In situ photoluminescence demonstrates improved gas sensing in In2O3 by modulating oxygen defects, indicating performance enhancements.
Oxygen defects, including oxygen vacancies (VO••) and interstitial oxygen (Oi″), are one of the main factors affecting the gas-sensing performance of metal oxide semiconductors. Therefore, in situ investigation of the intrinsic roles of oxygen defects during the gas sensing processes is of great importance to disclose the gas sensing mechanism for MOS-based gas sensors and improve the performance of the sensors. Herein, we synthesized pristine In2O3 single-crystal porous nanosheets by the hydrothermal method and subsequently modulated the oxygen defects via Ho/Pr single and binary doping. The evolution of the oxygen defects during the gas response of sensors was tracked in real time by in situ photoluminescence (PL). The gas sensing test indicated that the Ho/Pr-In2O3 gas sensor improved the response to 10 ppm of NO2 from 8.5 to 37.5 at lower power consumption than pristine In2O3 while providing higher stability and selectivity. In situ PL results also confirmed the functionality of oxygen defects: the facilitative impact of VO•• and the inhibitory effect of Oi″ on ion-adsorbed oxygen. Besides, a positive relationship between the sensor's response and the concentration of VO•• was established in this study.
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Bai et al. (2025) studied this question.
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