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Electrochemical Surface-Enhanced Raman Spectroscopy of acetaminophen: Adsorption dynamics and charge transfer mechanism

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F25%3A00638249" target="_blank" >RIV/61388955:_____/25:00638249 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985882:_____/25:00638249 RIV/60461373:22340/25:43932037

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0927775725017042?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0927775725017042?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.colsurfa.2025.137801" target="_blank" >10.1016/j.colsurfa.2025.137801</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electrochemical Surface-Enhanced Raman Spectroscopy of acetaminophen: Adsorption dynamics and charge transfer mechanism

  • Original language description

    Electrochemical Surface-Enhanced Raman Spectroscopy (EC-SERS) enables detailed study of molecular adsorption and charge transfer at metal surfaces. This work investigates acetaminophen (AAP) adsorption on a roughened copper electrode using EC-SERS combined with cyclic voltammetry (CV). CV confirms AAP´s electrochemical stability within1000 to 0 mV, allowing analysis of adsorption without redox interference. AAP rapidly adsorbs within eight CV cycles (similar to 13 min), forming stable surface complexes primarily through amine group interactions. Desorption is slower, indicated by gradual changes in electrochemical current and Raman signal during reverse scans. The highest SERS enhancement occurs at600 mV, where optimal charge transfer and molecular orientation maximize signal intensity. Density functional theory calculations support experimental findings, confirming the formation of metal-molecule ´complexes´ consistent with observed vibrational modes. The study highlights the influence of applied potential on adsorption/desorption dynamics and demonstrates copper's promise as an affordable EC-SERS substrate. Despite lower enhancement compared to noble metals, copper's biocompatibility and surface versatility make it suitable for biomedical and environmental sensing applications. These insights contribute to the advancement of electrochemical sensors based on EC-SERS for pharmaceutical and bioanalytical uses.

  • 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

    10403 - Physical chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Colloids and Surfaces A-Physicochemical and Engineering Aspects

  • ISSN

    0927-7757

  • e-ISSN

    1873-4359

  • Volume of the periodical

    726

  • Issue of the periodical within the volume

    Part 2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    137801

  • UT code for WoS article

    001542118000005

  • EID of the result in the Scopus database

    2-s2.0-105011479992