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Laser-induced graphene (LIG) on paper substrates is a desirable material for single-use point-of-care sensing with its high-quality electrical properties, low fabrication cost, and ease of disposal. While a prior study has shown how the repeated lasing of substrates enables the synthesis of high-quality porous graphitic films, however, the process-property correlation of lasing process on the surface microstructure and electrochemical behavior, including charge-transfer kinetics, is missing. The current study presents a systematic in-depth study on LIG synthesis to elucidate the complex relationship between the surface microstructure and the resulting electroanalytical properties. The observed improvements were then applied to develop high-quality LIG-based electrochemical biosensors for uric acid detection. We show that the optimal paper LIG produced via a dual pass (defocused followed by focused lasing) produces high-quality graphene in terms of crystallinity

The upstream effect of inlet contactors (T, Y, Cross-T, and Cross-Y) with splitting distributors for parallel microchannels on gas–liquid flow uniformity were studied. Splitting distributors were d...

The possibilities of the precise control of wetting properties of a series of laser-induced graphene (LIG) films consisting of microscale air pockets on top of nano-scale surface roughness using electrowetting are demonstrated. By application of a marginal DC bias (∼2 V), water can efficiently wet as well as can be pumped through the superhydrophobic LIG substrates. Interestingly, the electrowetting phenomenon is strongly dependent on the applied voltage polarity and it causes an abrupt wetting transition from superhydrophobic (contact angle ∼152°) Cassie state to superhydrophilic (contact angle ∼7°) Wenzel state on the LIG films. By analyzing the voltage polarity dependent electrowetting results with an equivalent electrical circuit model at the solid-liquid interface, and considering the hierarchical dual surface roughness (micro-nano scale), the transition between the “slippy” Cassie state and the “sticky” Wenzel states is explained. Furthermore, we demonstrate that the unique structural characteristics of the custom-designed micropatterned LIGs, with precisely tailored surface energy by simple post-annealing treatment, enable easy preparation of superhydrophobic LIG films. The approach to prepare stable superhydrophobic LIG with voltage polarity dependent wetting mode transition is used here to controllably transport of water through 3D porous LIG surfaces.

The persistent use of pesticides in the agriculture field remains a serious issue related to public health. In the present work, molecularly imprinted polymer thin films were developed using electropolymerization of pyrrole (py) onto gold microelectrodes followed by electrodeposition for the selective detection of chlorpyrifos (CPF). The molecularly imprinted polymer (MIP) was synthesized by the electrochemical deposition method, which allowed in-line transfer of MIP on gold microelectrodes without using any additional adhering agents. Various parameters such as pH, monomer ratio, scan rate, and deposition cycle were optimized for sensor fabrication. The sensor was characterized at every stage of fabrication using various spectroscopic, microscopic, and electrochemical techniques. The sensor requires only 2 μL of the analyte and its linear detection range was found to be 1 μM to 1 fM. The developed sensor’s limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.93 and 2.82 fM, respectively, with a sensitivity of 3.98 (μA/(μM)/ mm2. The sensor’s shelf life was tested for 70 days. The applicability of the sensor in detecting CPF in fruit and vegetable samples was also assessed out with recovery % between 91 and 97% (RSD < 5%). The developed sensor possesses a huge commercial potential for on-field monitoring of pesticides.

This work demonstrates the applicability of red mud-reduced graphene oxide (RM-rGO) nanocomposites, for the reliable and selective electrochemical detection of arsenic. The new nanocomposite materi...

