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Zinc (Zn) is an excellent material for use as an anode for rechargeable batteries in water-based electrolytes. Nevertheless, the high activity of water leads to Zn corrosion and hydrogen evolution, along with the formation of dendrites on the Zn surface during repeated charge-discharge (CD) cycles. To protect the Zn anode and limit parasitic side reactions, an artificial solid electrolyte interphase (ASEI) protective layer is an effective strategy. Herein, an ASEI made of a covalent organic framework (COFs: HqTp and BpTp) was fabricated on the surface of a Zn anode via Schiff base reactions of aldehyde and amine linkers. It is seen that COFs can regulate the Zn-ion flux, resulting in dendritic-free Zn. COFs can also mitigate the formation of an irreversible passive layer and the hydrogen evolution reaction (HER). Zn plating/stripping tests using a symmetrical cell suggest that HqTpCOF@Zn shows superior stability and greater coulombic efficiency (CE) compared to bare Zn. The full cell having COFs@Zn also displays much improved cyclability. As a result, the COF proves to be a promising ASEI material to enhance the stability of the Zn anode in aqueous media.

This study successfully created a portable acetylcholinesterase sensor on a printed hybrid electrode capable of detecting chlorpyrifos in the field. While a screen-printed electrode was chosen herein to enable a single-use and portable platform for the in-field application, the hybrid material was incorporated to ensure ultrasensitive detection at lower electrode potentials. The hybrid ink of gold nanoparticles (AuNPs) decorated on graphene (GP) sheets in poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) was synthesized through a simple completely-green one-pot process. The subsequent characterization was carried out via transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR). The synergy resulting from the greater surface area and enhanced transfer of electrons combined with high levels of electrocatalytic activity and superb conductivity offered by GP, AuNP, and PEDOT:PSS allows the sensor to exhibit ultrasensitive chlorpyrifos detection at the relatively low detection limit of 0.07 nM. The sensor demonstrated in this study also exhibits good reproducibility, desirable stability, and a successful application for the real sample with satisfactory recovery results of around 106 %, indicating its potential for use as a tool in the analysis of pesticides., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Sulfur composites consisting of electrochemical reactive catalysts/conductive materials are investigated for use in lithium-sulfur (Li-S) batteries (LSBs). In this paper, we report the synthesis, physicochemical and electrochemical properties of CuZnS quantum dots (CZSQDs) decorated with nickel-cobalt-sulfide ((NiCo)-S)) mixed with reduced graphene oxide (rGO)/oxidized carbon nanotube (oxdCNT) (rGO/oxdCNT) ((NiCo)-S@rGO/oxdCNT) composites. These composites are for the purpose of being the sulfur host cathode in Li-S batteries. The as-prepared composites showed a porous structure with the CZSQDs being uniformly found on the surface of the rGO/oxdCNT, which had a specific surface area of 26.54 m 2 /g. Electrochemical studies indicated that the (NiCo)-S@rGO/oxdCNT cells forming the cathode exhibited a maximum capacity of 1154.96 mAhg -1 with the initial discharge at 0.1 C. The smaller size of the CZSQDs (~10 nm) had a positive effect on the CZSQDs@(NiCo)-S@rGO/oxdCNT composites in that they had a higher initial discharge capacity of 1344.18 mAhg -1 at 0.1 C with the Coulombic efficiency being maintained at almost 97.62% during cycling. This latter property is approximately 1.16 times more compared to the absence of the Cu-Zn-S QD loading. This study shows that the CuZnS quantum dots decorated with a (NiCo)-S@rGO/oxdCNT supporting matrix-based sulfur cathode have the potential to improve the performance of future lithium-sulfur batteries.

Aqueous zinc-ion batteries (ZIBs) with exceptional safety and cost-effective features have captured researchers' attention, but the cathode materials available still need to be further explored. Herein, a flower-like W/WO 3 hybrid is developed as a cathode of ZIBs. Impressively, the W/WO 3 -ZIBs exhibit extraordinary rate performance (158 mA h g -1 under 0.1 A g -1 ) and remarkable cycling performance (96% over 1000 cycles). Additionally, an electrochemical mechanism based on reversible Zn 2+ insertion/extraction in W/WO 3 is firstly demonstrated, and the impressive flexibility and excellent capabilities of the soft-packaged batteries are also realized. Therefore, this research will pave a novel consideration of metal/metal oxide hybrids in designing cathodes of ZIBs with high electrochemical performance.

