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Structural Control over Bimetallic Core–Shell Nanorods for Surface-Enhanced Raman Spectroscopy

[Image: see text] Bimetallic nanorods are important colloidal nanoparticles for optical applications, sensing, and light-enhanced catalysis due to their versatile plasmonic properties. However, tuning the plasmonic resonances is challenging as it requires a simultaneous control over the particle sha...

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Detalles Bibliográficos
Autores principales: van der Hoeven, Jessi E. S., Deng, Tian-Song, Albrecht, Wiebke, Olthof, Liselotte A., van Huis, Marijn A., de Jongh, Petra E., van Blaaderen, Alfons
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970553/
https://www.ncbi.nlm.nih.gov/pubmed/33748617
http://dx.doi.org/10.1021/acsomega.0c06321
Descripción
Sumario:[Image: see text] Bimetallic nanorods are important colloidal nanoparticles for optical applications, sensing, and light-enhanced catalysis due to their versatile plasmonic properties. However, tuning the plasmonic resonances is challenging as it requires a simultaneous control over the particle shape, shell thickness, and morphology. Here, we show that we have full control over these parameters by performing metal overgrowth on gold nanorods within a mesoporous silica shell, resulting in Au–Ag, Au–Pd, and Au–Pt core–shell nanorods with precisely tunable plasmonic properties. The metal shell thickness was regulated via the precursor concentration and reaction time in the metal overgrowth. Control over the shell morphology was achieved via a thermal annealing, enabling a transition from rough nonepitaxial to smooth epitaxial Pd shells while retaining the anisotropic rod shape. The core–shell synthesis was successfully scaled up from micro- to milligrams, by controlling the kinetics of the metal overgrowth via the pH. By carefully tuning the structure, we optimized the plasmonic properties of the bimetallic core–shell nanorods for surface-enhanced Raman spectroscopy. The Raman signal was the most strongly enhanced by the Au core–Ag shell nanorods, which we explain using finite-difference time-domain calculations.