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New Insights into SERS Mechanism of Semiconductor-Metal Heterostructure: A Case Study on Vanadium Pentoxide Nanoparticles Decorated with Gold

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F24%3A10490065" target="_blank" >RIV/00216208:11320/24:10490065 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=1Ap0e9rh0n" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=1Ap0e9rh0n</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.jpcc.4c03080" target="_blank" >10.1021/acs.jpcc.4c03080</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    New Insights into SERS Mechanism of Semiconductor-Metal Heterostructure: A Case Study on Vanadium Pentoxide Nanoparticles Decorated with Gold

  • Original language description

    Recently, vanadium oxides and other semiconductor materials have been intensively studied to use them as nonplasmonic substrates for surface-enhanced Raman scattering (SERS) spectroscopy due to their advantages such as greater uniformity, stability, and spectral reproducibility compared to plasmonic ones. The combination of vanadium pentoxide nanoparticles (V(2)O(5) NPs) with nanostructures of noble metals has shown considerable promise for enhancing the SERS signal, while maintaining the aforementioned advantages. We prepared V(2)O(5)/Au NP films by a novel, simple, fully solvent- and linker-free method: the gas-phase synthesis of vanadium NPs followed by their thermal annealing at 550 degrees C to obtain V(2)O(5) NP films, which were subsequently decorated with Au nanoislands. Using methylene blue (MB) solution as a test analyte, we observed a significant enhancement of the SERS signal (up to 65 times) from the V(2)O(5)/Au composite compared to those from pure V(2)O(5) substrates. The SERS enhancement in this case arises from the synergy of electromagnetic and chemical (charge-transfer) enhancement. The deposition of Au on the V(2)O(5) surface increases the charge-transfer contribution. Moreover, the additional enhancement is achieved due to electromagnetic field coupling between V(2)O(5) and Au or between neighboring Au nanostructures. The observation of two maxima of MB SERS signal from the V(2)O(5)/Au heterostructure for various Au deposition times brings new insights into the SERS mechanism of the semiconductor-metal heterostructure. Spectral mapping across the V(2)O(5)/Au substrates shows excellent homogeneity and spectral reproducibility (RSD of the SERS signal less than 10%). This study introduces an important step in designing novel semiconductor-metal SERS-active substrates. Our V(2)O(5)/Au heterostructures represent highly attractive substrates with improved stability and spectral reproducibility as compared to other nonplasmonic and plasmonic ones.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10301 - Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect)

Result continuities

  • Project

    <a href="/en/project/GA22-16667S" target="_blank" >GA22-16667S: Synthesis of metal oxide-based nanomaterials for surface-enhanced Raman spectroscopy by plasma-based gas aggregation sources</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Physical Chemistry C

  • ISSN

    1932-7447

  • e-ISSN

    1932-7455

  • Volume of the periodical

    128

  • Issue of the periodical within the volume

    28

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    11732-11740

  • UT code for WoS article

    001265547500001

  • EID of the result in the Scopus database