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Quasi-two-dimensional (quasi-2D) molybdenum disulfide (MoS2) is a photoluminescence (PL) material with unique properties. The recent demonstration of its PL, controlled by the intercalation of positive ions, can lead to many opportunities for employing this quasi-2D material in ion-related biological applications. Here, we present two representative models of biological systems that incorporate the ion-controlled PL of quasi-2D MoS2 nanoflakes. The ion exchange behaviors of these two models are investigated to reveal enzymatic activities and cell viabilities. While the ion intercalation of MoS2 in enzymatic activities is enabled via an external applied voltage, the intercalation of ions in cell viability investigations occurs in the presence of the intrinsic cell membrane potential.

We demonstrate an active microfluidic platform that integrates dielectrophoresis for the control of silver nanoparticles spacing, as they flow in a liquid channel. By careful control of the nanoparticles spacing, we can effectively increase the surface-enhanced Raman scattering (SERS) signal intensity based on augmenting the number of SERS-active hot-spots, while avoiding irreversible aggregation of the particles. The system is benchmarked using dipicolinate (2,6-pyridinedicarboxylic acid) (DPA), which is a biomarker of Bacillus anthracis. The validity of the results is discussed using several complementing characterization scenarios.

A microfluidic dielectrophoresis platform consisting of curved microelectrodes was developed and integrated with a Raman spectroscopy system. The electrodes were patterned on a quartz substrate, which has insignificant Raman response, and integrated with a microfluidic channel that was imprinted in poly-dimethylsiloxane (PDMS). We will show that this novel integrated system can be efficiently used for the determination of suspended particle types and the direct mapping of their spatial concentrations. We will also illustrate the system's unique advantages over conventional optical systems. Nanoparticles of tungsten trioxide (WO(3)) and polystyrene were used in the investigations, as they are Raman active and can be homogeneously suspended in water.

This work demonstrates the application of dielectrophoretic (DEP) control of silica nanoparticles to form tuneable optical elements within a microfluidic system. The implementation consisted of a microfluidic channel with an array of curved microelectrodes along its base. Various DEP conditions were investigated at alternating current voltage amplitudes, flow rates and frequencies from 5 to 15 V, 2 to 10 microL/min and 0 to 20 MHz, respectively. The fluid channel was filled with deionized water suspending silica particles with diameters of 230 and 450 nm. Experiments were conducted to demonstrate DEP concentration and deflection of the particles and the impact of these particles distributions on the optical transmission through the fluid channel. Both confinement and scattering of the light were observed depending on the particle dimensions and the parameters of the DEP excitation. The results of this investigation illustrate the feasibility of DEP control in an optofluidic system and represent a significant step toward the dynamic formation of electrically controlled liquid optical waveguides.

This work describes the separation of polystyrene microparticles suspended in deionized (DI) water according to their dimensions using a dielectrophoretic (DEP) system. The DEP system utilizes curved microelectrodes integrated into a microfluidic system. Microparticles of 1, 6, and 15 μm are applied to the system and their response to the DEP field is studied at different frequencies of 100, 200, and 20 MHz. The microelectrodes act as a DEP barrier for 15 μm particles and retain them at all frequencies whereas the response of 1 and 6 μm particles depend strongly on the applied frequency. At 100 kHz, both particles are trapped by the microelectrodes. However, at 200 kHz, the 1 μm particles are trapped by the microelectrodes while the 6 μm particles are pushed toward the sidewalls. Finally, at 20 MHz, both particles are pushed toward the sidewalls. The experiments show the tunable performance of the system to sort the microparticles of various dimensions in microfluidic systems. [ABSTRACT FROM AUTHOR]

