Tuning conductivity while maintaining mechanical properties in perylene bisimide hydrogels at physiological pH.

By using different salts as a method to achieve gelation of two different amino-acid-functionalised perylene bisimides, we were able to tune reduction potentials while maintaining the mechanical and optical properties of the system all at pH 7.4.

Application of quasi solid electrolytes in organic based electrochromic devices: A mini review.

The interest in all solid organic based electrochromic devices (ECDs) is on the increase. This is because these devices offer the applicability of electrochromic materials in products such as smart sensors, smart windows, flexible wearables and energy storage devices. The use of quasi-solid electrolytes for the construction of these ECDs is attractive because of their ease of preparation, availability, low cost, improve electrochromic performance, good ionic conductivity and prevention of leakages in ECDs. Hence, in this review, a detailed discussion is presented on the progress in the development of semi-solid electrolytes for ECDs fabrication. The preparation of the most common electrolytes that have been applied for organic based ECDs are summarized. Particular attention is given to efforts and strategies that have been adopted to improve the efficiency of quasi-solid electrolytes. Importantly, knowledge gaps that warrant further research are clearly identified and recommendations for future works are suggested. This review will be very beneficial for both established and new researchers in the field of electrochromic devices and material science.

Advancements in electrochemical technologies for the removal of fluoroquinolone antibiotics in wastewater: A review.

In recent times, the need to make water safer and cleaner through the elimination of recalcitrant pharmaceutical residues has been the aim of many studies. Fluoroquinolone antibiotics such as ciprofloxacin, norfloxacin, enrofloxacin, and levofloxacin are among the commonly detected pharmaceuticals in wastewater. Since the presence of these pharmaceuticals in water bodies poses serious risks to living organisms, it is vital to adopt effective wastewater treatment techniques for their complete removal. Electrochemical technologies such as photoelectrocatalysis, electro-Fenton, electrocoagulation, and electrochemical oxidation have been established as techniques capable of the complete removal of organics including pharmaceuticals from wastewater. Hence, this review presents discussions on the recent progress (literature within 2018-2022) in the applications of common electrochemical processes for the degradation of fluoroquinolone antibiotics from wastewater. The fundamentals of these processes are highlighted while the results obtained using the processes are critically discussed. Furthermore, the inherent advantages and limitations of these processes in the mineralization of fluoroquinolone antibiotics are clearly emphasized. Additionally, appropriate recommendations are made toward improving electrochemical technologies for the complete removal of these pharmaceuticals with minimal energy consumption. Therefore, this review will serve as a bedrock for future researchers concerned with wastewater treatments to make informed decisions in the selection of suitable electrochemical techniques for the removal of pharmaceuticals from wastewater.

Using Nanomaterials as Excellent Immobilisation Layer for Biosensor Design.

The endless development in nanotechnology has introduced new vitality in device fabrication including biosensor design for biomedical applications. With outstanding features like suitable biocompatibility, good electrical and thermal conductivity, wide surface area and catalytic activity, nanomaterials have been considered excellent and promising immobilisation candidates for the development of high-impact biosensors after they emerged. Owing to these reasons, the present review deals with the efficient use of nanomaterials as immobilisation candidates for biosensor fabrication. These include the implementation of carbon nanomaterials-graphene and its derivatives, carbon nanotubes, carbon nanoparticles, carbon nanodots-and MXenes, likewise their synergistic impact when merged with metal oxide nanomaterials. Furthermore, we also discuss the origin of the synthesis of some nanomaterials, the challenges associated with the use of those nanomaterials and the chemistry behind their incorporation with other materials for biosensor design. The last section covers the prospects for the development and application of the highlighted nanomaterials.

Enhanced visible light driven photoelectrochemical degradation of tetracycline hydrochloride using a BiOI photoanode modified with MnO2 films.

Removal of pharmaceuticals in wastewater has been the focus of many research due to the recalcitrant nature and hazardous effects of these compounds. The photoelectrochemical degradation process has proven to be suitable to harness solar energy for the mineralization of organic compounds in wastewater. Herein, we report the application of BiOI/MnO2 heterostructured anode for the photoelectrochemical degradation of tetracycline hydrochloride in aqueous solution. The photoanode was prepared through electrodeposition technique and fully characterized through microscopic, spectroscopic and electrochemical techniques. The results showed that formation of p-n heterojunction between BiOI and MnO2 in the photoanode led to improved charge separation which was evident in improved optical and photoelectrochemical properties. The FTO-BiOI/MnO2 electrode attained a photocurrent density of 0.104 mA cm-2 with applied potential of 1.0 V (vs Ag/AgCl) which was almost double that of pristine BiOI suggesting efficient charge separation. The heterostructured photoanode achieved 94% removal of tetracycline hydrochloride after 120 min through the PEC degradation process with 61% mineralization efficiency. The electrode showed good reusability and stability with 92% PEC removal after eight cycles. Hence, the FTO-BiOI/MnO2 has a great potential as anode for PEC wastewater treatments.

