Monolayer Co3O4 Inverse Opals as Multifunctional Sensors for Volatile Organic Compounds

• Published in: Chemistry : a European journal Vol. 22; no. 21; pp. 7102 - 7107
• Main Authors: Lee, Chul-Soon, Dai, Zhengfei, Jeong, Seong-Yong, Kwak, Chang-Hoon, Kim, Bo-Young, Kim, Do Hong, Jang, Ho Won, Park, Joon-Shik, Lee, Jong-Heun
• Format: Journal Article
• Language: English
• Published: Weinheim Blackwell Publishing Ltd 17.05.2016; Wiley Subscription Services, Inc
• Subjects: Chemistry; monolayers; nanostructures; sensors; template synthesis; thin films
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.201505210

Monolayers of periodic porous Co3O4 inverse opal (IO) thin films for gas‐sensor applications were prepared by transferring cobalt‐solution‐dipped polystyrene (PS) monolayers onto sensor substrates and subsequent removal of the PS template by heat treatment. Monolayer Co3O4 IO thin films having periodic pores (d≈500 nm) showed a high response of 112.9 to 5 ppm C2H5OH at 200 °C with low cross‐responses to other interfering gases. Moreover, the selective detection of xylene and methyl benzenes (xylene+toluene) could be achieved simply by tuning the sensor temperature to 250 and 275 °C, respectively, so that multiple gases can be detected with a single chemiresistor. Unprecedentedly high ethanol response and temperature‐modulated control of selectivity with respect to ethanol, xylene, and methyl benzenes were attributed to the highly chemiresistive IO nanoarchitecture and to the tuned catalytic promotion of different gas‐sensing reactions, respectively. These well‐ordered porous nanostructures could have potential in the field of high‐performance gas sensors based on p‐type oxide semiconductors. Multi‐gas sensor: Co3O4 inverse opal (IO) thin films for gas sensing (see figure) were prepared by template synthesis. Unprecedentedly high ethanol response and temperature‐modulated selective detection of ethanol, xylene, and methyl benzenes were attributed to the highly chemiresistive IO nanoarchitecture and to the tuned catalytic promotion of different gas‐sensing reactions, respectively.