Synthesis of PDMS Chain Structure with Introduced Dynamic Covalent Bonding for High-Performance Rehealable Tactile Sensor Application.

In addressing the increasing demand for wearable sensing systems, the performance and lifespan of such devices must be improved by enhancing their sensitivity and healing capabilities. The present work introduces an innovative method for synthesizing a healable disulfide bond contained in a polydimethylsiloxane network (PDMS-SS) that incorporates ionic salts, which is designed to serve as a highly effective dielectric layer for capacitive tactile sensors. Within the polymer network structure, the cross-linking agent pentaerythritol tetrakis 3-mercaptopropionate (PTKPM) forms reversible disulfide bonds while simultaneously increasing polymer softness and the dielectric constant. The incorporation of dioctyl sulfosuccinate sodium salt (DOSS) significantly improves the capacitance and sensing properties by forming an electrical double-layer through interactions between the electrode charge and salt ions at the contact interface. The developed polymer material-based tactile sensor shows a strong response signal at low pressure (0.1 kPa) and maintains high sensitivity (0.175 kPa-1) over a wide pressure range (0.1-10 kPa). It also maintains the same sensitivity over 10 000 repeated applications of external pressure and is easily self-healed against mechanical deformation due to the dynamic disulfide covalent bonding, restoring ≈95% of its detection capacity.

Performance of angle shear connectors for U-shaped steel concrete infilled composite beams.

The current design codes i.e. AISC 360-16, CSA-S16-19, EC-04 etc. provide empirical relationships to estimate the capacity of shear connectors which were developed based on pushout tests of headed studs and channels connectors in exposed type sections. Therefore, these equations may result inaccurate predictions for strength of connectors in infilled-type sections. This study presents a detailed experimental study investigating the performance of angle connectors in composite sections. The testing program consisted two series of pushout tests. A total of 36 specimens were tested, considering the influence of several important parameters i.e. the length (Lc), height (hc), and web-thickness (tw) of angle connector, length of the weld (w) and the direction of shear connector (forward/backward) etc. The tests results demonstrated that with increasing connector height hs, and thickness, the maximum load Pmax and slip δu were increased. The connector direction didn't change much the load-slip behavior. The prediction accuracy of the existing shear capacity models was evaluated by comparing the predictions with experimental results. The current equations were noticed to be highly inconsistent in predicting the shear capacity of angle connectors, especially in case of infilled type sections. When the entire length of connector was taken as the effective length, the models overestimated the shear capacity. While in case when the welding length was taken as effective length in calculations, the models underestimated the shear strength of angle connectors.

Metastatic papillary renal cell carcinoma with portal vein tumor thrombosis confirmed on blind liver biopsy.

Portal vein tumor thrombosis (PVTT) is an uncommon condition in which tumor cells expand into the vessels, causing blood clot formation in the portal vein. PVTT is mainly associated with hepatocellular carcinoma, leading to an unfavorable prognosis; however, it can also develop in patients with other cancer types. Herein, we report a case of metastatic renal cell carcinoma diagnosed by a blind liver biopsy in a patient with dynamic computed tomography-confirmed portal vein thrombosis and cholangiopathy. This case illustrates the importance of systematic surveillance with routine laboratory tests and contrast-enhanced imaging studies on patients with cancer to detect potential liver infiltration of metastatic cancer.

Structural Control of Nanofibers According to Electrospinning Process Conditions and Their Applications.

Nanofibers have gained much attention because of the large surface area they can provide. Thus, many fabrication methods that produce nanofiber materials have been proposed. Electrospinning is a spinning technique that can use an electric field to continuously and uniformly generate polymer and composite nanofibers. The structure of the electrospinning system can be modified, thus making changes to the structure, and also the alignment of nanofibers. Moreover, the nanofibers can also be treated, modifying the nanofiber structure. This paper thoroughly reviews the efforts to change the configuration of the electrospinning system and the effects of these configurations on the nanofibers. Excellent works in different fields of application that use electrospun nanofibers are also introduced. The studied materials functioned effectively in their application, thereby proving the potential for the future development of electrospinning nanofiber materials.

Multiscale pore contained carbon nanofiber-based field-effect transistor biosensors for nesfatin-1 detection.

