Abstract
The combined effect of metal incorporated semiconductor nanostructures (NSs) provides hybrid, proficient and more functional properties that are difficult to be provided by single component NSs in modern applications and industry. A facile seed growth method is adapted for the synthesis of gold coated by cuprous oxide (Au@Cu2O) core@shell NSs that are functionalized in their shell thickness and surface states. As synthesized Au@Cu2O core@shell cubic NSs contain single cubic Au as a core material with varying Cu2O shell thickness, confirmed by their microscopic analysis. Various spectroscopic analyses are is accomplished to confirm the chemical structure, crystallinity, oxidation state and binding energy of the concerned material over the core's surface. Optical absorption properties of core@shell NSs are greatly affected causing a shift in the surface plasmon resonance (SPR) peaks intensities with increase of the shell size. Photoluminescence (PL) spectra explain influence of Cu2O shell morphology over the emission characteristics that an increasing shell thickness caused an enhancement in PL emission peak along with red-shift of the peak. The elemental quantifying is done by XPS technique to provide a detailed surface reaction chemistry about oxidation states of copper. The charge-transfer at the metal-semiconductor interface results in highly intense and selective enhanced SERS signals via PL quenching, using Rhodamine-6G as the probe. The results provide useful information for preparation of various Au@Cu2O NSs for applications involving charge-transfer and SPR based interaction.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.