Search Results (43)

Graphitic carbon nitride (CN) is a promising photocatalytic material, but its practical application is limited by small specific surface area, narrow light absorption range, and high photogenerated carrier recombination rate. To address these issues, this study synthesized boron-doped carbon nitride (BCN) and sulfuric acid-exfoliated boron-doped carbon nitride (BCND). X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results confirmed that boron was successfully doped into the CN skeleton via B-N bonds. Scanning electron microscopy (SEM) and N₂ adsorption–desorption (BET) characterizations showed that acid exfoliation significantly increased the specific surface area of BCND to 68.80 m²·g⁻¹, much higher than that of CN (9.54 m²·g⁻¹) and BCN (15.98 m²·g⁻¹). UV–visible diffuse reflectance spectroscopy (UV-Vis DRS) analysis revealed that BCND had the narrowest bandgap (2.59 eV) among the three materials, which enhanced its visible-light absorption efficiency. Photoelectrochemical tests demonstrated that BCND exhibited the smallest charge transfer resistance and the highest transient photocurrent density (eight times that of CN), indicating efficient separation of photogenerated electron–hole pairs. Photocatalytic water splitting experiments showed that BCND achieved the highest Hydrogen production rate of 792.34 μmol·g⁻¹·h⁻¹, which was about 4 times that of CN (158.41 μmol·g⁻¹·h⁻¹) and 1.36 times that of 2.5% BCN (584.30 μmol·g⁻¹·h⁻¹). Free-radical trapping experiments indicated that hydroxyl radicals (·OH) played a crucial promotional role in Hydrogen production, while superoxide anions (·O₂⁻) exerted an inhibitory effect. The enhanced performance of BCND was attributed to the synergistic effects of boron doping (narrowing bandgap) and acid exfoliation (increasing specific surface area). A possible photocatalytic Hydrogen production mechanism was proposed based on the experimental results. This study provides a feasible strategy for the structural modification and performance optimization of g-C₃N₄-based photocatalysts for water splitting. Full article

An effective strategy for significantly enhancing photocatalytic activity of composite materials is to construct heterojunctions. Herein, a series of imidazole-modified heterostructured g-C₃N₄/SnO (CNIS) Z-scheme photocatalysts were prepared by calcination methods, leading to superior photocatalytic performance than pure SnO and imidazole-modified g-C₃N₄. Rhodamine B (Rh B) aqueous solution was taken as the target pollutant, and the result presented that both imidazole modification and the Z-scheme heterojunction construction benefited from significant enhancement in photocatalytic activity. Moreover, it is revealed that electrons were transferred from imidazole-modified g-C₃N₄ to SnO through the interface of the composite by XPS analysis. Under visible light (>420 nm) irradiation, the built-in electric field, band edge bending, and Coulomb interaction work synergistically to drive the recombination of relatively useless electrons and holes in the hybrid. As a result, the residual electrons and holes, which possess enhanced reducibility and oxidizability, endow the composite with exceptional redox capability. This research can not only deepen our comprehension of designing and fabricating innovative Z-scheme heterojunction photocatalysts but also presents an effective approach to tackle environmental pollution issues in the future. Full article

To overcome the inherent limitations of graphitic carbon nitride (g-C₃N₄), specifically the rapid recombination of photogenerated electron–hole pairs and its confined light absorption range, a sulfur-doped g-C₃N₄ (S-g-C₃N₄) photocatalyst was developed in this work. The photocatalytic performance and its catalytic mechanism for rhodamine B (RhB) degradation were systematically investigated. Material characterization and performance tests revealed that S doping can narrow the band gap of g-C₃N₄ and effectively enhance the separation and transport efficiency of charge carriers. The as-prepared catalyst demonstrated excellent activity under simulated sunlight, achieving nearly complete degradation of 10 mg/L RhB within 15 min. Moreover, it exhibited robust stability across a pH range of 6 to 11 and in the presence of coexisting anions (Cl⁻, NO₃⁻, CO₃²⁻), with negligible activity loss after five consecutive cycles. Radical trapping experiments verified that ∙OH radicals served as the primary active species, with h⁺ playing a secondary role in the degradation process. This work provides practical guidance for designing durable g-C₃N₄-based photocatalysts with high performance for organic wastewater treatment. Full article

