Journal
ACS APPLIED NANO MATERIALS
Volume 3, Issue 9, Pages 8958-8971Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsanm.0c01702
Keywords
core-shell nanoparticles; doped tin oxide shells; gold-silver nanoshells; localized surface plasmon resonance; antimony-doped; zinc-doped
Funding
- Air Force Office of Scientific Research [AFOSR FA9550-18-1-0094]
- Robert A. Welch Foundation [E-1320, E-0024]
- Texas Center for Superconductivity
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This paper reports the synthesis and study of doped metal oxides as the shell in core-shell nanoparticle architectures. Specifically, the paper describes the synthesis of gold nanoparticles (Au NPs) and gold-silver nanoshells (GS-NSs) coated with antimony- and zinc-doped tin oxide (SnO2) shells (i.e., Au@ATO, Au@ZTO, GS-NS@ATO, and GS-NS@ZTO) with a comparison to the undoped SnO2-coated analogues Au@SnO2 and GS-NS@SnO2. The doped tin oxide core-shell nanoparticles prepared here were thoroughly characterized using scanning electron microscopy, transmission electron microscopy, dynamic light scattering, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. Separately, their optical properties were evaluated by UV-vis and photoluminescence spectroscopy. The results demonstrate that noble-metal nanoparticles such as Au NPs and GS-NSs, which exhibit strong surface plasmon resonances at visible-to-near-IR wavelengths, can be activated across a broader region of the solar spectrum when used in conjunction with wideband-gap semiconductors. In particular, utilization of a GS-NS core induces near-complete suppression in the electron-hole recombination processes in the tin oxide materials. Potential impacts on sensing and photonic applications are highlighted.
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