Silver nanoparticles (AgNPs) have been employed in various fields of biotechnology due to their proven properties as an antibacterial, antiviral and antifungal agent. AgNPs are generally synthesized through chemical, physical and biological approaches involving a myriad of methods. As each approach confers unique advantages and challenges, a trends analysis of literature for the AgNPs synthesis using different types of synthesis were also reviewed through a bibliometric approach. A sum of 10,278 publications were analyzed on the annual numbers of publication relating to AgNPs and biological, chemical or physical synthesis from 2010 to 2020 using Microsoft Excel applied to the Scopus publication database. Furthermore, another bibliometric clustering and mapping software were used to study the occurrences of author keywords on the biomedical applications of biosynthesized AgNPs and a total collection of 224 documents were found, sourced from articles, reviews, book chapters, conference papers and reviews. AgNPs provides an excellent, dependable, and effective solution for seven major concerns: as antibacterial, antiviral, anticancer, bone healing, bone cement, dental applications and wound healing. In recent years, AgNPs have been employed in biomedical sector due to their antibacterial, antiviral and anticancer properties. This review discussed on the types of synthesis, how AgNPs are characterized and their applications in biomedical field.

The unique properties of MXenes have been deemed to be of significant interest in various emerging applications. However, MXenes provide a major drawback involving environmentally harmful and toxic substances for its general fabrication in large-scale production and employing a high-temperature solid-state reaction followed by selective etching. Meanwhile, how MXenes are synthesized is essential in directing their end uses. Therefore, making strategic approaches to synthesize greener, safer, more sustainable, and more environmentally friendly MXenes is imperative to commercialize at a competitive price. With increasing reports of green synthesis that promote advanced technologies and non-toxic agents, it is critical to compile, summarize, and synthesize the latest development of the green-related technology of MXenes. We review the recent progress of greener, safer, and more sustainable MXene synthesis with a focus on the fundamental synthetic process, the mechanism, and the general advantages, and the emphasis on the MXene properties inherited from such green synthesis techniques. The emerging use of the so-called green MXenes in energy conversion and storage, environmental remediation, and biomedical applications is presented. Finally, the remaining challenges and prospects of greener MXene synthesis are discussed.

Carbon Quantum Dots (CQDs) have exceptionally solid and tuneable fluorescence properties which empower their application in vast fields. The hydrothermal approach is regarded as direct and efficient, through polymerization and carbonization reactions, and has been widely applied to prepare various materials due to the high reactivity of the reactants, easy control of the solution, little harm to the environment and low energy consumption under hydrothermal condition. The attracting feature of this route is that neither any strong acid nor post-synthetic surface passivation is necessary. As of now, a lot of important progress in the hydrothermal synthesis of carbon quantum dots such as materials use as precursors and influence of hydrothermal synthesis parameters. Hydrothermal synthesis is one of the most commonly used methods for preparation of nanomaterials. It is basically a solution reaction-based approach. In this review, the main focus is to review the hydrothermal route for carbon quantum dots using different source of materials and their fundamental characterizations, followed by the influence of hydrothermal synthesis conditions to carbon quantum dots.

This paper reported the uses of ark clam shell calcium precursor in order to form hydroxyapatite (HA) via the wet chemical precipitation method. The main objective of this research is to acquire better understanding regarding the effect of sintering temperature in the fabrication of HA. Throughout experiment, the ratio of Ca:P were constantly controlled, between 1.67 and 2.00. The formation of HA at these ratio was confirmed by means of energy-dispersive X-ray spectroscopy analysis. In addition, the effect of sintering temperature on the formation of HA was observed using X-ray diffraction analysis, while the structural and morphology was determined by means of field emission scanning electron microscopy. The formation of HA nanoparticle was recorded (~35–69 nm) in the form of as-synthesize HA powder. The bonding compound appeared in the formation of HA was carried out using Fourier transform infrared spectroscopy such as biomaterials that are expected to find potential applications in orthopedic and biomedical industries .

In the present study, the conversion of tea waste biomass was carried via carbonization at high temperature and further used as starting material to produce graphene oxide (GO). The oxidation and exfoliation of graphitized carbon was successfully achieved using modified Hummer’s method. The as synthesized GO have been loaded with titanium dioxide (TiO₂) using hydrothermal method to produce nanocomposite of rGO/TIO₂. The prepared nanocomposites were characterized by means of XRD, FTIR, Raman and FESEM analysis. The evaluation for rGO/TIO₂ nanocomposite photocatalytic activity was carried out based on degradation of methyl orange (MO) under the ultraviolet (UV) light irradiation. Results obtained using FTIR results revealed the successful oxidation of graphitized carbon with the presence of carboxyl and hydroxyl group. FESEM images suggested the changes of surface morphology from graphite flakes structure into few layers of graphene sheets. Therefore, it can be indicated that tea waste suitable to be sustainable alternative of graphite for the synthesis of GO. Moreover, GO obtained has immense potential for degradation of various water pollutions. Photocatalytic activity experiment inferred that the importance of optimum ratio between reduce GO to TiO₂ materials which can resulted in difference in the degradation efficiency; rGO/TiO₂ 1:8 > rGO/TiO₂ 1:4 > TiO₂ > rGO/TiO₂ 1:6 > rGO/TiO₂ 1:10.

In the current era of globalization, synthetic dyes are one of the key factors of water pollution. Photocatalysis constitutes a promising technology for the treatment of wastewater, especially to those containing hard-to-remove organic compounds. Zinc oxide nanoparticles (ZnONPs) play a vital role as a photocatalyst material. This research highlights the synthesized ZnONPs with roselle flower and oil palm leaf extract. The extracts and sodium hydroxide (NaOH) act as reducing agents during the synthesis process. Synthesis without the addition of plant extract is used as blank control for the experiment. Structural and optical studies of the three variants of ZnONPs were performed. High purity of ZnONPs with element Zn and O was obtained. The size of the three variants of ZnONPs was from 10–15 nm and found in agglomerated spherical shape. Large band gap, 3.2 eV was obtained by UV-Vis and high thermal stability was proven by TGA. Oxygen vacancies that assist in the degradation phenomenon were found in ZnONPs. Five percent of ZnONPs with the presence of 10 W UV light could effectively degrade 10 ppm MO in 5 h and MB in 3 h. Besides, high antioxidant properties and low toxicity demonstrated the ability of ZnONPs to be used as photocatalysts. In conclusion, ZnONPs can be further developed for pharmaceutical and industrial use.