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.

Color-tunable stable quasi-2D hybrid metal halide perovskites: synthesis, characterization, and optical analysis.

Metal halide perovskites show remarkable optical properties and useful applications in optoelectronic devices. However, the instability of three-dimensional (3D) metal halide perovskites limits their applications, leading to the emergence of more stable two-dimensional (2D) metal halide perovskites. Herein, we present a facile synthesis of the 2D hybrid metal halide perovskite (EDA)(MA)n-1PbnBr3n+1 (EDA: ethylene diammonium, MA: methylammonium), where n = 1-6, and MAPbBr3 perovskite layers using an anti-solvent co-precipitation technique. The synthesized materials exhibited tunable optical properties, and the color emissions of pure EDAPbBr4 and (EDA)(MA)2Pb3Br10 perovskites were successfully tailored by altering halide anion layers. The band gap decreases as the value of n in the (EDA)(MA)n-1PbnBr3n+1 compound increases from 1 to 6. The as-prepared materials were characterized using X-ray diffraction (XRD) technique, Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-Vis), photoluminescence spectroscopy (PL), scanning electron microscopy (SEM), and energy dispersive X-ray analysis (EDX). Finally, the stability of the 2D hybrid metal halide perovskite structures was evaluated under ambient conditions over different periods. Their tunable color emission was investigated and robust fluorescence was observed after 55 days. Thus, this study provides valuable insights into the synthesis and characterization of 2D hybrid metal halide perovskites for tunable color emission, highlighting their potential for use in various optoelectronic applications.

Fundamentals of Hysteresis in Perovskite Solar Cells: From Structure-Property Relationship to Neoteric Breakthroughs.

Perovskite solar cells (PSC) have shown a rapid increase in efficiency than other photovoltaic technology. Despite its success in terms of efficiency, this technology is inundated with numerous challenges hindering the progress towards commercial viability. The crucial one is the anomalous hysteresis observed in the photocurrent density-voltage (J-V) response in PSC. The hysteresis phenomenon in the solar cell presents a challenge for determining the accurate power conversion efficiency of the device. A detailed investigation of the fundamental origin of hysteresis behavior in the device and its associated mechanisms is highly crucial. Though numerous theories have been proposed to explain the causes of hysteresis, its origin includes slow transient capacitive current, trapping, and de-trapping process, ion migrations, and ferroelectric polarization. The remaining issues and future research required toward the understanding of hysteresis in PSC device is also discussed.

Assessment of Foodborne Bacterial Pathogens in Buffalo Raw Milk Using Polymerase Chain Reaction Based Assay.

Milk is a putrescible commodity that is extremely prone to microbial contamination. Primarily, milk and dairy products are believed to be easily contaminated by pathogenic microorganisms, including Listeria monocytogenes, Salmonella spp., and Staphylococcus aureus. The microbiological quality of raw milk and dairy products regarding foodborne pathogens is of paramount importance due to concern of human health. In this study 400 buffalo raw milk samples were screened for assessing the prevalence of L. monocytogenes, Salmonella spp., and S. aureus. This study implemented uniplex-polymerase chain reaction (u-PCR) and multiplex-polymerase chain reaction (m-PCR) assays for the fast simultaneous detection of these pathogens comparing to the conventional culturing methods. Raw milk samples were found contaminated with the prevalence of 2.2%, 4.0%, and 14.2% for L. monocytogenes, Salmonella spp., and S. aureus, respectively. These pathogens were detected with the optimized polymerase chain reaction assays after 6 h of enrichment. u-PCR and m-PCR demonstrated the limit of detection as 104, 102, and 10 cells/mL after 6, 12, 18, and 24 h for each culture of the pathogens. A high sensitivity (10 colony-forming unit [CFU]/mL) of the m-PCR protocol was noted. The developed protocol is a cost-effective and rapid method for the simultaneous detection of pathogens associated with raw milk and dairy industries.