To improve the production rate of MoS

The origin of nitrogen-incorporated boron-doped nanocrystalline diamond (NB-NCD) nanowires as a function of substrate temperature (Ts) in H2/CH4/B2H6/N2 reactant gases is systematically addressed. Because of Ts, there is a drastic modification in the dimensional structure and microstructure and hence in the several properties of the NB-NCD films. The NB-NCD films grown at low Ts (400 °C) contain faceted diamond grains. The morphology changes to nanosized diamond grains for NB-NCD films grown at 550 °C (or 700 °C). Interestingly, the NB-NCD films grown at 850 °C possess one-dimensional nanowire-like morphological grains. These nanowire-like NB-NCD films possess the co-existence of the sp3-diamond phase and the sp2-graphitic phase, where diamond nanowires are surrounded by sp2-graphitic phases at grain boundaries. The optical emission spectroscopy studies stated that the CN, BH, and C2 species in the plasma are the main factors for the origin of nanowire-like conducting diamond grains and the materialization of graphitic phases at the grain boundaries. Moreover, conductive atomic force microscopy studies reveal that the NB-NCD films grown at 850 °C show a large number of emission sites from the grains and the grain boundaries. While boron doping improved the electrical conductivity of the NCD grains, the nitrogen incorporation eased the generation of graphitic phases at the grain boundaries that afford conducting channels for the electrons, thus achieving a high electrical conductivity for the NB-NCD films grown at 850 °C. The microplasma devices using these nanowire-like NB-NCD films as cathodes display superior plasma illumination properties with a threshold field of 3300 V/μm and plasma current density of 1.04 mA/cm2 with a supplied voltage of 520 V and a lifetime stability of 520 min. The outstanding plasma illumination characteristics of these conducting nanowire-like NB-NCD films make them appropriate as cathodes and pave the way for the utilization of these materials in various microplasma device applications.

Synthesis of stable hybrid carbon nanostructure for high-performance supercapacitor electrode with long life-cycle for electronic and energy storage devices is a real challenge. Here, we present a ...

Direct synthesis of a nano-structured carbon hybrid consisting of vertically aligned carbon nanograsses on top of boron-doped nanocrystalline diamond is demonstrated and the carbon hybrid is further applied as an electrode material for the fabrication of supercapacitors. The hybrid film combines the dual advantages of sp2 (carbon nanograss) and sp3 (nanocrystalline diamond) bonded carbon, possessing not only the excellent electrical characteristics of sp2 carbon but also the exceptional electrochemical stability of sp3 carbon. As a result, the specific capacitance of the as-prepared hybrid material reaches up to 0.4 F cm−2, one of the highest reported in diamond-based supercapacitors. The entire electrochemical results exhibit enhanced electron transfer efficiency with remarkable stability of 95% of capacitance retention even after 10 000 cycles.

The possibilities of precise control over the wetting characteristics of carbon-based hybrid nanostructures consisting of both sp2 and sp3 hybridized carbons using the electrowetting technique were demonstrated. An excellent polarity-dependent electrowetting behavior in the presence of an electrolyte followed an abrupt transition from the highly hydrophobic (contact angle ∼ 142°) Cassie–Baxter states to a hydrophilic (∼30°) Wenzel state, where diamond films acted as the anode. In addition, we also reported a remarkable transition from weakly hydrophobic to nearly superhydrophobic diamond nanostructures by chemical and morphological manipulations. The unique structural properties with precisely tailored morphology and surface roughness enabled such transitions on the nanostructured surface. This approach of preparing environmental stable hydrophobic surfaces with polarity-dependent wetting and precise control of the wetting mode transition could be used in numerous applications such as the electrochemical transport of liquids, supercapacitors, and low-friction microfluidics.

The aluminum industrial waste red mud was successfully utilized as a novel adsorbent for the removal of arsenic (As) ions from water. The arsenate (As (V)) adsorption efficacy of red mud nanoparticles was also investigated. Red mud nanoparticles were prepared by ball milling raw red mud for 10 h, yielding particles’ size of 20 nm on average. The As (V) adsorption on these nanoparticles strongly depended on the size of the nanoparticles. As (V) removal increased from 58 to 83% by reducing the size of red mud particles from 200 to 20 nm. Detail kinetics and transport study confirmed the pseudo-second-order kinetic process which was governed by external mass transport. The Freundlich (and Langmuir) isotherms confirm that the arsenate adsorption capacity changes from 2.28 mg/g (1.84 mg/g) to 2.54 mg/g (1.96 mg/g) for reduction of particles from size 200 nm to 20 nm. Water filter columns made with red mud nanoparticles prepared by ball milling for 10 h showed better filtration performance than the filter packed with raw red mud. Both the hydraulic conductivity and the As (V) removal (8 mm/h and 61% respectively) of influent 1 mg/L As (V) by red mud nanoparticles were greater than the raw red mud (3.2 mm/h and 54%). The modified red mud column filters also exhibited a higher efficiency than the raw red mud filters to remove Escherichia coli and Staphylococcus aureus from the water. Overall, this research shows that nanomaterials derived from aluminum processing waste can be a promising material for water filtration.

