4.8 Article

Humidity-Independent Gas Sensors Using Pr-Doped In2O3 Macroporous Spheres: Role of Cyclic Pr3+/Pr4+ Redox Reactions in Suppression of Water-Poisoning Effect

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 28, Pages 25322-25329

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b06386

Keywords

oxide semiconductor gas sensor; indium oxide; praseodymium; humidity dependence; cyclic redox reactions

Funding

  1. International Research & Development Program of the National Research Foundation of Korea (NRF) - Ministry of Science, ICT, and Future Planning (MSIP) of Korea [NRF-2017K1A3A1A49069947]
  2. Industrial Strategic Technology Development Program - Ministry of Trade, Industry & Energy (MOTIE, Korea) [10073068]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [10073068] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Pure and 3-12 at. % Pr-doped In2O3 macroporous spheres were fabricated by ultrasonic spray pyrolysis and their acetone sensing characteristics under dry and humid conditions were investigated to design humidity-independent gas sensors. The 12 at. % Pr-doped In2O3 sensor exhibited approximately the same acetone responses and sensor resistances at 450 degrees C regardless of the humidity variation, whereas the pure In2O3 exhibited significant deterioration in gas-sensing characteristics upon the change in the atmosphere, from dry to humid (relative humidity: 80%). Moreover, the 12 at. % Pr-doped In2O3 sensor exhibited a high response to acetone with negligible cross responses to interfering gases (NH3, CO, benzene, toluene, NO2, and H-2) under the highly humid atmosphere. The mechanism for the humidity-immune gas-sensing characteristics was investigated by X-ray photoelectron and diffuse reflectance infrared Fourier transform spectroscopies together with the phenomenological gas-sensing results and discussed in relation with Pr3+/Pr4+ redox pairs, regenerative oxygen adsorption, and scavenging of hydroxyl groups.

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