| Literature DB >> 30347729 |
Tao Guo1, Tianhao Zhou2,3, Qiulin Tan4,5, Qianqian Guo6,7, Fengxiang Lu8,9, Jijun Xiong10,11.
Abstract
A carbon nanotube/Fe₃O₄ thin film-based wireless passive gas sensor with better performance is proposed. The sensitive test mechanism of LC (Inductance and capacitance resonant) wireless sensors is analyzed and the reason for choosing Fe₃O₄ as a gas sensing material is explained. The design and fabrication process of the sensor and the testing method are introduced. Experimental results reveal that the proposed carbon nanotube (CNT)/Fe₃O₄ based sensor performs well on sensing ammonia (NH₃) at room temperature. The sensor exhibits not only an excellent response, good selectivity, and fast response and recovery times at room temperature, but is also characterized by good repeatability and low cost. The results for the wireless gas sensor's performance for different NH₃ gas concentrations are presented. The developed device is promising for the establishment of wireless gas sensors in harsh environments.Entities:
Keywords: NH3; carbon nanotube/Fe3O4 thin film; gas sensor; wireless passive
Year: 2018 PMID: 30347729 PMCID: PMC6210953 DOI: 10.3390/s18103542
Source DB: PubMed Journal: Sensors (Basel) ISSN: 1424-8220 Impact factor: 3.576
Figure 1Sensor coupling model.
Figure 2(a) Sensor model. (b) Sensor circuit model. (c) Ammonia molecule model. (d) Diagram of adsorbed gas molecules. (e) Trend of resonant frequency.
Figure 3Model of the intermolecular binding force.
Figure 4(a) Design of the LC (Inductance and capacitance resonant) wireless sensor. (b) Simulation results for the designed sensor. (c) Schematic of the fabrication procedure of the gas sensor.
Figure 5Schematic of the wireless gas sensing measurement setup.
Figure 6(a) Diagram of the change in the resonant frequency of the gas sensor at 40 ppm atmospheric ammonia at room temperature. (b) Amplified view into the trend of change plot in panel (a).
Figure 7(a) Variation in the resonant frequency of the sensor for different concentrations of atmospheric ammonia. (b) Linearity curve of the sensor.
Figure 8(a) Repeatability of the gas sensor exposed to 20, 40, and 60 ppm of atmospheric ammonia, at room temperature. (b) Long-term stability of the gas sensor exposed to 20, 40, and 60 ppm of acetone gas.
Figure 9(a) Responses of different gas sensitive films to ammonia. (b) Response of the proposed sensor to different gases.
Comparison of response of the developed sensor in this work with those of other materials-based gas sensors to ammonia at room temperature.
| Materials | NH3 Concentration | Response Time | Recovery Time | Reference |
|---|---|---|---|---|
| Fe3O4/CNTs | 20 ppm | 290 s | 100 s | This work |
| PANI/HCSA | 100 ppm | 20 s | 80 s | [ |
| RGO-A (aniline reducing) | 20 ppm | 1200 s | 300 s | [ |
| single ZnO-T−CNT | 100 ppm | 20 s | 420 s | [ |
| MWCNT/PEDOT:PSS | 30 ppm | 1200 s | 300 s | [ |
| Natural Carbonized Sugar | 100 ppm | 50 s | 42 s | [ |