Graphene quantum dots (GQDs) possess excellent optical and electrical properties that can be used in a wide variety of application. Synthesis of hybrid nanoparticles with GQDs have been known to improve the properties further. Therefore, in this method, graphene quantum dots –gold (GQD-Au) hybrid nanoparticles were synthesized using GQDs which reduces HAuCl4.3H2O to Au nanoparticles on its surface at room temperature. The GQDs with self-passivated layers were synthesized by microwave assisted hydrothermal method using glucose as a single precursor. The synthesis process does not involve the use of harmful chemicals. The whole synthesis process of GQD and GQD-Au hybrid nanoparticles takes only five minutes. The synthesized GQDs have been extracted using citrate in order to increase the stability of the hybrid nanoparticles for up to four weeks. The size of the synthesized GQD-Au hybrid nanoparticles is in the range of 5–100 nm and were found to be luminescent under UV-A illumination. The merit of the following method over other synthesis techniques include its rapidity, ease of preparation, and no requirement of elaborate synthesis procedures and/or harmful chemicals. The GQD-Au hybrid nanoparticles can be used in several applications such as luminescent coatings for glass and windowpanes for automobiles, etc. The reducing property of GQDs can further be utilized for the reduction of various metal salts (AgNO3) and organic dyes (methylene blue and methyl orange). . It presents a method/protocol-development of the luminescent GQD-Au hybrid particles of size ~ 5–100 nm. . The GQD-Au hybrid particles find potential applications in luminescent coating applications., Graphical abstract Image, graphical abstract

Free-standing films of graphene oxide (GO) are regarded as potential materials for numerous applications in different fields. However, fabricating macroscopic free-standing GO films with high throughput is a bottleneck in large-scale application of these films. Here we introduce a method suitable for the mass-scale fabrication of free-standing GO films by exploring paraffin film (Parafilm M®) as a sacrificial substrate. The method involves deposition of GO on a paraffin film and peeling of the paraffin film after swelling it with toluene to obtain free-standing film of GO. Furthermore, the GO films were reduced into highly conductive RGO films using a green reducing agent ascorbic acid. A strategy of treating GO films with CuSO4 solution prior to reduction is also designed to avoid the possible disintegration of GO films in ascorbic acid solution. A detailed comparative study on the properties of RGO films prepared via thermal and chemical treatment and through the combination of both is also reported. An investigation of the variation in the electrical conductivity of the RGO films based on the reduction method is also carried out. The hydrophobic nature of the thermally reduced RGO films is explored for the oil/water separation.

Herein, we report the effect of incorporation of two types of plasmonic nanocomposites, TiO2–Au and TiO2–Ag in different ratios, in the TiO2 photoanode of dye-sensitized solar cells (DSSCs). Electrophoretic deposition technique (EPD) has been utilized for the deposition of these nanocomposite photoanodes. The high-resolution transmission electron microscopy reveals that the nanocomposites, TiO2–Au and TiO2–Ag, have a wide size distribution of Au (5–60 nm) and Ag (20–130 nm) nanoparticles embedded in the TiO2 matrix. The UV–Visible absorption spectra of these nanocomposite films reveal the enhancement in the optical density due to the plasmonic effect. The DSSC based on photoanode consists of plasmonic nanocomposite TiO2–Au:TiO2–Ag (3:1 ratio) showed power conversion efficiency (PCE) of 10.9% which is 187% higher than that pristine TiO2 counterpart. The enhancement in the PCE has been confirmed by the photoluminescence and electro-impedance spectroscopy indicating that both Au and Ag play an important role in enhancing the PCE of DSSCs due to the plasmonic effect.

