Chemical interface damping (CID) is the most recently suggested plasmon damping pathway induced by adsorbate molecules in gold nanoparticles. Despite recent advances in this field, CID has not been studied in gold nanorods coated with mesoporous silica shells (AuNRs@mSiO2). Herein, we conducted a single‐particle correlation study to elucidate CID using p‐nitrothiophenol (p‐NTP) as adsorbates in single AuNRs@mSiO2. Through surface‐enhanced Raman spectroscopy studies, we confirmed that p‐NTP with a strong electron‐withdrawing group was effectively adsorbed on the AuNR cores. Following the chemisorption of p‐NTP, a strong CID was observed with localized surface plasmon resonance (LSPR) linewidth broadening through the preferred interaction between sulfur and the Au surfaces. Furthermore, we presented the molecular binding effect on the LSPR linewidth of single AuNRs@mSiO2 during the reaction with p‐NTP in real‐time. Thus, the result further supported that the CID could be used to develop LSPR sensors having low sensitivity to the medium dielectric constant.
Herein, we investigated the photoreduction of silver (Ag) ions on gold nanorods coated with mesoporous silica shell (AuNRs@mSiO2) induced by hot electrons generated in Au via localized surface plasmon resonance (LSPR) excitation. In addition, we investigated chemical interface damping (CID) using pyridine as the adsorbate in single Ag‐coated AuNRs@mSiO2. The Ag deposition caused a blue shift and linewidth broadening of the LSPR peak of the AuNRs@mSiO2. The subsequent chemisorption of pyridine on Ag‐coated AuNRs@mSiO2 resulted in a red shift and additional LSPR linewidth broadening. Finally, we demonstrated real‐time time‐dependent changes in LSPR peak wavelength and linewidth during the sequential processes of hot electron‐mediated Ag deposition and pyridine adsorption on a single AuNR@mSiO2 in a flow cell. Therefore, we provided a deep understanding of hot electron‐triggered Ag coating and CID induced by pyridine adsorption in single AuNRs@mSiO2 coated with Ag.
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