalytic reduction of O₂ at metal catalysts either follows a 2-electron transfer pathway to the formation of H₂O₂ or a 4-electron transfer pathway to the formation of H₂O. The branching ratio of this reaction has a significant impact on the applicability of catalyst materials. The previously introduced oxygen competition mode of SECM, which allows high-resolution imaging of local O₂ consumption, has been extended to a potential-pulse sequence enabling the sequential detection of O₂ reduction followed by the detection of local H₂O₂ formation. Thus, not only the local catalytic activity of a catalyst can be visualised but, additionally, the degree of the branching can be estimated. The selectivity of a catalyst candidate can thereby be visualised sequentially to the elucidation of its activity. First results on the properties of electrodeposited Pt and Au test structures are shown demonstrating the feasibility to clearly distinguish catalyst activity and selectivity under variation of the polarisation potential.