Vertically aligned nitrogen-doped nanocrystalline diamond nanorods are fabricated from nitrogen-doped nanocrystalline diamond films using reactive ion etching in oxygen plasma. These nanorods show enhanced thermionic electron emission (TEE) characteristics, viz.. a high current density of 12.0 mA/cm(2) and a work function value of 4.5 eV with an applied voltage of 3 Vat 923 K. The enhanced TEE characteristics of these nanorods are ascribed to the induction of nanographitic phases at the grain boundaries and the field penetration effect through the local field enhancement from nanorods owing to a high aspect ratio and an excellent field enhancement factor.

The increasing need of on-demand power for enabling portable low-power devices and sensors has necessitated work in novel energy harvesting materials and devices. In a recent work, we demonstrated the production and suitability of three-dimensional (3-D) spacer all fibre piezoelectric textiles for converting mechanical energy into electrical energy for wearable and technical applications. The current work investigates the textile performance properties of these 3-D piezoelectric fabrics including porosity, air permeability, water vapour transmission and bursting strength. Furthermore, as these textiles are intended for wearable applications, we have assessed their wear abrasion and consequently provide surface resistance measurements which can affect the lifetime and efficiency of charge collection in the piezoelectric textile structures. The results show that the novel smart fabric with a measured porosity of 68% had good air (1855l/m(2)/s) and water vapour permeability (1.34g/m(2)/day) values, good wear abrasion resistance over 60,000 rotations applied by a load of 12kPa and bursting strength higher than 2400kPa. Moreover, the antibacterial activity of 3-D piezoelectric fabrics revealed that owing to the use of Ag/PA66 yarns, the textiles exhibit excellent antibacterial activity against not only Gram-negative bacteria E. coli but they are also capable of killing antibiotic methicillin-resistant bacteria S. aureus.

Polystyrene is a chemically inert synthetic aromatic polymer. This widely used form of plastic is recalcitrant to biodegradation. The exponential production and consumption of polystyrene in various sectors has presented a great environment risk and raised the problem of waste management. Biodegradation by bacteria has previously shown great potential against various xenobiotics but there are only a few reports concerning polyolefins. By screening wetland microbes, we found two bacterial species – Exiguobacterium sibiricum strain DR11 and Exiguobacterium undae strain DR14 which showed promising biodegradation potential against polystyrene. In this study, we report the degradation of non-irradiated solid polystyrene material after incubation with these isolates. Growth studies suggested that the Exiguobacterium strains utilize polystyrene as a carbon source. Moreover, our data suggest that polymer degradation was initiated by biofilm formation over the PS surface leading to alteration in the physical properties of the material. Surface property analysis by AFM revealed significantly enhanced roughness resulting in reduced surface hydrophobicity of polystyrene. Fourier-transfer infrared (FT-IR) spectroscopic analysis showed breakdown of polystyrene backbone by oxidation. The extent of deterioration was further determined by percent weight reduction of polystyrene after incubation with bacteria. Our data support the fact that strains of extremophile bacterium Exiguobacterium are capable of degrading polystyrene and can be further used to mitigate the environmental pollution caused by plastics.

Single-step synthesis of core-shell diamond-graphite hybrid electrodes is demonstrated by a mere variation of CH4 concentration (CC) in the microwave growth plasma. The excellent electrochemical stability of diamond and high surface area/electrical conductivity of graphite make the hybrid electrode suitable for supercapacitor application. The supercapacitor study of the hybrid electrode is carried out using both aqueous and redox species contained electrolytes. A brilliant supercapacitor performance (specific capacitance 0.19 F cm−2) with high energy and power density and remarkable electrode retention (96% after 10,000 cycles) is obtained and discussed in the light of different electrochemical techniques such as cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. The supercapacitor performance is explained by analyzing the microstructural evolution of diamond films from a well-faceted geometry dominated with pure diamond phase to an entirely different needle-like structure having diamond-graphite mixed phase. The CC-dependent phase transition is confirmed by X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy study. Finally, the core-shell structure of the hybrid nano-needles is confirmed by transmission electron microscopy investigations.

