Room Temperature Phosphorescence of Chlorine Doped Carbon Nitride Dots.

Metal free room temperature phosphorescent materials have been the subject of considerable attention due to their potential applications in optoelectronic devices sensing, and security and safety signage. This study discusses how efficient fluorescent and phosphorescent chlorine doped carbon nitride dots (Cl-CNDs) were prepared by thermal treatment of guanidine hydrochloride. The Cl-CNDs prepared were characterized by field emission scanning electron microscope, dynamic light scattering, PXRD, EDX, Thermo gravimetric analysis, FT-IR, and UV-Visible spectroscopy. The Cl-CNDs exhibit a long phosphorescence lifetime of 657 ms and the phosphorescence quantum yield was found to be 2.32% upon being excited at 360 nm in ambient conditions. Formation of compact coreparticles via condensation along with hydrogen bonding of Cl-CNDs by its functional groups facilitate intersystem crossing and stabilizes the triplet states, favoring room temperature phosphorescence. The cost effective preparation and tunable optical properties of Cl-CNDs may find applications in security encryption and optoelectronic devices.

Green Synthesis of Silver Nanoparticles Using Diospyros malabarica Fruit Extract and Assessments of Their Antimicrobial, Anticancer and Catalytic Reduction of 4-Nitrophenol (4-NP).

The green synthesis of silver nanoparticles (AgNPs) has currently been gaining wide applications in the medical field of nanomedicine. Green synthesis is one of the most effective procedures for the production of AgNPs. The Diospyros malabarica tree grown throughout India has been reported to have antioxidant and various therapeutic applications. In the context of this, we have investigated the fruit of Diospyros malabarica for the potential of forming AgNPs and analyzed its antibacterial and anticancer activity. We have developed a rapid, single-step, cost-effective and eco-friendly method for the synthesis of AgNPs using Diospyros malabarica aqueous fruit extract at room temperature. The AgNPs began to form just after the reaction was initiated. The formation and characterization of AgNPs were confirmed by UV-Vis spectrophotometry, XRD, FTIR, DLS, Zeta potential, FESEM, EDX, TEM and photoluminescence (PL) methods. The average size of AgNPs, in accordance with TEM results, was found to be 17.4 nm. The antibacterial activity of the silver nanoparticles against pathogenic microorganism strains of Staphylococcus aureus and Escherichia coli was confirmed by the well diffusion method and was found to inhibit the growth of the bacteria with an average zone of inhibition size of (8.4 ± 0.3 mm and 12.1 ± 0.5 mm) and (6.1 ± 0.7 mm and 13.1 ± 0.5 mm) at 500 and 1000 µg/mL concentrations of AgNPs, respectively. The anticancer effect of the AgNPs was confirmed by MTT assay using the U87-MG (human primary glioblastoma) cell line. The IC50 value was found to be 58.63 ± 5.74 µg/mL. The results showed that green synthesized AgNPs exhibited significant antimicrobial and anticancer potency. In addition, nitrophenols, which are regarded as priority pollutants by the United States Environmental Protection Agency (USEPA), can also be catalytically reduced to less toxic aminophenols by utilizing synthesized AgNPs. As a model reaction, AgNPs are employed as a catalyst in the reduction of 4-nitrophenol to 4-aminophenol, which is an intermediate for numerous analgesics and antipyretic drugs. Thus, the study is expected to help immensely in the pharmaceutical industries in developing antimicrobial drugs and/or as an anticancer drug, as well as in the cosmetic and food industries.

Long Afterglow Room-Temperature Phosphorescence from Nanopebbles: A Urea Pyrolysis Product.

Materials having long afterglow are highly sought after for various applications such as light-emitting diodes, security signs and bioimaging. Herein, we report a simple, low-cost synthesis of a purely organic room-temperature phosphorescent nanomaterial with a pebble-like structure by heating urea, a biocompatible and easily available precursor, at 200 °C with a high phosphorescence lifetime of 1.0365 s and a visible afterglow for up to 10 s. This urea derived phosphorescent nanocomposite (UPNC) can be mixed with commercially available acrylic paint base and common gum, which can be readily used as a phosphorescent pigment.

