Unveiling the Unprecedented Optical Properties of Citrate‐Stabilized Hollow AgAu Nanoshells Under Photothermal Irradiation

Metallic nanoshells heat efficiently on excitation of the localized surface plasmon resonance (LSPR). Whilst investigating the photothermal properties of citrate-stabilized hollow gold nanoshells (HGNs) synthesized using a sacrificial silver nanoparticle (AgNPs), the LSPR undergoes a distinct blueshift (70 ± 20 nm (0.20 ± 0.06 eV)) when photothermally irradiated. Notably, when functionalized with a Raman reporter, the surface-enhanced Raman scattering (SERS) signal unexpectedly and dramatically increases 8 ± 2-fold upon plasmonic heating, despite the LSPR shifting away from the excitation wavelength. This unprecedented enhancement of the SERS signal is absent in samples lacking citrate or prepared using a cobalt nanoparticle template, underscoring the importance of citrate, heat, and AgNPs in eliciting these effects. It is hypothesized that aqueous silver ions near the surface of the HGNs react with the citrate and form a complex that is both light and temperature sensitive. The formation of silver deposits, observed by electron microscopy, alters the core-to-shell thickness ratio, resulting in a blueshift in the LSPR, and change the scattering to absorption properties, enabling an improved SERS performance. This new optical phenomenon has now been understood and will be of significant interest to future studies in harnessing the properties of HGNs.