Thin film micro carbon dioxide sensor using MEMS process

Pt/Na + ion conductive ceramic thin film/Pt/carbonate (Na 2CO 3:BaCO 3=1:1.7 mol) system CO 2 micro gas sensor was fabricated and the sensing properties were investigated. The Na + ion conductive thin film was prepared by RF magnetron sputtering method. The thin film micro carbon dioxide sensor was...

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Published inSensors and actuators. B, Chemical Vol. 102; no. 1; pp. 20 - 26
Main Authors Bang, Yeung-Il, Song, Kap-Duk, Joo, Byung-Su, Huh, Jeung-Soo, Choi, Soon-Don, Lee, Duk-Dong
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.09.2004
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Summary:Pt/Na + ion conductive ceramic thin film/Pt/carbonate (Na 2CO 3:BaCO 3=1:1.7 mol) system CO 2 micro gas sensor was fabricated and the sensing properties were investigated. The Na + ion conductive thin film was prepared by RF magnetron sputtering method. The thin film micro carbon dioxide sensor was prepared by using silicon process combined with MEMS technology. A NASICON thin film (2000–2500 Å) as main layer of the device was formed on N/O/N film using magnetron sputtering system. In order to simplify the device process, both the heater and lower electrode were formed on the same plane. And carbonate thin film as a sensing layer was formed on the upper electrode by sputtering sodium–barium carbonate target (Na 2CO 3:BaCO 3=1:1.7 molar ratio). The area of the sensing layer was 0.55 mm×0.4 mm and that of total device was 3.2 mm×4.5 mm. The study of NASICON thin film conductivity was carried out using AC impedance spectroscopy. The properties of NASICON thin film for various temperatures were investigated. The NASICON thin film showed a higher ionic conductivity (0.43 S/cm) compared to that of bulk NASICON material. The Nernst’s slope of 57 mV per decade for CO 2 concentrations from 1000 to 10,000 ppm was obtained at operating temperature of 400 °C. The power consumption of the fabricated sensor was about 52 mW at 400 °C. As results, it is supposed that the fabricated sensor could be applied for monitoring CO 2 gas in environment.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2003.11.039