Electrochemical biosensors employing nano-transduction surfaces are considered highly sensitive to the morphology of nanomaterials. Various interfacial parameters namely charge transfer resistance, double layer capacitance, heterogeneous electron transfer rate and diffusion limited processes, depend strongly on the nanostructure geometry which eventually affects the biosensor performance. The present work deals with a comparative study of electrochemical impedance-based detection of L-tyrosine (or simply tyrosine) by employing carbon nanostructures (graphene quantum dots, single walled carbon nanotubes (CNTs) and graphene) along with tyrosinase as the bio-receptor. Specifically, the role of carbon nanostructures (i.e. 0D, 1D and 2D) on charge transfer resistance is investigated by applying time-varying electric field at the nano-bioelectrode followed by calculating the heterogeneous electron transfer rate, double layer capacitor current and their effects on limits of detection and sensitivities towards tyrosine recognition. A theoretical model based on Randel’s equivalent circuit is proposed to account for the redox kinetics at various carbon nanostructure/enzyme hybrid surfaces. It was observed that, the 1D morphology (single walled CNTs) exhibited lowest charge transfer resistance ∼2.62 kΩ (lowest detection limit of 0.61 nM) and highest electron transfer rate ∼0.35 μm s−1 (highest sensitivity 0.37 kΩ nM−1 mm−2). Our results suggest that a suitable morphology of carbon nanostructure would be essential for efficient and sensitive detection of tyrosine.

We have studied the optimum deposition conditions for the improvement of oxygen and carbon dioxide gas barrier performance of functional diamond-like carbon (DLC) thin films. The a-C:H: a-C:H:Si, a-C:H:N and ta-C:N thin films with 10–400 nm thickness were deposited on polyethylene terephthalate (PET) substrates by the radio frequency plasma-enhanced chemical vapour deposition method. To study the microstructure of the PET coated films, we have used the Raman spectroscopy, X-ray photoelectron spectroscopy, nano-indentation and surface profilometry. The gas barrier property were analysed and found that the a-C:H:N's are 5–10 times better gas barrier properties than that of uncoated PET substrates. These thin layer PET coated thin films could be use in food packaging and biomedical applications.

One-dimensional diamond nanorods (DNRs) were fabricated from nanocrystalline diamond films using a facile combination of microwave plasma enhanced chemical vapor deposition and reactive ion etching (RIE) techniques. Structural and electrochemical properties of undoped and nitrogen doped DNRs were thoroughly investigated. A cyclic voltammetry study revealed the increase in density of charge carriers when doped with nitrogen. Mott Schottky analysis was implemented for the quantitative determination of the flat band potential, effective density of charge carriers and energy band diagram, which revealed that the undoped sample exhibit p-type behavior, whereas the nitrogen doped sample showed n-type behavior. Defect related damage due to graphitization and hydrogen termination in the undoped DNRs (during RIE) was correlated with the p-type conductivity. Nitrogen doping induces n-type conductivity and enhances effective density of charge carriers.

In this article, we report the modification of the electronic and magnetic properties of few-layered graphene (FLG) nanoflakes by nitrogen functionalization carried out using radio-frequency plasma-enhanced chemical vapor deposition (rf-PECVD) and electron cyclotron resonance (ECR) plasma processes. Even though the rf-PECVD N2 treatment led to higher N-doping levels in the FLG (4.06 atomic %) as compared to the ECR process (2.18 atomic %), the ferromagnetic behavior of the ECR FLG (118.62 × 10–4 emu/g) was significantly higher than that of the rf-PECVD FLG (0.39 × 10–4 emu/g) and pristine graphene (3.47 × 10–4 emu/g). Although both plasma processes introduce electron-donating N atoms into the graphene structure, distinct dominant nitrogen bonding configurations (pyridinic, pyrrolic) were observed for the two FLG types. Whereas the ECR plasma introduced more sp2-type nitrogen moieties, the rf-PECVD process led to the formation of sp3-coordinated nitrogen functionalities, as confirmed through Raman measurem...