Abstract: Plasmonic biosensors based on noble metals generally suffer from low sensitivities if the perturbation of refractive‐index in the ambient is not significant. By contrast, the features of degenerately doped semiconductors offer new dimensions for plasmonic biosensing, by allowing charge‐based detection. Here, this concept is demonstrated in plasmonic hydrogen doped molybdenum oxides (HxMoO3), with the morphology of 2D nanodisks, using a representative enzymatic glucose sensing model. Based on the ultrahigh capacity of the molybdenum oxide nanodisks for accommodating H+, the plasmon resonance wavelengths of HxMoO3 are shifted into visible‐near‐infrared wavelengths. These plasmonic features alter significantly as a function of the intercalated H+ concentration. The facile H+ deintercalation out of HxMoO3 provides an exceptional sensitivity and fast kinetics to charge perturbations during enzymatic oxidation. The optimum sensing response is found at H1.55MoO3, achieving a detection limit of 2 × 10−9 m at 410 nm, even when the biosensing platform is adapted into a light‐emitting diode‐photodetector setup. The performance is superior in comparison to all previously reported plasmonic enzymatic glucose sensors, providing a great opportunity in developing high performance biosensors. [ABSTRACT FROM AUTHOR]

Assembled nanofin heat sinks, nanostructures which are formed via external forces in a cooling microfluidic to remove heat from hot spots, are a new concept that has recently been introduced. In this work, we investigate nanofin structures formed by CrO2 and Fe2O3 magnetic nanoparticles and compare their performance. Thermal imaging is used for comparison of three cases including: (i) DI water as the coolant liquid, (ii) suspension of magnetic particles in DI water, and (iii) suspension of magnetic particles in DI water in the presence of a magnetic field. For each case, the experiments are conducted at three different flow rates of 10, 40 and 120 μl min−1. Our results suggest that the high thermal conductivity of the nanofins composed of CrO2 significantly enhances the heat exchange across the microchannel. The proof-of-concept magnetophoretic system can offer a practical solution for the cooling of future compact electronics. [ABSTRACT FROM AUTHOR]

Metal foams are highly sought‐after porous structures for heterogeneous catalysis, which are fabricated by templating, injecting gas, or admixing blowing agents into a metallic melt at high temperatures. They also require additional catalytic material coating. Here, a low‐melting‐point liquid metal is devised for the single‐step formation of catalytic foams in mild aqueous environments. A hybrid catalytic foam fabrication process is presented via simultaneous chemical foaming, melting, and sintering reaction of liquid metal nanoparticles. As a model, nanoparticles of tertiary low‐melting‐point eutectic alloy of indium, bismuth, and tin (Field's metal) are processed with sodium hydrogen carbonate, an environmentally benign blowing agent. The competing endothermic foaming and exothermic sintering reactions are triggered by an aqueous acidic bath. The overall foaming process occurs at a localized temperature above 200 °C, producing submicron‐ to micron‐sized open‐cell pore foams with conductive cores and semiconducting surface decorations. The catalytic properties of the metal foams are explored for a range of applications including photo‐electrocatalysis, bacteria electrofiltration, and CO2 electroconversion. In particular, the Field's metal‐based foams show exceptional CO2 electrochemical conversion performance at low applied voltages. The facile process presented here can be extended to other low‐temperature post transition and transition metal alloys. [ABSTRACT FROM AUTHOR]

We demonstrate photochemically induced actuation of liquid metal marbles, which are liquid metal droplets encased in micro/nanoparticles. The WO3 nanoparticles coated marbles are placed in H2O2 solution, and their surfaces are illuminated with UV light. The semiconducting WO3 coating behaves as a photocatalyst to trigger a photochemical reaction, generating oxygen bubbles that propel the marble. The actuation of the marbles is investigated under different H2O2 concentrations, light intensities, and marble dimensions. Equations describing the fundamentals of such actuations are presented. [ABSTRACT FROM AUTHOR]

The advent of optofluidic systems incorporating suspended particles has resulted in the emergence of novel applications. Such systems operate based on the fact that suspended particles can be manipulated using well-appointed active forces, and their motions, locations and local concentrations can be controlled. These forces can be exerted on both individual and clusters of particles. Having the capability to manipulate suspended particles gives users the ability for tuning the physical and, to some extent, the chemical properties of the suspension media, which addresses the needs of various advanced optofluidic systems. Additionally, the incorporation of particles results in the realization of novel optofluidic solutions used for creating optical components and sensing platforms. In this review, we present different types of active forces that are used for particle manipulations and the resulting optofluidic systems incorporating them. These systems include optical components, optofluidic detection and analysis platforms, plasmonics and Raman systems, thermal and energy related systems, and platforms specifically incorporating biological particles. We conclude the review with a discussion of future perspectives, which are expected to further advance this rapidly growing field. [ABSTRACT FROM AUTHOR]

