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We report the development of a 3G microswimmer, namely, CNT-bot, capable of undergoing acid-, alkali-, magneto- and phototaxis inside acidic or alkaline baths of peroxide fuel and/or water. The use of carboxyl-functionalised multi-walled carbon nanotubes (MWCNTs) facilitated the propulsion of CNT-bots in an alkaline-water solution by ejecting carbon-dioxide bubbles. Furthermore, doping of magnetite nanoparticles (FeONPs), ferrous ions (Fe2+) and titanium dioxide nanoparticles (TiONPs) induces magnetic, chemical and photonic modes of propulsion. While FeONPs stimulated magnetotaxis at a rate of up to ~10 body lengths per second under the influence of a bar magnet, chemotaxis of a similar speed in a peroxide fuel was achieved by bubble-propulsion of oxygen gas originating from the Fenton reaction. In addition, the light-stimulated photo-Fenton reaction led to phototaxis of CNT-bots. A thin coating of magnesium imparted a half-faced Janus appearance to the CNT-bots, which facilitated motion in normal or acidic water media through the ejection of hydrogen gas bubbles. This chemotaxis could be transformed into pH-stimulated directional motion by establishing an acid or alkali concentration gradient across the peroxide and/or water baths. The capacity of CNT-bots to produce oxygen (hydrogen) bubbles in peroxide (acidic water) fuel was exploited to power a PEM fuel cell to generate electricity. The pure oxygen and hydrogen gases generated by CNT-bots in separate chambers were fed directly into the fuel cell in which the incessant motions of the particle facilitated the creation and release of the pure gases to achieve on-demand electricity generation. The motor could also induce dye degradation through advanced oxidation owing to the production of intermediate hydroxyl radicals during the Fenton reaction. Self-propelling objects have been increasingly used for a wide range of applications. Thus far, the first- (1G) and second-generation (2G) motors have served the purpose of achieving diverse motions under a directional trigger. A team headed by Shirsendu Mitra and Dipankar Bandyopadhyay at the Indian Institute of Technology Guwahati, India, has developed a third-generation (3G) artificial microswimmer composed of chemically modified multi-walled carbon nanotubes (MW CNTs)—namely the CNT-bots. Such microbots can move in response to acidic, alkaline, magnetic, and light stimuli. The team used the capacity of the CNT-bots to produce pure oxygen and hydrogen, allowing a proton-exchange membrane (PEM) fuel cell to generate an electric field. The authors believe that their study highlights the potential of a 3G CNT-bot for energy harvesting.

A paper based chemiresistor has been fabricated to selectively sense ethanol in human breath. The chemiresistor was composed of a sensing mixture of multiwall-carbon-nano-tubes (MWCNTs), poly (diallyl-dimethyl-ammonium chloride) (PDDA), alcohol dehydrogenase (ADH), and coenzyme (NADH). The aluminum electrode was deposited on the paper surface, followed by drop-casting of the aforementioned sensing mixture. The resistance of the sensors was measured by exposing the same in gas-vapor mixture as well as the sample solution. The surface-modified MWCNTs specifically broke down ethanol present in the gas-vapor mixture or in a solution to generate a quantitative electronic response proportional to the ethanol concentration. Subsequently, the interference of other volatile organic materials was also tested to prove the selectivity and sensitivity of the sensor towards ethanol in the presence of different volatile organic compounds (VOCs). The variation of the resistance during the interaction between sensor and ethanol was also characterized by measuring the surface potential of the channel material under ethanol exposure using Kelvin probe force microscopy (KPFM). The sensor was integrated with a voltage divider circuit, a display, and a microcontroller unit to make a proof-of-concept prototype for the point-of-care (POC) detection of ethanol in human breath.

Contamination of water bodies due to the disposal of natural and anthropogenic pollutants is one of the major global concerns in the recent times. Regular on-spot monitoring of water quality has become mandatory wherein diverse classes of materials such as organic, inorganic, heavy metals, or biological wastes are detected employing standard protocols. However, most of the existing laboratory techniques are either costly and/or time consuming owing to the process involving the expert driven sophisticated analysis techniques. Herein, we report the development of three paper based colorimetric sensors for the on-spot quantitative detection of the levels of fluoride (F−), lead (Pb2+), and pH in drinking water. The variations in the color-intensities of the paper sensors with the variation in the concentration of fluoride (F−), lead (Pb2+), and pH were converted into electronic signals to enable the development of a point-of-care-testing (POCT) device. For this purpose, initially, the sensors were characterized and calibrated with known concentrations of contaminates before successful validations with real samples. Thereafter, the sensors were illuminated with a light emitting diode from one side while the transmitted rays passing through the sensor was captured by a light dependent resistor (LDR) from the other side. The variation in the color intensity of the paper-sensor with the contaminant loading was found linearly varying with the resistance of the LDR. The sensor was then translated into a specific, stable and user friendly POCT device, which enabled inexpensive spot detection of pollutants in drinking water.

