Polymeric Graphitic Carbon Nitride Research Articles

Sensitizer created defective metal organic framework as a new platform for boosting visible-light photocatalysis of g-C3N4

We developed herein for the first time a sensitizer created defective MOF (SCD-MOF), simultaneously possessing sensitizers and defects as visible-light harvester and electron trapper, respectively, which can synergistically improve the visible-light photocatalysis of polymeric graphitic carbon nitride (g-C3N4). Based on this discovery, the resulting 5.0 wt% FeTCPP⊂UiO-66@g-C3N4 shows a significant 6.6 and 3.9 times improvement in catalytic efficiency compared with its parent materials of FeTCPP⊂UiO-66 and g-C3N4 in degrading organic pollutants. Moreover, it shows a 10.4 times enhancement in catalytic efficiency compared with commercial TiO2 (P25). Mechanism studies suggest that sensitizer molecules and defects in SCD-MOF can synergistically improve photocatalytic efficiency because of broadening the visible-light response and strengthening the charge carrier separation. This work illustrates a remarkably triple synergetic effect among visible-light harvester, electron/hole separator, and semiconductor and thus established SCD-MOF as a class of new platform to greatly improve the visible-light photocatalytic performance of conventional semiconductors.

Elevating Supercapacitor Performance of Co3O4-g-C3N4 Nanocomposites Fabricated via the Hydrothermal Method.

The hydrothermal method has been utilized to synthesize graphitic carbon nitride (g-C3N4) polymers and cobalt oxide composites effectively. The weight percentage of g-C3N4 nanoparticles influenced the electrochemical performance of the Co3O4-g-C3N4 composite. In an aqueous electrolyte, the Co3O4-g-C3N4 composite electrode, produced with 150 mg of g-C3N4 nanoparticles, revealed remarkable electrochemical performance. With an increase in the weight percentage of g-C3N4 nanoparticles, the capacitive contribution of the Co3O4-g-C3N4 composite electrode increased. The Co3O4-g-C3N4-150 mg composite electrode shows a specific capacitance of 198 F/g. The optimized electrode, activated carbon, and polyvinyl alcohol gel with potassium hydroxide were used to develop an asymmetric supercapacitor. At a current density of 5 mA/cm2, the asymmetric supercapacitor demonstrated exceptional energy storage capacity with remarkable energy density and power density. The device retained great capacity over 6k galvanostatic charge-discharge (GCD) cycles, with no rise in series resistance following cyclic stability. The columbic efficiency of the asymmetric supercapacitor was likewise high.

A Coordination Polymer Based on Nickel(II)–Cyamelurate: A Robust Catalyst with Highly Dispersed Nickel Sites for Nitrophenol Reduction under Ambient Conditions

Cyamelurate anions obtained from the hydrolysis of polymeric graphitic carbon nitride were used for the preparation of a water-stable and crystalline coordination polymer based on nickel(II)–cyamelurate. The polymer was prepared and applied as a catalyst for the reduction of 4-nitrophenol to 4-aminophenol in the presence of borohydride under ambient conditions. The catalyst was prepared by a simple and environmentally friendly method in an aqueous medium, and it was completely characterized by a variety of techniques, including FTIR, UV–Vis, XRD, TGA, TEM, and STEM. The obtained catalyst was able to catalyze the reaction of 4-nitrophenol to 4-aminophenol with a good kinetic constant. In addition, the catalyst proved to be significantly robust, maintaining a conversion rate greater than 80% after five minutes of reaction for eight consecutive catalytic cycles. In addition, the catalytic activity of the coordination polymer was much higher than that observed for a homogeneous catalyst based on aqueous Ni2+ ions, suggesting the importance of the structure of the coordination sphere formed by the cyamelurate anions. The results presented here can contribute to the application of other coordination polymers anchored with cyamelurate-like ligands and derivatives, as well as to new catalyst designs based on this coordination site formed by oxygen and nitrogen donor atoms.

