4.7 Article

H2 and C2H5OH sensing characteristics of mesoporous p-type CuO films prepared via a novel precursor-based ink solution route

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 178, Issue -, Pages 395-403

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2012.12.096

Keywords

Cupric oxide (CuO); p-Type; Gas sensor; Mesoporous film; Solution process

Funding

  1. World Class University (WCU) program through the National Research Foundation (NRF) of Korea Grant
  2. Ministry of Education, Science and Technology (MEST) [2012-0008669]
  3. LG Display Co., Ltd.
  4. NRF of Korea Grant
  5. MEST [2012-008226]
  6. Research Institute of Advanced Materials (RIAM)
  7. National Research Foundation of Korea [2009-0092779, 2012R1A2A4A01008226, R31-2012-000-10075-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The p-type semiconducting CuO mesoporous films were fabricated with a novel ink solution formulated optimally with an organometallic precursor and a polymer additive. The films were calcined at 200-600 degrees C in air and their crystallinity, morphology, pore structure and chemical composition were investigated by X-ray diffraction (XRD), focused ion beam scanning electron microscopy (FIB-SEM) and X-ray photoelectron spectroscopy (XPS). H-2 and C2H5OH gas sensing properties of the films calcined above 400 degrees C were investigated as a function of operating temperature, and were correlated with crystallinity, hole concentration and morphological factors of each film. The calcination-temperature dependence of the p-type gas sensing properties regarding the films suggested that higher hole concentration/crystallinity/surface-to-volume ratio and better crystallinity/lower grain boundary density in the sensing films lead to higher and faster p-type gas responses, respectively. In addition, to the best of our knowledge, the responses toward H-2 and C2H5OH gases regarding these CuO gas sensors are comparable to the values previously reported. (c) 2012 Elsevier B.V. All rights reserved.

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