The thermal stability and tribological performance of silicon- and oxygen-incorporated diamond-like carbon (DLC) and silicon doped-DLC films were investigated. The DLC and DLC:Si are deposited on various (silicon, stainless steel and aluminium) substrates within the thickness range 200–400 nm by radio frequency plasma-enhanced chemical vapour deposition (PECVD) method. Carbon dioxide (CO2) precursor gas is used to reduce the hydrogen content and to increase the adhesion of the films to the substrate. The X-ray photoelectron spectroscopy, Raman spectroscopy, surface profilometry and nano-indentation are used to study the chemical composition, microstructure, thermal stability and mechanical properties of the films. For CO2 precursor made DLC samples, Raman parameters did not show any significant change up to temperature 500 °C. The lowest coefficient of friction was found to be 0.298 for the DLC:Si film prepared with CO2 at room temperature and corresponded lowest wear rate of 1.77 × 10− 10 mm3/Nm. The micro-structural properties at various annealing temperature were critically analysed by monitoring graphitization behaviour and oxidation of the film surface.

This work describes a simple wet chemical synthesis of iron oxide (Fe3O4) nanoparticles (NPs) capped with terephthalic acid (TA) and their application for the individual detection of Hg(II), Pb(II) and Cd(II) ions as well as simultaneous and selective detection of Hg(II), Pb(II) and Cd(II) ions by electrochemical approach. Terephthalic acid capped Fe3O4 NPs were first characterized by cyclic voltammetry (CV) using redox couples Fe(CN)63 −/4 −, thereafter square wave anodic stripping voltammetry (SWASV) was utilized for the detection of Hg(II), Pb(II) and Cd(II) ions. Optimization of experimental parameters such as deposition time, deposition potential and pH value of the electrolyte towards electrochemical detection of target heavy metal ions was also carried out in SWASV method. Under optimized experimental conditions limit of detection (LOD) values for individual analysis of Hg(II), Pb(II) and Cd(II) ions were found to be 0.1, 0.05 μM and 0.01 μM respectively, whereas the LOD values for the simultaneous analysis of Hg(II), Pb(II) and Cd(II) ions were found to be 0.3 μM, 0.04 μM and 0.2 μM respectively.

Titania–zeolite Y composites were synthesized by a facile solid-state dispersion method. The synergistic effects of porous zeolite structure and novel photocatalysis properties of titania nanoparticles were exploited. The physical properties of the composites were characterized by scanning electron microscopy, energy-dispersive X-ray, X-ray diffraction, diffuse reflectance spectroscopy, fourier transform infra-red spectroscopy and photoluminescence spectroscopy. Porosity and surface area of the composites were determined from Brunauer–Emmett–Teller studies. The antibacterial effect and the photocatalysis properties of these composites were studied. Composites exhibited higher growth reduction of Escherichia coli and Staphylococcus aureus as compared with the pure forms (P25 titania and zeolite Y). Maximum growth reduction of both types of bacterial cells (gram-positive as well as gram-negative) was observed with 20% titania–zeolite composite. The composite demonstrated 40 and 30% enhancement in the growth reduction of E. coli and S. aureus, respectively, as compared with the pure forms; 10% composite exhibited 50% enhancement in the photocatalysis efficiency of methylene blue dye degradation as compared with P25 titania nanoparticles and led to a complete removal of the dye in the first 60 min of photocatalysis process. Mechanisms for both applications have been proposed in light of the observed results.

Disposable devices for sensing biomarkers like Na+ ion in sweat was developed using UV-Ozone irradiated laser-induced graphene (LIG) based electrodes. Solid-state ion-selective electrodes (ISEs) sensitive to Na+ ions were fabricated by a two-step drop-coating process of polyvinyl chloride solution containing plasticizer, ionophore and ion-exchanger on LIG electrode. Hydrophobic to hydrophilic transition induced by UV-Ozone treatment reduced the contact angle, resulting in better permeation of the ion-selective membrane into the ozonized LIG film. Raman spectroscopy and IR absorption studies indicate physisorption of ozone on LIG. Performance of ozonized LIG (O-LIG) electrodes was much better than pristine LIG and screen-printed carbon electrodes. Sensitivity of 60.2 ± 0.9 mV/ decade to Na+ ions and a lower limit of detection of 1 × 10−6 M was achieved using O-LIG based ISEs. Response time of the devices were around 1 min.

