Nanodiamonds: A Cutting-Edge Approach to Enhancing Biomedical Therapies and Diagnostics in Biosensing.

Nanodiamonds (NDs) have garnered attention in the field of nanomedicine due to their unique properties. This review offers a comprehensive overview of NDs synthesis methods, properties, and their uses in biomedical applications. Various synthesis techniques, such as detonation, high-pressure, high-temperature, and chemical vapor deposition, offer distinct advantages in tailoring NDs' size, shape, and surface properties. Surface modification methods further enhance NDs' biocompatibility and enable the attachment of bioactive molecules, expanding their applicability in biological systems. NDs serve as promising nanocarriers for drug delivery, showcasing biocompatibility and the ability to encapsulate therapeutic agents for targeted delivery. Additionally, NDs demonstrate potential in cancer treatment through hyperthermic therapy and vaccine enhancement for improved immune responses. Functionalization of NDs facilitates their utilization in biosensors for sensitive biomolecule detection, aiding in precise diagnostics and rapid detection of infectious diseases. This review underscores the multifaceted role of NDs in advancing biomedical applications. By synthesizing NDs through various methods and modifying their surfaces, researchers can tailor their properties for specific biomedical needs. The ability of NDs to serve as efficient drug delivery vehicles holds promise for targeted therapy, while their applications in hyperthermic therapy and vaccine enhancement offer innovative approaches to cancer treatment and immunization. Furthermore, the integration of NDs into biosensors enhances diagnostic capabilities, enabling rapid and sensitive detection of biomolecules and infectious diseases. Overall, the diverse functionalities of NDs underscore their potential as valuable tools in nanomedicine, paving the way for advancements in healthcare and biotechnology.

A NiO-nanostructure-based electrochemical sensor functionalized with supramolecular structures for the ultra-sensitive detection of the endocrine disruptor bisphenol S in an aquatic environment.

Herein, NiO nanoparticles (NPs) functionalized with a para-hexanitrocalix[6]arene derivative (p-HNC6/NiO) were synthesized by using a facile method and applied as a selective electrochemical sensor for the determination of bisphenol S (BPS) in real samples. Moreover, the functional interactions, phase purities, surface morphologies and elemental compositions of the synthesized p-HNC6/NiO NPs were investigated via advanced analytical tools, such as Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). Additionally, the synthesized p-HNC6/NiO NPs were cast on the surface of a bare glassy carbon electrode (GCE) via a drop casting method, which resulted in uniform deposition of p-HNC6/NiO/GCE over the surface of the GCE. Additionally, the developed p-HNC6/NiO/GCE sensor demonstrated an outstanding electrochemical response to BPS under optimized conditions, including a supporting electrolyte, a Briton-Robinson buffer electrolyte at pH 4, a scan rate of 110 mV s-1 and a potential window of between -0.2 and 1.0 V. The wide linear dynamic range was optimized to 0.8-70 µM to obtain a brilliant linear calibration curve for BPS. The limit of detection (LOD) and limit of quantification (LOQ) of the developed sensor were estimated to be 0.0059 and 0.019 µM, respectively, which are lower than those of reported sensors for BPS. The feasibility of the developed method was successfully assessed by analyzing the content of BPS in waste water samples, and good recoveries were achieved.

Highly Efficient Arginine Intercalated Graphene Oxide Composite Membranes for Water Desalination.

Graphene oxide-based composite membranes have received enormous attention for highly efficient water desalination. Herein, we prepare arginine/graphene oxide (Arg/GO) composite membranes by surface functionalizing GO nanosheets with arginine amino acid. Arginine has a unique combination of hydroxyl and amino functional groups that cross-link GO nanosheets through hydrogen bonding and electrostatic interactions. The as-prepared Arg@GO composite membranes with different thicknesses are used to separate the salt and dye molecules. The 900-nm-thick Arg@GO composite membrane shows high rejection of 98% for NaCl and 99.8% for MgCl2, Ni(NO3)2, and Pb(NO3)2 with good water permeance. Such a membrane also shows a high separation efficiency (100%) for methylene blue, rhodamine B, and Evans blue dyes. At the same time, the ultrathin Arg@GO composite membrane (220 ± 10 nm) exhibits high water permeance of up to 2100 ± 10 L m-2 h-1 bar-1. Furthermore, the 900-nm-thick Arg@GO composite membrane is stable in an aqueous environment for 40 days with significantly less swelling. Therefore, these membranes can be utilized in future desalination and separation applications.

Fabrication of para-dimethylamine calix[4]arene functionalized self-assembled graphene oxide composite material for effective removal of 2, 4, 6-tri-Cholorphenol from aqueous environment.

