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Solar-driven photocatalysis offers an environmentally friendly and sustainable approach for the removal of air pollutants such as nitric oxides without chemical addition. However, the low specific surface area and adsorption capacity of common photocatalysts restrict the surface reactions with NO at the ppb-level. In this study, imidazolium-based hyper-cross-linked polymer (IHP) was introduced to modify the surface of TiO 2 to construct a porous TiO 2 /IHP composite photocatalyst. The as-prepared composite with hierarchical porous structure achieves a larger specific surface area as 309 m 2 /g than that of TiO 2 (119 m 2 /g). Meanwhile, the wide light absorption range of the polymer has brought about the strong visible-light absorption of the TiO 2 /IHP composite. In consequence, the composite photocatalyst exhibits excellent performance toward NO oxidation at a low concentration of 600 ppb under visible-light irradiation, reaching a removal efficiency of 51.7%, while the generation of the toxic NO 2 intermediate was suppressed to less than 1 ppb. The enhanced NO adsorption and the suppressed NO 2 generation on the TiO 2 /IHP surface were confirmed by in situ monitoring technology. This work demonstrates that the construction of a porous structure is an effective approach for efficient NO adsorption and photocatalytic oxidation.

An alternative electrosynthesis of PdTe, using the electrochemical atomic layer deposition (E-ALD) method, is reported. The cyclic voltammetry technique was used to analyze Au substrate in copper (Cu 2+ ), and a tellurous (Te 4+ ) solution was used to identify UPDs and set the E-ALD cycle program. Results obtained using atomic force microscopy (AFM) and scanning electron microscopy (SEM) techniques reveal the nanometer-sized flat morphology of the systems, indicating the epitaxial characteristics of Pd and PdTe nanofilms. The effect of the Pd:Te ratio on the crystalline structure, electronic properties, and magnetic properties was investigated using a combination of density functional theory (DFT) and X-ray diffraction techniques. Te-containing electrocatalysts showed improved peak current response and negative onset potential toward ethanol oxidation (5 mA; -0.49 V) than Pd (2.0 mA; -0.3 V). Moreover, DFT ab initio calculation results obtained when the effect of Te content on oxygen adsorption was studied revealed that the d-band center shifted relative to the Fermi level: -1.83 eV, -1.98 eV, and -2.14 eV for Pd, Pd 3 Te, and Pd 3 Te 2 , respectively. The results signify the weakening of the CO-like species and the improvement in the PdTe catalytic activity. Thus, the electronic and geometric effects are the descriptors of Pd 3 Te 2 activity. The results suggest that Pd 2 Te 2 is a potential candidate electrocatalyst that can be used for the fabrication of ethanol fuel cells.

Purification and detection of algal toxins is the most effective technique to ensure that people have clean and safe drinking water. To achieve these objectives, various state-of-the-art technologies were designed and fabricated to decontaminate and detect algal toxins in aquatic environments. Amongst these technologies, aptamer-functionalized hybrid nanomaterials conjugates have received significant consideration as a result of their several benefits over other methods, such as good controllable selectivity, low immunogenicity, and biocompatibility. Because of their excellent properties, aptamer-functionalized hybrid nanomaterials conjugates are one of several remarkable agents. Several isolated aptamer sequences for algal toxins are addressed in this review, as well as aptasensor and decontamination aptamer functionalized metal nanoparticle-derived hybrid nanocomposites applications. In addition, we present diverse aptamer-functionalized hybrid nanomaterial conjugates designs and their applications for sensing and decontamination., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)

Pt-supported carbon material-based electrocatalysts are formidably suffering from carbon corrosion when H 2 O and O 2 molecules are present at high voltages in polymer electrolyte membrane fuel cells (PEMFCs). In this study, we discovered that the edge site of a fluorine-doped graphene nanoribbon (F-GNR) was slightly adsorbed with H 2 O and was thermodynamically unfavorable with O atoms after defining the thermodynamically stable structure of the F-GNR from DFT calculations. Based on computational predictions, the physicochemical and electrochemical properties of F-GNRs with/without Pt nanoparticles derived from a modified Hummer's method and the polyol process were investigated as support materials for electrocatalysts and additives in the cathode of a PEMFC, respectively. The Pt/F-GNR showed the lowest degradation rate in carbon corrosion and was effective in the cathode as additives, resulting from the enhanced carbon corrosion durability owing to the improved structural stability and water management. Notably, the F-GNR with highly stable carbon corrosion contributed to achieving a more durable PEMFC for long-term operation.

