The implementation of plasmonic materials in heterogeneous catalysis was limited due to the lack of experimental access in managing the plasmonic hot carriers. Herein, we propose a liquid-state surface-enhanced Raman scattering (SERS) technique to manipulate and visualize heterogeneous photocatalysis with transparent plasmonic chips. The liquid-state measurement conquers the difficulties that arise from the plasmon-induced thermal effects, and thus the plasmon based strategies can be extended to investigate a wider range of catalytic reactions. We demonstrated the selection of reaction products by modulating the plasmonic hot carriers and explored the mechanisms in several typical C−C coupling reactions with 4bromothiophenol (4-BTP) as reactants. The real-time experimental results suggest brand new mechanisms of the formation of C−C bonds on plasmonic metal nanoparticles (NPs): the residue of 4-BTP, but not thiophenol (TP), is responsible for the C−C coupling. Furthermore, this technique was extended to study the evolution of the Suzuki−Miyaura reaction on nonplasmonic palladium metals by establishing the charge transfer channels between palladium and Au NPs. The cleavage and formation of chemical bonds in each individual reaction step were discerned, and the corresponding working mechanisms were clarified.

The plasmonic metal/semiconductor heterojunction provides a unique paradigm for manipulating light to improve the efficiency of plasmonic materials. Previous studies suggest that the improvement originates from the enhanced carrier exchanges between the plasmonic component of the heterojunction and molecules. This viewpoint, known as the chemical mechanism, is reasonable but insufficient, because the construction of the heterojunction will lead to a charge redistribution in the plasmonic component and cause changes in its physical characteristics. Herein, we will try to clarify that these changes are decisive factors in specific applications by investigating the surface-enhanced Raman scattering (SERS) behavior of a typical Ag/TiO 2 heterojunction. We observed significant changes in SERS spectra by modulating the band alignment of the heterojunction in a loop. Identical trends in SERS spectra were observed despite the fact that the charge transfer from the heterojunction to molecules was blocked, suggesting that the major SERS enhancement originates from electromagnetic mechanisms rather than chemical ones.

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Molecular orientation provides fundamental images to understand the molecular behaviors in chemistry. Herein, we propose and demonstrate sandwich plasmonic nanocavity as a surface-selection ruler to illustrate the molecular orientations by...