Fabricating a 3D floating porous PDMS − Ag/AgBr decorated g-C3N4 nanocomposite sponge as a re-usable visible light photocatalyst

In this study, polymeric graphitic carbon nitride (g-C3N4) semiconductors was synthesized via a thermal condensation method. Subsequently, Ag/AgBr nanoparticles with varying ratios were decorated onto the g-C3N4 surface using the water/oil emulsion method. The resulting nanocomposites were characterized using XRD for phase identification and structural analysis, HR-TEM and SEM&EDAX for morphological structure, particle size, and elemental composition analysis, and XPS for investigating the chemical state and electronic structure. The impact of Ag/AgBr content on the optical properties of g-C3N4 were also studied such as (optical bandgap (Eg), refractive index (n), extinction coefficient (k), optical conductivity (σopt) and dielectric function (ε*)), Electrochemical impedance spectroscopy (EIS), PL spectroscopy and Chrono-amperometric investigations were conducted to assess the charge transfer capabilities and long-term durability of the prepared nanocomposites. The results revealed a reduction in Ag/AgBr particle size with an increase in g-C3N4 content, accompanied by a decrease in the optical bandgap from 2.444 eV to 2.393 eV. Furthermore, the nanocomposites exhibited enhanced degradation efficiencies of RhB dye, with the highest tested content of Ag/AgBr achieving 100% degradation after 120 min of irradiation. However, the challenge of catalyst separation after the degradation process remained. To address this issue, we developed a novel approach by impregnating Ag/AgBr@g-C3N4 photocatalyst onto a floating porous sponge using a simple sugar-template technique, offering potential as a reusable photocatalyst material. Furthermore, the 3D PDMS − Ag/AgBr@g-C3N4 photocatalyst was evaluated and found to maintain nearly the same photocatalytic efficiency for up to 5 consecutive cycles.

Preconcentration and selective extraction of trace Hg(ii) by polymeric g-C3N4 nanosheet-packed SPE column.

In this study, we successfully synthesized polymeric graphitic carbon nitride (g-C3N4) nanosheets through thermal means and proposed their application in solid-phase extraction (SPE) for the enrichment of trace Hg(ii). The nanosheets underwent characterization using scanning electron microscopy, tunnelling electron microscopy, and energy-dispersive X-ray spectroscopy. The column packed with polymeric carbon nitride nanosheets demonstrated effective extraction of trace Hg(ii) ions from complex samples. The g-C3N4 nanosheets possess a zeta potential value of -20 mV, enabling strong interaction with positively charged divalent Hg(ii) ions. This interaction leads to the formation of stable chelates with the nitrogen atoms present in the polytriazine and heptazine units of the material. The proposed method exhibited a high preconcentration limit of 0.33 μg L-1, making it suitable for analysing trace amounts of Hg(ii) ions. Moreover, the method's applicability was confirmed through successful analysis of real samples, achieving an impressive preconcentration factor of 200. The detection limit for trace Hg(ii) ions was determined to be 0.6 μg L-1. To assess the accuracy of the method, we evaluated its performance by recovering spiked amounts of Hg(ii) and by analysing certified reference materials. The results indicated excellent precision, with RSD consistently below 5% for all the analyses conducted. In conclusion, the thermally synthesized polymeric carbon nitride nanosheets present a promising approach for solid-phase extraction and preconcentration of trace Hg(ii) from real samples. The method showcases high efficiency, sensitivity, and accuracy, making it a valuable tool for environmental and analytical applications.

