Carbon Nitride Nanoparticles Research Articles

Enhancing the performance of unitized regenerative proton exchange membrane fuel cells through microwave-synthesized chitosan based nanocomposites

The membrane electrode assembly (MEA) is a core component of unitized regenerative proton exchange membrane fuel cells (UR-PEMFCs). The studies aimed to improve the cell performance and reduce the cost of the MEAs for the widespread adoption of UR-PEMFCs. The present study focuses on modifications of MEA. For this purpose, an innovative nanocomposite electrocatalyst was developed by using a carbon-based support material containing platinum nanoparticles with a diameter of approximately 20–30 nm via microwave synthesis technique. The electrocatalyst was developed by a single-step process, consist of multi-walled carbon nanotubes (MWCNT), graphitic carbon nitride (g-C3N4), chitosan (Chi), and platinum nanoparticles (MWCNT/g-C3N4/Chi/Pt nanocomposite). With the development of this support material, a relatively economical and effective electrocatalyst was obtained by large surface area and using the platinum on this surface at the nano level. The prepared catalyst was applied to commercially available membrane electrode assemblies with an active area of 100 cm2. Single-cell and triple-stack performance tests were conducted, and an increase of 17.13 % in the electrolyzer mode and 16.98 % in the fuel cell mode was achieved in single-cell performance with this applied electrocatalyst. Furthermore, an enhancement of 16.96 % in the electrolyzer mode and 16.81 % in the fuel cell mode was discerned in the UR-PEMFC stack. Beside the experimental studies, a numerical model of the modified membrane properties has been developed and validated through experimental data.

From aromatic rings to aliphatic compounds - degradation of duloxetine with the use of visible light driven Z-scheme photocatalyst

The growing consumption of antidepressants, associated with their high chemical stability and low biodegradability, become a serious problem for aquatic environment. Many of their components are resistant to conventional water treatment technologies. The photocatalytic processes with the use of semiconductors becoming attractive methods of drugs degradation because the highly reactive species: electrons, holes, hydroxyl radicals (⦁OH) and superoxide anion radicals (O2⦁−) generated under illumination may be involved directly or indirectly in decomposition of complicated organic molecules.In this work we have shown for the first time that Z-scheme photocatalyst, consisted of bismuth vanadate (BiVO4), graphitic-like carbon nitride (g-C3N4) and Au nanoparticles (Au NPs) as a charge transfer mediator, is very efficient in degradation of duloxetine (DLX). We performed the comprehensive evaluation focused not only on degradation rate, mechanism of photocatalytic process, but also identification of decomposition products and the pathways of DLX degradation. Due to application of the elaborated Z-scheme photocatalyst, the degradation rate constant was more than 2-3 times higher than that obtained for photolysis, but more important, the final compounds were mainly aliphatic products, formed by opening of aromatic rings. The chemical structure of the degradation products were determined with the use of HPLC and LC-MS. The toxicity of photoproducts with respect to water organisms was tested by means of Spirotox and Microtox assays. The Microtox test indicated that toxicity of the products after 6h of the solution irradiation in the presence of Z-scheme photocatalyst is about 4 times lower than that after photolysis.

Glassy carbon electrodes modified with graphitic carbon nitride nanosheets and CoNiO2 bimetallic oxide nanoparticles as electrochemical sensor for Sunitinib detection in human fluid matrices and pharmaceutical samples.

