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Graphitic Carbon Nitride as a Platform for the Synthesis of Silver Nanoclusters.

ABSTRACT: Graphitic carbon nitride (CN) synthetized by the thermal polycondensation of melamine at 550 °C for 4 h was further exfoliated by heating at 500 °C for 3 h. Silver cations were adsorbed on the exfoliated graphitic carbon nitride (CNE) and then reduced by sodium borohydride forming silver nanoclusters (NCs) with a size of less than 1 nm. The NCs were located on the CNE surface and did not change the CNE properties except for its pore size distribution and thereby specific surface area (SSA). The Ag NCs were able to collect the photoinduced electrons of CNE and thus reduce their recombination with the holes. It was also documented by the increase in the CNE photocatalytic activity in terms of the degradation of antibiotic Ofloxacin. This study demonstrates the ability of CNE to serve as a platform for a simple and fast synthesis of Ag NCs without any stabilizing compounds.

SUBMITTER: Starukh H

PROVIDER: S-EPMC8613329 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Synthesis of Silver Nanoparticles-Modified Graphitic Carbon Nitride Nanosheets for Highly Efficient Photocatalytic Hydrogen Peroxide Evolution.

Project description:As a promising metal-free photocatalyst, graphitic carbon nitride (g-C3N4) is still limited by insufficient visible light absorption and rapid recombination of photogenerated carriers, resulting in low photocatalytic activity. Here, we adjusted the microstructure of the pristine bulk-g-C3N4 (PCN) and further loaded silver (Ag) nanoparticles. Abundant Ag nanoparticles were grown on the thin-layer g-C3N4 nanosheets (CNNS), and the Ag nanoparticles decorated g-C3N4 nanosheets (Ag@CNNS) were successfully synthesized. The thin-layer nanosheet-like structure was not only beneficial for the loading of Ag nanoparticles but also for the adsorption and activation of reactants via exposing more active sites. Moreover, the surface plasmon resonance (SPR) effect induced by Ag nanoparticles enhanced the absorption of visible light by narrowing the band gap of the substrate. Meanwhile, the composite band structure effectively promoted the separation and transfer of carriers. Benefiting from these merits, the Ag@CNNS reached a superior hydrogen peroxide (H2O2) yield of 120.53 μmol/g/h under visible light irradiation in pure water (about 8.0 times higher than that of PCN), significantly surpassing most previous reports. The design method of manipulating the microstructure of the catalyst combined with the modification of metal nanoparticles provides a new idea for the rational development and application of efficient photocatalysts.

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The role of guanidine hydrochloride in graphitic carbon nitride synthesis.

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Biogenic Synthesis of Graphitic Carbon Nitride for Photocatalytic Degradation of Organic Dyes.

Project description:A simple approach of template growth of graphitic-carbon nitride (g-CN), a polymeric unit consisting of C, N, O, and H elements derived from extracts of green plant Aloe vera, which are rich in several chemical constituents, has been successfully experimented in this work. Comparing several other methods used for synthesizing g-CN involving a large amount of toxic components, here, we propose the simplest route economically and environmentally highly viable for near future. Green plants are highly rich in natural carbon and nitrogen compounds, such as acemannan, glucose, aloin, protein, etc. Way before g-CN research, many carbon-based materials have been synthesized for multifunctional properties, but g-CN has much benefit over them due to the presence of elements such as C, N, O, and H, thus making it electron-rich. Multifunctional properties of graphitic-carbon nitride interface bonding as a supercapacitor or as a metal-free catalyst thus help degrade dyes. Violet-blue broad band emission was even noticed when excited at 240 nm via C-C bonding (π-π* transition) in the absorption band with an extinction coefficient of ∼104 M-1 cm-1. With our research, we want to pave new ways of synthesizing such materials present in our nature in a biological form, which can protect our environment, thus causing less harm to mankind.