C3N4-interlayer-mediated interfacial polymerization of homopolymer nanofiltration membranes for efficient water purification

Interlayered thin film composite (TFNi) membranes have been shown to achieve high-quality polyamide (PA) skin layers with enhanced permeability and selectivity. Herein, we demonstrate the construction of a hydrophilic interlayer by polymeric graphitic carbon nitride (g-C3N4) for optimizing the interfacial polymerization of the nanofiltration membrane. Due to the effective enrichment and the slowed diffuse rate of amine monomer solutions, g-C3N4 modification decreases the thickness of the PA skin layer and increases the electronegativity of membranes. The best TFNi membrane exhibits a high water permeance of 31.82 L m−2 h−1 bar−1, nearly twice as high as that of the membrane without g-C3N4 interlayer, while maintaining a comparably Na2SO4 rejection efficiency. The stronger hydrophilicity and more negatively charged surface of the TFNi membrane effectively retarded membrane fouling, contributing to the high-efficiency removal of harmful drugs from actual surface water, with more than two times higher water flux that of commercialized NF270 membrane. This work provides a facile strategy to synthesize TFNi membranes with great application potential for high-performance nanofiltration.

Improving photocatalytic hydrogen generation of g-C3N4 via efficient charge separation imposed by Bi2O2Se nanosheets

Enabling highly efficient photocatalytic hydrogen production from solar-driven water splitting is of immense potential and environmental significance. However, the crucial issue of the low utilization efficiency of photogenerated charges in most photocatalysts, such as polymeric graphitic carbon nitride, g-C3N4 (CN), hampers the overall photocatalytic activity and hinders practical applications. To surmount this parasitic phenomenon, we develop a heterojunction-based strategy that improves the charge separation efficiency in CN. The heterostructure is constructed between thermally exfoliated CN and liquid phase exfoliated Bi2O2Se (BOS) via a solution-phase, electrostatically driven self-assembly process. The properly aligned band positions between the two components create a built-in electric field, which endows the composite with an enhanced charge separation efficiency. The optimized Pt-deposited heterostructure photocatalyst exhibits a hydrogen production rate of 6481 μmol h−1 g−1, and an apparent quantum efficiency of 11.65% at 420 nm, compared to those of Pt-deposited ECN (4595 μmol h−1 g−1, 6.64 %). We validate the efficient charge separation effect and the prolonged lifetime of photogenerated carriers in the heterostructure using a series of comprehensive characterizations across multiple timescales, thus, elucidating the origin of the observed photocatalytic activity. This demonstration offers valuable insights into improving the utilization efficiency of photogenerated charges for photocatalysis by heterostructure engineering with materials of distinct electronic configurations.

Synthesis of Graphene Based Graphitic Carbon Nitride Hybrid Nanocomposite Photocatalysts for Hydrogen Generation: A Mini Review

The discovery of visible active photocatalysts for H2 evolution via water splitting is the most awaited and critical goal of many researchers in recent years. Novel polymeric graphitic carbon nitride (GCN/g-CN) has emerged as a versatile material which has attracted the scientific community and industrialist because of its distinctiveness and outstanding electronic properties. g-CN is a metal free semiconductor as well as non-toxic, biodegradable polymeric material with low band gap energy which makes it a promising candidate as a photocatalyst and its efficiency as a catalyst can be modified by forming a hybrid nanocomposite with other semiconducting materials. Reduced graphene oxide, another metal free 2D material is a very good choice for this purpose. This review is an outlook for the synthesis processes and various properties of both g-CN and graphene. Further, it gives the approaches attempted towards the modifications required and done towards the development of a metal-free nano-hybrid material which is cost-effective, eco-friendly, and highly active visible light catalyst for the water- splitting process.

Nickel supported on polymeric graphitic carbon nitride for electrocatalytic in reduction of carbon dioxide

This study explores the potential of carbon-based materials, specifically CN-Ni-doped, as catalysts for CO2 reduction to methanol in a PEM-R. The research investigates the impact of Ni incorporation on CN's structure, resulting in increased interlayer spacing and reduced crystallite size. Additionally, the introduction of Ni modifies the samples' morphology, creating a more compact structure with smaller sheets. The findings indicate that CN-Ni displays promising catalytic activity, achieving a 25% Faradaic Efficiency (FE) with a methanol production rate of approximately 1.1 mol L−1 h−1. The study underscores the significance of optimizing reactor operational parameters to enhance CO2RR. In conclusion, this research contributes to the advancement of efficient and sustainable approaches for CO2 utilization and methanol synthesis.