Asophisticated electrochemical sensoris presented employing a glassy carbon electrode (GCE) modified with a novel composite of synthesized graphitic carbon nitride (g-C3N4) and CoNiO2 bimetallic oxide nanoparticles (g-C3N4/CoNiO2). The sensor's electrocatalytic capabilities for Sunitinib (SUNI) oxidation were demonstratedexceptional performance with a calculated detection limit (LOD) of 52.0nM. The successful synthesis and integrity of the composite were confirmed through meticulous characterization using various techniques. FT-IR analysis affirmed the successful synthesis of g-C3N4/CoNiO2 by providing insights into its molecular structure. XRD, FE-SEM, SEM-EDX, and BET analyses collectively validated the material's structural integrity, surface morphology, and electrocatalytic performance. Optimization of key analytical parameters, such as loading volume, concentration, electrolyte solution type, and pH, enhanced the electrocatalytic sensing capabilities of g-C3N4/CoNiO2. The synergistic interaction between g-C3N4 and CoNiO2 bimetallic oxide nanoparticles executed the sensor highly effective in the electrical oxidation of SUNI. Across a concentration range of 0.1-83.8µMSUNI, the anodic peak current exhibited a linear increasewith good precision. Application of the newly developed g-C3N4/CoNiO2 system to detect SUNI in a variety of samples, including urine, human serum, and capsule dosage forms, obtained satisfactory recoveries ranging from 97.1 to 103.0%. This methodology offers a novel approach to underscore the potential of the developed sensor for applications in biological and pharmaceutical monitoring.

Sensitive Electrochemical Sensor for Gallic Acid Determination in Honey Based on g-C3N4/AuNPs Modified Carbon Paste Electrode

Gallic acid (GA) is a well-known polyphenol that occurs naturally in plants and is used as a chemical marker or standard antioxidant in analytical research. Here, a carbon paste electrode was modified with a nanocomposite of graphitic carbon nitride and gold nanoparticles (g-C3N4/AuNPs/CPE). The g-C3N4/AuNPs was characterized by Fourier transform infrared spectroscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. Electrochemical impedance spectroscopy, cyclic voltammetry, and differential pulse voltammetry methods were used to investigate the electrochemical behavior of GA on the electrode. EIS analysis exhibited lower charge-transfer resistance in g-C3N4/AuNPs/CPE than CPE; 250 vs 1500 Ω, respectively. The g-C3N4/AuNPs/CPE was used to GA sensing with limit of detection and linear response range of 0.025 and 0.16–4.10 μM, respectively via DPV. Then, the GA content in Iranian honey samples with different floral origins such as Ziziphus, Barberry, Thyme, Astragalus, Eucalyptus and Coriander was successfully determined. According to result, the fabricated electrochemical sensor could be useful for GA evaluation in food samples.

Radiant synergy: Illuminating methyl orange dye removal with g-C3N4/ZnO heterojunction photocatalyst

In this study, a robust hybrid heterojunction composite of g-C3N4/ZnO was successfully synthesized using a straightforward and cost-effective coprecipitation method. The resulting composite amalgamates the properties of graphitic carbon nitride (g-C3N4) and zinc oxide nanoparticles (ZnO NPs). Thorough characterization using techniques such as XRD, FT-IR, FE-SEM, HR-TEM, UV-DRS, EIS, PL, and EDX confirmed the structural and elemental composition of the catalyst. The challenge of using photons as the sole energy source for the activation of photocatalysts under ambient conditions was addressed. The photocatalytic potential of the hybrid heterojunctions was assessed by degrading the methyl orange (MO) dye under sunlight. The 10 wt% g-C3N4/ZnO composite exhibited effective suppression of charge recombination during photocatalytic degradation. Notably, the heterojunction 10 wt% g-C3N4/ZnO composite displayed remarkable photocatalytic performance, achieving a substantial 98 % degradation of MO within 90 min of solar irradiation, outperforming other materials. Moreover, the synthesized composites exhibited favorable attributes in terms of recyclability and mechanical stability, retaining their efficacy over five cycles. This substantiates their promising role as potential candidates for future photocatalyst applications. In essence, g-C3N4/ZnO heterojunction composites offer a robust solution for efficient and sustainable photocatalytic degradation of organic pollutants.

Aggregation-Induced Emission CN-Based Nanoparticles to Alleviate Hypoxic Liver Fibrosis via Triggering HSC Ferroptosis and Enhancing Photodynamic Therapy.

