Surface enhanced resonance Raman and luminescence on plasmon active nanostructured cavities

Presented here are studies of the impact of excitation angle on surface enhanced Raman and luminescence spectroscopy of dye immobilised on a plasmon active nanocavity array support. Results show that both Raman and luminescence intensities depend on the angle of incidence consistent with the presence of cavity supported plasmon modes. Dependence of scattering or emission intensity with excitation angle occurs over the window of observation

Self-Powered Microfluidic Device for Rapid Assay of Antiplatelet Drugs

We report the development of a microfluidic device for the rapid assay in whole blood of platelet-protein interactions indicative of the efficacy of antiplatelet drugs—e.g., aspirin and Plavix, two of the world’s most widely used drugs—in cardiovascular patients. Because platelet adhesion to surface-confined protein matrices is modulated by fluid shear rates at the blood/protein interface, and because such binding is a better indicator of platelet function than platelet self-aggregation, we designed, fabricated, and characterized the performance of a family of disposable, self-powered microfluidic chips with well-defined flow and interfacial shear rates suitable for small blood volumes (≤ 200 µL). We report a simple technique to fabricate single-use self-powered chips incorporating shear control, “SpearChips”. These parallel-plate flow devices integrate on-chip vacuum-driven blood flow, using a pre-degassed elastomer component to obviate active pumping, with microcontact-printed arrays of 6-µm-diameter fluorescently-labeled fibrinogen dots on a poly(cycloolefin) base plate as a means to quantitatively count platelet-protein binding events. The use of SpearChips to assess in whole blood samples the effects of GPIIb/IIIa and P2Y12 inhibitors—two important classes of “antiplatelet” drugs—is reported

Hydrothermal syntheses of tungsten doped TiO 2 and TiO 2 /WO 3 composite using metal oxide precursors for charge storage applications

Synthesis of advanced functional materials through scalable processing routes using greener approaches is essential for process and product sustainability. In this article, syntheses of nanoparticles of titanium dioxide (TiO₂), tungsten trioxide (WO₃), WO₃-doped titanium dioxide (W-TiO₂) and TiO₂/WO₃ composite at hydrothermal conditions using corresponding metal oxide precursors are described. Electrochemical charge storage capabilities of the above materials are measured using cyclic voltammetry, charge-discharge cycling and electrochemical impedance spectroscopy in aqueous KOH electrolyte. The TiO₂ and the WO₃ nanoparticle showed a specific charge (Q) of ∼12 and ∼36 mA h g⁻¹ at a current density of 2 A g⁻¹ in 6 M KOH, respectively. The Q of TiO₂ increased upon W doping up to 25 mA h g−1 for 5 wt% W-TiO2 and the WO₃/TiO₂ composite showed the highest storage capability (Q ∼40 mA h g⁻¹). Changes in the charge storage capabilities of the doped and composite materials have been correlated to materials properties.Bhupender Pal acknowledges the Research & Innovation Department of Universiti Malaysia Pahang (http://ump.edu.my) for award of Postdoctoral Fellowship. This project is funded under Flagship Strategic Leap 3 of Universiti Malaysia Pahang (Grant Number # RDU 172201)

Modification of Capacitive Charge Storage of TiO2 with Nickel Doping

For practical deployment of supercapacitors characterized by high energy density, power density and long cycle life, they must be realized using low cost and environmentally benign materials. Titanium dioxide (TiO2) is largely abundant in the earth's crust; however, they show inferior supercapacitive electrochemical properties in most electrolytes for practical deployment. In this paper, we show that nickel doped TiO2 (Ni:TiO2) nanowires developed by electrospinning showed five times larger capacitance (∼200 F g−1) than the undoped analogue (∼40 F g−1). Electrochemical measurements show that the Ni:TiO2 nanowires have 100% coulombic efficiency. The electrodes showed no appreciable capacitance degradation for over 5000 cycles. The superior charge storage capability of the Ni:TiO2 could be due to its high electrical conductivity that resulted in five orders of magnitude higher ion diffusion as determined by cyclic voltammetry and electrochemical impedance spectroscopy measurements

Lithium-ion adsorption on surface modified porous carbon

Lithium-ion storage in porous carbon electrodes offers challenges due to poor electrode kinetics and limited storability. In this article, we demonstrate improved lithium-ion storage kinetics and rate capability in carbon electrode with appropriate surface or void modifications. The surface of porous carbon is modified by developing a thin film of either a metal oxide (Mn2O3) or a metal (cobalt) or the large voids in them are filled using hierarchical MnCo2O4 or TiO2 nanoflowers. Lithium-ion capacitors are fabricated in the Carbon//LiPF6//Li configuration and evaluated their lithium storage performance using cyclic voltammetry, galvanostatic charge discharge cycling, and electrochemical impedance spectroscopy. While the surface or void modification nominally increased the specific capacitance, the potential window and rate capability of the resulting devices remarkably increased. Among all the tested devices, the MnCo2O4 flowers filled electrode showed the largest capacitance and capacity retention, which are ascribed to its lower lithium transfer resistance

Facile fabrication of thin metal oxide films on porous carbon for high density charge storage