Synthesis and characterization of enhanced visible light-driven C-doped ZnO-2D GO/g-C3N4 heterojunction photocatalyst

Well-designed 2D graphene oxide-modified polymeric graphitic carbon nitride composite nanosheets (GO/g-C3N4) as desirable sensitizers and catalytic substrates for optimising the visible light-driven photocatalytic performance of ZnO-based photocatalysts have been investigated. Herein, 2D GO/g-C3N4 composite nanosheets are first developed by ultrasonic and hydrothermal methods, and then coupled with ZnO nanoparticles to prepare a series of ternary GO/g-C3N4-ZnO heterojunction composites with vary GO loading concentrations. Characterization of the photocatalysts was carried out by SEM, TEM, XPS, XRD, DRS, photoluminescence (PL) spectroscopy; evaluation of the visible light photocatalytic activity was performed by degrading an aqueous methylene blue (MB) solution. XPS studies showed that the formation of a ZnC bond in 15 % GO/g-C3N4-ZnO is due to the replacement of oxygen by carbon, indicating the construction of a hybrid heterojunction composed of C-doped ZnO and visible light sensitive GO/g-C3N4 composite nanosheets. The photodegradation performance of 15 % GO/g-C3N4-ZnO is 5.3, 2.9, and 2.2 times higher than that of pure ZnO, g-C3N4, and g-C3N4-ZnO, respectively. Due to the increase of GO loading in GO/g-C3N4 composite nanosheets, some characteristics of efficient visible light photocatalysis, such as a wider light absorption range, fluorescence quenching in the PL spectrum, excellent optical response in photocurrent measurement, and good stability，were confirmed and can be attributed to the electronic interaction between heterostructures and the effective transfer of photogenerated electrons in these ternary nanocomposites. This work may provide a new promising pathway for the construction of easily prepared 2D GO/g-C3N4 hybrid-modified nanocomposites, which is a hopeful material for wastewater control.

Gas template mediated exfoliation of polymeric graphitic carbon nitride; what contributes more to hydrogen production, a higher specific surface area, or defect sites?

Polymeric graphitic carbon nitride (g-C3N4) has emerged as a promising photocatalyst for various applications; however, the optimization of its performance remains a challenge. In this study, we investigate the influence of specific surface area and nitrogen content on the photocatalytic activity of g-C3N4. Our findings reveal that a highly nitrogen-deficient g-C3N4 demonstrates superior photocatalytic activity in the absence of a co-catalyst. Conversely, a g-C3N4 sample with a higher surface area and reduced nitrogen deficiency performs better when coupled with a co-catalyst such as platinum. We attribute these differences to the concurrent introduction of nitrogen defects and oxygen species, which modify the conduction band position and improve the separation efficiency of photogenerated charge carriers. These outcomes suggest that the optimization of specific surface area and nitrogen defects could be a promising strategy for tailoring g-C3N4 performance in photocatalytic applications. Such an approach holds significant implications for developing highly efficient photocatalytic systems.

Disulfide bond cross-linked three-dimensional graphitic carbon nitride nanocomposites with glutathione responsive fluorescence for cancer-cell specific bioimaging

