Operando monitoring of a room temperature nanocomposite methanol sensor

被引:14
|
作者
Maqbool, Qaisar [1 ]
Yigit, Nevzat [2 ]
Stoeger-Pollach, Michael [3 ]
Ruello, Maria Letizia [1 ]
Tittarelli, Francesca [1 ]
Rupprechter, Guenther [2 ]
机构
[1] Univ Politecn Marche, Dept Mat Environm Sci & Urban Planning SIMAU, INSTM Res Unit, Via Brecce Bianche 12, I-60131 Ancona, Italy
[2] TU Wien, Inst Mat Chem, Getreidemarkt 9 BC, A-1060 Vienna, Austria
[3] TU Wien, Univ Serv Ctr Transmiss Electron Microscopy, Wiedner Hauptstr 8-10, A-1040 Vienna, Austria
基金
奥地利科学基金会;
关键词
ANATASE TIO2; NANOPARTICLES; GAS; ADSORPTION; FILM; ZNO; SPECTROSCOPY; GENERATION; REACTIVITY; CATALYSTS;
D O I
10.1039/d2cy01395a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 (TiO2@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 CO2 and H2O.
引用
收藏
页码:624 / 636
页数:14
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