Water pollution caused by the release of organic pollutants is a major environmental concern worldwide. These pollutants can have harmful effects on aquatic ecosystems and the organisms living within them, as well as on human health when contaminated water is consumed. It is essential to implement proper treatment and management strategies to prevent and mitigate water pollution. Moreover, the major untreated industrial effluents are synthetic organic compounds especially 2,4,6-trichlorophenol (TCP) which cause several environmental issues and heath related problems in humans. To cope with this problem, an excellent 2D porous material based on p-DMAC4/GO composite has been synthesized as adsorbent material for the effective removal of 2,4,6-trichlorophenol pollutant from wastewater. In this regard, the advanced analytical tools such as Fourier-Transform infrared (FT-IR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy-Dispersive X-ray spectroscopy (EDS) were used for its characterization. The results justified the chemical composition, excellent crystalline nature, surface morphology and elemental composition of the synthesized composite material. The synthesized adsorbent material showed 95% adsorption of TCP from wastewater system at optimal conditions i.e., pH (6), adsorbent dosage (30 mg) and shaking time (60 min). The mathematical models such as isotherms, thermodynamics and kinetics studies validate the nature of adsorption process of TCP pollutant. The adsorption data found to be best fitted with Langmuir isotherms (R2 = 0.99); whereas kinetic study suggested the pseudo-second-order nature of reaction with R2 = 0.99. The thermodynamics study confirmed the spontaneous and endothermic nature of the TCP pollutant onto the surface of p-DMAC4/GO material. Moreover, the results of current work were also compared with existing reported adsorbents and data suggested the higher efficiency, feasibility, and reusability of p-DMAC4/GO material to remove the TCP pollutant from the wastewater system.

Functionalized graphene oxide-based lamellar membranes for organic solvent nanofiltration applications.

In this study, two-dimensional graphene oxide-based novel membranes were fabricated by modifying the surface of graphene oxide nanosheets with six-armed poly(ethylene glycol) (PEG) at room conditions. The as-modified PEGylated graphene oxide (PGO) membranes with unique layered structures and large interlayer spacing (∼1.12 nm) were utilized for organic solvent nanofiltration applications. The as-prepared 350 nm-thick PGO membrane offers a superior separation (>99%) against evans blue, methylene blue and rhodamine B dyes along with high methanol permeance ∼ 155 ± 10 L m-2 h-1, which is 10-100 times high compared to pristine GO membranes. Additionally, these membranes are stable for up to 20 days in organic solvent. Hence the results suggested that the as-synthesized PGO membranes with superior separation efficiency for dye molecules in organic solvent can be used in future for organic solvent nanofiltration application.

Lamellar Graphene Oxide-Based Composite Membranes for Efficient Separation of Heavy Metal Ions and Desalination of Water.

Sufficient efforts have been carried out to fabricate highly efficient graphene oxide (GO) lamellar membranes for heavy metal ion separation and desalination of water. However, selectivity for small ions remains a major problem. Herein, GO was modified by using onion extractive (OE) and a bioactive phenolic compound, i.e., quercetin. The as-prepared modified materials were fabricated into membranes and used for separation of heavy metal ions and water desalination. The GO/onion extract (GO/OE) composite membrane with a thickness of 350 nm shows an excellent rejection efficiency for several heavy metal ions such as Cr6+ (∼87.5%), As3+ (∼89.5%), Cd2+ (∼93.0%), and Pb2+ (∼99.5%) and a good water permeance of ∼460 ± 20 L m-2 h-1 bar-1. In addition, a GO/quercetin (GO/Q) composite membrane is also fabricated from quercetin for comparative studies. Quercetin is an active ingredient of onion extractives (2.1% w/w). The GO/Q composite membranes show good rejection up to ∼78.0, ∼80.5, ∼88.0, and 95.2% for Cr6+, As3+, Cd2+, and Pb2+, respectively, with a DI water permeance of ∼150 ± 10 L m-2 h-1 bar-1. Further, both membranes are used for water desalination by measuring rejection of small ions such as NaCl, Na2SO4, MgCl2, and MgSO4. The resulting membranes show >70% rejection for small ions. In addition, both membranes are used for filtration of Indus River water and the GO/Q membrane shows remarkably high separation efficiency and makes river water suitable for drinking purpose. Furthermore, the GO/QE composite membrane is highly stable up to ∼25 days under acidic, basic, and neutral environments as compared to GO/Q composite and pristine GO-based membranes.

Influence of Operating and Electrochemical Parameters on PEMFC Performance: A Simulation Study.