The polymeric graphitic carbon nitride (g-C3N4) nanomaterials with non-toxicity, high stability, and photoluminescence property have promising application in bioimaging and biosensing. In this work, smart three-dimensional (3D) disulfide bond cross-linked g-C3N4 (CL-g-C3N4) nanocomposites with glutathione (GSH)-responsive fluorescence property were designed and developed for cancer cell-specific imaging. The g-C3N4 layered nanosheets with an average lateral size of 80–120 nm and mean thickness of ca. 0.5–1.0 nm were fabricated and used as building blocks. By combining several g-C3N4 nanosheets with non-fluorescent redox-sensitive disulfide bond-contained cross-linker, CL-g-C3N4 nanocomposites with a hydrodynamic particle size of ca. 270.5 nm were synthesized. The fluorescence of the CL-g-C3N4 nanocomposites was initially quenched due to the assembly of 2D g-C3N4 nanosheets into 3D structured nanocomposite caused by the crosslinking process. However, upon stirring them in a GSH solution with a concentration of 2 mM, which simulates the content in the cytoplasm of cells, the fluorescence was recovered to 89.3 % of its original intensity. This recovery was achieved through a thiol-disulfide exchange reaction, highlighting the GSH-responsive fluorescence recovery property of the nanocomposites. The cellular uptake traced images of CL-g-C3N4 in human cervix carcinoma (HeLa) cancer cells exhibited almost 3.5 times higher fluorescence intensity than that in human embryonic kidney (HEK 293 T) healthy cells owing to higher GSH concentration in cancer cells than that in healthy cells. The constructed CL-g-C3N4 nanocomposites should hold great promise as a fluorescence detector of cancer cells for early cancer diagnose.

Fabrication of copper molybdate nanoflower combined polymeric graphitic carbon nitride heterojunction for water depollution: Synergistic photocatalytic performance and mechanism insight

In the scope, developed a novel copper molybdate decorated polymeric graphitic carbon nitride (CuMoO4@g-C3N4 or CMC) heterojunction nanocomposite in an easy solvothermal environment for the first time. The synthesized CMC improved the photocatalytic degradation of an antibiotic drug [ciprofloxacin (CIP)] and organic dye [Rhodamine B (RhB)]. Consequently, the CMC demonstrates a marvelous crystalline nature with ∼26 nm size, as obtained from XRD analysis. Besides, the surface morphology studies confirm the large-scale construction of flower-like CMC with a typical size of 10–15 nm. The CMC showed efficient catalytic activity for both the pollutants, achieving the degradation of 98% for RhB and 97% for CIP in 35 and 60 min, respectively. The reaction parameters including the concentration of pollutants, catalyst dosages, and scavengers are optimized for the best photocatalytic results. Notably, the trapping tests showed that the •OH and O2•− radicals are the primary oxidative species liable for the photocatalytic process. The recyclability test of the photocatalyst infers that the photocatalyst is highly stable up to the fifth recycle. Our work affords an efficient and ideal path to constructing the new g-C3N4-based architected photocatalyst for toxic wastewater treatment in the near future.

Engineering morphology and nitrogen content on graphitic carbon nitrides for efficient solar to hydrogen conversion reaction

Semiconducting polymeric graphitic carbon nitride (g-C3N4; GCN) has emerged as low-cost and robust photocatalyst to convert solar to chemical energy. Unfortunately, the preparation of GCN is carried out via thermal polymerization of melamine, results the GCN with low specific surface area and poor charge separation efficiency. Herein, we report the synthesis of high-quality one-dimensional g-C3N4 nanobelts with rich amino groups and higher surface area by treating melamine precursors with hydrochloric acid and subsequent thermal polymerization reaction. The GCN nanobelts produced after optimizing the HCl treatment can effectively generate H2 evolution rate of 2912.6 μmol/g/h, which is six times higher than that of bulk GCN obtained via direct thermal polymerization reaction without any treatment. Meanwhile, the quantum efficiency of 3.8% at 420 nm toward solar to hydrogen conversion was achieved, prominently surpassing the many g-C3N4 nanostructures. Such one-dimensional g-C3N4 nanobelt semiconductors are predicted to hold great potential for solar energy conversion reactions.