Advances in polymer-based detection of environmental ibuprofen in wastewater.

Globally, ibuprofen is the third most consumed drug and its presence in the environment is a concern because little is known about its adverse effects on humans and aquatic life. Environmentalists have made monitoring and the detection of ibuprofen in biological and environmental matrices a priority. For the detection and monitoring of ibuprofen, sensors and biosensors have provided rapid analysis time, sensitivity, high-throughput screening, and real-time analysis. Researchers are increasingly seeking eco-friendly technology, and this has led to an interest in developing biodegradable, bioavailable, and non-toxic sensors, or biosensors. The integration of polymers into sensor systems has proven to significantly improve sensitivity, selectivity, and stability and minimize sample preparation using bioavailable and biodegradable polymers. This review provides a general overview of perspectives and trends of polymer-based sensors and biosensors for the detection of ibuprofen compared to non-polymer-based sensors.

The application of photoelectrocatalysis in the degradation of rhodamine B in aqueous solutions: a review.

The pollution of the water environment by industrial effluents is an ongoing challenge due to the rate of industrialisation and globalisation. Photoelectrocatalysis (PEC), an electrochemical advanced oxidation process, has proven to be an effective method for removing organics from wastewater. Photoelectrocatalysis is environmentally benign, cost-effective and easy to operate. In this present review, we examine the recent progress in the removal of rhodamine B dye, a common constituent of textile effluent released into the environment, through photoelectrocatalytic degradation. We present a detailed discussion on the use of different kinds of unmodified and modified photoanodes that have been explored for the photoelectrocatalytic removal of this dye. More importantly, discussions are presented on the mechanisms and kinetics of the degradation of rhodamine B dye using these photoanodes. Hence, this review will be beneficial for researchers in developing future projects in the area of wastewater treatments through photoelectrocatalysis.

Enhanced photoelectrocatalytic degradation of diclofenac sodium using a system of Ag-BiVO4/BiOI anode and Ag-BiOI cathode.

We report the photoelectrocatalysis of diclofenac sodium using a reactor consisting of Ag-BiVO4/BiOI anode and Ag-BiOI cathode. The electrodes were prepared through electrodeposition on FTO glass and modified with Ag nanoparticles through photodeposition. The structural and morphological studies were carried out using XRD, SEM, and EDS which confirmed the successful preparation of the materials. The optical properties as observed with UV-DRS revealed that the electrodes were visible light active and incorporation of metallic Ag particles on the surface increased the absorption in the visible light region. Presence of p-n heterojunction in the anode led to decrease in the spontaneous recombination of photoexcited electron-hole pairs as seen in the photocurrent response. The results from photoelectrocatalytic degradation experiments revealed that replacing platinum sheet with Ag-BiOI as counter electrode resulted in higher (92%) and faster removal of diclofenac sodium as evident in the values of apparent rate constants. The reaction mechanism further revealed that efficiently separated photogenerated holes played a major role in the degradation of the pharmaceutical. The prepared electrodes showed good stability and impressive reusability. The reports from this study revealed that the dual photoelectrodes system has a great potential in treating pharmaceutical polluted wastewater using visible light irradiation.

Recent advances in degradation of pharmaceuticals using Bi2WO6 mediated photocatalysis - A comprehensive review.

The pollution of water bodies by residual pharmaceuticals is a major problem globally. Bismuth tungstate mediated photocatalysis has been effective in the removal of these organics from water. Bismuth tungstate (Bi2WO6) has proven to be an excellent visible light active photocatalyst because of its non-toxicity, low band gap energy and ease of preparation. It has been widely applied for the removal of a wide array of organic pollutants, particularly dyes, from wastewater. However, recently, much attention has been channelled to its application for the degradation of pharmaceuticals. In this present review, the recent trends in the applications of Bi2WO6 based photocatalysts for the removal of pharmaceuticals in wastewater are comprehensively discussed. The fabrication of Bi2WO6 based photocatalysts with enhanced photocatalytic performances through morphology control, doping and formation of heterojunctions are highlighted. Much discussion centres on the mechanisms and possible degradation pathways of antibiotic pharmaceuticals in wastewater. Finally, areas needing more attention and investigation on the use of Bi2WO6 based photocatalysts for removal of pharmaceuticals from wastewater especially towards real-life applications are presented for future research directions.