Nesfatin-1 (NES1) is a potential biomarker found in serum and saliva that indicates hyperpolarization and depolarization in the hypothalamic ventricle nucleus as well as an increase in epileptic conditions. However, real-time investigations have not been carried out to detect changes in the concentration of NES1. In this study, we develop a multiscale pore contained carbon nanofiber-based field-effect transistor (FET) biosensor to detect NES1. The activated multiscale pore contained carbon nanofiber (a-MPCNF) is generated using a single-nozzle co-electrospinning method and a subsequent steam-activation process to obtain a signal transducer and template for immobilization of bioreceptors. The prepared biosensor exhibits a high sensitivity to NES1. It can detect levels as low as 0.1 fM of NES1, even in the presence of other interfering biomolecules. Furthermore, the a-MPCNF-based FET sensor has significant potential for practical applications in non-invasive real-time diagnosis, as indicated by its sensing performance in artificial saliva.

Comparative Studies on Crystallinity, Thermal and Mechanical Properties of Polyketone Grown on Plasma Treated CVD Graphene.

In this work, we report a facile way to control crystalline structures of polyketone (PK) films by combining plasma surface treatment with chemical vapor deposition (CVD) technique. The crystalline structure of PKs grown on plasma-treated graphene and the resulting thermal and mechanical properties were systematically discussed. Every graphene sheet used in this work was produced by CVD method and the production of PKs having different crystallinity were performed on the O2- and N2-doped graphene sheets. It was evident that the CVD-grown graphene sheets acted as the nucleating agents for promoting the crystallization of ß-form PK, while suppressing the growth of α-form PK crystals. Regardless of the increase in surface roughness of graphene, surface functionality of the CVD-grown graphene was found to be an important factor in determining the crystalline structure of PK. N2 plasma treatment of the CVD-grown graphene promoted growth of the ß-form PK, whereas the O2 plasma treatment of CVD graphene led to transformation of the unoriented ß-form PK into the oriented α-form PK. Thus, the resulting thermal and mechanical properties of the PKs were highly dependent on the surface functionality of the CVD graphene. The method of controlling crystalline structure of the PKs suggested in this study, is expected to be very effective in realizing the PK with good processability, heat resistance and mechanical properties.

Freestanding and Flexible ß-MnO2@Carbon Sheet for Application as a Highly Sensitive Dimethyl Methylphosphonate Sensor.

Research on wearable sensor systems is mostly conducted on freestanding polymer substrates such as poly(dimethylsiloxane) and poly(ethylene terephthalate). However, the use of these polymers as substrates requires the introduction of transducer materials on their surface, which causes many problems related to the contact with the transducer components. In this study, we propose a freestanding flexible sensor electrode based on a ß-MnO2-decorated carbon nanofiber sheet (ß-MnO2@CNF) to detect dimethyl methylphosphonate (DMMP) as a nerve agent simulant. To introduce MnO2 on the surface of the substrate, polypyrrole coated on poly(acrylonitrile) (PPy@PAN) was reacted with a MnO2 precursor. Then, phase transfer of PPy@PAN and MnO2 to carbon and ß-MnO2, respectively, was induced by heat treatment. The ß-MnO2@CNF sheet electrode showed excellent sensitivity toward the target analyte DMMP (down to 0.1 ppb), as well as high selectivity, reversibility, and stability.

Recent Development of Flexible Tactile Sensors and Their Applications.

With the rapid development of society in recent decades, the wearable sensor has attracted attention for motion-based health care and artificial applications. However, there are still many limitations to applying them in real life, particularly the inconvenience that comes from their large size and non-flexible systems. To solve these problems, flexible small-sized sensors that use body motion as a stimulus are studied to directly collect more accurate and diverse signals. In particular, tactile sensors are applied directly on the skin and provide input signals of motion change for the flexible reading device. This review provides information about different types of tactile sensors and their working mechanisms that are piezoresistive, piezocapacitive, piezoelectric, and triboelectric. Moreover, this review presents not only the applications of the tactile sensor in motion sensing and health care monitoring, but also their contributions in the field of artificial intelligence in recent years. Other applications, such as human behavior studies, are also suggested.

Ruthenium Decorated Polypyrrole Nanoparticles for Highly Sensitive Hydrogen Gas Sensors Using Component Ratio and Protonation Control.

Despite being highly flammable at lower concentrations and causing suffocation at higher concentrations, hydrogen gas continues to play an important role in various industrial processes. Therefore, an appropriate monitoring system is crucial for processes that use hydrogen. In this study, we found a nanocomposite comprising of ruthenium nanoclusters decorated on carboxyl polypyrrole nanoparticles (Ru_CPPy) to be successful in detecting hydrogen gas through a simple sonochemistry method. We found that the morphology and density control of the ruthenium component increased the active surface area to the target analyte (hydrogen molecule). Carboxyl polypyrrole (CPPy) in the nanocomposite was protonated to increase the charge transfer rate during gas detection. This material-based sensor electrode was highly sensitive (down to 0.5 ppm) toward hydrogen gas and had a fast response and recovery time under ambient conditions. The sensing ability of the electrode was maintained up to 15 days without structure deformations.

