H₂S and NH₃ Detection with Langmuir-Schaefer Monolayer Organic Field-Effect Transistors

In this work gas sensing properties of Langmuir-Schaefer monolayer organic field-effect transistors (LS OFETs) prepared from organosilicon derivative of [1]benzothieno[3,2-b][1]-benzothiophene (BTBT) have been investigated. The monolayer has been deposited using Langmuir-Schaefer method, which results in a uniform low-defect monolayer with excellent electrical performance, hole mobility up to 7 × 10−2 cm2 V−1 s−1, the threshold voltage around 0 V and on-off ratio of 104. Developed sensors demonstrate a long-term stability of a half-year storage under ambient conditions. Preliminary investigations demonstrated that the LS OFETs give instantaneous response on ammonia and hydrogen sulfide at low concentrations. The results reported open new perspectives for the OFET-based gas-sensing technology

Applying of C8-BTBT-Based EGOFETs at Different pH Values of the Electrolyte

Electrolyte-gated organic field-effect transistors (EGOFETs) is a popular platform for numerous sensing and biosensing applications in aqueous media. In this work, the variation of electrical characteristics of EGOFETs based on small-molecule organic semiconductor C8-BTBT and polystyrene blend in water solutions at different pH values was investigated. A positive shift of the threshold voltage with near-Nernstian pH sensitivity was demonstrated in the pH range from 4.9 to 2.8, while no measurable pH dependence in the range from 4.9 to 8.6 pH was registered. These results indicate chemical doping of the molecules of organic semiconductors by protons from the electrolyte in the acidic region. In order to check the applicability of the EGOFETs in a flow mode, a flow chamber was designed and assembled. The preliminary results obtained in the flow mode measurements showed a fast response to pH variation

Applying of C8-BTBT-Based EGOFETs at Different pH Values of the Electrolyte

Electrolyte-gated organic field-effect transistors (EGOFETs) is a popular platform for numerous sensing and biosensing applications in aqueous media. In this work, the variation of electrical characteristics of EGOFETs based on small-molecule organic semiconductor C8-BTBT and polystyrene blend in water solutions at different pH values was investigated. A positive shift of the threshold voltage with near-Nernstian pH sensitivity was demonstrated in the pH range from 4.9 to 2.8, while no measurable pH dependence in the range from 4.9 to 8.6 pH was registered. These results indicate chemical doping of the molecules of organic semiconductors by protons from the electrolyte in the acidic region. In order to check the applicability of the EGOFETs in a flow mode, a flow chamber was designed and assembled. The preliminary results obtained in the flow mode measurements showed a fast response to pH variation

Quantitative Detection of the Influenza a Virus by an EGOFET-Based Portable Device

Elaboration of biosensors on the base of organic transistors with embedded biomolecules which can operate in an aqueous environment is of paramount importance. Electrolyte-gated organic field-effect transistors demonstrate high sensitivity in detection of various analytes. In this paper, we demonstrated the possibility of quantitative fast specific determination of virus particles by an aptasensor based on EGOFET. The sensitivity and selectivity of the devices were examined with the influenza A virus as well as with control bioliquids like influenza B, Newcastle disease viruses or allantoic fluid with different dilutions. The influence of the semiconducting layer thickness on EGOFETs sensory properties is discussed. The fabrication of a multi-flow cell that simultaneously registers the responses from several devices on the same substrate and the creation of a multi-sensor flow device are reported. The responses of the elaborated bioelectronic platform to the influenza A virus obtained with application of the portable multi-flow mode are well correlated with the responses obtained in the laboratory stationary mode

Polymer Surface Engineering for Efficient Printing of Highly Conductive Metal Nanoparticle Inks

An approach to polymer surface modification using self-assembled layers (SALs) of functional alkoxysilanes has been developed in order to improve the printability of silver nanoparticle inks and enhance adhesion between the metal conducting layer and the flexible polymer substrate. The SALs have been fully characterized by AFM, XPS, and WCA, and the resulting printability, adhesion, and electrical conductivity of the screen-printed metal contacts have been estimated by cross-cut tape test and 4-point probe measurements. It was shown that (3-mercaptopropyl)­trimethoxysilane SALs enable significant adhesion improvements for both aqueous- and organic-based silver inks, approaching nearly 100% for PEN and PDMS substrates while exhibiting relatively low sheet resistance up to 0.1 Ω/sq. It was demonstrated that SALs containing functional −SH or −NH₂ end groups offer the opportunity to increase the affinity of the polymer substrates to silver inks and thus to achieve efficient patterning of highly conductive structures on flexible and stretchable substrates

Easily Processable Highly Ordered Langmuir-Blodgett Films of Quaterthiophene Disiloxane Dimer for Monolayer Organic Field-Effect Transistors

Self-assembly of highly soluble water-stable tetramethyldisiloxane-based dimer of α,α′-dialkylquaterthiophene on the water–air interface was investigated by Langmuir, grazing incidence X-ray diffraction, and X-ray reflectivity techniques. The conditions for formation of very homogeneous crystalline monolayer Langmuir-Blodgett (LB) films of the oligomer were found. Monolayer organic field-effect transistors (OFETs) based on these LB films as a semiconducting layer showed hole mobilities up to 3 × 10^–3 cm²/(V s), on–off ratio of 10⁵, small hysteresis, and high long-term stability. The electrical performance of the LB films studied is close to that for the same material in the bulk or in the monolayer OFETs prepared from water vapor sensitive chlorosilyl derivatives of quaterthiophene by self-assembling from solution. These findings show high potential of disiloxane-based LB films in monolayer OFETs for large-area organic electronics

Luminescent Organic Semiconducting Langmuir Monolayers

In recent years, monolayer organic field-effect devices such as transistors and sensors have demonstrated their high potential. In contrast, monolayer electroluminescent organic field-effect devices are still in their infancy. One of the key challenges here is to create an organic material that self-organizes in a monolayer and combines efficient charge transport with luminescence. Herein, we report a novel organosilicon derivative of oligothiophene–phenylene dimer <b>D2-Und-PTTP-TMS</b> (D2, tetramethyldisiloxane; Und, undecylenic spacer; P, 1,4-phenylene; T, 2,5-thiophene; TMS, trimethylsilyl) that meets these requirements. The self-assembled Langmuir monolayers of the dimer were investigated by steady-state and time-resolved photoluminescence spectroscopy, atomic force microscopy, X-ray reflectometry, and grazing-incidence X-ray diffraction, and their semiconducting properties were evaluated in organic field-effect transistors. We found that the best uniform, fully covered, highly ordered monolayers were semiconducting. Thus, the ordered two-dimensional (2D) packing of conjugated organic molecules in the semiconducting Langmuir monolayer is compatible with its high-yield luminescence, so that 2D molecular aggregation per se does not preclude highly luminescent properties. Our findings pave the way to the rational design of functional materials for monolayer organic light-emitting transistors and other optoelectronic devices