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[Display omitted] • Bimetallic MOFs-derived hierarchical WO 3 /ZnWO 4 /CoWO 4 heterostructures are gained. • Morphology and sensing behavior of the samples are tuned by the amounts of ZIFs. • Good selectivity and stability of WO 3 -based composites can be observed at 25 °C. • Abundant polyoxometalate electron acceptors are distributed on the coarse surface. • Sensing mechanism is relied on the rapid transport of carriers and plentiful POMs. Bimetallic MOFs-derived hierarchical WO 3 /ZnWO 4 /CoWO 4 heterostructures were prepared by electrospinning for achieving superior n-butanol-sensing property at low operating temperatures. Porous chain-like structures can gradually transformed into porous mulberry-like structures composed of various accumulated particles as increasing the additive amount of Zn/Co-ZIFs. High selectivity and stability of WO 3 -based composites to 100 ppm n-butanol can be observed at 25 °C, including the large sensitivity of 32 and the fast response/recovery times of 115/179 s. The enhanced gas-sensing performance is primarily ascribed to the increased specific surface area, plentiful polyoxometalate, and effective heterojunctions, obviously promoting surface/interface absorption behavior and electron transport process. [ABSTRACT FROM AUTHOR]

Porous double-channel α-Fe 2 O 3 /SnO 2 heterostructures with tunable surface/interface transport mechanism have been originally fabricated by the electrospinning and subsequent calcination process. With the increase of Sn content from 0 to 5 mol%, the morphology of α-Fe 2 O 3 -based materials changed from porous fibers to ribbons with both sides curled inward. Double-channel structure can provide more active sites and enhanced adsorption capacity with the large specific surface areas of 233.2 m2/g. The optimal α-Fe 2 O 3 /SnO 2 composites exhibit the highest response value (32.38) and fastest response/recovery times (33/58 s) than those of other samples to 100 ppm N,N-dimethylformamide (DMF) at 360 °C. Meanwhile, good cycling and long-term stability and high gas selectivity of the composites are conductive to the feasible detection to DMF under high temperature (≥360 °C) condition. The enhanced gas-sensitive properties of α-Fe 2 O 3 /SnO 2 composites at high temperature are closely related to phase composition, unique morphology, efficient n-n heterojunction and accelerated surface/interface charge transfer process. Significantly, the porous double-channel α-Fe 2 O 3 /SnO 2 composite is expected to be a potential candidate for DMF vapor detection in the dye or pesticide industry to prevent DMF explosion under high temperature conditions in the future. [Display omitted] • Porous double-channel α-Fe 2 O 3 /SnO 2 heterostructures is gained by electrospinning. • The special structure can provide more active sites and enhanced adsorption capacity. • Superior gas-sensing properties to DMF are obtained at high temperature (≥360 °C). • Fe/Sn-0.03 shows the highest response (32.38) and low detection limit (1 ppm) to DMF. • Sensing behavior depends on surface/interface multiple electronic transport routes. [ABSTRACT FROM AUTHOR]

Currently, the construction of three-dimensional (3D) flower-like SnS 2 /In 2 S 3 heterostructures has been primarily developed for low-temperature gas-sensing detection of triethylamine (TEA) by a facile hydrothermal treatment. The thickness of nanosheets and the number of folds of self-assembled products can be well regulated as the introduction of In component increasing, as well as the distribution of effective SnS 2 –In 2 S 3 heterojunctions. All the as-prepared SnS 2 -based sensors can exhibit good gas sensitive response behavior to TEA at various low operating temperatures, even for the first time at room temperature. For example, the optimal SnS 2 -1% In have the highest response (21.01), the relatively fast response/recovery times, and superior gas selectivity and stability to 100 ppm TEA at 40 °C, compared with other samples. Besides the combination of the formation of SnS 2 –In 2 S 3 heterojunctions, abundant active sites of the self-assembled structures, and unique surface/interface transmission mechanism is beneficial to the enhanced gas-sensing performance, significantly, the generation of state density resonance effect can be employed for improving the electron transport efficiency due to the adjustment of state density near the Femi level. The available long-term, cycling, and humidity stabilities and the linear response relationship of the sensors greatly contribute for the potential application of seafood storage evaluation. • Flower-like SnS 2 /In 2 S 3 self-assembly with effective heterojunctions is obtained. • SnS 2 -based sensors can exhibit superior TEA-sensing behavior at low temperatures. • Available state density resonance effect plays the key role of sensing behavior. • SnS 2 /In 2 S 3 sensors can be used for the application of seafood storage evaluation. • Construction of new TEA sensors with state density resonance effect is provided. [ABSTRACT FROM AUTHOR]

[Display omitted] • An effective surface double oxygen defect strategy is gained for CeO 2 /WO 2.9 sensors. • Tunable button-shaped porous CeO 2 /WO 2.9 composites are initially fabricated. • CeO 2 /WO 2.9 sensors exhibit the excellent n -butanol detection at room temperature. • Gas-sensing mechanism deeply depends on surface double oxygen defect engineering. • New insight for constructing double oxygen defect induced gas sensors is provided. In the present work, a series of CeO 2 /WO 2.9 composites with a tunable structure and thickness are originally fabricated by innovating different additional quantities of H 2 WO 4 during the hydrothermal process. Optimal Ce/W-0.25 sensors have a higher response value of 23.68 to 100 ppm n -butanol at room temperature than that of pure CeO 2 (1.26) at 200 ℃. The unique surface double oxygen defect engineering between CeO 2 and WO 2.9 has a remarkable role in enhanced gas sensing, formation of the CeO 2 -WO 2.9 heterojunction, and effective surface/interface transport mechanism. The electron transfer between WO 2.9 and CeO 2 driven by oxygen defects on the surface of CeO 2 can easily facilitate the interconversion between Ce3+ and Ce4+. This work provides a new insight and the facile fabrication pathway for constructing double oxygen defects-derived CeO 2 -based heterostructures for developing novel n -butanol gas sensors with excellent sensing performance at room temperature. [ABSTRACT FROM AUTHOR]