The hematite phase decorated with iron-doped cerium oxide nanoparticles (F@FC) was precipitated from cerium and iron oxalate intermediate products. The photocatalytic composite of graphitic carbon nitride (gCN) and F@FC was prepared by a simple method involving mixing the two components, followed by thermal treatment at 400 °C. According to electron microscopy, F@FC is composed of a submicron iron oxide (hematite) phase decorated with iron-doped cerium oxide nanoparticles deposited on gCN substrate. A hierarchically structured composite was observed instead of a simple mechanical mixture of α-Fe₂O₃, Fe-CeO₂, and gCN. To observe two types of degradation activity, photocatalytic and Photo-Fenton degradation activity, Rhodamine B (RhB) was applied as the model water pollutant. The influence of the amount of photocatalyst, the RhB concentration, the presence of cations and anions, the pH, and the effect of e⁻, h⁺, •OH, and •O₂⁻ scavenging reactants were studied. The Photo-Fenton degradation exhibited high efficiency across the entire tested pH range, whereas photocatalytic degradation showed comparable activity only at acidic pH. The F@FC-gCN composite catalyst exhibited a high degree of recyclability. The degradation pathways of photocatalytic and Photo-Fenton reactions were suggested by HPLC-MS analysis of the reaction products. A notable finding of this study was the observation that the green-yellow, fluorescent intermediate Rhodamine 110 was formed during the photocatalytic degradation of RhB. However, the high reactivity of the generated •OH radicals during Photo-Fenton degradation has been demonstrated to inhibit the formation of intermediate Rhodamine 110. Full article

Deoxynivalenol (DEOX), a dangerous mycotoxin, causes serious health problems for humans and animals. Hence, the on-site monitoring of DEOX has begun to be important in the health and food sectors in recent years. In the present study, a molecularly imprinted surface plasmon resonance (SPR) sensor based on sulfur-doped boron graphitic carbon nitride (S-B-g-C₃N₄) was developed and applied for detecting DEOX in drinking water and orange juice samples, achieving high recovery. After the S-B-g-C₃N₄ nanocomposite was synthesized via thermal polycondensation and microwave treatment with a highly environmentally friendly approach, a SPR chip was modified with the S-B-g-C₃N₄ nanocomposite considering the high affinity between gold and sulfur. Then, the molecularly imprinted SPR sensor based on the S-B-g-C₃N₄ nanocomposite was prepared in the presence of methacryloylamidoglutamic acid (MAGA) as the monomer and N,N′-azobisisobutyronitrile (AIBN) as the initiator. The DEOX-imprinted SPR sensor based on the S-B-g-C₃N₄ nanocomposite showed linearity from 1.0 to 10.0 ng L⁻¹, with a limit of quantification (LOQ) of 1.0 ng L⁻¹ and a limit of detection (LOD) of 0.30 ng L⁻¹. Finally, the selectivity, repeatability, and reproducibility of the DEOX-imprinted SPR sensor based on the S-B-g-C₃N₄ nanocomposite were investigated. Full article

With the escalating challenges of global warming and the energy crisis, electrocatalytic CO₂ reduction reaction (CO₂RR) has emerged as a promising strategy to mitigate atmospheric CO₂ concentrations while converting it into high-value-added chemicals. Among various CO₂RR catalysts, copper-based materials exhibit unique capabilities for C-C coupling, yet their practical application remains constrained by several limitations: Low selectivity for C₂₊ products (typically <60%); Catalyst instability due to dynamic reconfiguration of active sites under high overpotentials; poor energy efficiency caused by competing hydrogen evolution reactions (HERs), etc. Recent studies demonstrate that nonmetallic heteroatom doping or functionalized ligand incorporation can effectively modulate the electronic structure and surface microenvironment of Cu-based catalysts, thereby enhancing CO₂RR performance. In this review, we comprehensively summarize recent advances in such strategies. We first systematically elucidate the unique advantages of copper-based catalysts as benchmark materials for multi-carbon (C₂₊) product synthesis, along with the current challenges they face. Subsequently, we highlight recent advances in modulating copper-based catalysts through the incorporation of diverse nonmetallic heteroatoms (e.g., N, S, B, P, halogens) or the introduction of functionalized ligands, with a particular focus on mechanistic insights and characterization methods aimed at enhancing C-C coupling efficiency and improving C₂₊ product selectivity. Finally, we present perspectives on the remaining opportunities and challenges in this research field. Full article

