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Operando monitoring of a room temperature nanocomposite methanol sensor

The sensing of volatile organic compounds by composites containing metal oxide semiconductors is typically explained via adsorption–desorption and surface electrochemical reactions changing the sensor's resistance. The analysis of molecular processes on chemiresistive gas sensors is often based...

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Detalles Bibliográficos
Autores principales: Maqbool, Qaisar, Yigit, Nevzat, Stöger-Pollach, Michael, Ruello, Maria Letizia, Tittarelli, Francesca, Rupprechter, Günther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900598/
https://www.ncbi.nlm.nih.gov/pubmed/36760342
http://dx.doi.org/10.1039/d2cy01395a
Descripción
Sumario:The sensing of volatile organic compounds by composites containing metal oxide semiconductors is typically explained via adsorption–desorption and surface electrochemical reactions changing the sensor's resistance. The analysis of molecular processes on chemiresistive gas sensors is often based on indirect evidence, whereas in situ or operando studies monitoring the gas/surface interactions enable a direct insight. Here we report a cross-disciplinary approach employing spectroscopy of working sensors to investigate room temperature methanol detection, contrasting well-characterized nanocomposite (TiO(2)@rGO-NC) and reduced-graphene oxide (rGO) sensors. Methanol interactions with the sensors were examined by (quasi) operando-DRIFTS and in situ-ATR-FTIR spectroscopy, the first paralleled by simultaneous measurements of resistance. The sensing mechanism was also studied by mass spectroscopy (MS), revealing the surface electrochemical reactions. The operando and in situ spectroscopy techniques demonstrated that the sensing mechanism on the nanocomposite relies on the combined effect of methanol reversible physisorption and irreversible chemisorption, sensor modification over time, and electron/O(2) depletion–restoration due to a surface electrochemical reaction forming CO(2) and H(2)O.