Selective Synthesis of Bismuth or Bismuth Selenide Nanosheets from a Metal Organic Precursor: Investigation of their Catalytic Performance for Water Splitting.

The development of cost-effective, functional materials that can be efficiently used for sustainable energy generation is highly desirable. Herein, a new molecular precursor of bismuth (tris(selenobenzoato)bismuth(III), [Bi(SeOCPh)3]), has been used to prepare selectively Bi or Bi2Se3 nanosheets via a colloidal route by the judicious control of the reaction parameters. The Bi formation mechanism was investigated, and it was observed that the trioctylphosphine (TOP) plays a crucial role in the formation of Bi. Employing the vapor deposition method resulted in the formation of exclusively Bi2Se3 films at different temperatures. The synthesized nanomaterials and films were characterized by p-XRD, TEM, Raman, SEM, EDX, AFM, XPS, and UV-vis spectroscopy. A minimum sheet thickness of 3.6 nm (i.e., a thickness of 8-9 layers) was observed for bismuth, whereas a thickness of 4 nm (i.e., a thickness of 4 layers) was observed for Bi2Se3 nanosheets. XPS showed surface oxidation of both materials and indicated an uncapped surface of Bi, whereas Bi2Se3 had a capping layer of oleylamine, resulting in reduced surface oxidation. The potential of Bi and Bi2Se3 nanosheets was tested for overall water-splitting application. The OER and HER catalytic performances of Bi2Se3 indicate overpotentials of 385 mV at 10 mA cm-2 and 220 mV, with Tafel slopes of 122 and 178 mV dec-1, respectively. In comparison, Bi showed a much lower OER activity (506 mV at 10 mA cm-2) but a slightly better HER (214 mV at 10 mA cm-2) performance. Similarly, Bi2Se3 nanosheets were observed to exhibit cathodic photocurrent in photoelectrocatalytic activity, which indicated their p-type behavior.

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.

Cesium Lead Halide Perovskite Nanostructures: Tunable Morphology and Halide Composition.

Inorganic halide perovskite (CsPbX3 ) nanostructures have gained considerable interest in recent years owing to their enhanced stability and optoelectronic applications. Recent developments in the synthesis of nanostructures are reviewed. The impact of the precursor and ligand nature, temperature and growth time on the morphology and shape tuning of CsPbX3 nanostructures is described in relation to their optical properties. The presynthetic and postsynthetic anion exchange strategies to retain pre-existing crystal phase and shape are discussed in this minireview.

A comparative study of the influence of N,N'-dialkyl vs. N,N'-diaryl-based electron donor ancillary ligands on photocurrent and photovoltage in dye-sensitized solar cells (DSSCs).

In this study, we report the synthesis of a novel heteroleptic Ru(ii)-sensitizer, (Ru(2,2'-bipyridine-4,4'-dicarboxylic acid)-4,4'-bis(4-piperidin-1-yl)phenyl ethenyl)-(2,2'-bipyridine) (NCS)2, denoted as SD-1; moreover, its photophysical, electrochemical, and photovoltaic performances were compared with those of N719 and K77-7 (N,N'-diaryl Ru-sensitizer, namely Ru(2,2'-bipyridine-4,4'-dicarboxylic-acid)-4,4'-bis(2-(4-N,N'-diphenylaminophenyl)ethenyl)-2,2'-bipyridine (NCS)2). The photovoltaic performance of SD-1 outperformed those of N-719 and K77-7, particularly in the red region, and the overall efficiency of SD-1 was 8.5% as compared to 8.0% of K77-7 and 7.7% of N719 under the same experimental device conditions. The superior light harvesting efficiency of SD-1 can be attributed to the strong electron donor sp3-nitrogen, which is attached to two sp3-carbons (dialkyl), whereas in the case of K77-7, all carbon atoms attached to the sp3-nitrogen are sp2, which decrease the electron density on the latter and minimize the electron-donating power of the ancillary ligand in K77-7. To gain a quantitative understanding of the electron density on nitrogen in SD-1 and K77-7, first-principle calculations using molecular and thermodynamic descriptors, such as frontier molecular orbitals, ground-state oxidation potential (GSOP), excited-state oxidation potential (ESOP), optical gap (E0-0), and charge distributions, were conducted in solution. In addition, for understanding the anchored structures of dyes on Ti24O48, density functional theory (DFT) and time-dependent density functional theory (TD-DFT) were utilized. Results of computational studies are in excellent agreement with the experimental results, which can be used as a screening tool for the design of more efficient molecular motifs for DSSCs.