Nitrogen-doped carbon dots as fluorescence ON-OFF-ON sensor for parallel detection of copper(ii) and mercury(ii) ions in solutions as well as in filter paper-based microfluidic device.

Due to improper garbage disposal and rapid industrialization, concentrations of different metal ions are rising to toxic levels in natural water sources. Development of novel, selective and sensitive sensors for different metal ions is in high demand for rapid detection and remediation. Herein, we report nitrogen-doped carbon dots (NCDs) with high blue fluorescence, synthesized by a new one-step pyrolytic method using urea and ethylenediaminetetraacetic (EDTA) acid as precursors. The NCDs were used for parallel detection of Hg2+ and Cu2+ ions in aqueous medium through a fluorescence ON-OFF-ON process. The minimum detection limit for Hg2+ and Cu2+ were 6.2 nM and 2.304 nM, respectively, in aqueous medium, which is close to or below the allowed levels of Hg2+ and Cu2+ ions, i.e., 6 ppb and 2 ppm, respectively, in drinking water as per World Health Organisation (WHO). Hg2+ and Cu2+ ions were discriminated with vitamin C (ascorbic acid) and trisodium citrate by a fluorescence turn on process. A filter paper based microfluidic device loaded with NCDs, vitamin C and trisodium citrate was developed using candle wax channels on a filter paper as a proof of principle, projecting NCDs as a promising material for parallel detection of multiple metal ions. The device demonstrated herein is capable of detecting Hg2+ and Cu2+ ions up to 0.1 µM. This simple, low cost, disposable paper-based device will be very useful for rapid onsite analysis.

Stimuli-responsive aggregation-induced fluorescence in a series of biphenyl-based Knoevenagel products: effects of substituent active methylene groups on π-π interactions.

A series of three biphenyl-based Knoevenagel products (denoted 1a, 1b, 1c) with active methylene groups has been synthesized. Compounds 1a and 1b show strong solid-state fluorescence, whereas 1c displays low emission. Effects of substituent groups in condensed phase packing of the molecules have been investigated and correlated with their photophysical properties. Interestingly, compound 1a exhibits mechanofluorochromism with emission color changes from yellow to green (wavelength shift of 40 nm) after mechanical grinding. Furthermore, fluorescence of 1a and 1b is turned off under alkaline conditions, making them potential candidates for aggregation-enhanced emission-based pH sensors.

An Interactive Quantum Dot and Carbon Dot Conjugate for pH-Sensitive and Ratiometric Cu2+ Sensing.

Herein we report the photoinduced electron transfer from Mn2+ -doped ZnS quantum dots (Qdots) to carbon dots (Cdots) in an aqueous dispersion. We also report that the electron transfer was observed for low pH values, at which the oppositely charged nanoparticles (NPs) interacted with each other. Conversely, at higher pH values the NPs were both negatively charged and thus not in contact with each other, so the electron transfer was absent. Steady-state and time-resolved photoluminescence studies revealed that interacting particle conjugates were responsible for the electron transfer. The phenomenon could be used to detect the presence of Cu2+ ions, which preferentially, ratiometrically, and efficiently quenched the luminescence of the Qdots.

Optically definable reaction-diffusion-driven pattern generation of Ag-Au nanoparticles on templated surfaces.

We introduce a new lithographic method for the generation of 2D patterns of composite nanoparticles (NPs) of Ag and Au by taking recourse to combine top-down and bottom-up approaches. Micrometer-scale and submicrometer-scale patterned Ag foils of commercially available compact disks (CDs) and digital versatile disks (DVDs), respectively, were used as templates. The galvanic replacement reaction of Ag by HAuCl(4) in the presence of the dye coatings on the foils led to the formation of patterned NP composites of Ag and Au, in addition to the formation of AgCl. The resultant structures appeared in the form of cross patterns of particles with micrometer and submicrometer dimensions. The AgCl crystals thus formed could be removed by using either a saturated NaCl solution or aqueous ammonia. In addition, AgCl could be converted to Ag by electrochemical reduction, thus generating Ag-coated Au NPs. Interestingly, the digital writing on CDs led to the formation of tertiary imprints on the patterns, based on the original writing patterns. This provided an additional handle in generating hierarchical patterns using light in combination with a chemical reaction diffusion process and the nearly parallel line patterns originally present in commercial CDs. The reactions could be carried out in aqueous solution, and the method does not require any additional curing. Also, the density of patterned particles is scalable on the basis of the choice of the original line patterns as present in CDs and DVDs.

