Two-dimensional titanium carbide MXenes, TiCT, possess high surface area coupled with metallic conductivity and potential for functionalization. These properties make them especially attractive for the highly sensitive room-temperature electrochemical detection of gas analytes. However, these extraordinary materials have not been thoroughly investigated for the detection of volatile organic compounds (VOCs), many of which hold high relevance for disease diagnostics and environmental protection. Furthermore, the insufficient interlayer spacing between MXene nanoflakes could limit their applicability and the use of heteroatoms as dopants could help overcome this challenge. Here, we report that S-doping of TiCT MXene leads to a greater gas-sensing performance to VOCs compared to their undoped counterparts, with unique selectivity to toluene. After S-doped and pristine materials were synthesized, characterized, and used as electrode materials, the as-fabricated sensors were subjected to room-temperature dynamic impedimetric testing in the presence of VOCs with different functional groups (ethanol, hexane, toluene, and hexyl-acetate). Unique selectivity to toluene was obtained by both undoped and doped TiCT MXenes, but an enhancement of response in the range of ∼214% at 1 ppm to ∼312% at 50 ppm (3-4 folds increase) was obtained for the sulfur-doped sensing material. A clear notable response to 500 ppb toluene was also obtained with sulfur-doped TiCT MXene sensors along with excellent long-term stability. Our experimental measurements and density functional theory analysis offer insight into the mechanisms through which S-doping influences VOC analyte sensing capabilities of TiCT MXenes, thus opening up future investigations on the development of high-performance room-temperature gas sensors.

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http://dx.doi.org/10.1021/acssensors.0c01287DOI Listing

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