Metal based drugs: design, synthesis and in-vitro antimicrobial screening of Co(II), Ni(II), Cu(II) and Zn(II) complexes with some new carboxamide derived compounds: crystal structures of N-[ethyl(propan-2-yl)carbamothioyl]thiophene-2-carboxamide and its copper(II) complex.

A new series of compounds derived from thiophene-2-carboxamide were synthesized and characterized by IR, (1)H-NMR and (13)C-NMR, mass spectrometry and elemental analysis. These compounds were further used to prepare their Co(II), Ni(II), Cu(II) and Zn(II) metal complexes. All metal(II) complexes were air and moisture stable. Physical, spectral and analytical data have shown the Ni(II) and Cu(II) complexes to exhibit distorted square-planar and Co(II) and Zn(II) complexes tetrahedral geometries. The ligand (L(1)) and its Cu(II) complex were characterized by the single-crystal X-ray diffraction method. All the ligands and their metal(II) complexes were screened for their in-vitro antimicrobial activity. The antibacterial and antifungal bioactivity data showed that the metal(II) complexes were found to be more potent than the parent ligands against one or more bacterial and fungal strains.

Metal-based carboxamide-derived compounds endowed with antibacterial and antifungal activity.

A series of three bioactive thiourea (carboxamide) derivatives, N-(dipropylcarbamothioyl)-thiophene-2-carboxamide (L(1)), N-(dipropylcarbamothioyl)-5-methylthiophene-2-carboxamide (L(2)) and 5-bromo-N-(dipropylcarbamothioyl)furan-2-carboxamide (L(3)) and their cobalt(II), copper(II), nickel(II) and zinc(II) complexes (1)-(12) have been synthesized and characterized by their IR,(1)H-NMR spectroscopy, mass spectrometry and elemental analysis data. The Crystal structure of one of the ligand, N-(dipropylcarbamothioyl)thiophene-2-carboxamide (L(1)) and its nickel(II) and copper(II) complexes were determined from single crystal X-ray diffraction data. All the ligands and metal(II) complexes have been subjected to in vitro antibacterial and antifungal activity against six bacterial species (Escherichia coli. Shigella flexneri. Pseudomonas aeruginosa. Salmonella typhi. Staphylococcus aureus and Bacillus subtilis) and for antifungal activity against six fungal strains (Trichophyton longifusus. Candida albicans. Aspergillus flavus. Microsporum canis. Fusarium solani and Candida glabrata). The in vitro antibacterial and antifungal bioactivity data showed the metal(II) complexes to be more potent than the parent ligands against one or more bacterial and fungal strains.

Silver-infused TiO2 nanowires and unveiling their potential for superior wastewater dye remediations.

Silver infused ultrathin TiO2 nanowires (NWs) were synthesized via a single step solvothermal approach. The crystallinity, structure, and morphology were determined to understand the physicochemical nature of the nanocomposites. The catalytic efficiency of the newly synthesized nanocatalysts was tested for the textile waste treatment taking methylene blue (MB) as model pollutant under solar light irradiations. Nearly 96% photodegradation efficiency for MB was achieved within 20 min. Furthermore, the recyclability of the photocatalyst was also studied, and the material remained stable and effective up to four consecutive runs. RESEARCH HIGHLIGHTS: Precise size-controlled synthesis of Ag-incorporated titania nanowires (ATNWs) Controlled aspect ratios, with tunable lengths and diameters (100-3 nm) via precursor and surfactant optimization Demonstrated ATNWs' efficiency in degrading toxic dye, methylene blue (MB) 96% photodegradation efficiency for MB achieved within 20 min using 3 nm thick annealed TiO2 NWs Recyclability efficiency of photocatalyst, which remained stable and effective for up to four consecutive runs.

