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- W2754657639 startingPage "1701633" @default.
- W2754657639 abstract "Designing controlled hybrid nanoarchitectures between plasmonic and catalytic materials is of paramount importance to fully exploit each function of constituent materials. This study reports a new synthetic strategy for the realization of colloidal clusters of core–shell nanoparticles with plasmonic cores and catalytically active shells. The Au@M (M = Pd or Pt) nanoparticle clusters (NPCs) with a high density of sub-1 nm interparticle gaps are successfully prepared by the deposition of M shells onto thermally activated Au NPCs. NPCs with other metal, metal sulfide, and metal oxide shells can also be synthesized by using the present approach. The prepared Au@M NPCs show remarkably enhanced plasmonic performance compared to their Au@M nanoparticle counterparts due to the localization of a strong electromagnetic field at the interparticle gaps, while the inherent catalytic function of shells is intact. In situ real-time Raman spectroscopy and plasmon-enhanced electrocatalysis experiments demonstrate that the controlled assembly of core–shell nanoparticles is a very effective route for the synergistic integration of plasmonic and catalytic functions in a single platform." @default.
- W2754657639 created "2017-09-25" @default.
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- W2754657639 date "2017-09-13" @default.
- W2754657639 modified "2023-09-25" @default.
- W2754657639 title "Core-Shell Nanoparticle Clusters Enable Synergistic Integration of Plasmonic and Catalytic Functions in a Single Platform" @default.
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- W2754657639 doi "https://doi.org/10.1002/smll.201701633" @default.
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