Hypoxia can lead to liver fibrosis and severely limits the efficacy of photodynamic therapy (PDT). Herein, carbon nitride (CN)-based hybrid nanoparticles (NPs) VPSGCNs@TSI for light-driven water splitting were utilized to solve this problem. CNs were doped with selenide glucose (Se-glu) to enhance their red/NIR region absorption. Then, vitamin A-poly(ethylene glycol) (VA-PEG) fragments and aggregation-induced emission (AIE) photosensitizers TSI were introduced into Se-glu-doped CN NPs (VPSGCNs) to construct VPSGCNs@TSI NPs. The introduction of VA-PEG fragments enhanced the targeting of the NPs to activated hepatic stellate cells (HSCs) and reduced their toxicity to ordinary liver cells. VPSGCN units could trigger water splitting to generate O2 under 660 nm laser irradiation, improve the hypoxic environment of the fibrosis site, downregulate HIF-1α expression, and activate HSC ferroptosis via the HIF-1α/SLC7A11 pathway. In addition, generated O2 could also increase the reactive oxygen species (ROS) production of TSI units in a hypoxic environment, thereby completely reversing hypoxia-triggered PDT resistance to enhance the PDT effect. The combination of water-splitting materials and photodynamic materials showed a 1 + 1 > 2 effect in increasing oxygen levels in liver fibrosis, promoting ferroptosis of activated HSCs and reversing PDT resistance caused by hypoxia.

Fluorescent Carbon Nitride Nanoparticles for Picric Acid Sensing.

Detection of nitroaromatic explosives is essential in the area of environmental safety. Fluorescent carbon nitride nanoparticles is a promising material for this purpose. Herein, we have prepared fluorescent carbon nitride nanoparticles (CNNPs) by one step thermal treatment of formamide. These fluorescent CNNPs is sensitive towards picric acid (PA) than other analytes both in aqueous medium and on test paper which is witnessed by fluorescence quenching based on inner filter effect (IFE). The PA detection with the fluorescent CNNPs is observed in the concentration ranges, 0 µM to 60 µM with linear range of 10 nM to 25 µM. The minimum detection limit in aqueous medium and solid phase are determined to be 26.20 nM and 10 µM respectively. Finally, the fluorescent CNNPs is applied for detection of PA in real water samples. The recoveries are in the ranges from 99.54 to 116.35% with relative standard deviation less than 3.85%. This proposed fluorescent method can act as suitable analytical technique to monitored PA concentration in water samples.

Manipulating interface-induced multi-channel charge transfers toward highly hierarchical synchronous g-C3N4/STO@Pt modulation for boosting artificial photosynthesis