The application of FTO-Cu2O/Ag3PO4 heterojunction in the photoelectrochemical degradation of emerging pharmaceutical pollutant under visible light irradiation.

We report the photoelectrochemical application of a visible light active FTO-Cu2O/Ag3PO4 photoanode for the abatement of sulfamethoxazole in water. The as-synthesised photoanodes were characterised using XRD, field emission SEM, EDX, diffuse reflectance UV-vis, impedance spectroscopy and chronoamperometry. The results obtained confirmed a successful formation of p-n heterojunction at the Cu2O/Ag3PO4 interface. The highest photocurrent response of 0.62 mAcm-2 was obtained for the composite photoanode which was four times higher than pure Cu2O and about three times higher than pristine Ag3PO4. The photoanode gave 67% removal efficiency within 2 h upon its photoelectrochemical application in the degradation of sulfamethoxazole with 1.5 V bias potential at pH 6.2. The FTO-Cu2O/Ag3PO4 electrode was also applied in the treatment of a cocktail of synthetic organics containing sulfamethoxazole and orange II dye. The photogenerated holes was found to be the major oxidant and the photoanodes was stable and reusable.

Towards visible light driven photoelectrocatalysis for water treatment: Application of a FTO/BiVO4/Ag2S heterojunction anode for the removal of emerging pharmaceutical pollutants.

Pharmaceuticals have been classified as emerging water pollutants which are recalcitrant in nature. In the quest to find a suitable technique in removing them from contaminated water, photoelectrocatalytic oxidation method has attracted much attention in recent years. This report examined the feasibility of degrading ciprofloxacin and sulfamethoxazole through photoelectrocatalytic oxidation using FTO-BiVO4/Ag2S with p-n heterojunction as anode. BiVO4/Ag2S was prepared through electrodeposition and successive ionic layer adsorption/reaction on FTO glass. Structural and morphological studies using XRD, SEM, EDS and diffusive reflectance UV-Vis confirmed the successful construction of p-n heterojunction of BiVO4/Ag2S. Electrochemical techniques were used to investigate enhanced charge separation in the binary electrode. The FTO-BiVO4/Ag2S electrode exhibited the highest photocurrent response (1.194 mA/cm-2) and longest electron lifetime (0.40 ms) than both pristine BiVO4 and Ag2S electrodes which confirmed the reduction in recombination of charge carriers in the electrode. Upon application of the prepared FTO-BiVO4/Ag2S in photoelectrocatalytic removal of ciprofloxacin and sulfamethoxazole, percentage removal of 80% and 86% were achieved respectively with a low bias potential of 1.2 V (vs Ag/AgCl) within 120 min. The electrode possesses good stability and reusability. The results obtained revealed BiVO4/Ag2S as a suitable photoanode for removing recalcitrant pharmaceutical molecules in water.

Interrogating solar photoelectrocatalysis on an exfoliated graphite-BiVO4/ZnO composite electrode towards water treatment.

A novel photoanode consisting of an exfoliated graphite-BiVO4/ZnO heterostructured nanocomposite was fabricated. The material was characterised with scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and X-ray diffraction (XRD). Photoelectrochemical studies were carried out with cyclic/linear sweep voltammetry and chronoamperometry. The solar photoelectrochemical properties of the heterojunction photoanode were investigated through the degradation of rhodamine B in water. The results revealed that the nanoparticles of BiVO4 and ZnO were well entrapped within the interlayers of the exfoliated graphite (EG) sheets. Improved charge separation was achieved in the EG-BiVO4/ZnO composite electrode which resulted in superior photoelectrochemical performance than individual BiVO4 and ZnO electrodes. A higher degradation efficiency of 91% of rhodamine B was recorded using the composite electrode with the application of 10 mA cm-2 current density and a solution pH of 7. The highest total organic carbon removal of 74% was also recorded with the EG-BiVO4/ZnO. Data from scavenger studies were used to support the proposed mechanism of degradation. The electrode has high stability and reusability and hence lends itself to applications in photoelectrocatalysis, especially in water treatment.