Carbon dioxide (CO 2 ) is considered a useful greenhouse gas that can be captured and be used in the electro-syntheses of useful chemicals or fuels. On the other hand, there's also a tremendous interest on ethanol beneficiation as it is largely produced from crops, and it is regarded as a potential candidate for low temperature fuel cell applications. Although ethanol possesses good advantages, its resistant to oxidation poses a threat. The main objective of the study is to synthesis bio-inspired metal oxide-support catalyst which will help enhance the activity, efficiency and selectivity of Pd catalyst in CO 2 reduction, Fuel cell performance and ethanol oxidation. Here, Pd nanoparticles were supported on NiO/C through a green facile one-step process using pomegranate peel extracts as reducing agent. A series of characterizations were carried out to provide proof for and to quantify the presence of Pd, Ni, O and C in the prepared sample. Microscopic methods confirmed the successful preparation of pure NiO/C and (%5 Pd) Pd-NiO/C, evident by the key elemental components, mixed nanostructures and co-existence of Pd and NiO/C. The resultant Pd-NiO/C nanocatalyst revealed higher activity towards the oxidation of ethanol and that the nanocatalyst is more tolerant to poising by intermediate oxidation species. Enhanced cell performance with current and power densities of 66 mA cm -2 and 26 mW cm -2 relative to the commercial Pd/C were obtained under passive conditions at 1 M ethanol in 1MKOH. In addition, the nanocatalyst showed good selectivity to HCOOH with enhanced current efficiencies of 45%., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Recent studies have suggested that certain nanomaterials can interfere with optically based cytotoxicity assays resulting in underestimations of nanomaterial toxicity. As a result there has been growing interest in the use of whole cell electrochemical biosensors for nanotoxicity applications. Herein we report application of an electrochemical cytotoxicity assay developed in house (TOXOR) in the evaluation of toxic effects of mercaptosuccinic acid capped cadmium telluride quantum dots (MSA capped CdTe QDs), toward mammalian cells. MSA capped CdTe QDs were synthesized, characterized, and their cytotoxicity toward A549 human lung epithelial cells investigated. The internalization of QDs within cells was scrutinized via confocal microscopy. The cytotoxicity assay is based on the measurement of changes in cellular enzyme acid phosphatase upon 24 h exposure to QDs. Acid phosphatase catalyzes dephosphorylation of 2-naphthyl phosphate to 2-naphthol (determined by chronocoulometry) and is indicative of metabolic activity in cells. The 24 h IC50 (concentration resulting in 50% reduction in acid phosphatase activity) value for MSA capped CdTe QDs was found to be 118 ± 49 μg/mL using the TOXOR assay and was in agreement with the MTT assay (157 ± 31 μg/mL). Potential uses of this electrochemical assay include the screening of nanomaterials, environmental toxins, in addition to applications in the pharmaceutical, food, and health sectors.

An electrochemical method based on a cytochrome c biosensor was developed, for the detection of selected arsenic and cyanide compounds. Boron doped diamond (BDD) electrode was used as a transducer, onto which cytochrome c was immobilised and used for direct determination of Prussian blue, potassium cyanide and arsenic trioxide. The sensitivity as calculated from cyclic voltammetry (CV) and square wave voltammetry (SWV), for each analyte in phosphate buffer (pH=7) was found to be in the range of (1.1-4.5)×10(-8) A μM(-1) and the detection limits ranged from 4.3 to 9.1 μM. The biosensor is therefore able to measure significantly lower than current Environmental Protection Agency (EPA) and World Health Organisation (WHO) guidelines, for these types of analytes. The protein binding was monitored as a decrease in biosensor peak currents by SWV and as an increase in biosensor charge transfer resistance by electrochemical impedance spectroscopy (EIS). EIS provided evidence that the electrocatalytic advantage of BDD electrode was not lost upon immobilisation of cytochrome c. The interfacial kinetics of the biosensor was modelled as equivalent electrical circuit based on electrochemical impedance spectroscopy data. UV-vis spectroscopy was used to confirm the binding of the protein in solution by monitoring the intensity of the soret bands and the Q bands. FTIR was used to characterise the protein in the immobilised state and to confirm that the protein was not denatured upon binding to the pre-treated bare BDD electrode. SNFTIR of cyt c immobilised at platinum electrode, was used to study the effect of oxidation state on the surface bond vibrations. The spherical morphology of the immobilised protein, which is typical of native cytochrome c, was observed using scanning electron microscopy (SEM) and confirmed the immobilisation of the cytochrome c without denaturisation., (Copyright © 2012 Elsevier B.V. All rights reserved.)