Recent studies shows laser-induced graphene (LIG) based electrodes can be very effective for electrochemical sensing applications. In this work, we aim to develop a stable ion selective membrane (ISM) based sweat sensor using laser-induced graphene (LIG) as the electrode material. However, the surface of pristine LIG is hydrophobic. Hence, coating these hydrophobic LIG films with ISM produces low sensitivity in sensing applications. In this study, UV-Ozone irradiated laser-induced graphene (LIG) based electrodes were explored for sensing biomarkers like ion in sweat. Solid-state ion-selective electrodes (ISEs) sensitive to ions were fabricated by a two-step drop-coating process of polyvinyl chloride solution containing plasticizer, ionophore, and ion-exchanger on the LIG electrode. We found the ozone treatment process significantly increased the electrochemical active surface area (EASA) and porosity of the pristine LIG. Hydrophobic to hydrophilic transition induced by UV-Ozone treatment reduced the contact angle (CA), resulting in better permeation of the ion-selective membrane (ISM) into the ozonized LIG film. Raman spectroscopy and IR absorption studies indicate physisorption of ozone on LIG. The concentration of the ISM solution has a great influence on attachment to the O-LIG film. Here, we report the applicability of O-LIG as an electrochemical sensor towards the detection of sodium ion () using the open circuit potential (OCP) method. The performance of ozonized LIG (O-LIG) electrodes was much better than pristine LIG and screen printed carbon electrodes. The sensitivity of 60.2 ± 0.9 mV/ decade to Na+ ions and a lower limit of detection of 1 × 10-6 M was achieved using O-LIG based ISEs. Response time of the O-LIG based electrodes were around 1 min. The current study demonstrates that the LIG-based electrodes can be used as a flexible electrochemical sensing platform and is suitable for future wearable sensing devices. Keywords Laser-induced graphene; ion-selective electrode; wearable sensors; electrochemical sensor; sweat sensor.

3-D vertically aligned few-layered graphene (FLGs) nanoflakes synthesised using microwave plasma enhanced chemical vapour deposition are melt-impregnated with partially reduced graphene oxide-sulfur (PrGO-S) nanocomposites for use in lithium–sulfur batteries. The aligned structure and the presence of interconnected micro voids/channels in the 3-D FLG/PrGO-S electrodes serves as template not only for the high sulfur loading (up to 80 wt%, areal loading of 1.2 mg cm−2) but also compensates for the volume changes occurring during charge–discharge cycles. The inter-connectivity of the electrode system further facilitates fast electronic and ionic transport pathways. Consequently, the binder-free 3-D FLG/PrGO-S electrodes display a high first-cycle capacity (1320 mA h g−1 at C/20), along with excellent rate capability of ∼830 mA h g−1 and 700 mA h g−1 at 2C and 5C rates, respectively. The residual functional groups of PrGO (–OH, –C–O–C– and –COOH) facilitate fast and reversible capture of Li+ ions while confining the polysulfide shuttles, thus, contributing to excellent cycling capability and retention capacity. The 3D electrodes demonstrate excellent capacity retention of ∼80% (1040 mA h g−1 at C/10) over 350 charge–discharge cycles. Comparatively, the 2-D planar PrGO-S electrodes displayed poor electronic conductivity and can only provide 560 mA h g−1 after 150 cycles, thereby further highlighting the vital role of the electrode morphology in improving the electrochemical performance of Li–S batteries.