In an effort to minimize the usage of non-renewable materials and to enhance the functionality of the renewable materials, we have developed thin metal oxide coated porous carbon derived from a highly abundant non-edible bio resource, i.e., palm kernel shell, using a one-step activation-coating procedure and demonstrated their superiority as a supercapacitive energy storage electrode. In a typical experiment, an optimized composition contained ~10 wt.% of Mn2O3 on activated carbon (AC); a supercapacitor electrode fabricated using this electrode showed higher rate capability and more than twice specific capacitance than pure carbon electrode and could be cycled over 5000 cycles without any appreciable capacity loss in 1 M Na2SO4 electrolyte. A symmetric supercapacitor prototype developed using the optimum electrode showed nearly four times higher energy density than the pure carbon owing to the enhancements in voltage window and capacitance. A lithium ion capacitor fabricated in half-cell configuration using 1 M LiPF6 electrolyte showed larger voltage window, superior capacitance and rate capability in the ~10 wt.% Mn2O3@AC than the pure analogue. These results demonstrate that the current protocol allows fabrication of superior charge storing electrodes using renewable materials functionalized by minimum quantity of earthborn materials

Large Scale Synthesis of Binary Composite Nanowires in the Mn2O3-SnO2 System with Improved Charge Storage Capabilities

Large scale production of electrochemical materials in non-conventional morphologies such as nanowires has been a challenging issue. Besides, functional materials for a given application do not often offer all properties required for ideal performance; therefore, a composite is the most sought remedy. In this paper, we report large scale production of a composite nanowire, viz. Mn2O3-SnO2, and their constituent binary nanowires by a large scale electrospinning pilot plant consisting of 100 needles. Electrochemical characterization of thus produced composite nanowires showed nearly threefold increase in the discharge capacity compared to their single component counterparts: Mn2O3-SnO2 ∼53 mA h g−1 (specific capacitance, CS ∼384 F g−1); Mn2O3 ∼18 mA h g−1 (CS ∼164 F g−1); and SnO2 ∼14 mA h g−1 (CS ∼128 F g−1) at 1 A g−1 in 6 M KOH. The EIS studies showed that the characteristic resistances and time of the composite electrode are appreciably lower than their constituents. Owing to the scalability of the synthesis processes and promising capacitive properties achieved would lead the composite material as a competitive low-cost and high-performance supercapacitor electrode

Standard versus simplified radiofrequency ablation protocol for Barrett's esophagus: comparative analysis of the whole treatment pathway.

Background and study aims  The standard radiofrequency ablation (RFA) protocol for Barrett's esophagus (BE) encompasses an intermediary cleaning phase between two ablation sessions. A simplified protocol omitting the cleaning phase is less labor-intensive but equally effective in studies based on single ablation procedures. The aim of this study was to compare efficacy and safety of the standard and simplified RFA protocols for the whole treatment pathway for BE, including both circumferential and focal devices. Patients and methods  We performed a retrospective analysis of prospectively collected data on patients receiving RFA between January 2007 and August 2017 at two institutions. Outcomes assessed were: 1) complete remission of dysplasia (CR-D) and intestinal metaplasia (CR-IM) at 18 months; and 2) rate of esophageal strictures. Results  One hundred forty-five patients were included of whom 73 patients received the standard and 72 patients received the simplified protocol. CR-D was achieved in 94.5 % and 95.8 % of patients receiving the standard and simplified protocol, respectively ( P  = 0.71). CR-IM was achieved in 84.9 % and 77.8 % of patients treated with the standard and simplified protocol, respectively ( P  = 0.27). Strictures were significantly more common among patients who received the simplified protocol (12.5 %) compared to the standard protocol (1.4 %; P  = 0.008). The median number of esophageal dilations was one. Conclusion  The simplified RFA protocol is as effective as the standard protocol in eradicating BE but carries a higher risk of strictures. This needs to be taken into account, particularly in patients with higher pretreatment risk of strictures, such as those with esophageal narrowing from previous endoscopic mucosal resection (EMR)

Pulsed plasma physical vapour deposition approach towards the facile synthesis of multilayer and monolayer graphene for anticoagulation applications

We demonstrate the growth of multilayer and single layer graphene on copper foil using bipolar pulsed direct current (DC) magnetron sputtering of a graphite target in pure Ar atmosphere. Single layer and few layer graphene films (SG and FLG) are deposited at temperatures ranging from 700-920 °C in less than 30 minutes. We find that the deposition and post-deposition annealing temperatures influence the layer thickness and quality of the graphene films formed. The films were characterized using atomic force microscopy (AFM), scanning electron microscopy (SEM), High resolution transmission electron microscopy (HRTEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and optical transmission spectroscopy techniques. Based on the above studies, a diffusion controlled mechanism was proposed for the graphene growth. A single step whole blood assay was used to investigate the anticoagulant activity of graphene surfaces. Platelet adhesion, activation and morphological changes on the graphene/glass surfaces compared to bare glass were analysed using fluorescence microscopy and SEM techniques. We have found significant suppression of the platelet adhesion, activation and aggregation on the graphene covered surfaces compared to the bare glass, indicating the anticoagulant activity of the deposited graphene films. Our production technique represents an industrially relevant method for the growth of single and few layer graphene for various applications including the biomedical field