Plasmonic metal nanostructures are essential for plasmon‐mediated chemical reactions (PMCRs) and surface‐enhanced Raman spectroscopy (SERS). The nanostructures are commonly made from the coinage metals gold and silver. Copper (Cu) is less used mainly due to the difficulties in fabricating stable nanostructures. However, Cu is an attractive option with its strong plasmonic properties, high catalytic activities, and relatively cheap price. Herein, we fabricated tunable, reliable, and efficient Cu nanoelectrodes (CuNEs). Using time‐resolved electrochemical SERS, we have comprehensively studied the reversible chemical transformations between aromatic amine and nitro groups modified on the CuNE surface. Their PMCRs are well‐controlled by changing the surface roughness, the oxidation states of Cu, and the applied electrode potential. We thus demonstrate that the Cu nanostructures enable better investigations in the interplays between PMCR, electrochemistry, and Cu catalysis.
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Abstract -
Ghimire, Govinda ; Guo, Jing ; Halmagian, Robert ; He, Jin ( , Angewandte Chemie International Edition)
Abstract Plasmonic metal nanostructures are essential for plasmon‐mediated chemical reactions (PMCRs) and surface‐enhanced Raman spectroscopy (SERS). The nanostructures are commonly made from the coinage metals gold and silver. Copper (Cu) is less used mainly due to the difficulties in fabricating stable nanostructures. However, Cu is an attractive option with its strong plasmonic properties, high catalytic activities, and relatively cheap price. Herein, we fabricated tunable, reliable, and efficient Cu nanoelectrodes (CuNEs). Using time‐resolved electrochemical SERS, we have comprehensively studied the reversible chemical transformations between aromatic amine and nitro groups modified on the CuNE surface. Their PMCRs are well‐controlled by changing the surface roughness, the oxidation states of Cu, and the applied electrode potential. We thus demonstrate that the Cu nanostructures enable better investigations in the interplays between PMCR, electrochemistry, and Cu catalysis.