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Project description:Bulk graphitic carbon nitride (CN) was synthetized by heating of melamine at 550 °C, and the exfoliated CN (ExCN) was prepared by heating of CN at 500 °C. Sulfur-doped CN was synthesized by heating of thiourea (S-CN) and by a novel procedure based on the post-synthetic derivatization of CN with methanesulfonyl (CH3SO2-) chloride (Mes-CN and Mes-ExCN). The obtained nanomaterials were investigated by common characterization methods and their photocatalytic activity was tested by means of the decomposition of acetic orange 7 (AO7) under ultraviolet A (UVA) irradiation. The content of sulfur in the modified CN decreased in the sequence of Mes-ExCN > Mes-CN > S-CN. The absorption of light decreased in the opposite manner, but no influence on the band gap energies was observed. The methanesulfonyl (mesyl) groups connected to primary and secondary amine groups were confirmed by high resolution mass spectrometry (HRMS). The photocatalytic activity decreased in the sequence of Mes-ExCN > ExCN > CN ≈ Mes-CN > S-CN. The highest activity of Mes-ExCN and ExCN was explained by the highest amounts of adsorbed Acetic Orange 7 (AO7). In addition, in the case of Mes-ExCN, chloride ions incorporated in the CN lattice enhanced the photocatalytic activity as well.

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Nitrogen-doped Carbon Nanospheres-Modified Graphitic Carbon Nitride with Outstanding Photocatalytic Activity.

Project description:Metals and metal oxides are widely used as photo/electro-catalysts for environmental remediation. However, there are many issues related to these metal-based catalysts for practical applications, such as high cost and detrimental environmental impact due to metal leaching. Carbon-based catalysts have the potential to overcome these limitations. In this study, monodisperse nitrogen-doped carbon nanospheres (NCs) were synthesized and loaded onto graphitic carbon nitride (g-C3N4, GCN) via a facile hydrothermal method for photocatalytic removal of sulfachloropyridazine (SCP). The prepared metal-free GCN-NC exhibited remarkably enhanced efficiency in SCP degradation. The nitrogen content in NC critically influences the physicochemical properties and performances of the resultant hybrids. The optimum nitrogen doping concentration was identified at 6.0 wt%. The SCP removal rates can be improved by a factor of 4.7 and 3.2, under UV and visible lights, by the GCN-NC composite due to the enhanced charge mobility and visible light harvesting. The mechanism of the improved photocatalytic performance and band structure alternation were further investigated by density functional theory (DFT) calculations. The DFT results confirm the high capability of the GCN-NC hybrids to activate the electron-hole pairs by reducing the band gap energy and efficiently separating electron/hole pairs. Superoxide and hydroxyl radicals are subsequently produced, leading to the efficient SCP removal.

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| S-EPMC8182687 | biostudies-literature

Palladium Nanoparticles/Graphitic Carbon Nitride Nanosheets-Carbon Nanotubes as a Catalytic Amplification Platform for the Selective Determination of 17α-ethinylestradiol in Feedstuffs.

Project description:A new kind of nanocomposite, graphitic carbon nitride (g-C3N4)-carbon nanotubes (CNTs), has been synthesized via solid grinding, and followed by thermal polymerization process of melamine and CNTs. Pd nanoparticles were loaded on the as-prepared nanocomposite by the self-assembly method. The Pd/g-C3N4-CNTs nanocomposite exhibited excellent electrocatalytic activity toward the oxidation of 17α-ethinylestradiol (EE2), and compared with other detection methods of EE2, such as HPLC, this detection platform does not need the samples for further purification processing. And this detection platform was compared with HPLC, there is no significant difference between two methods, and the accuracy and precision of the determination of EE2 in feedstuff sample by differential pulse voltammetry (DPV) to a satisfactory level. Thus, the Pd/g-C3N4-CNTs nanocomposite can be used as a signal amplification platform for the detection of EE2 in feedstuffs samples. Under the optimum condition, the current response increased linearly with EE2 concentration from 2.0 × 10-6 ~ 1.5 × 10-4 M with a detection limit of 5.0 × 10-7 M (S/N = 3) by DPV. The Pd/g-C3N4-CNTs showed good reproducibility and excellent anti-interference ability that the relative standard deviation was 3.3% (n = 5). This strategy may find widespread and promising applications in other sensing systems involving EE2.

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Project description:Photoelectrochemical (PEC) conversion of solar light into chemical fuels is one of the most promising solutions to the challenge of sustainable energy. Graphitic carbon (IV) nitride polymer (g-CN) is an interesting sustainable photocathode material due to low-cost, visible-light sensitivity, and chemical stability up to 500 °C in air. However, grain boundary effects and limited active sites greatly hamper g-CN activity. Here, we demonstrate biopolymer-activation of g-CN through simultaneous soft-templating of a sponge-like structure and incorporation of active carbon-dopant sites. This facile approach results in an almost 300% increase in the cathodic PEC activity of g-CN under simulated solar-irradiation.

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