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[Display omitted] • Synthesis of atomically thin 2D metal oxide NSs by a chemical exfoliation process. • A comparative study on the humidity sensing performances of 2D Ru oxide and Mn oxide NSs. • Demonstration of real-time breath humidity monitoring using a wearable sensing module. Collecting real-time breath humidity data is important for calibrating gas sensors from interfering signals in breath components, ultimately for accurately monitoring a patient's physiological information for applications in non-invasive and point-of-care diagnostics. In this work, atomically thin 2D metal oxide nanosheets (NSs) were synthesized by a liquid phase exfoliation process and their humidity sensing properties were investigated. Interestingly, Opposite humidity sensing responses (R D /R H) were observed between semiconducting oxide and metallic oxide NSs. For the semiconducting manganese (Mn) oxide NSs, decreasing resistance transitions were obtained with the response of 24.01 at 44.5% RH at low humidity levels (i.e., 6.1–45% RH), which was governed by proton (H+) conduction. On the other hand, the metallic ruthenium (Ru) oxide NSs exhibited increasing resistance transitions with the response of 0.28 at 96.3% RH at a high humidity range (i.e., 50–99.9% RH) as a result of proton trapping by accepting electrons upon the exposure to excess water molecules. Ru oxide NSs exhibited the response and recovery times of 68 sec and 8 sec, respectively, at 96.3% RH. Real-time breath humidity monitoring is demonstrated by integrating Ru oxide NSs with a wristband-type wireless sensing module, which can transmit the sensing data to a mobile device. [ABSTRACT FROM AUTHOR]

Electrospinning–etching strategy was employed to synthesize Pt-loaded SnO 2 hollow microbelts (Pt_SnO 2 HBLs) based chemiresistive-type sensor demonstrating high sensitivity and selectivity toward acetone gas. This strategy overcomes a major hurdle toward achieving ubiquitous gas diffusion in electrospun structures, and provides highly porous thin-walled HBLs with large surface area and small crystallites. [Display omitted] • In situ templating of SnO 2 with SiO 2 was employed to form Pt-loaded SiO 2 @SnO 2 core–shell microbelts. • Etching away of SiO 2 in the Pt-loaded SiO 2 @SnO 2 microbelts yielded Pt-loaded SnO 2 hollow microbelts. • The Pt-loaded SnO 2 hollow microbelts exhibited good response (R a /R g = 93.5) and selectivity toward 2 ppm acetone at 350 °C. Challenges for ubiquitous diffusion of gas analytes into semiconducting metal oxides (SMOs) based sensing layers have necessitated the introduction of unprecedented synthesis techniques for thin, porous and high-performance gas sensing materials. In this work, electrospinning and calcination were employed to prepare unprecedented SiO 2 –SnO 2 core–shell microbelts (hereinafter referred to as SiO 2 @SnO 2 BLs) followed by etching away of SiO 2 in NaOH solution (pH 12) to achieve hollow SnO 2 BLs (hereinafter referred to as SnO 2 HBLs) with mean crystal size of 14.01 nm, large BET surface area (143.5 m2‧g–1), high porosity (mean pore size of 5.7 nm), and shell thickness of 58.3 ± 11.4 nm. Sensitization of SnO 2 HBLs with apoferritin-templated platinum nanoparticles (Pt NPs) enhanced their detection capability toward acetone. Response (defined as R a /R g , where R a and R g are sensor resistances in air and target gas, respectively) of Pt(0.12 %)_SnO 2 HBLs toward 2 ppm acetone was up to 7.8 times higher compared to that of pristine SnO 2 HBLs, and exhibited faster response (9.2 s). The Pt(0.12 %)_SnO 2 HBLs based sensor indicated a promising long-term stability, and outstanding repeatability of response (R a /R g = 93.7 ± 0.89) toward 25 cycles of 2 ppm acetone exposure in a humid environment of 90 % relative humidity. This performance could be attributed to the unique morphology of HBLs, sensitization effects of catalytic Pt NPs, and enlargement of the electron-depleted layer resulting from a Schottky barrier between Pt NPs and SnO 2 grains. [ABSTRACT FROM AUTHOR]