A bimetallic co-doped iron and copper in polymeric graphitic carbon nitride to enhance catalytic activity and reusability of Fenton-like oxidation

In this study, a new Fenton-like catalyst was developed through incorporating iron and copper in polymeric graphitic carbon nitride (FeCu/CN) for catalytic activity and reusability enhancement. With theoretical Fe/Cu ratio of 7:3 (Fe7Cu3/CN) and pH of 5, the bimetallic catalyst system showed a pseudo-first-order rate constant of 0.07294 min−1 for bisphenol S (BPS) degradation, which was near double the sum of values in monometallic catalyst systems. Moreover, the new catalyst showed much better performance for reuse, BPS removal of which catalyzed system decreased from 98.0 % to 87.3 % after five cycles used. Comparatively, BPS removal declined from 69.5 % to 45.0 % in Fe/CN catalyzed system. Characterization results indicate the superiority of Fe7Cu3/CN for Fenton-like catalysis is mainly attributed to the intrinsic advantage of CN support, Fe(II) formation, copper catalysis, and synergistic effect between iron and copper. Furthermore, hydroxyl radicals were determined as the main species for pollutant degradation, and their accumulation was monitored. The destruction pathways of BPS were analyzed by detection of degradation intermediates, and the results further confirm the main active species of hydroxyl radicals. Moreover, the new Fenton-like system also exhibited good performance for different pollutant removal and real wastewater treatment. This study provided a new catalyst with superior catalytic activity and favorable reusability, and also sheds new light on supported bimetallic catalyst development.

Polymeric graphitic carbon nitride layers decorated with erbium oxide and enhanced photocatalytic performance under visible light irradiation.

Developing and implementing visible light active organic-inorganic hybrid semiconductor nanomaterials with enhanced photocatalytic properties find newer environmental and energy treatment capabilities. Here, we are reporting polymeric g-C3N4 layers coated with different propositions of erbium oxide nanoparticles, characterized using XPS, UV-Vis-DRS, FT-IR, HR-TEM, FE-SEM, elemental mapping, XRD and surface area techniques and its photocatalytic activities were evaluated under visible light irradiations. The hybrid nanocomposite materials possess better crystalline nature and erbium oxide particles were on the surface of polymeric g-C3N4. The surface area and bandgap energy of the polymeric g-C3N4-erbium oxide (5 wt%) nanohybrid composite were 99.9 m2/g and 2.52eV. The photocatalytic activities as prepared nanohybrid composites were assessed for the oxidation of orange G dye molecules in the presence of visible light and were highly active in a broader range of pH with the presence of various inorganic anions. The rate of photocatalytic oxidation of dye molecules varied from 4.79 × 10-4 to 1.77 × 10-4min-1 for the initial concentration of 5 to 20ppm and retained its activities above 95% up to three cycles of reusability. Hence, the organic-inorganic novel catalytic nanohybrid composite may find more comprehensive applications in the area of environmental and energy applications.

Single-Step Synthesis of Graphitic Carbon Nitride Nanomaterials by Directly Calcining the Mixture of Urea and Thiourea: Application for Rhodamine B (RhB) Dye Degradation

Recently, polymeric graphitic carbon nitride (g-C3N4) has been explored as a potential catalytic material for the removal of organic pollutants in wastewater. In this work, graphitic carbon nitride (g-C3N4) photocatalysts were synthesized using mixtures of low-cost, environment-friendly urea and thiourea as precursors by varying calcination temperatures ranging from 500 to 650 °C for 3 h in an air medium. Different analytical methods were used to characterize prepared g-C3N4 samples. The effects of different calcination temperatures on the structural, morphological, optical, and physiochemical properties of g-C3N4 photocatalysts were investigated. The results showed that rhodamine B (RhB) dye removal efficiency of g-C3N4 prepared at a calcination temperature of 600 °C exhibited 94.83% within 180 min visible LED light irradiation. Photocatalytic activity of g-C3N4 was enhanced by calcination at higher temperatures, possibly by increasing crystallinity that ameliorated the separation of photoinduced charge carriers. Thus, controlling the type of precursors and calcination temperatures has a great impact on the photocatalytic performance of g-C3N4 towards the photodegradation of RhB dye. This investigation provides useful information about the synthesis of novel polymeric g-C3N4 photocatalysts using a mixture of two different environmentally benign precursors at high calcination temperatures for the photodegradation of organic pollutants.