For the transformation of energy conversion and photocatalytic decomposition, photocatalyst-based artificial photosynthesis for solar-to green fuels and environmental treatment has aroused great attention. Herein, a novel ternary heterojunction based on constructing an interaction between 2D-graphitic carbon nitride (CN), 3D-strontium titanate (STO) and Pt nanoparticles (NPs) (2D/3D CN/STO@Pt) is designed for the first time to greatly promote photocatalytic water cracking hydrogen (H2) evolution in an alkalescent environment, such as triethanolamine (TEO) as well as integrating with Rhodamin B (RhB) decomposition. Under optimized conditions, the H2 productivity over 3D/2D CN/STO@Pt-3 heterostructures (10,005 μmol h−1 g−1) with an apparent quantum yield of H2 production approaching 47.5% is found to be ∼29.7, 8.5, 1.1, and 1.5-fold as much as that in the CN, CN/STO, CN/STO@Pt-1, and CN/STO@Pt-5 heterojunctions, respectively. An up to 2.5-fold enhancement in the photocatalytic RhB decomposition rate, obtaining 90% within 60 min under visible-light-driven is observed for 3D/2D CN/STO@Pt-3 heterostructures, surpassing that of other samples. The CN/STO@Pt-3 sample shows the highest degradation rate of 3.5 min−1, which is 1.8, 2.8, 4.27 and 4.9 -time higher than that of the CN/STO@Pt-1, CN/STO@Pt-5, CN, and STO samples, respectively. The improved photocatalytic behavior of the heterogeneous structures could be ascribed to i) the type II-heterojunction between 2D CN and 3D STO; and ii) the creation of the Schottky contacts between semiconductors and Pt NPs. The configuration of the type-II heterojunction formed by the two semiconductors of 2D g-C3N4 and 3D STO contributes to improved light absorption ability, and rapid separation and transfer of photoinduced charges. At the same time, the close junction of Pt establishes the Schottky barrier to facilitate efficient electron transfer in the ternary nanostructures, impeding the quick recombination of photoexcited charge carriers, and offering abundant reactive sites, contributing multiple electron pathways for the photoreaction strategy. Increased photocurrent density from the LSV measurement and a declined in PL intensity confirmed the enhanced interfacial charge separation in the tertiary photocatalyst. Furthermore, the CN/STO@Pt-3 ternary heterostructure presents outstanding photocatalytic performance after five cycles, indicating good stability and reusability. This work gives a valuable modification pathway for the establishing multi-channel charge carrier transport for energy conversion and environmental remediation processes.

Correlation between existential form of ruthenium cocatalyst and photocatalytic hydrogen evolution of carbon nitride

Catalysts composed of nanocluster and single-atom (SA) were extensively used to enhance electrocatalytic water splitting performance, whereas study of their photocatalytic hydrogen (H2) evolution activity was limited. Herein, carbon nitride (CN) decorated by ruthenium (Ru) cocatalysts existed as SA + cluster, cluster + nanoparticles (NPs), and NPs were prepared by impregnation and calcination processes. The correlation between existential form, content of Ru cocatalyst and H2 evolution rate were carefully discussed. It was found that Ru NPs were favor for water molecule adsorption, whereas Ru SAs and clusters facilitated H2 desorption. Theoretical calculations revealed that Ru clusters + NPs cocatalyst were beneficial for H* intermediate formation. Water splitting tests found that 1.07 wt% Ru NPs + cluster modified CN showed the highest H2 evolution rate of 13.64 mmol h−1 g−1, which was 266.4 and 1.5 times higher than those of CN and Ru NPs (2.33 wt%) decorated CN, respectively. This work deeply reveals the influences of existential form of Ru cocatalysts on photocatalytic water splitting of CN, and provides thought in designing new cocatalysts to largely enhance H2 evolution.

Ultrasensitive detection of Ag+ and Ce3+ ions using highly fluorescent carboxyl-functionalized carbon nitride nanoparticles

The fluorescence quenching of carboxyl-rich g-C3N4 nanoparticles was found to be selective to Ag+ and Ce3+ with a limit of detection as low as 30 pM for Ag+ ions. A solid-state thermal polycondensation reaction was used to produce g-C3N4 nanoparticles with distinct green fluorescence and high water solubility. Dynamic light scattering indicated an average nanoparticle size of 95 nm. The photoluminescence absorption and emission maxima were centered at 405 nm and 540 nm respectively which resulted in a large Stokes shift. Among different metal ion species, the carboxyl-rich g-C3N4 nanoparticles were selective to Ag+ and Ce3+ ions, as indicated by strong fluorescence quenching and a change in the fluorescence lifetime. The PL sensing of heavy metal ions followed modified Stern–Volmer kinetics, and CNNPs in the presence of Ag+/Ce3+ resulted in a higher value of K app (8.9 × 104 M−1) indicating a more efficient quenching process and stronger interaction between CNNP and mixed ions. Sensing was also demonstrated using commercial filter paper functionalized with g-C3N4 nanoparticles, enabling practical on-site applications.