Proton exchange membrane fuel cell, or polymer electrolyte fuel cell, (PEMFC) has received a significant amount of attention for green energy applications due to its low carbon emission and less other toxic pollution capacity. Herein, we develop a three-dimensional (3D) computational fluid dynamic model. The values of temperature, pressure, relative humidity, exchange coefficient, reference current density (RCD), and porosity values of the gas diffusion layer (GDL) were taken from the published literature. The results demonstrate that the performance of the cell is improved by modifying temperature and operating pressure. Current density is shown to degrade with the rising temperature as explored in this study. The findings show that at 353 K, the current density decreases by 28% compared to that at 323 K. In contrast, studies have shown that totally humidified gas passing through the gas channel results in a 10% higher current density yield, and that an evaluation of a 19% higher RCD value results in a similar current density yield.

Ultrathin Graphene Oxide-Based Nanocomposite Membranes for Water Purification.

Two-dimensional graphene oxide (GO)-based lamellar membranes have been widely developed for desalination, water purification, gas separation, and pervaporation. However, membranes with a well-organized multilayer structure and controlled pore size remain a challenge. Herein, an easy and efficient method is used to fabricate MoO2@GO and WO3@GO nanocomposite membranes with controlled structure and interlayer spacing. Such membranes show good separation for salt and heavy metal ions due to the intensive stacking interaction and electrostatic attraction. The as-prepared composite membranes showed high rejection rates (˃70%) toward small metal ions such as sodium (Na+) and magnesium (Mg2+) ions. In addition, both membranes also showed high rejection rates ˃99% for nickel (Ni2+) and lead (Pb2+) ions with good water permeability of 275 ± 10 L m-2 h-1 bar-1. We believe that our fabricated membranes will have a bright future in next generation desalination and water purification membranes.

Functionalized Graphene Oxide-Based Lamellar Membranes with Tunable Nanochannels for Ionic and Molecular Separation.

Graphene oxide (GO)-based membranes with tunable microstructure and controlled nanochannels have attracted an increasing interest for various applications in wastewater treatment, desalination, gas separation, organic nanofiltration, etc. However, they showed limited use in water desalination due to their lower stability and separation efficiency. In this work, a class of two-dimensional (2D) GO lamellar membranes have been prepared with controlled pores for efficient and fast separation of ions and dye molecules. The GO membranes are fucntionalized with a star-like 6-armed poly(ethylene oxide) using the simple amidation route under mild conditions. The as-prepared covalently cross-linked networks are chemically steady in aqueous medium and show remarkable selectivity (∼100%) for several probe molecules and 10-100 higher permeance than those of the reported GO-based membranes. Further, such membranes are also used for salt separation and show more than 80% rejection for Pb2+ and Ni2+ salts. Moreover, a 1360 nm-thick membrane shows >99% rejection for NaCl with a good water permeance of up to 120 L m-2 h-1 bar-1. Additionally, these membranes are stable for more than 20 days under different conditions.

Regenerated Silk Nanofibers for Robust and Cyclic Adsorption-Desorption on Anionic Dyes.

In recent years, adsorption-based membranes have been widely investigated to remove and separate textile pollutants. However, cyclic adsorption-desorption to reuse a single adsorbent and clear scientific evidence for the adsorption-desorption mechanism remains challenging. Herein, silk nanofibers were used to assess the adsorption potential for the typical anionic dyes from an aqueous medium, and they show great potential toward the removal of acid dyes from the aqueous solution with an adsorption rate of ∼98% in a 1 min interaction. Further, we measured the filtration proficiency of a silk nanofiber membrane in order to propose a continuous mechanism for the removal of acid blue dye, and a complete rejection was observed with a maximum permeability rate of ∼360 ± 5 L·m-2·h-1. The Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy studies demonstrate that this fast adsorption occurs due to multiple interactions between the dye molecule and the adsorbent substrate. The as-prepared material also shows remarkable results in desorption. A 50-time cycle exhibits complete adsorption and desorption ability, which not only facilitates high removal aptitude but also produces less solid waste than other conventional adsorbents. Additionally, fluorescent 2-bromo-2-methyl-propionic acid (abbreviated as EtOxPY)-silk nanofibers can facilitate to illustrate a clear adsorption and desorption mechanism. Therefore, the above-prescribed results make electrospun silk nanofibers a suitable choice for removing anionic dyes in real-time applications.

Facile synthesis of Zn-doped CdS nanowires with efficient photocatalytic performance.

In this study, one-dimensional zinc (Zn)-doped cadmium sulphide (CdS) nanowires were synthesised by a solvothermal method. The Zn doping concentrations were varied from 1 to 5 mol% (ZnxCd1-xS where x = 0.001, 0.003 and 0.005). As-prepared materials were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy and UV-visible spectroscopy. Electrochemical impedance spectroscopy (EIS) was conducted to measure the charge transfer resistance. The photocatalytic performance of prepared materials was evaluated by the photodegradation of methylene blue (MB) dye. The result showed that 5% Zn-doped CdS is more photoactive as compared to other corresponding doped and undoped CdS. The increase in photocatalytic performance is due to improvement in the charge separation.