Facile Synthesis of Co3O4-Incorporated Multichannel Carbon Nanofibers for Electrochemical Applications.

Considering their superior electrochemical performances, extensive studies have been carried out on composite nanomaterials based on porous carbon nanofibers. However, the introduction of inorganic components into a porous structure is complex and has a low yield. In this study, we propose a simple synthesis of cobalt-oxide-incorporated multichannel carbon nanofibers (P-Co-MCNFs) as electrode materials for electrochemical applications. The cobalt oxide component is directly formed in the carbon structure by a simple oxygen plasma exposure of the phase-separated polymer nanofibers. P-Co-MCNF displays high specific capacitance (815 F g-1 at 2.0 A g-1), rate capability (821 F g-1 at 1 A g-1 and 786 F g-1 at 20 A g-1), and cycle stability (92.1% for 5000 cycles) as a supercapacitor electrode. Moreover, excellent sensitivity (down to 1 nM) and selectivity to the glucose molecule is demonstrated for nonenzyme sensor applications.

Aptamer-Functionalized Three-Dimensional Carbon Nanowebs for Ultrasensitive and Free-Standing PDGF Biosensor.

Research on flexible biosensors is mostly focused on their use in obtaining information on physical signals (such as temperature, heart rate, pH, and intraocular pressure). Consequently, there are hardly any studies on using flexible electronics for detecting biomolecules and biomarkers that cause diseases. In this study, we propose a flexible, three-dimensional carbon nanoweb (3DCNW)-based aptamer sensor to detect the platelet-induced growth factor (PDGF), which is an oncogenic biomarker. As a template for the 3D structure, poly(acrylonitrile) (PAN) nanowebs were synthesized using a facile electrospinning process. The PAN nanowebs were then subjected to chemical vapor deposition with copper powder. This was followed by Cu etching to generate carbon protrusions on the web surface. As an active site, PDGF-B binding aptamer was introduced on the 3DCNW surface to form biosensor electrodes. The 3DCNW-based aptasensor exhibited excellent sensitivity (down to 1.78 fM), with high selectivity, reversibility, and stability to PDGF-BB.

Comparative Study on the Formation and Oxidation-Level Control of Three-Dimensional Conductive Nanofilms for Gas Sensor Applications.

Investment in wearable monitoring systems is increasing rapidly for realizing their practical applications, for example, in medical treatment, sports, and security systems. However, existing wearable monitoring systems are designed to measure a real-time physical signal and abnormal conditions rather than harmful environmental characteristics. In this study, a flexible chemical sensor electrode based on a three-dimensional conductive nanofilm (3D CNF) is fabricated via facile polymerization with temperature control. The morphology and chemical state of the 3D CNF are modified via electrochemical doping control to increase the carrier mobility and the active surface area of the sensor electrode. The sensor electrode is highly sensitive (up to 1 ppb), selective, and stable for an analyte (NH3) at room temperature owing to the three-dimensional morphology of polypyrrole and the oxidation-level control.

Recent Developments of the Solution-Processable and Highly Conductive Polyaniline Composites for Optical and Electrochemical Applications.

Solution-processable conducting polymers (CPs) are an effective means for producing thin-film electrodes with tunable thickness, and excellent electrical, electrochemical, and optical properties. Especially, solution-processable polyaniline (PANI) composites have drawn a great deal of interest due to of their ease of film-forming, high conductivity up to 103 S/cm, excellent redox behaviors, processability, and scalability. In this review, basic principles, fabrication methods, and applications of solution-processable PANI composites will be discussed. In addition, recent researches on the PANI-based electrodes for solar cells (SCs), electrochromic (EC) windows, thermoelectric (TE) materials, supercapacitors, sensors, antennas, electromagnetic interference (EMI) shielding, organic field-effect transistors (OFETs), and anti-corrosion coatings will be discussed. The presented examples in this review will offer new insights in the design and fabrication of high-performance electrodes from the PANI composite solutions for the development of thin-film electrodes for state-of-art applications.

Comparative Studies on Two-Electrode Symmetric Supercapacitors Based on Polypyrrole:Poly(4-styrenesulfonate) with Different Molecular Weights of Poly(4-styrenesulfonate).