High-performance gas sensor utilizing g-C3N4/In2O3 composite for low concentration prediction to NO2

The demand for gas sensors is experiencing rapid growth, driven by the increasing need for air quality detection in the face of environmental pollution and industrial emissions. However, the widely used metal oxide semiconductor (MOS) gas sensors suffer from drawbacks such as low ability to predict gas concentration and poor selectivity. In this work, a sensor array was fabricated consisting of 10 various gas sensors and combined with an advanced deep learning algorithm to achieve precise predictions of nitrogen dioxide (NO2) at low concentrations. First, graphitic carbon nitride (g-C3N4) and In2O3 nanoparticles were composited with different mass ratios, resulting in the formation of distinct g-C3N4/In2O3 composites as sensing materials. Afterward, SEM, TEM, and XRD were employed to characterize the morphology, structure, and elemental composition of the samples. Furthermore, sensing properties including response, selectivity, and repeatability, are studied for 10 gas sensors based on g-C3N4/In2O3 composites. Finally, the convolutional neural network-efficient channel attention-gate recursive unit (CNN-AGRU) model was proposed to analyze the patterns of the signals collected from the sensor array when exposed to various NO2 concentrations from 1 to 9 ppm. The results demonstrated the integration of high-selectivity sensing materials to NO2 and an advanced deep learning algorithm CNN-AGRU enables to realize a high concentration prediction accuracy of about 97.04% and a low prediction error of 0.20527 ppm for NO2 gas.

Portable analysis of tract mercury ions by a hydrogel-based ratiometric fluorescence sensor using C3N4-CdTe0.16S0.84 QDs nanocomposites

The portable detection of trace mercury ions (Hg2+) in water is crucial for preventing and controlling mercury pollution. In this study, graphitic carbon nitride nanoparticles (CNNPs) with green fluorescence as the self-calibration signal were synthesized by a one-pot solvothermal method. Cadmium telluride sulfide quantum dots (CdTe0.16S0.84 QDs) with red fluorescence as a response signal were prepared using an oxidation-reduction method. Thus, a new ratiometric fluorescence sensor based on CNNPs-CdTe0.16S0.84 QDs was constructed for the visual detection of trace Hg2+. The linear range of the sensor was from 0.05 to 2525 nM, with a detection limit of 0.009 nM. The sensor displayed higher sensitivity to Hg2+ compared to copper ions and silver ions. The fluorescence quenching behavior and the source of sensitivity for the three metal ions were investigated using the Stern-Volmer equation and density functional theory. The results suggest that the high sensitivity to Hg2+ may arise from electron transfer and electrostatic interactions between Hg2+ and CdTe0.16S0.84 QDs. Building on this proposed strategy, a new smartphone-assisted CNNPs-CdTe0.16S0.84 QDs hydrogel-based fluorescence sensor was constructed for portable on-site analysis of trace Hg2+. This new method will facilitate the on-site monitoring of hazardous substances in environmental water.

Multicolour room temperature phosphorescence of carbon nitride nanoparticles in sodium borohydride and borax matrix

Carbon nitride based materials find applications in photocatalysis, sensing, and bioimaging. The fluorescence properties of carbon nitride based nanomaterials is widely studied. However, its phosphorescence phenomenon is relatively less explored. Herein, we report a simple and economic one step thermal synthesis of highly fluorescent pure carbon nitride nanoparticles (CNNPs) from organic solvent formamide at 220 °C, just above its boiling point without any further passivation or purification.The fluorescent CNNPs is dispersed in sodium borohydride and borax which act as suitable host matrix resulting in activation of persistent room temperature phosphorescence of CNNPs with high phosphorescence lifetimes of 1.144 s and 0.737 s respectively. Moreover, the CNNPs-Sodium borohydride composite display tricolour, blue, green and yellow-orange phosphorescence under 254 nm, 365 nm and 400 nm light respectively while CNNPs-Borax composite show dual blue and green phosphorescence under 254 nm and 365 nm UV light respectively. Hence, these CNNPs-Composite may be used as multicolour anti-counterfeiting materials in future.