We present the employment of the Keggin ion 12-phosphotungsticacid as a UV-switchable reducing agent for the decoration of Au, Ag,Pt, and Cu nanoparticles onto the surface of TiO2nanotubessynthesized by electrochemical anodization. The synthesized compositeswere studied using SEM, GADDS XRD, and EDX, and the photocatalyticactivity of the composites was examined by measuring the photodegradationof the organic dye “Congo red” under simulated solarlight. Decoration with metal nanoparticles was observed to enhancethe activity of the photocatalytic process by upward of 100% withrespect to unmodified TiO2nanotubes. [ABSTRACT FROM AUTHOR]

In research on alternative photoanode materials for dye-sensitized solar cells (DSCs), there is rarely any report on WO3, probably due to its acidic surface and more positive (vs NHE) conduction band edge position compared to TiO2and ZnO. For the first time, dye-sensitized solar cells based on porous WO3nanoparticle films were successfully fabricated with efficiency of up to 0.75%. The multicrystalline structure of WO3was examined by Raman spectroscopy and X-ray diffraction analysis. It was found that significant performance enhancement can be obtained from treating the WO3nanoparticle film with TiCl4; the TiCl4-treated WO3DSCs were recorded with efficiency reaching 1.46%. [ABSTRACT FROM AUTHOR]

Abstract: We report an efficient solar-light-driven photocatalyst based on three-dimensional nanoporous tungsten trioxide (WO3) films. These films are obtained by anodizing W foils in fluoride-containing electrolytes at room temperature and under low applied voltages with an efficient growth rate of 2μmh−1. The maximum thickness of the films is ~3μm that exceeds those of previously reported anodized WO3 films in fluoride-containing electrolytes. By investigating the photocatalytic properties of the films with thicknesses ranging from ~0.5 to ~3μm, the optimum thickness of the nanoporous film is found to be ~1μm, which demonstrates an impressive 120% improvement in the photocatalytic performance compared to that of a RF-sputtered nanotextured film with similar weights. We mainly ascribe this to large surface area and smaller bandgap. [Copyright &y& Elsevier]

Abstract: Highly dispersed gold nanoparticles (AuNPs) supported on nitrogen-doped multiwalled carbon nanotubes (NCNTs) were synthesized using an electrochemical method. Size of AuNPs and their dispersion profile were tuned in a facile manner by controlling the applied potential and deposition time. The structure of the films was characterized using SEM, HRTEM, XRD and Raman spectroscopy. Electron microscopy revealed that the nanoparticles were deposited homogeneously on the outer surface of the NCNTs in high density. The average dimensions of the AuNPs could be tuned by varying the applied voltage and the duration of the electrochemical process. The XRD patterns confirmed the presence of metallic fcc gold along with disordered graphitic phases. The Raman spectroscopy showed that NCNTs possess 3–5at.% nitrogen with a heterogeneous distribution profile, which is consistent with nitrogen incorporation in both graphitic and pyridinic moieties within the carbon sp2 network of disordered NCNTs. SERS enhancement was also observed for AuNPs/NCNTs prepared at 10V/20min condition. Conductometric gas sensors were developed from the thin films of AuNPs/NCNTs nanocomposites and evaluated towards H2 gas. The sensors were exposed to different concentrations of H2 in synthetic air at room temperature. The highest sensitivity of 75% was measured towards 1% H2 when average size of AuNPs on NCNTs is about 4–6nm. [Copyright &y& Elsevier]

Abstract: Conductometric, optical and surface acoustic wave gas sensors based on sol–gel silica porous films doped with NiO and Au nanoparticles are studied. The nanocomposite films are characterized by optical absorption in the visible and near-infrared region, spectroscopic ellipsometry, X-ray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray (EDX) analysis and X-ray photoemission spectroscopy (XPS). They show poor conductometric gas sensing response toward CO and H2. However, both optical and surface acoustic wave (SAW) responses are reversible and stable to H2. Moreover, exploiting the wavelength dependence of the optical sensor response it is possible to selective recognition of H2. Choosing the appropriate wavelength, almost no variation in absorption is observed when introducing different gases into the testing chamber. [Copyright &y& Elsevier]