Two-Dimensional Transition Metal Carbides and Nitrides (MXenes) for Water Purification and Antibacterial Applications.

Two-dimensional (2D) materials such as graphene, graphene oxide (GO), metal carbides and nitrides (MXenes), transition metal dichalcogenides (TMDS), boron nitride (BN), and layered double hydroxide (LDH) metal-organic frameworks (MOFs) have been widely investigated as potential candidates in various separation applications because of their high mechanical strength, large surface area, ideal chemical and thermal stability, simplicity, ease of functionalization, environmental comparability, and good antibacterial performance. Recently, MXene as a new member of the 2D polymer family has attracted significant attention in water purification, desalination, gas separation, antibacterial, and antifouling applications. Herein, we review the most recent progress in the fabrication, preparation, and modification methods of MXene-based lamellar membranes with the emphasis on applications for water purification and desalination. Moreover, the antibacterial properties of MXene-based membranes show a significant potential for commercial use in water purification. Thus, this review provides a directional guide for future development in this emerging technology.

CdPS3 nanosheets-based membrane with high proton conductivity enabled by Cd vacancies.

Proton transport in nanochannels under humid conditions is crucial for the application in energy storage and conversion. However, existing materials, including Nafion, suffer from limited conductivity of up to 0.2 siemens per centimeter. We report a class of membranes assembled with two-dimensional transition-metal phosphorus trichalcogenide nanosheets, in which the transition-metal vacancies enable exceptionally high ion conductivity. A Cd0.85PS3Li0.15H0.15 membrane exhibits a proton conduction dominant conductivity of ~0.95 siemens per centimeter at 90° Celsius and 98% relative humidity. This performance mainly originates from the abundant proton donor centers, easy proton desorption, and excellent hydration of the membranes induced by cadmium vacancies. We also observed superhigh lithium ion conductivity in Cd0.85PS3Li0.3 and Mn0.77PS3Li0.46 membranes.

Laminar Graphene Oxide Membranes Towards Selective Ionic and Molecular Separations: Challenges and Progress.

Resolution of resources and environmental crises requires an efficient separation technologies, consequently, scientists and engineers are working vigorously for ideal separation materials. Laminar graphene oxide (GO) is a two-dimensional (2D) material offers considerable interest in this field due to its single atomic layer thickness, good stability, chemical inertness, and variety of functional groups. Recently, GO have emerged as a novel membrane material for molecular and ionic separation of gases, solvent, water, and desalination applications. This tutorial review aims to discuss the various approaches used to control the stacking of GO-based membrane with emphasis of advantages and drawbacks associated with each approach. Further, attention will also be given to describe the recent progress in GO based membranes for ionic and molecular separations. Meanwhile, challenges and opportunities will also be discussed in detail. We hope this review expected to provide a compact source of information that will be of great interest to chemists, material scientists, physicists, and engineers working or planning to work in GO based membranes for separation applications.

Highly stable graphene-oxide-based membranes with superior permeability.

Increasing fresh water demand for drinking and agriculture is one of the grand challenges of our age. Graphene oxide (GO) membranes have shown a great potential for desalination and water purification. However, it is challenging to further improve the water permeability without sacrificing the separation efficiency, and the GO membranes are easily delaminated in aqueous solutions within few hours. Here, we report a class of reduced GO membranes with enlarged interlayer distance fabricated by using theanine amino acid and tannic acid as reducing agent and cross-linker. Such membranes show water permeance over 10,000 L m-2 h-1 bar-1, which is 10-1000 times higher than those of previously reported GO-based membranes and commercial membranes, and good separation efficiency, e.g., rhodamine B and methylene blue rejection of ~100%. Moreover, they show no damage or delamination in water, acid, and basic solutions even after months.

Controlling reduction degree of graphene oxide membranes for improved water permeance.

Tailoring the pore structure and surface chemistry of graphene-based laminates is essentially important for their applications as separation membranes. Usually, pure graphene oxide (GO) and completely reduced GO (rGO) membranes suffer from low water permeance because of the lack of pristine graphitic sp2 domains and very small interlayer spacing, respectively. In this work, we studied the influence of reduction degree on the structure and separation performance of rGO membranes. It was found that weak reduction retains the good dispersion and hydrophilicity of GO nanosheets. More importantly, it increases the number of pristine graphitic sp2 domains in rGO nanosheets while keeping the large interlayer spacing of the GO membranes in most regions at the same time. The resultant membranes show a high water permeance of 56.3 L m-2 h-1 bar-1, which is about 4 times and over 104 times larger than those of the GO and completely reduced rGO membranes, respectively, and high rejection over 95% for various dyes. Furthermore, they show better structure stability and more superior separation performance than GO membranes in acid and alkali environments.