Porous boron-doped graphitic carbon nitride-based label-free electrochemical immunoassay of vascular endothelial cadherin.

As a main connecting protein between endothelial cells, vascular endothelial cadherin (CD144) is involved in regulating vascular remodeling and maintaining vascular integrity. It is regarded as a marker of endothelial dysfunction and injury. Quantitative determination of CD144 is of importance in pathology research, diagnosis and treatment of vascular diseases. A label-free electrochemical method for the immunoassay of CD144 was developed in this work. CD144 antibodies were assembled on a glassy carbon electrode modified with porous boron-doped carbon nitride (B-GCN) and gold nanoparticles (AuNPs) in the presence of protein A. The binding of CD144 on the antibody-modified electrode induced serious steric hindrance, inhibiting the diffusion of ferri-/ferrocyanide from the bulk electrolyte to the electrode interface. The change of the differential pulse voltammetric response displayed a linear relationship with the concentration of CD144 between 0.500 and 400 ng mL-1. The new electrochemical sensor showed some good performances including good selectivity, high stability and satisfactory reproducibility. The cellular morphology observation and activity measurement showed that the dysfunction of vascular endothelial cells appeared in the presence of high-content NaCl. The electrochemical analysis reveals a positive correlation between the release amount of CD144 from the dysfunctional cells and the NaCl concentration in the growth medium.

Visible Light Driven CO2 Photoreduction Using TiO2 Nanotube Arrays Embedded with Low Bandgap Carbon Nitride Nanoparticles

The extraordinary thermal and photochemical stability, superior charge transport, and tunable band positions of graphitic carbon nitride (g-CN), which is constituted of elements that are plentiful on Earth, renders g-CN an important semiconductor photocatalyst for heterogeneous catalysis [1,2]. Despite these advantages, carbon nitride-based semiconductors do not function effectively as freestanding photocatalysts or photoelectrodes due to a rapid carrier recombination rate and a slightly wide bandgap that only enables them to capture blue and UV photons [3,4]. Anodically formed TiO2 nanotube arrays (TNTAs) are semiconducting wide bandgap scaffolds with excellent photocatalytic properties due to the intrinsic orthogonalization of charge generation/transport and charge transfer processes. Herein, we use a novel in situ electrophoretic anodization to embed low bandgap carbon nitride nanoparticles (CNNPs) in the walls of titania nanotubes. The likelihood of the CNNPs leaching off the TNTA photoanode during photoelectrochemical processes was eliminated by encapsulating CN inside a TiO2 matrix. CNNPs were formed by the thermal condensation polymerization of carbon nitride utilizing citric acid and urea as the precursors, and exhibited some unusual properties, including a lower bandgap of 2.1 eV, a highly redshifted fluorescence emission maximum at 2.35 eV, surface carboxylate groups, and the emergence of unique structural characteristics corresponding to amorphous yet graphitic carbon [5]. In contrast to bulk g-CN, which has a C:N ratio of 0.75, the CNNPs possessed an elevated C:N ratio as high as 1.87 at the surface. The additional carbon was found to be both amorphous and graphitic, although the structural characteristics of g-CN were mostly unaffected, as validated by diffractometric and spectroscopic data. Even in the absence of a sacrificial agent, the CNNP@TNT nanocomposite demonstrated enhanced performance in sunlight-driven CO2 photoreduction. When compared to the freestanding TNT photocatalyst, the CO yield of photoreduction for the CN@TNT hybrid was more than three times higher. UV-filtered illumination of the CNNP@TNT heterojunction photocatalyst generated appreciable quantities of methane and CO (3.41 and 8.78 μmolg–1h–1 respectively). In situ electrophoretic anodization is an innovative approach to incorporate semiconductor quantum dots into TiO2 nanotubes or other electrochemically grown nanostructures.REFERENCES1. Kessler, F. K. et al., Nature Reviews Materials (2017) 2 (6), 1.2. Chaulagain, N. et al., ACS Applied Materials & Interfaces (2022) 14 (21), pp.24309-24320.3. Kumar, P. et al., Advanced Optical Materials (2020) 8 (4), Art. No. 1901275.4. Fu, J. et al., Advanced Energy Materials (2018) 8 (3), Art. No. 1701503.5. Alam, K.M. et al., Chemical Engineering Journal (2023) 456, Art. No. 141067.