Electrowetting-on-dielectric (EWOD) is a microfluidic technology used for manipulating liquid droplets at microliter to nanoliter scale. EWOD has the ability to facilitate the accurate manipulation of liquid droplets, i.e., transporting, dispensing, splitting, and mixing. In this work, EWOD fabrication with suitable and affordable materials is proposed for creating EWOD lab-on-a-chip platforms. The EWOD platforms are applied for the diagnosis of early mortality syndrome (EMS) in shrimp by utilizing the colorimetric loop-mediated isothermal amplification method with pH-sensitive xylenol orange (LAMP-XO) diagnosis technique. The qualitative sensitivity is observed by comparing the limit of detection (LOD) while performing the LAMP-XO diagnosis test on the proposed lab-on-a-chip EWOD platform, alongside standard LAMP laboratory tests. The comparison results confirm the reliability of EMS diagnosis on the EWOD platform with qualitative sensitivity for detecting the EMS DNA plasmid concentration at 10 2 copies in a similar manner to the common LAMP diagnosis tests.

α-MnO 2 nanofibers combined with nitrogen and sulfur co-doped reduced graphene oxide (α-MnO 2 /N&S-rGO) were prepared through simple hydrothermal and ball milling processes. Structural characterization results by X-ray diffraction, X-ray photoemission spectroscopy, electron microscopy and Raman spectroscopy demonstrated that α-MnO 2 nanofibers with the average diameter of ~40 nm were well dispersed on N&S-rGO nanoflakes. The synthesized material was incorporated into supercapacitor (SC) electrodes and assembled with the quasi-solid-state electrolyte comprising N,N-Diethyl-N-methyl-N-(2-methoxy-ethyl)ammonium bis (trifluoromethyl-sulfonyl)amide [DEME][TFSA]/polyvinylidene fluoride-hexafluoropropylene (PVDF-co-HFP) to produce coin-cell SCs. Electrochemical performances of SCs were measured by cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. From the electrochemical data, SC using α-MnO 2 /N&S-rGO exhibited a good specific capacitance of 165F g -1 at 0.25 A g -1 with a wide potential window of 0-4.5 V, corresponding to a high energy density of 110 Wh kg -1 and a power density of 550 W kg -1 . In addition, it exhibited good electrochemical stability with a capacitance retention of 75% after 10,000 cycles at 1 A g -1 and a low self-discharge loss. The attained energy-storage performances indicated that the α-MnO 2 /N&S-rGO composite could be highly promising for high-performance ionic liquid-based quasi solid-state supercapacitors., Competing Interests: Declaration of Competing Interest The authors declared that there is no conflict of interest., (Copyright © 2020. Published by Elsevier Inc.)

Fully printable perovskite solar cells (PPSCs) attract attention in the photovoltaic industry and research owing to their controllable and scalable production with reduced material waste during manufacturing. However, the commercialization of PPSCs has been impeded by their inherent vulnerability to ambient moisture, leading to a rapid loss of device efficiency and lifetime. Here, we propose a novel idea to enhance the photovoltaic performance and stability of PPSCs in humid air (relative humidity exceeding 80%) using electrospun hydrophobic polymer membranes, i.e., polylactic acid (PLA), polycaprolactone (PCL), and PLA/PCL blends, as moisture-resistant layers for PPSCs. After optimizing the morphologies, hydrophobicity, and thermal properties of the electrospun membranes by varying the contents of the polymer components in the membranes, the unencapsulated devices with these membranes demonstrated power conversion efficiencies of up to 8.2%, which was significantly higher than for devices without the membranes (6.8%). Moreover, devices with the optimum electrospun membrane retained more than 85% of their original efficiency after being stored in humid air for over 35 days. In comparison, devices without the electrospun membranes lost about 50% of their initial efficiency over the same time. Our work is very useful for the development of highly efficient and stable commercial PPSCs.

A molecularly imprinted polymer (MIP) and a nanocomposite prepared from gold nanoparticles (AuNP) and poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT:PSS) were deposited on a screen-printed carbon electrode (SPCE). The nanocomposite was prepared by one-pot simultaneous in-situ formation of AuNPs and PEDOT:PSS and was then inkjet-coated onto the SPCE. The MIP film was subsequently placed on the modified SPCE by co-electrodeposition of o-phenylenediamine and resorcinol in the presence of the antibiotic nitrofurantoin (NFT). Using differential pulse voltammetry (DPV), response at the potential of ~ 0.1 V (vs. Ag/AgCl) is linear in 1 nM to 1000 nM NFT concentration range, with a remarkably low detection limit (at S/N = 3) of 0.1 nM. This is two orders of magnitude lower than that of the control MIP sensor without the nanocomposite interlayer, thus showing the beneficial effect of AuNP-PEDOT:PSS. The electrode is highly reproducible (relative standard deviation 3.1% for n = 6) and selective over structurally related molecules. It can be re-used for at least ten times and was found to be stable for at least 45 days. It was successfully applied to the determination of NFT in (spiked) feed matrices and gave good recoveries. Graphical abstract Schematic representation of a voltammetric sensor for the determination of nitrofurantoin. The sensor is based on a screen-printed carbon electrode (SPCE) modified with an inkjet-printed gold nanoparticles-poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) nanocomposite and a molecularly imprinted polymer.

