By means of experiments and theory, the gas-sensing properties of tin diselenide (SnSe2) were elucidated. We discover that, while the stoichiometric single crystal is chemically inert even in air, the… Click to show full abstract
By means of experiments and theory, the gas-sensing properties of tin diselenide (SnSe2) were elucidated. We discover that, while the stoichiometric single crystal is chemically inert even in air, the nonstoichiometric sample assumes a subnanometric SnO2 surface oxide layer once exposed to ambient atmosphere. The presence of Se vacancies induces the formation of a metastable SeO2-like layer, which is finally transformed into a SnO2 skin. Remarkably, the self-assembled SnO2/SnSe2-x heterostructure is particularly efficient in gas sensing, whereas the stoichiometric SnSe2 sample does not show sensing properties. Congruently with the theoretical model, direct sensing tests carried out on SnO2/SnSe2-x at an operational temperature of 150 °C provided sensitivities of (1.06 ± 0.03) and (0.43 ± 0.02) [ppm]-1 for NO2 and H2, respectively, in dry air. The corresponding calculated limits of detection are (0.36 ± 0.01) and (3.6 ± 0.1) ppm for NO2 and H2, respectively. No detectable changes in gas-sensing performances are observed in a time period extended above six months. Our results pave the way for a novel generation of ambient-stable gas sensor based on self-assembled heterostructures formed taking advantage on the natural interaction of substoichiometric van der Waals semiconductors with air.
               
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