Rapid and precise discrimination of various odorants is vital to fabricating enhanced sensing devices in the fields of disease diagnostics, food safety, and environmental monitoring. Here, we demonstrate an ultrasensitive and flexible field-effect transistor (FET) olfactory system, namely, a bioelectronic nose (B-nose), based on plasma-treated bilayer graphene conjugated with an olfactory receptor. The stable p- and n-type behaviors from modified bilayer graphene (MBLG) took place after controlled oxygen and ammonia plasma treatments. It was integrated with human olfactory receptors 2AG1 (hOR2AG1: OR), leading to the formation of the liquid-ion gated FET-type platform. ORs bind to the particular odorant amyl butyrate (AB), and their interactions are specific and selective. The B-noses behave as flexible and transparent sensing devices and can recognize a target odorant with single-carbon-atom resolution. The B-noses are ultrasensitive and highly selective toward AB. The minimum detection limit (MDL) is as low as 0.04 fM (10(-15); signal-to-noise: 4.2), and the equilibrium constants of OR-oxygen plasma-treated graphene (OR-OG) and ammonia plasma-treated graphene (-NG) are ca. 3.44 × 10(14) and 1.47 × 10(14) M(-1), respectively. Additionally, the B-noses have long-term stability and excellent mechanical bending durability in flexible systems.
Mercury (Hg) is highly toxic but has been widely used for numerous domestic applications, including thermometers and batteries, for decades, which has led to fatal outcomes due to its accumulation in the human body. Although many types of mercury sensors have been developed to protect the users from Hg, few methodologies exist to analyze Hg(2+) ions in low concentrations in real world samples. Herein, we describe the fabrication and characterization of liquid-ion gated field-effect transistor (FET)-type flexible graphene aptasensor with high sensitivity and selectivity for Hg. The field-induced responses from the graphene aptasensor had excellent sensing performance, and Hg(2+) ions with very low concentration of 10 pM could be detected, which is 2-3 orders of magnitude more sensitive than previously reported mercury sensors using electrochemical systems. Moreover, the aptasensor showed a highly specific response to Hg(2+) ions in mixed solutions. The flexible graphene aptasensor showed a very rapid response, providing a signal in less than 1 s when the Hg(2+) ion concentration was altered. Specificity to Hg(2+) ions was demonstrated in real world samples (in this case samples derived from mussels). The aptasensor was fabricated by transferring chemical vapor deposition (CVD)-grown graphene onto a transparent flexible substrate, and the structure displayed excellent mechanical durability and flexiblility. This graphene-based aptasensor has potential for detecting Hg exposure in human and in the environment.
Tailoring the morphology of materials in the nanometer regime is vital to realizing enhanced device performance. Here, we demonstrate flexible nerve agent sensors, based on hydroxylated poly(3,4-ethylenedioxythiophene) (PEDOT) nanotubes (HPNTs) with surface substructures such as nanonodules (NNs) and nanorods (NRs). The surface substructures can be grown on a nanofiber surface by controlling critical synthetic conditions during vapor deposition polymerization (VDP) on the polymer nanotemplate, leading to the formation of multidimensional conducting polymer nanostructures. Hydroxyl groups are found to interact with the nerve agents. Representatively, the sensing response of dimethyl methylphosphonate (DMMP) as a simulant for sarin is highly sensitive and reversible from the aligned nanotubes. The minimum detection limit is as low as 10 ppt. Additionally, the sensor had excellent mechanical bendability and durability.
Ultrafine metal-oxide-decorated hybrid carbon nanofibers (CNFs) were fabricated by a single-nozzle co-electrospinning process using a phase-separated mixed polymer composite solution and heat treatment. To decorate metal oxides on the CNF surface, core (PAN) and shell (PVP) structured nanofibers (NFs) were fabricated as starting materials. The core-shell NF structure was prepared by single-nozzle co-electrospinning because of the incompatibility of the two polymers. Ultrafine hybrid CNFs were then formed by decomposing the PVP phase, converting the metal precursors to metal oxide nanonodules, and transforming the PAN to CNFs of ca. 40 nm diameter during heat treatment. The decoration morphology of the metal oxide nanonodules could be controlled by precursor concentration in the PVP solution. These ultrafine hybrid CNFs were applied to a dimethyl methylphosphonate (DMMP) chemical sensor at room temperature with excellent sensitivity. The minimum detectable level (MDL) of hybrid CNFs was as low as 0.1 ppb, which is 10-100 times higher than for a chemical sensor based on carbon nanotubes. This is because the metal oxide nanonodules of hybrid CNFs increase the surface area and affinity to DMMP vapor. Our new synthetic methodology promises to be an effective approach to fabricating hybrid CNF/inorganic nanostructures for future sensing technologies.
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