A single step wet chemical approach to bifunctional ultrathin (ZnO)62(Fe2O3)38 dendritic nanosheets.

At the ultrathin scale, nanomaterials exhibit interesting chemical and physical properties, like flexibility, and polymer-like rheology. However, to limit the dimensions of composite nanomaterials at the ultrathin level is still a challenging task. Herein, by adopting a new low temperature single step and single pot wet chemical approach, we have successfully fabricated two dimensional (2D) mixed oxide ZnO-Fe2O3 dendritic nanosheets (FZDNSs). Various control experimental outcomes demonstrate that precursor salts of both the metals are crucial for the formation of stable 2D FZDNSs. The obtained FZDNSs not only exhibit the best photoreduction performance but also much enhanced electrocatalytic performance. This work will provide a promising avenue for the synthesis of cost effective transition metal mixed oxide based 2D nanosheets having wide ranging applications.

Green synthesis of Cu-Mn co-incorporated ZnO nanoparticles for antibacterial and photocatalytic applications.

The synergistic effect of bimetallic co-incorporated metal oxides have gained enormous attention due to their unique optoelectronic properties. Herein, we present the green synthesis of ZnO, Cu-incorporated ZnO, Mn-incorporated ZnO, and Cu-Mn co-incorporated nanoparticles (ZnO NPs, CuZnO NPs, MnZnO NPs, MnCuZnO NPs) for antimicrobial and photocatalytic reduction applications using corn silk extract and industrial metal wastes. The as-synthesized NPs were characterized by using UV-visible absorption spectroscopy (UV-Vis), photoluminescence (PL) spectroscopy, Fourier-transformed infrared spectroscopy (FT-IR), powdered x-ray diffraction (XRD), and scanning electron microscopy (SEM). CuZnO, MnZnO, and MnCuZnO NPs efficiently inhibited bacterial culture growth. The photocatalytic reduction activity of as-synthesized NPs against the different concentrations of 4-nitrophenol (4-NP) in water was also investigated. CuZnO and MnCuZnO nanoparticles were to be efficient photocatalysts for reducing 4-NP into 4-aminophenol (4-AP). RESEARCH HIGHLIGHTS: Green synthesis of nanomaterials by agricultural and industrial wastes Cu and Mn co-incorporated ZnO NPs have shown good photocatalysis and antimicrobial activities Green approach for waste conversion to value-added products.

A single-source precursor route to unusual PbSe nanostructures by a solution-liquid-solid method.

PbSe nanowires (NWs) have been synthesized by using a single-source precursor route. Carefully controlling the conditions of individual reactions leads to PbSe NWs with well-defined diameters (8-25 nm) and lengths (100 nm-1 µm). The as-grown PbSe NWs are highly crystalline, defect free, and readily dispersible in organic solvents. The NWs have been characterized by X-ray diffraction and high-resolution transmission electron microscopy.

Controlled synthesis of tuned bandgap nanodimensional alloys of PbS(x)Se(1-x).

Truly alloyed PbS(x)Se(1-x) (x = 0-1) nanocrystals (∼5 nm in size) have been prepared, and their resulting optical properties are red-shifted systematically as the sulfur content of the materials increases. Their optical properties are discussed using a modified Vegard's approach and the bowing parameter for these nanoalloys is reported for the first time. The alloyed structure of the nanocrystals is supported by the energy-filtered transmission electron microscope images of the samples, which show a homogeneous distribution of sulfur and selenium within the nanocrystals. X-ray photoelectron spectroscopy studies on ligand-exchanged nanocrystals confirmed the expected stoichiometry and various oxidized species.