Poly(4-styrenesulfonate)-conducting polymer (PSS-CP) is advantageous for thin-film electrode manufacturing due to its high conductivity, high charge storage, structural stability, and excellent ink dispersion. In this work, comparative studies of two-electrode symmetric supercapacitors using Polypyrrole:Poly(4-styrenesulfonate) (PPy:PSS), with different molecular weights (Mw's) of Poly(4-styrenesulfonate) (PSS) as the electrodes, were performed. PPy:PSS can be easily prepared using a simple solution process that enables the mass production of thin-film electrodes with improved electrical and electrochemical properties. As-prepared PPy:PSS, with different PSS molecular weights, were assembled into two-electrode supercapacitors based on coin cell structures. It was confirmed that the electrical and electrochemical properties of PPy:PSS were improved with increasing PSS molecular weight. The coin cell, using PPy:PSS with a PSS molecular weight of 1.0 × 106 g/mol, exhibited higher areal capacitance (175.3 mF/cm²), higher volumetric capacitance (584.2 F/cm³), and longer cycling stability (86.3% after 5000 cycles) compared to those of PPy:PSS with PSS molecular weights of 2.0 × 105 and 7.0 × 104 g/mol. This work provides an efficient approach for producing cost-effective and miniaturized supercapacitors with high conductivity and high specific capacitance for practical applications in a variety of electronic devices.

Highly porous structured polyaniline nanocomposites for scalable and flexible high-performance supercapacitors.

Recently, flexible energy devices have been used to power up portable electronics such as E-skins, smart clothes, and bendable displays. However, the usage of rigid and inactive components in electrode materials limits the application in flexible energy devices. Here, we report a novel method to fabricate porous polyaniline composites (Pt_CPPy/PANI:CSA) using Pt decorated carboxyl polypyrrole nanoparticles (Pt_CPPyNPs) as a nucleating agent for electrodes of supercapacitors. The specific capacitance and electrical conductivity of the Pt_CPPy/PANI:CSA film are 325.0 F g-1 and 814 S cm-1, respectively, which are much higher than those of the pristine PANI:CSA film. Furthermore, the porous PANI:CSA composites exhibit excellent rate capability and cycling stability as the pores in the PANI structure enhance the active surface area between PANI and the ions of the electrolytes. This unique fabrication technique is an effective approach for preparing large scale highly porous polyaniline nanomaterials for diverse electrochemical applications.

Development of a Predictive Model Using Endoscopic Features for Gastric Cytomegalovirus Infection in Renal Transplant Patients.

BACKGROUND: Cytomegalovirus (CMV) is a common viral pathogen in transplant patients which often targets the stomach. However, the endoscopic characteristics of gastric CMV infection are not well established. We aimed to develop a predictive model using endoscopic findings for gastric CMV infection in renal transplant patients. METHODS: A retrospective study of 287 kidney transplant recipients who underwent endoscopy with biopsy for suspected CMV infection from January 2006 to November 2015 at a tertiary referral hospital was performed. CMV infection was defined based on inclusion bodies in hematoxylin and eosin and immunohistochemical staining. Endoscopic and clinical parameters related to gastric CMV infection were selected by univariate analyses. Multivariate logistic regression was used to create a predictive model from ß-coefficients. RESULTS: CMV was present in 107 (37.7%) of the 287 patients. Multivariate analysis found age (odds ratio [OR], 0.964; 95% confidence interval [CI], 0.938-0.99; P = 0.008), erosions with surface exudate (OR, 5.34; 95% CI, 2.687-10.612; P < 0.001), raised shape of erosions (OR, 3.957; 95% CI, 1.937-8.083; P < 0.001), and antral location of ulcers (OR, 15.018; 95% CI, 5.728-39.371; P < 0.001) as independent predictive factors for gastric CMV infection. Using the predictive model created from this analysis, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy were 71.03%, 85.56%, 74.51%, 83.24%, and 80.14%, respectively. The area under the receiver operating characteristic curve of this model for detecting CMV infection was 0.850 (95% CI, 0.803-0.889; P < 0.001). CONCLUSIONS: The predictive model with typical endoscopic findings may be useful for detecting gastric CMV infection in renal transplant patients.

Multidimensional Conductive Nanofilm-Based Flexible Aptasensor for Ultrasensitive and Selective HBsAg Detection.

