We fabricated a sensing layer from ink-printed WS2 flakes and utilized it for UV-activated gas sensing. The optical imaging of the structure made by repeated printing revealed the continuous layer comprising sub-µm flakes, confirmed independently by small-area AFM images (1×1 µm2). The activity of the sensing surface was investigated locally via AFM scanning of the surface with a polarized probing tip. The results indicated that the applied UV light amplifies the existing conducting paths in the dark. These hot spots are associated with the sensing activity of the WS2 surface (local adsorption-desorption centers). Gas sensing experiments revealed that the DC resistance of the WS2 sensor changes in the opposite direction for increasing concentrations of NO2 and NH3, which correlates with the electron-accepting and electron-donating properties of these species. On the contrary, low-frequency noise intensifies gradually in both gases, and relative changes in noise responses are higher than DC resistance responses for all investigated concentrations. The lowest detection limit obtained was 103 ppb from DC responses for NO2 and 168 ppb from noise responses for NH3. The studies of sensing responses for mixtures of the mentioned target gases revealed that the amplitude of resistance fluctuations is not a direct summation of spectra obtained for pure compounds. Such an effect observed for mixed gases indicates that the intermittent reactions between both species before adsorbing at the sensing surface or in the adsorption centers impact their detection.
Autorzy
Informacje dodatkowe
- DOI
- Cyfrowy identyfikator dokumentu elektronicznego link otwiera się w nowej karcie 10.1016/j.snb.2024.136923
- Kategoria
- Publikacja w czasopiśmie
- Typ
- artykuły w czasopismach
- Język
- angielski
- Rok wydania
- 2025
Źródło danych: MOSTWiedzy.pl - publikacja "UV light-activated gas mixture sensing by ink-printed WS2 layer" link otwiera się w nowej karcie