Ammonia (NH) is an irritant gas with a unique pungent odor; sub-parts per million-level breath ammonia is a medical biomarker for kidney disorders and Helicobacter pylori bacteria-induced stomach infections. The humidity varies in both ambient environment and exhaled breath, and thus humidity dependence of gas-sensing characteristics is a great obstacle for real-time applications. Herein, flexible, humidity-independent, and room-temperature ammonia sensors are fabricated by the thermal evaporation of CuBr on a polyimide substrate and subsequent coating of a nanoscale moisture-blocking CeO overlayer by electron-beam evaporation. CuBr sensors coated with a 100 nm-thick CeO overlayer exhibits an ultrahigh response (resistance ratio) of 68 toward 5 ppm ammonia with excellent gas selectivity, rapid response, reversibility, and humidity-independent sensing characteristics at room temperature. In addition, the sensing performance remains stable after repetitive bending and long-term operation. Moreover, the sensors exhibit significant response to the simulated exhaled breath of patients with H. pylori infection; the simulated breath contains 50 ppb NH. The sensors thus show promising potential in detecting sub-parts per million-level NH, regardless of humidity fluctuations, which can open up new applications in wearable devices for in situ medical diagnosis and indoor/outdoor environment monitoring.
The use of composite materials and polynary compounds is a promising strategy to promote conductometric sensor performances. The perovskite oxides provide various compositional combinations between different oxides for tuning gas-sensing reaction and endowing rich oxygen deficiencies for preferable gas adsorption. Herein, a sacrificial colloidal template approach is exploited to fabricate crystalline ternary LaFeO3 perovskite porous thin films, by transferring a La(3+)-Fe(3+) hybrid solution-dipped template onto a substrate and sequent heat treatment. The honeycomb-like LaFeO3 film consisted of monolayer periodic pore (size: ∼ 500 nm) array can be successfully in situ synthesized in a homogeneous layout with a single phase of perovskite. This periodic porous LaFeO3 film with p-type semiconductivity exhibits a high gas response, fast response (∼4 s), trace detection capacity (50 ppb), and favorable ethanol selectivity from similar acetone. It exhibits enhanced sensing performances compared to those of a binary n-type Fe2O3 film and a nontemplated dense LaFeO3 film. In addition, a five-axe spiderweb diagram is introduced to make a feasible evaluation of the optimal practical work condition, comprehensively regarding the response/recovery rate, gas response, selectivity and operating temperature. The enhanced ethanol sensing mechanism of honeycomb-like LaFeO3 periodic porous film is also addressed. This novel and facile route to fabricate well-ordered porous LaFeO3 thin film can also be applied to many fields to obtain special performances, such as solar cells, ion conductors, gas separation, piezoelectricity, and self-powered sensing device system.
Ultra-selective and sensitive detection of benzene was achieved using Pd-loaded SnO2 yolk–shell micro-reactor sensing films coated with a catalytic Co3O4 overlayer.
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