Due to water shortage and increased water pollution, various methods are being explored to improve water quality by treating contaminants. Sonophotocatalysis is a combination of two individual water treatment processes i.e., photocatalysis and sonocatalysis. With advantages including shorter reaction times and enhanced activity, this technique shows possible futuristic applications as an efficient water treatment technology. Herein, background insight on sonophotocalysis as a water and wastewater treatment technique as well as the general mechanism of activity is explained. The commonly used catalysts for sonophotocatalytic applications as well as their synthesis pathways are also briefly discussed. Additionally, the utilisation of sonophotocatalysis for the disinfection of various microbial species as well as treatment of wastewater pollutants including organic (dyes, pharmaceuticals and pesticides) and inorganic species (heavy metals) is deliberated. This review also gives a critical analysis of the efficiency, enhancement strategies as well as challenges and outlooks in this field. It is thus intended to give insight to researchers in the context of facilitating future developments in the field of water treatment, and advancing sonophotocatalysis towards large-scale implementation and commercialization.

Millions of people worldwide are affected by diabetes, a chronic disease that continuously grows due to abnormal glucose concentration levels present in the blood. Monitoring blood glucose concentrations is therefore an essential diabetes indicator to aid in the management of the disease. Enzymatic electrochemical glucose sensors presently account for the bulk of glucose sensors on the market. However, their disadvantages are that they are expensive and dependent on environmental conditions, hence affecting their performance and sensitivity. To meet the increasing demand, non-enzymatic glucose sensors based on chemically modified electrodes for the direct electrocatalytic oxidation of glucose are a good alternative to the costly enzymatic-based sensors currently on the market, and the research thereof continues to grow. Nanotechnology-based biosensors have been explored for their electronic and mechanical properties, resulting in enhanced biological signaling through the direct oxidation of glucose. Copper oxide and copper sulfide exhibit attractive attributes for sensor applications, due to their non-toxic nature, abundance, and unique properties. Thus, in this review, copper oxide and copper sulfide-based materials are evaluated based on their chemical structure, morphology, and fast electron mobility as suitable electrode materials for non-enzymatic glucose sensors. The review highlights the present challenges of non-enzymatic glucose sensors that have limited their deployment into the market.

Cancer is a persistent global disease and a threat to the human species, with numerous cases reported every year. Over recent decades, a steady but slowly increasing mortality rate has been observed. While many attempts have been made using conventional methods alone as a theragnostic strategy, they have yielded very little success. Most of the shortcomings of such conventional methods can be attributed to the high demands of industrial growth and ever-increasing environmental pollution. This requires some high-tech biomedical interventions and other solutions. Thus, researchers have been compelled to explore alternative methods. This has brought much attention to nanotechnology applications, specifically magnetic nanomaterials, as the sole or conjugated theragnostic methods. The exponential growth of nanomaterials with overlapping applications in various fields is due to their potential properties, which depend on the type of synthesis route used. Either top-down or bottom-up strategies synthesize various types of NPs. The top-down only branches out to one method, i.e., physical, and the bottom-up has two methods, chemical and biological syntheses. This review highlights some synthesis techniques, the types of nanoparticle properties each technique produces, and their potential use in the biomedical field, more specifically for cancer. Despite the evident drawbacks, the success achieved in furthering nanoparticle applications to more complex cancer stages and locations is unmatched.

In this work, iron based 1, 3, 5-tricarboxylic acid (FeBTC) was prepared via microwave-assisted method and incorporated into TiO₂ via ultrasonic assisted method. The TiO₂–FeBTC nanocomposites were characterized by XRD, FTIR, Raman, BET, FESEM, HRTEM, TGA, UV‒vis DRS and PL to understand their crystallographic, surface morphology, and optical characteristics. The Raman spectra showed a blue shift of E_g, A_1g, and B_1g peaks upon incorporation of FeBTC MOF onto TiO₂. HRTEM and XRD analysis confirmed a mixture of TiO₂ nanospheres and hexagonal FeBTC MOF morphologies with high crystallinity. The incorporation of FeBTC onto TiO₂ improved the surface area as confirmed by BET results, which resulted in improved absorption in the visible region as a results of reduced bandgap energy from 3.2 to 2.84 eV. The PL results showed a reduced intensity for TiO₂–FeBTC (6%) sample, indicating improved separation of electron hole pairs and reduced recombination rate. After fabrication of the TiO₂–FeBTC MOF photoanode, the charge transfer kinetics were enhanced at TiO₂–FeBTC MOF (6%) with Rp value of 966 Ω, as given by EIS studies. This led to high performance due to low charge resistance. Hence, high power conversion efficiency (PCE) value of 0.538% for TiO₂–FeBTC (6%) was achieved, in comparison with other loadings. This was attributed to a relatively high surface area which allowed more charge shuttling and thus better electrical response. Conversely, upon increasing the FeBTC MOF loading to 8%, significant reduction in efficiency (0.478%) was obtained, which was attributed to sluggish charge transfer and fast electron–hole pair recombination rate. The TiO₂–FeBTC (6%) may be a good candidate for use in DSSCs as a photoanode materials for improved efficiency.