Electronic and surface properties of PbS nanoparticles exhibiting efficient multiple exciton generation.

Ultrafast transient absorption measurements have been used to study multiple exciton generation in solutions of PbS nanoparticles vigorously stirred to avoid the effects of photocharging. The threshold and slope efficiency of multiple exciton generation are found to be 2.5 ± 0.2 ×E(g) and 0.34 ± 0.08, respectively. Photoemission measurements as a function of nanoparticle size and ageing show that the position of the valence band maximum is pinned by surface effects, and that a thick layer of surface oxide is rapidly formed at the nanoparticle surfaces on exposure to air.

Transient optical studies of interfacial charge transfer at nanostructured metal oxide/PbS quantum dot/organic hole conductor heterojunctions.

We report a transient absorption and luminescence study addressing the charge separation, recombination, and regeneration reactions at nanostructured metal oxide/PbS quantum dot/organic hole conductor heterojunctions. We show that yields of charge separation are significantly higher at PbS/SnO(2) interfaces relative to PbS/TiO(2) interfaces, and conclude that this behavior is a result of the ca. 300-500 meV lower conduction band edge in SnO(2) as compared to TiO(2). We also report a correlation between the PbS particle size and the yield of charge separation at PbS/SnO(2) interfaces, with a smaller PbS particle radius resulting a higher yield of charge separation. Finally we investigated the regeneration of the photooxidized PbS by an organic hole transporting material, namely, spiro-OMeTAD. The overall spiro-OMeTAD(+) yield is found to be 27% at a SnO(2)/PbS (approximately 3 nm diameter)/spiro-OMeTAD heterojunction. The addition of a lithium salt was found to raise the overall spiro-OMeTAD(+) yield from its initial value of 27% (where no Li(+) is present) to 50%. We believe this to be a result of an increase in the primary charge injection yield to near unity as the SnO(2) conduction band is lowered (with increasing [Li(+)]), increasing the driving force for electron injection. The present findings are discussed with relevance to the design of PbS-sensitized metal oxide layers for DSSCs.

Electronic Tuning of Zinc Oxide by Direct Fabrication of Chromium (Cr) incorporated photoanodes for Visible-light driven Water Splitting Applications.

Herein, we report the synthesis of Cr incorporated ZnO sheets arrays microstructures and construction of photoelectrode through a direct aerosol assisted chemical vapour deposition (AACVD) method. The as-prepared Cr incorporated ZnO microstructures were characterized by transmission electron microscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, powdered X-ray spectroscopy, X-ray photoelectron spectroscopy and UV-Vis diffused reflectance spectroscopy. The Cr incorporation in ZnO red shifted the optical band gap of as-prepared photoanodes. The 15% Cr incorporation in ZnO has shown enhanced PEC performance. The AACVD method provides an efficient in situ incorporation approach for the manipulation of morphological aspects, phase purity, and band structure of photoelectrodes for an enhanced PEC performance.

Synthesis of ZnO hexagonal single-crystal slices with predominant (0001) and (0001) facets by poly(ethylene glycol)-assisted chemical bath deposition.

ZnO hexagonal single-crystal slices with predominant (0001) and (0001) facets have been fabricated by poly(ethylene glycol)-assisted chemical bath deposition.

5-(2-Methoxy-benz-yl)-4-(2-methoxy-phen-yl)-4H-1,2,4-triazol-3-ol.

In the mol-ecule of the title compound, C(17)H(17)N(3)O(3), the triazole ring is oriented at dihedral angles of 88.09 (3) and 83.72 (3)° with respect to the 2-methoxy-benzyl and 2-methoxy-phenyl rings, respectively. The dihedral angle between the 2-methoxy-benzyl and 2-methoxy-phenyl rings is 52.95 (3)°. In the crystal structure, inter-molecular N-H⋯O hydrogen bonds link the mol-ecules into centrosymmetric dimers. There is a π-π contact between the 2-methoxy-phenyl rings [centroid-centroid distance = 3.811 (3) Å].