Synergy of crystallinity modulation and intercalation engineering in carbon nitride for boosted H2O2 photosynthesis

Photosynthesis of hydrogen peroxide (H2O2) by selective oxygen reduction is a green and cost-effective alternative to the energy-intensive anthraquinone process. Although inexpensive polymeric graphitic carbon nitride (g-C3N4) exhibits the ability to produce H2O2, its disordered and amorphous structure leads to a high recombination rate of photogenerated carriers and hinders charge transfer between layers. Herein, we predict that stacked polymeric g-C3N4 with ion intercalation (K+ and I-) can improve carrier separation and transfer by multiscale computational simulations. The electronic structures of g-C3N4 were tailored and modified by intercalating K+ and I- into the layer-by-layer structures. Guided by the computational predictions, we achieved efficient solar-driven H2O2 production by employing this facile and ion-intercalated crystalline g-C3N4. An H2O2 production rate of 13.1 mM g-1 h-1 and an apparent quantum yield of 23.6% at 400 nm were obtained. The synergistic effects of crystallinity regulation and dual interstitial doping engineering triggered the formation of new light absorption centers, the establishment of rapid charge diffusion channels, and the enhancement of two-electron oxygen reduction characteristics. This work sheds light on the dual tuning of crystallinity and electronic structure and broadens the design principles of organic-conjugated polymer photocatalysts for environmental remediation and energy conservation.

Phosphorus modified graphitic carbon nitride activated by guanidine phosphate enables fast, efficient and selective immobilization of aquatic lead

With the assistance of preinstalled silica templates, polymeric graphitic carbon nitride with enhanced porosity suffers from complicated procedures and by-product wastes. Besides, it is still difficult to achieve the incorporation of phosphate groups with high contents on carbon-based materials (mostly < 1.0 at.% of P) via a one-step preparation since phosphate species on the surfaces of sorbents could complex heavy metals strongly from wastewaters. Given the porosity engineering of guanidine phosphate (GP) for carbonaceous materials, GP activated graphitic carbon nitrides (GPCNs) with developed surface area (4.2–4.8 fold of enhancement than inactivated one) and abundant phosphate groups (9.9–16.7 at.% of P) were fabricated via a one-step pyrolysis at 450, 500, and 550 °C. On this basis, the sorption of Pb(II) on GPCNs were studied under geochemical conditions including contact time, solution pH, ionic strength, humic acid concentration, interfering cations and anions, and temperature. GPCN pyrolyzed at 500 °C could capture Pb(II) rapidly (20.0 min) with superior maximum capacities (81.8–217.1 mg/g at pH 5.0, T 298 K), excellent selectivity coefficients (8.10–16.54) and favorable reusability (81.4% of capacity remained). The formation of minerals was dominant for the selectivity rather than ion exchange or surface coordination, etc. This work starts up the facile activation of carbon nitride with developed porosity and surface functionality to manage aquatic pollutants.

Post-functionalization of graphitic carbon nitride for highly efficient photocatalytic hydrogen evolution

In this work we report the feasible modification of graphitic carbon nitride (g-C3N4) polymer through a post-functionalization progress. The resultant photocatalyst exhibits boron doping and mesoporous structure with a high surface area of 125 m2/g, leading in an increased surface activity for photocatalytic water splitting reaction. X-ray diffraction, X-ray photoelectron spectroscopy, PL emission spectra and UV-Vis spectra were used to detect the properties of as-prepared samples. Based on X-ray photoelectron spectroscopy analysis, boron is proposed to dope in the g-C3N4 lattice. Optical studies indicated that boron doped g-C3N4 exhibits enhanced and extended light absorbance in the visible-light region and a much lower intensity of PL emission spectra compared to pure g-C3N4. As a result, boron doped g-C3N4 shows activity of 10.2 times higher than the pristine g-C3N4 for photocatalytic hydrogen evolution. This work may provide a way to design efficient and mesoporous photocatalysts through post modification.