Related Experiment Video
Updated: Sep 19, 2025

Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition
Published on: May 2, 2014
Deciphering the Humidity Resistance and Oxygen-Content Independence of Conductometric Hydrogen Sulfide Sensors Based
Yanjie Wang1,2, Mengqing Wang1, Xinke Jiang1
1Key Laboratory of Optoelectronic Technology and System of Ministry of Education, College of Optoelectronic Engineering, Chongqing University, Chongqing 400044, People's Republic of China.
Abstract:
Limited by inherent physicochemical properties and surface-adsorption-dominated gas-sensing behavior, traditional metal oxides are susceptible to ambient humidity levels and oxygen content within test environments. To overcome this issue, we proposed one highly sensitive MEMS-type H2S sensor featuring electrospun cerium oxide (CeO2)/copper oxide (CuO) nanotubes as the sensing layer. The constituent ratio-optimized sensors (CeO2/CuO-5) exhibited superior H2S-sensing performance over pure CeO2 counterparts, including lower operation temperature, more than two times stronger response (7.4 vs 3.1@4 ppm), and favorable selectivity. Density functional theory calculations and a series of characterization methods found that the increased oxygen vacancies and abundant CeO2/CuO n-p heterojunctions jointly contributed to the promotion of receptor and transducer function. In addition, a humidity-resistant and oxygen content-independent sensor performance was demonstrated. On the one hand, the self-refreshing effect of CeO2 endowed the CeO2/CuO-5 sensor with 75.6% retention of response toward 4 ppm of H2S under 70% RH with respect to the dry case, thus showcasing an excellent humidity tolerance. On the other hand, the decent oxygen storage ability of CeO2 favored a high response even under oxygen-lean environments. Furthermore, a patrol monitor apparatus loaded with the as-prepared sensor was designed, which showed efficient detection and alerting for on-site H2S leakage.