A novel nanocomposite consisting of π-conjugated 2-aminoterephthalic acid (ATA) coated iron oxide (Fe3O4) nanoparticles and reduced graphene oxide (RGO) has been synthesized using a facile combination of wet-chemistry and low-power sonication. The ATA–Fe3O4/RGO nanocomposites exhibited a high specific capacitance of the order of 576 F g−1; significantly higher than that of pristine Fe3O4 (132 F g−1) and RGO (60 F g−1) counterparts, indicative of a synergistic effect between the ATA–Fe3O4 and RGO components. Furthermore, the maximum energy storage density was calculated to be 75 W h kg−1 (at a current density of 6 A g−1). The charging–discharging analysis showed promising long-term stability with nearly 86% retention of the capacitance after 5000 cycles. The superior capacitive behaviour of these ATA–Fe3O4/RGO nanocomposites is attributed to the synergistic effect of the π-conjugated ATA coating on Fe3O4 which enhances the pseudo-capacitive charge transfer process of Fe3O4 and works in conjunction with the surface functional groups (such as carboxylic, amino and amide) present on the RGO surface, providing enhanced double layer capacitance. Thus, the current system exploits the advantages of both the double layer capacitors and pseudocapacitors in a hybrid structure.

In the present work, the suitability of Aloe vera (AV) as a ‘green reducing agent’ has been investigated for the reduction of graphene oxide (GO). The extent of reduction was studied by varying the amount of AV. The physical and chemical properties of the GO and reduced graphene oxide (rGO) were investigated using UV-Vis spectrophotometry, FT-IR spectroscopy, High Resolution Transmission Electron Microscopy (HRTEM) and Selected Area Electron Diffraction (SAED). Partially reduced graphene oxide sheets obtained with 7.5 g of AV (rGO-7.5) demonstrated a maximum reduction efficiency of about 73% as evident from FT-IR data. Cyclic voltammetry and electrochemical impedance spectroscopy studies revealed a significant enhancement in current density and a decrease in charge transfer resistance for the rGO-7.5 sample. Moreover, the as prepared rGO-7.5 sample showed a remarkable dye removal ability with a maximum efficiency of ∼98%. The enhanced surface area, π–π interaction and strong electrostatic attraction were correlated with the dye removal capability. The adsorption kinetics were also studied and pseudo second order adsorption phenomena were confirmed. The recyclability of the rGO-7.5 sample was further investigated and an excellent desorption capability was established.

In this paper, a theoretical model is developed to investigate the performance of the hybrid solar thermoelectric generator (HSTEG) system, which is designed without (B-HSTEG) and with an evacuated glass tube (V-HSTEG). The heat loss, power output, thermal efficiency, and electrical efficiency of the B-HSTEG/V-HSTEG system are evaluated by analyzing the design parameters such as geometric solar concentration ratio, thermoelectric figure of merit, and cold-side inlet fluid temperature. The performance of the B-HSTEG is compared with the V-HSTEG system using two heat transfer fluids: water and Therminol VP-1. The maximum electrical efficiency of the B-HSTEG and V-HSTEG is estimated to be 12.2 and 15.6% (ZT = 3) with a corresponding thermal efficiency of about 61.9 and 60.3%, respectively. Overall, this paper provides a systematic performance analysis of HSTEG systems.

Metals (Zr, Zn and Cu) containing oil swollen surfactant gels have been utilized as precursors for the preparation of metal oxides (ZrO2, ZnO and CuO) nanoparticles. No metal alkoxide, external gelating agent or any other intricate molecule have been utilized to reinforce gelation; gel stage has been achieved simply through judicial adjustment of water to surfactant ratio and salinity of the reaction mixture. Unlike, several previously published reports, in this approach surfactant has been added not to just increase the viscosity of solution but it has also formed rod shaped gelatinous micelles in response to the variation in water to surfactant ratio, which endowed mechanical strength to the gel. The effect of nature of metal salt on mechanical properties of gel has also been investigated. Zn and Cu containing cetyltrimethylammonium bromide (CTAB) gels have been found to be strongest and weakest, respectively. Metal containing CTAB gels were heat treated at various temperatures (600, 700 and 800 °C) in order to obtain metal oxides nanoparticles. The effect of calcination temperature on crystallinity, particle size and morphology of the metal oxides nanoparticles has also been investigated. A comparison between ZrO2 nanoparticles prepared using conventional sol gel and oil swollen surfactant gel method has also been carried out in terms of crystallinity, particle size and optical property.