| Autor: |
Pfisterer JHK; Molecular Spectroscopy Department, Electrochemical Surface Science Group, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Baghernejad M; Molecular Spectroscopy Department, Electrochemical Surface Science Group, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Giuzio G; Molecular Spectroscopy Department, Electrochemical Surface Science Group, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Domke KF; Molecular Spectroscopy Department, Electrochemical Surface Science Group, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany. domke@mpip-mainz.mpg.de. |
| Abstrakt: |
Electrocatalysts often show increased conversion at nanoscale chemical or topographic surface inhomogeneities, resulting in spatially heterogeneous reactivity. Identifying reacting species locally with nanometer precision during chemical conversion is one of the biggest quests in electrochemical surface science to advance (electro)catalysis and related fields. Here, we demonstrate that electrochemical tip-enhanced Raman spectroscopy can be used for combined topography and reactivity imaging of electro-active surface sites under reaction conditions. We map the electrochemical oxidation of Au nanodefects, a showcase energy conversion and corrosion reaction, with a chemical spatial sensitivity of about 10 nm. The results indicate the reversible, concurrent formation of spatially separated Au 2 O 3 and Au 2 O species at defect-terrace and protrusion sites on the defect, respectively. Active-site chemical nano-imaging under realistic working conditions is expected to be pivotal in a broad range of disciplines where quasi-atomistic reactivity understanding could enable strategic engineering of active sites to rationally tune (electro)chemical device properties. |