Hepatitis B virus (HBV) infection is a major worldwide health issue causing serious liver diseases, including liver cirrhosis and hepatocellular carcinoma. Monitoring the serum hepatitis B surface antigen (HBsAg) level is pivotal to the diagnosis of HBV infection. In this study, we describe multidimensional conductive nanofilm (MCNF)-based field-effect transistor (FET) aptasensor for HBsAg detection. The MCNF, composed of vertically oriented carboxylic polypyrrole nanowires (CPPyNW) and graphene layer, is formed using electropolymerization of pyrrole on the graphene surface and following acid treatment. The amine-functionalized HBsAg-binding aptamers are then immobilized on the CPPyNW surface through covalent bonding formation (i.e., amide group). The prepared aptasensor presents highly sensitive to HBsAg as low as 10 aM among interfering biomolecules with various deformations. Moreover, the MCNF-based aptasensor has great potential for practical application in the noninvasive real-time diagnosis because of its improved sensing ability to the human serum and artificial saliva.

Platinum nanoparticles immobilized on polypyrrole nanofibers for non-enzyme oxalic acid sensor.

Oxalic acid (OA), naturally available in many fruits and vegetables, reacts easily with Ca2+ and Mg2+ ions to produce an insoluble salt. In renal systems, this insoluble salt brings about various renal diseases. As such, the OA excretion level in urine has been utilized as an index parameter in healthcare settings. Here, we report the fabrication of platinum nanoparticle-immobilized polypyrrole-3-carboxylated nanofibers (Pt_cPPyNFs) to apply as a transducer material for a non-enzyme field-effect transistor (FET)-type OA sensor. To achieve uniformly decorated Pt on carboxylated polypyrrole nanofibers (cPPyNFs), ultrasonication and chemical reduction were introduced as a Pt immobilization process. The Pt_cPPyNFs were immobilized on an interdigitated array (IDA) electrode for our sensor application. The resulting Pt_cPPyNF based non-enzyme FET-type OA sensor exhibited high sensitivity at unprecedentedly low concentrations (10-14 M); this was attributed to the uniformity of the Pt-nanoparticle decoration and distinct properties of the FET configuration. In addition, high stability was achieved in repeated experiments and under ambient storage conditions.

Facile synthesis of size-controlled Fe2O3 nanoparticle-decorated carbon nanotubes for highly sensitive H2S detection.

Hydrogen sulfide (H2S) is one of the most plentiful toxic gases in a real-life and causes a collapse of the nervous system and a disturbance of the cellular respiration. Therefore, highly sensitive and selective H2S gas sensor systems are becoming increasingly important in environmental monitoring and safety. In this report, we suggest the facile synthesis method of the Fe2O3 particles uniformly decorated on carbon nanotubes (Fe2O3@CNT) to detect H2S gas using oxidative co-polymerization (pyrrole and 3-carboxylated pyrrole) and heat treatment. The as prepared Fe2O3@CNT-based sensor electrode is highly sensitive (as low as 1 ppm), selective and stable to H2S gas at 25 °C, which shows promise for operating in medical diagnosis and environment monitoring. Excellent performance of the Fe2O3@CNT is due to the unique morphology of the nanocomposites made from uniformly dispersed Fe2O3 nanoparticles on the carbon surface without aggregation.

Ultrasensitive and Selective Organic FET-type Nonenzymatic Dopamine Sensor Based on Platinum Nanoparticles-Decorated Reduced Graphene Oxide.

Dopamine (DA), a catecholamine hormone, is an important neurotransmitter that controls renal and cardiovascular organizations and regulates physiological activities. Abnormal concentrations of DA cause unfavorable neuronal illnesses such as Parkinson's disease, schizophrenia, and attention deficit hyperactivity disorder/attention deficit disorder. However, the DA concentration is exceedingly low in patients and difficult to detect with existing biosensors. In this study, we developed an organic field-effect-transistor-type (OFET) nonenzyme biosensor using platinum nanoparticle-decorated reduced graphene oxide (Pt_rGO) for ultrasensitive and selective DA detection. The Pt_rGOs were fabricated by reducing GO aqueous solution-containing Pt precursors (PtCl4) with a chemical reducing agent. The Pt_rGOs were immobilized on a graphene substrate by π-π interactions and a conducting-polymer source-drain electrode was patterned on the substrate to form the DA sensor. The resulting OFET sensor showed a high sensitivity to remarkably low DA concentrations (100 × 10-18 M) and selectivity among interfering molecules. Good stability was expected for the OFET sensor because it was fabricated without an enzymatic receptor, and π-π conjugation is a part of the immobilization process. Furthermore, the OFET sensors are flexible and offer the possibility of wide application as wearable and portable sensors.