Elucidating different NO2 sensing mechanisms in oxidized PbS nanocrystals

Abstract

In this work we provide an in-depth analysis of the sensing mechanisms of NO2 by lead-sulfide nanocrystals (PbS-NCs). A detailed model for the sorption mechanism is proposed, and the correlation is established between experimental sensing characteristics and the surface composition, based on both experimental characterization and ab initio (DFT) simulations. We demonstrated how the sensitivity and the sensing dynamic response can be tuned by a post-deposition multistep dry-thermal process at mild temperature, that alternates vacuum-assisted annealing and heating in open-air. Sensors with different surface compositions were fabricated, and their dynamic response was characterized at low concentration of NO2 (0.5 ppm) in air, at ambient temperature. DFT simulations indicate that both surface stoichiometry and oxidation critically govern NO2 interaction on PbS, with sulfur-rich terminations favoring weaker binding and faster desorption, while intermediate oxidation enhances interaction and overoxidation leads to surface passivation, in agreement with the measured experimental sensing dynamics. By linking surface composition, adsorption chemistry, and resistance transduction within a single framework, this work provides clear indications to design room-temperature, low-ppm NO2 microsensors fabricated through a simple and scalable processes.

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