Few-layered graphene networks composed of phosphorus and nitrogen dual-doped porous graphene (PNG) are synthesized via a MgO-templated chemical vapor deposition (CVD) using (NH4)3PO4 as N and P source. P and N atoms have been substitutionally doped in graphene networks since the doping takes place at the same time with the graphene growth in the CVD process. Raman spectra show that the amount of defects or disorders increases after P and N atoms are incorporated into graphene frameworks. The doping levels of P and N measured by X-ray photoelectron spectroscopy are 0.6 and 2.6 at %, respectively. As anodes for Li ion batteries (LIBs), the PNG electrode exhibits high reversible capacity (2250 mA h g(-1) at the current density of 50 mA g(-1)), excellent rate capability (750 mA h g(-1) at 1000 mA g(-1)), and satisfactory cycling stability (no capacity decay after 1500 cycles), showing much enhanced electrode performance as compared to the undoped few-layered porous graphene. Our results show that the PNG is a promising candidate for anode materials in high-rate LIBs.
We investigated the development of spontaneous (resting state) cerebral electric fields and their network organization from early to late childhood in a large community sample of children. Critically, we examined electrocortical maturation across one-year windows rather than creating aggregate averages that can miss more subtle maturational trends. We implemented several novel methodological approaches including a more fine grained examination of spectral features across multiple electrodes, the use of phase-lagged functional connectivity to control for the confounding effects of volume conduction and applying topological network analyses to weighted cortical adjacency matrices. Overall, there were major decreases in absolute EEG spectral density (particularly in the slow wave range) across cortical lobes as a function of age. Moreover, the peak of the alpha frequency increased with chronological age and there was a redistribution of relative spectral density towards the higher frequency ranges, consistent with much of the previous literature. There were age differences in long range functional brain connectivity, particularly in the alpha frequency band, culminating in the most dense and spatially variable networks in the oldest children. We discovered age-related reductions in characteristic path lengths, modularity and homogeneity of alpha-band cortical networks from early to late childhood. In summary, there is evidence of large scale reorganization in endogenous brain electric fields from early to late childhood, suggesting reduced signal amplitudes in the presence of more functionally integrated and band limited coordination of neuronal activity across the cerebral cortex.
Nanoparticle synthesis using microorganisms and plants by green synthesis technology is biologically safe, cost-effective, and environment-friendly. Plants and microorganisms have established the power to devour and accumulate inorganic metal ions from their neighboring niche. The biological entities are known to synthesize nanoparticles both extra and intracellularly. The capability of a living system to utilize its intrinsic organic chemistry processes in remodeling inorganic metal ions into nanoparticles has opened up an undiscovered area of biochemical analysis. Nanotechnology in conjunction with biology gives rise to an advanced area of nanobiotechnology that involves living entities of both prokaryotic and eukaryotic origin, such as algae, cyanobacteria, actinomycetes, bacteria, viruses, yeasts, fungi, and plants. Every biological system varies in its capabilities to supply metallic nanoparticles. However, not all biological organisms can produce nanoparticles due to their enzymatic activities and intrinsic metabolic processes. Therefore, biological entities or their extracts are used for the green synthesis of metallic nanoparticles through bio-reduction of metallic particles leading to the synthesis of nanoparticles. These biosynthesized metallic nanoparticles have a range of unlimited pharmaceutical applications including delivery of drugs or genes, detection of pathogens or proteins, and tissue engineering. The effective delivery of drugs and tissue engineering through the use of nanotechnology exhibited vital contributions in translational research related to the pharmaceutical products and their applications. Collectively, this review covers the green synthesis of nanoparticles by using various biological systems as well as their applications.
In the present work, we reported the luminescence of a green-emitting carbon dots (CDs) synthesized via solid state reaction method using diammonium hydrogen citrate and urea as a starting materials. The obtained green-emitting CDs shows strong absorption in the 350–450 nm region and gives intense green emission (λmax = 537 nm) with quantum yield as high as 46.4% under 420 nm excitation. The obtained green-emitting CDs also demonstrates high photo-stability, which is evidenced by the fact that its emission intensity almost has no change under irradiation by a 365 nm UV lamp for 2 hours. Moreover, the obtained green-emitting CDs shows high sensitivity and selectivity for the detection of Fe3+, and their emission intensity response towards Fe3+ ions is highly linear (R2 = 0.995) over the concentration range from 25 to 300 µM, which could provide an effective platform for detection of Fe3+. Mostly important, we further demonstrate that such photoluminescent green-emitting CDs exhibits low toxicity and are biocompatible for use with in cellular imaging. Combining with low cytotoxicity, good water solubility and excellent luminescence properties, green-emitting CDs could be used as a biocompatible fluorescent ink in future applications.
Monodispersed metastable cubic AgInS2 nanocrystals with an average size of around 2.5 nm are obtained via a solution-phase reaction. In contrast with the usual chalcopyrite and orthorhombic phase, Ag+ and In3+ cations in metastable cubic AgInS2 are randomly coordinated by four S2− anions. A phase transition from cation-disordered cubic to orthorhombic AgInS2 occurs with the increased reaction temperature or elongated reaction time. The photoluminescence quantum yield of cation-disordered cubic AgInS2 nanocrystals could reach 10% at room temperature, which is much higher than that of orthorhombic AgInS2 nanocrystals obtained via a similar approach.
A novel and facile soft-chemical method has been proposed for the synthesis of Ag 3 PO 4 crystals with various new morphologies (branch, tetrapod, nanorod, triangular prism), and the morphological effect on the photocatalytic activity of the obtained Ag 3 PO 4 crystals has been investigated. It is demonstrated that the morphology of Ag 3 PO 4 crystals can be controlled by simply adjusting external experimental conditions such as static and ultrasonic conditions. Photocatalytic results indicate that the branched Ag 3 PO 4 crystal with porous structure shows the highest photocatalytic activity among these Ag 3 PO 4 crystals with multiform morphologies, and the photocatalytic rate constants of branched Ag 3 PO 4 are 2.8 and 4 times those of irregular spherical Ag 3 PO 4 for degradation of methylene blue (MB) and rhodamine B (RhB) dye solutions under visible light irradiation, respectively.
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