Towards Surface-Enhanced Raman Scattering using electroless substrate for trace arsenic detection and speciation
- Others:
- Institut Lumière Matière [Villeurbanne] (ILM) ; Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)
- Institut de Physique de Nice (INPHYNI) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
- Laboratoire Hubert Curien [Saint Etienne] (LHC) ; Institut d'Optique Graduate School (IOGS)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS)
- Institut des Matériaux, de Microélectronique et des Nanosciences de Provence (IM2NP) ; Aix Marseille Université (AMU)-Université de Toulon (UTLN)-Centre National de la Recherche Scientifique (CNRS)
Description
Arsenic is one of the most toxic elements present in the environment, especially in water. The World Health Organization (WHO) recommends a maximum concentration of arsenic in drinkable water of 10 µg/L (10 ppb). Sensors implementing Surface Enhanced Raman Scattering (SERS) can detect chemical species at low concentrations. The aim of this study is to compare two kinds of silver-coated SERS substrates for detection and speciation of trace, trivalent and pentavalent, inorganic arsenic compounds. One type of substrates were prepared by a classical thermal evaporation technique, the second type by an electroless process. The electroless substrates allow to differentiate As(3) and As(5) with a limit of detection (LOD) 1 µg/L (1 ppb) equal for each valency, below WHO recommendation. Though the SERS intensity shows a non linear behaviour over a large analyte concentration range of five orders of magnitude, these preliminary results are discussed the framework of the demonstration of a trace As SERS sensor in drinkable water.
Additional details
- URL
- https://hal.archives-ouvertes.fr/hal-03577648
- URN
- urn:oai:HAL:hal-03577648v1
- Origin repository
- UNICA