A composite coating based on Ti3C2Tx MXene and M16 corrosion inhibitor for self-healing anti-corrosion and wear resistance

In this study, two-dimensional transition metal carbides and carbon nitride (MXene) and mesoporous silica nanoparticles (SiO2) loaded with corrosion inhibitor 1-(3-((N-n-butyl) aminecarboxamido) propyl)-3-hexadecyl imidazolidin bromide (M16) were used to prepare a M16@MXene-SiO2 nanocomposite with good anti-corrosion and wear resistance. The structure and composition of the nanocomposites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). The synthesized M16@MXene-SiO2 nanocomposite was then added to an epoxy coating on Q235 carbon steel. The uniform distribution of M16@MXene-SiO2 in the coating was confirmed by SEM and atomic force microscopy (AFM). The electrochemical impedance spectroscopy (EIS) test showed that the corrosion resistance of epoxy coating was the best when the addition amount of M16@MXene-SiO2 was 5 wt%, and its electrochemical impedance could reach 5.98 × 109 Ω∙cm2. After 144 h immersion, the coating resistance (Rc) of the epoxy coating decreased to 3.88 × 103 Ω∙cm2, and that of the epoxy coating with M16@MXene-SiO2 increased to 1.01 × 104 Ω∙cm2. The corrosion inhibition efficiency of M16@MXene-SiO2 was tested by potentiodynamic polarization. After immersion for 24 h, the corrosion current density (Icorr) of the epoxy coating was 2.23 × 10−7 A∙cm−2, which reduced to 4.38 × 10−8 A∙cm−2 after adding M16@MXene-SiO2 and the corrosion inhibition efficiency increased by 80.36 %. In addition, the wear resistance of the epoxy coating was tested by reciprocating friction experiment. The friction coefficient of the epoxy coating decreased from 0.44 to 0.12 after adding 5 wt% M16@MXene-SiO2. The results showed that the composite coating had excellent corrosion resistance, self-healing properties and wear resistance. The improvement in corrosion could be explained by the filling of coating defects with MXene-SiO2 and the formation of corrosion inhibitor films. The improvement of friction performance was mainly attributed to the friction transfer film formed by MXene-SiO2 and M16.

Rapid charge migration of hierarchical S-Scheme g-C3N4/CdS@C for efficient photocatalytic hydrogen evolution

Photocatalytic H2 evolution as a resultful way to figure out energy problems is still inhibited by carrier separation efficiency and catalyst service life. Here, we report a hierarchical S-Scheme heterostructure of layered graphite carbon nitride and CdS nanoparticles coated with carbon film (g-C3N4/CdS@C) by a simple hydrothermal method for highly efficient visible-light-driven H2 evolution. The S-Scheme, comprising g-C3N4 and CdS, synergistically enhances the efficiency of carrier separation while maintaining the redox capacity of both components. The introduction of carbon film enhances the migration rate of carriers, in the meantime inhibits the photo corrosion of CdS to enhance the stability of catalyst. The g-C3N4/CdS@C achieves the H2 generation rate of 6.4 mmol g−1 h−1 and the apparent quantum yield of 12.7%, superior to most works on g-C3N4. This work provides a delicate S-Scheme photocatalyst and offers a valid strategy for prolonging the lifetime of transition metal sulfide-based materials.