A facile one-pot and green method was developed to prepare a nanocomposite of gold nanoparticle (AuNP), graphene (GP) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). Graphene was first electro-exfoliated in a polystyrene sulfonate solution, followed by a one-step simultaneous in situ formation of gold nanoparticle and PEDOT. The as-synthesized aqueous dispersion of AuNP-GP-PEDOT:PSS was thereafter used to modify the glassy carbon electrode (GCE). For the first time, the quaternary composite between AuNP, GP, PEDOT and PSS was used for selective determination of dopamine (DA) and uric acid (UA) in the presence of ascorbic acid (AA). In comparison to a bare GCE, the nanocomposite electrode shows considerably higher electrocatalytic activities toward the oxidation of DA and UA due to a synergistic effect between AuNP, GP, PEDOT and PSS. Using differential pulse voltammetry (DPV), selective determination of DA and UA in the presence of AA could be achieved with a peak potential separation of 110 mV between DA and UA. The sensor exhibits wide linear responses for DA and UA in the ranges of 1 nM to 300 μM and 10 μM to 1 mM with detection limits (S/N = 3) of 100 pM and 10 μM, respectively. Furthermore, the proposed sensor was also successfully used to determine DA in a real pharmaceutical injection sample as well as DA and UA in human serum with satisfactory recovery results., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

In this work, flame-spray-made undoped SnO2 nanoparticles were loaded with 0.1-5 wt % electrolytically exfoliated graphene and systematically studied for NO2 sensing at low working temperatures. Characterizations by X-ray diffraction, transmission/scanning electron microscopy, and Raman and X-ray photoelectron spectroscopy indicated that high-quality multilayer graphene sheets with low oxygen content were widely distributed within spheriodal nanoparticles having polycrystalline tetragonal SnO2 phase. The 10-20 μm thick sensing films fabricated by spin coating on Au/Al2O3 substrates were tested toward NO2 at operating temperatures ranging from 25 to 350 °C in dry air. Gas-sensing results showed that the optimal graphene loading level of 0.5 wt % provided an ultrahigh response of 26,342 toward 5 ppm of NO2 with a short response time of 13 s and good recovery stabilization at a low optimal operating temperature of 150 °C. In addition, the optimal sensor also displayed high sensor response and relatively short response time of 171 and 7 min toward 5 ppm of NO2 at room temperature (25 °C). Furthermore, the sensors displayed very high NO2 selectivity against H2S, NH3, C2H5OH, H2, and H2O. Detailed mechanisms for the drastic NO2 response enhancement by graphene were proposed on the basis of the formation of graphene-undoped SnO2 ohmic metal-semiconductor junctions and accessible interfaces of graphene-SnO2 nanoparticles. Therefore, the electrolytically exfoliated graphene-loaded FSP-made SnO2 sensor is a highly promising candidate for fast, sensitive, and selective detection of NO2 at low operating temperatures.

In this work, flame-spray-made SnO2 nanoparticles are systematically studied by doping with 0.1-2 wt % nickel (Ni) and loading with 0.1-5 wt % electrolytically exfoliated graphene for acetone-sensing applications. The sensing films (∼12-18 μm in thickness) were prepared by a spin-coating technique on Au/Al2O3 substrates and evaluated for acetone-sensing performances at operating temperatures ranging from 150 to 350 °C in dry air. Characterizations by X-ray diffraction, transmission/scanning electron microscopy, Brunauer-Emmett-Teller analysis, X-ray photoelectron spectroscopy and Raman spectroscopy demonstrated that Ni-doped SnO2 nanostructures had a spheriodal morphology with a polycrystalline tetragonal SnO2 phase, and Ni was confirmed to form a solid solution with SnO2 lattice while graphene in the sensing film after annealing and testing still retained its high-quality nonoxidized form. Gas-sensing results showed that SnO2 sensing film with 0.1 wt % Ni-doping concentration exhibited an optimal response of 54.2 and a short response time of ∼13 s toward 200 ppm acetone at an optimal operating temperature of 350 °C. The additional loading of graphene at 5 wt % into 0.1 wt % Ni-doped SnO2 led to a drastic response enhancement to 169.7 with a very short response time of ∼5.4 s at 200 ppm acetone and 350 °C. The superior gas sensing performances of Ni-doped SnO2 nanoparticles loaded with graphene may be attributed to the large specific surface area of the composite structure, specifically the high interaction rate between acetone vapor and graphene-Ni-doped SnO2 nanoparticles interfaces and high electronic conductivity of graphene. Therefore, the 5 wt % graphene loaded 0.1 wt % Ni-doped SnO2 sensor is a promising candidate for fast, sensitive and selective detection of acetone.