This study reveals various unexplored pathways to energy storage in parallel and curved plate supercapacitors (SCs). The spatiotemporal variations in the electric field intensity of such SCs were found to have a significant influence on their performance. The observations unearth the limitations associated with the previous theoretical models, which are routinely employed to analyze the performance of SCs by considering electrical double layers (EDLs) as capacitors near the electrodes. The time-dependent electrochemical behaviors of SCs obtained from the Nyquist and Bode diagrams of electrochemical impedance spectroscopy showed (i) electrode polarization at the higher-frequency sweeps, (ii) immobile Helmholtz layer formation at the mid-frequency zone, and (iii) formation of diffuse layer of EDL in the low-frequency regime. The results suggest that charge storage of SCs heavily depend on electrode geometry, type of electrolyte, electrolyte concentration, electrode separation, separator type, and dielectric...

Self-organization of large-area micro- or nanoscale patterns, using an inexpensive one-step process, is proposed for the fabrication of low-cost, high-performance organic solar cells. The authors employ spin dewetting of a conductive polymer to fabricate an array of micro- to nanoscale ordered heterojunctions, and demonstrate improvements in the key performance indicators of the resulting organic photovoltaic devices. A theoretical study with appropriate boundary conditions is carried out to understand the pattern formation, and simulations are performed to probe the effects of varying active-layer geometry on device characteristics.

We explore the improvements in yield and conversion of a chemical reaction inside a two-phase microfluidic reactor when subjected to an externally applied alternating current (AC) electric field. A computational fluid dynamic (CFD) framework has been developed to incorporate the descriptions of the two-phase flow, multicomponent transport and reaction, and the Maxwell's stresses generated at oil-water interface owing to the presence of the externally applied electric field. The CFD model ensures that the reactants are flown into a microchannel together with the oil and water phases before the reaction takes place at the interface and products diffuse back to the bulk phases. The study unveils that the variation in the intensity of the AC field helps in converting a two-phase stratified flow into an oil-in-water microemulsion composed of oil slugs, plugs, or droplets. Importantly, the results also suggest that harnessing the vortices inside or outside these flow patterns helps in the improvement in mass transfer across the interface, which can be employed to improve the yield and conversion of a reaction. We have shown an example case of a pseudo-first order reaction for which the variation in frequency and intensity of AC field is found to form higher surface-to-volume-ratio flow patterns having a higher throughput. The convective recirculation in and around these miniaturized flow morphologies increase the rate of mass transfer, mixing of reactant and products, conversion of reactant, and yield of products. The results reported can be of significance in the design and development of future advanced-flow rector technologies.

Chemical pattern directed spin-dewetting of a macroscopic droplet composed of a dilute organic solution of liquid crystal (LC) formed an ordered array of micro- and nanoscale LC droplets. Controlled evaporation of the spin-dewetted droplets through vacuum drying could further miniaturize the size to the level of ∼90 nm. The size, periodicity, and spacing of these mesoscale droplets could be tuned with the variations in the initial loading of LC in the organic solution, the strength of the centripetal force on the droplet, and the duration of the evaporation. A simple theoretical model was developed to predict the spacing between the spin-dewetted droplets. The patterned LC droplets showed a reversible phase transition from nematic to isotropic and vice versa with the periodic exposure of a solvent vapor and its removal. A similar phase transition behavior was also observed with the periodic increase or reduction of temperature, suggesting their usefulness as vapor or temperature sensors. Interestingly, when the spin-dewetted droplets were confined between a pair of electrodes and an external electric field was applied, the droplets situated at the hydrophobic patches showed light-reflecting properties under the polarization microscopy highlighting their importance in the development of micro- or nanoscale LC displays. The digitized LC droplets, which were stationary otherwise, showed dielectrophoretic locomotion under the guidance of the external electric field beyond a threshold intensity of the field. Remarkably, the motion of these droplets could be restricted to the hydrophilic zones, which were confined between the hydrophobic patches of the chemically patterned surface. The findings could significantly contribute in the development of futuristic vapor or temperature sensors, light reflectors, and self-propellers using the micro- or nanoscale digitized LC droplets.