Comparative catalytic reduction and degradation with biodegradable sodium alginate based nanocomposite: Zinc oxide/N-doped carbon nitride/sodium alginate

Sodium alginate (SA) is a biodegradable macromolecule which is used to synthesize nanocomposites and their further use as catalysis. Zinc oxide (ZnO) and nitrogen doped carbon nitride (ND-C3N4) nanoparticles are prepared using solvothermal and hydrothermal methods, respectively. ZnO/ND-C3N4/SA nanocomposites are successfully synthesized by employing in-situ polymerization. The presence of essential functional groups is confirmed by Fourier transform infrared (FTIR) spectroscopic analysis. Controlled spherical morphology for ZnO nanoparticles, with an average diameter of ∼52 nm, is shown by Scanning electron microscopic (SEM) analysis, while rice-like grain structure with an average grain size ∼62 nm is exhibited by ND-C3N4 nanoparticles. The presence of required elements is confirmed by Energy dispersive X-ray spectroscopic (EDX) analysis. The crystalline nature of nanocomposites is verified by X-ray diffraction spectroscopic (XRD) analysis. The investigation of the catalytic efficiency for degradation and reduction of various organic dyes is carried out on nanoparticles and nanocomposites. Thorough examination and comparison of parameters, such as apparent rate constant (kapp), reduction time, percentage reduction, reduced concentration and half-life, are conducted for all substrates. The nanocomposites show greater efficiency than nanoparticles in both reactions: catalytic reduction and catalytic degradation.

Eco-conscious nanofluids: exploring heat transfer performance with graphitic carbon nitride nanoparticles

Abstract The work explores the heat transfer capabilities of semiconducting graphitic carbon nitride (g-C3N4) nanofluids. Also, it presents a sustainable and eco-friendly method for synthesizing g-C3N4 nanoparticles using commercially available rice flour as a natural carbon precursor through hydrothermal treatment. The synthesized sample subjected to various characterizations, including analysis of their structure, morphology, thermal properties, and optical properties. The optical bandgap (2.66 eV) is deduced through Tauc plot analysis and reveals the semiconducting nature of the sample. The formation of g-C3N4 is confirmed by various spectroscopic techniques, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), and Raman spectroscopy. Thermogravimetric analysis (TGA) demonstrates the nanoparticles’ excellent thermal stability up to 550 °C, indicating potential applications in heat transfer fluids. The investigation of concentration-dependent thermal diffusivity variation using the sensitive mode mismatched dual beam thermal lens technique highlights the potential of g-C3N4 semiconductor nanofluid as an organic and metal-free additive in industry-demanding coolant applications.

Enhanced photocatalytic degradation of polycyclic aromatic hydrocarbon by graphitic carbonitride-nickel (g–C3N4–Ni) nanocomposite

The objective of the present study is to synthesize g-C3N4–Ni nanocomposites composed of graphitic carbon nitride and magnetic nickel nanoparticles for benzopyrene degradation, which is one of the most potent polycyclic aromatic hydrocarbons (PAH) molecules. The concocted g-C3N4–Ni nanocomposites contained confined nanospheres with a mean particle dimension of 22 nm. Batch adsorption studies revealed that a rise in adsorbent dosage elevates benzopyrene degradation percentage in both water and soil samples with respect to time. The increase in the benzopyrene concentration did not have much influence on the degradation efficiency, and hence, the minimal concentration of PAH molecule is essential for the effective adsorption by g-C3N4–Ni nanocomposites. The rise in pH tends to increase the degradation of Benzopyrene till 3 h of the incubation period, and beyond 3 h, the degradation percentage declines. With regard to the effect of light source, UV light has been shown to accelerate the degradation of benzopyrene by g-C3N4–Ni nanocomposites than sunlight. The adsorption kinetic and isotherm investigations have proven that the Pseudo-second order kinetic model and Freundlich isotherm model were appropriate for our study. Thus, the g-C3N4–Ni nanocomposites were found to be efficient as a photocatalyst for the adsorption of benzopyrene from environmental samples.