Signaling gene cascade in silver nanoparticle induced apoptosis.

Nanoscale materials are presently gaining much importance for biological applications especially in the field of medicine. The large numbers of nanomaterial based products that are currently being developed - with projected applications in medicine - have inspired a growing interest in exploring their impact on cellular gene expression. The present study examines the effects of silver nanoparticles (NPs) on genes expression in an endeavor to assess the fundamental mechanisms that contribute to silver NP induced programmed cell death. Here, we have used RT-PCR to study the gene expression, flow cytometry analyses to probe the extent of apoptosis (FACS) and atomic force microscopy (AFM) to follow the cell membrane topology change induced by Ag NPs. The gene expression study revealed that Ag NP induced p53-mediated apoptotic pathway through which most of the chemotherapeutic drugs trigger apoptosis (programmed cell death). The results also suggest that Ag NPs could be attributed as therapeutic agent for biomedical and pharmaceutical applications.

Implications of silver nanoparticle induced cell apoptosis for in vitro gene therapy.

The impact of manufactured nanomaterials on human health and the environment is a major concern for commercial use of nanotechnology based products. A judicious choice of selective usage, lower nanomaterial concentration and use in combination with conventional therapeutic materials may provide the best solution. For example, silver nanoparticles (Ag NPs) are known to be bactericidal and also cytotoxic to mammalian cells. Herein, we investigate the molecular mechanism of Ag NP mediated cytotoxicity in both cancer and non-cancer cells and find that optimum particle concentration leads to programmed cell death in vitro. Also, the benefit of the cytotoxic effects of Ag NPs was tested for therapeutic use in conjunction with conventional gene therapy. The synergistic effect of Ag NPs on the uracil phosphoribosyltransferase expression system sensitized the cells more towards treatment with the drug 5-fluorouracil. Induction of the apoptotic pathway makes Ag NPs a representative of a new chemosensitization strategy for future application in gene therapy.

Green fluorescent protein-expressing Escherichia coli as a model system for investigating the antimicrobial activities of silver nanoparticles.

Recombinant Escherichia coli (E. coli) bacteria expressing green fluorescent protein (GFP) was used as a model system to investigate the antimicrobial activities of Ag nanoparticles (NPs). A convenient in situ method of Ag NP synthesis using sodium borohydride, in the bacterial growth medium, was developed to produce preformed NPs for the study. Fluorescence spectroscopic and microscopic techniques allowed rapid detection of time-dependent changes in bacterial growth as well as fluorescence characteristics in the presence of Ag NPs. In addition, X-ray diffraction, UV-vis spectroscopic, and transmission electron microscopic measurements were carried out to understand the effect of Ag NPs on the bacteria. Our observations indicated that Ag NPs, above a certain concentration, not only were bactericidal but also were found to reduce the sizes of treated bacteria in comparison to untreated ones. Cell lysis of Ag NP-treated bacteria was suggested by the increased GFP fluorescence obtained in the medium. In vitro DNA-Ag NP interaction was detected by spectrophotometric analysis. However, electrophoresis studies indicated no direct effect of Ag NPs on DNA or protein profiles.

Lithography for imprinting colored patterns with quantum dots.

In this article, we report a new form of lithography that involves a reaction between a gas and an ion embedded in a polymer film. The principle is based on a combination of top-down and bottom-up approaches in which a transmission electron microscope grid is placed on a poly(vinylpyrrolidone) film containing Cd2+ ions, which is then exposed to H2S gas. This leads to the generation of a fluorescent yellow pattern due to the formation of CdS nanoparticles on exposed parts of the film. Also, we have used the same method to generate patterns in two colors by starting with a green fluorescent dye incorporated into the film and following the same procedure in which patterned yellow-orange CdS nanoaparticles are distributed over the background fluorescence of the dye. We have used fluorescence microscopy, UV-vis and fluorescence spectroscopy, transmission electron microscopy, atomic force microscopy, and X-ray diffraction methods for the characterization of the products and patterns. This method could possibly be a fairly general method of generating patterned materials on 2D and 3D substrates.