Room Temperature UV-Activated NO2 and NO Detection by ZnO/rGO Composites

被引:6
|
作者
Platonov, Vadim [1 ]
Malinin, Nikolai [2 ]
Vasiliev, Roman [1 ,2 ]
Rumyantseva, Marina [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Chem Dept, Moscow 119991, Russia
[2] Moscow MV Lomonosov State Univ, Fac Mat Sci, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
rGO; ZnO; heterostructure nanocomposites; nitrogen dioxide; nitrogen monoxide; photoactivated gas sensor; electrospinning; GAS-SENSING PROPERTIES; GRAPHENE OXIDE; WORK FUNCTION; LIGHT IRRADIATION; SENSOR; PERFORMANCE; FUNCTIONALIZATION; HETEROJUNCTIONS; REDUCTION; NANOWIRES;
D O I
10.3390/chemosensors11040227
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Nanocomposites, including nanoparticles of semiconductor metal oxide (MO) and reduced graphene oxide (rGO), are of exceptional interest for light-activated gas sensors functioning without thermal heating. In this paper, we discuss the sensor properties of electrospun ZnO nanofibers and ZnO/rGO composites. The materials were characterized by transmission and scanning electron microscopy (TEM, SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and IR spectroscopy (FTIR). The sensor characteristics were studied when detecting reducing gases CO, H-2, and NH3 and oxidizing gases NO and NO2 at 25-150 degrees C in dark conditions and under UV illumination. ZnO nanofibers and ZnO/rGO composites have no sensitivity when detecting CO, NH3, and H-2 either in dark conditions or under UV illumination. At T = 25 degrees C, UV illumination is a necessary condition for the appearance of a sensor response when detecting both NO and NO2. The increased sensitivity of ZnO/rGO composites when detecting nitrogen oxides at T = 25 degrees C is discussed in terms of the heterojunction formation. Observed at T = 150 degrees C, opposite trends in the UV illumination influence on the sensor response toward NO and NO2 are due to the participation of chemisorbed oxygen in the processes responsible for the sensor response formation when detecting NO.
引用
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页数:17
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