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Abstract Pseudomonas aeruginosa(P. aeruginosa) is an opportunistic pathogen causing infections in blood and implanted devices. Traditional identification methods take more than 24 h to produce results. Molecular biology methods expedite detection, but require an advanced skill set. To address these challenges, this work demonstrates functionalization of laser‐induced graphene (LIG) for developing flexible electrochemical sensors forP. aeruginosabased on phenazines. Electrodeposition as a facile approach is used to functionalize LIG with molybdenum polysulfide (MoS_x). The sensor's limit of detection (LOD), sensitivity, and specificity are determined in broth, agar, and wound simulating medium (WSM). Control experiments withEscherichia coli, which does not produce phenazines, demonstrate specificity of sensors forP. aeruginosa. The LOD for pyocyanin (PYO) and phenazine‐1‐carboxylic acid (PCA) is 0.19 × 10⁻⁶ and 1.2 × 10⁻⁶ m, respectively. Furthermore, the highly stable sensors enable real‐time monitoring ofP. aeruginosabiofilms over several days. Comparing square wave voltammetry data over time shows time‐dependent generation of phenazines. In particular, two configurations—“Normal” and “Flipped”—are studied, showing that the phenazines time dynamics vary depending on how cells interact with sensors. The reported results demonstrate the potential of the developed sensors for integration with wound dressings for early diagnosis ofP. aeruginosainfection. 

To fully capitalize on the unique properties of 2D materials, cost-effective techniques for producing high-quality 2D flakes at scale are crucial. In this work, we show that dry ball-milling, a commonly used powder-processing technique, can be effectively and efficiently upgraded into an automated exfoliation technique. It is done by adding polymer as adhesives into a ball mill to mimic the well-known tape exfoliation process, which is known to produce 2D flakes with the highest quality but is limited by its extremely low efficiency on large-scale production. Seventeen types of commonly seen polymers, including both artificial and natural ones, have been examined as additives to dry ball-mill hexagonal boron nitride. A parallel comparison between different additives identifies low-cost natural polymers such as starch as promising dry ball-mill additives to produce ultrathin flakes with the largest aspect ratio. The mechanical, thermal, and surface properties of the polymers are proposed as key features that simultaneously determine the exfoliation efficiency, and their ranking of importance in the mechanical exfoliation process is revealed using a machine learning model. Finally, the potential of the polymer-assisted ball-mill exfoliation method as a universal way to produce ultra-thin 2D nanosheets is also demonstrated. 

W e present a scalable solution-processing method for fabricating high-quality graphene and graphene/1T-MoS 2 heterostructure films. The process begins with the synthesis of potassium-intercalated graphite (KC 8 ), which is exfoliated in tetrahydrofuran (THF) to produce stable dispersions of negatively charged (electron rich) graphene sheets. The graphene is subsequently transferred to water, forming a surfactant-free aqueous dispersion suitable for creating homogenous graphene films via vacuum filtration and stamping. Additionally, graphene is combined with 1T-MoS 2 nanosheets to fabricate graphene/1T-MoS 2 bulk heterostructure films. Comprehensive characterization, including X-ray diffraction (XRD), absorption spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy ( TEM), Raman spectroscopy, and X-ray photon emission spectroscopy (XPS), reveals that the heterostructure films exhibit enhanced optical and electronic properties, including improved light absorption, which could lead to novel photo-responsive devices. Raman spectroscopy shows significant changes in the graphene’s structural a nd electronic properties upon interaction with MoS 2 , indicating strong interlayer coupling and potential charge transfer between the layered components. The g raphene films demonstrate highly sensitive detection of dopamine (DA), while the graphene/1T-MoS 2 b ulk heterostructure films exhibit capacitance values up to 3 8.3 Fg − 1 at 5 mV/s in non-aqueous electrolytes. These results highlight the potential of these films for advanced applications in molecular sensing and energy storage. 

As the feature size of microelectronic circuits is scaling down to nanometer order, the increasing interconnect crosstalk, resistance-capacitance (RC) delay and power consumption can limit the chip performance and reliability. To address these challenges, new low-kdielectric (k < 2) materials need to be developed to replace current silicon dioxide (k = 3.9) or SiCOH, etc. However, existing low-kdielectric materials, such as organosilicate glass or polymeric dielectrics, suffer from poor thermal and mechanical properties. Two-dimensional polymers (2DPs) are considered promising low-kdielectric materials because of their good thermal and mechanical properties, high porosity and designability. Here, we report a chemical-vapor-deposition (CVD) method for growing fluoride rich 2DP-F films on arbitrary substrates. We show that the grown 2DP-F thin films exhibit ultra-low dielectric constant (in plane k = 1.85 and out-of-plane k = 1.82) and remarkable mechanical properties (Young’s modulus > 15 GPa). We also demonstrated the improved performance of monolayer MoS₂field-effect-transistors when utilizing 2DP-F thin films as dielectric substrates. 

Recent advances in graphene-based electroanalytical biodevices: different methods for graphene synthesis, functionalization, device fabrication, and transduction mechanisms are discussed for various healthcare applications.