The CO₂ capture from flue gas using biomass-derived porous carbons presents an environmentally friendly and sustainable strategy for mitigating carbon emissions. However, the conventional fabrication of porous carbons often relies on highly corrosive activating agents like KOH and ZnCl₂, posing environmental and safety concerns. To address this challenge, in the present work sodium metaborate tetrahydrate (NaBO₂·4H₂O) has been utilized as an alternative, eco-friendly activating agent for the first time. Moreover, a water chestnut shell (WCS) is used as a sustainable precursor for boron-doped porous carbons with varied microporosity and boron concentration. It was found out that pyrolysis temperature significantly determines the textural features, elemental composition, and CO₂ adsorption capacity. With a narrow micropore volume of 0.27 cm³/g and a boron concentration of 0.79 at.% the representative adsorbent presents the maximum CO₂ adsorption (2.51 mmol/g at 25 °C, 1 bar) and a CO₂/N₂ selectivity of 18 in a 10:90 (v/v) ratio. Last but not least, the as-prepared B-doped carbon adsorbent possesses a remarkable cyclic stability over five cycles, fast kinetics (95% equilibrium in 6.5 min), a modest isosteric heat of adsorption (22–39 kJ/mol), and a dynamic capacity of 0.80 mmol/g under simulated flue gas conditions. This study serves as a valuable reference for the fabrication of B-doped carbons using an environmentally benign activating agent for CO₂ adsorption application. Full article

The electrochemical reduction of CO₂ (CO₂RR) to valuable chemicals and fuels is a promising strategy for addressing environmental challenges. Graphitic carbon nitride (g-C₃N₄) is a promising electrocatalyst for CO₂ reduction. However, poor electron transfer and low CO₂ affinity often limit its catalytic performance. In this study, we employ density functional theory (DFT) calculations to systematically investigate the effect of various non-metal dopants (B, P, O, and S) on the electronic structure and CO₂ adsorption properties of g-C₃N₄. Our results demonstrated that O-C₃N₄ preferentially catalyzes the formation of HCOOH with a low limiting potential of −0.12 V. Meanwhile, S-C₃N₄ efficiently promotes the generation of CH₂O, CH₃OH, and CH₄ at a limiting potential of −0.58 V, as well as CO at −0.77 V. These findings provide valuable insights toward the rational design of effective non-metal-doped g-C₃N₄ catalysts for efficient CO₂ conversion. Full article

In this study, Bi₂MoO₆ nanoflowers with different molybdenum sources were in situ grown on the surface of g-C₃N₄ nanosheets (OCN) by a simple one-step solvothermal method. The effects of doping and different molybdenum sources on the photocatalytic degradation and bactericidal activity of Bi₂MoO₆/OCN were discussed. Among them, the solvothermal preparation of P-Bi₂MoO₆/OCN using phosphomolybdic acid as molybdenum source can make up for the shortcomings caused by the destruction of OCN structure by generating more lattice defects to promote charge separation and constructing Lewis acid/base sites to effectively improve the photocatalytic performance. In addition, by adding phosphoric acid to increase the P-doped content, more exposed alkaline active sites are induced on the surface of P-Bi₂MoO₆/OCN, as well as larger specific surface area and charge transfer efficiency, which further improve the photocatalytic performance. Finally, the optimized 16P-Bi₂MoO₆/OCN showed a degradation rate of 99.7% for 20 mg/L rhodamine B (RhB) within 80 min under visible light, and the antibacterial rates against E. coli, S. aureus and P. aeruginosa within 300 min were 99.58%, 98.20% and 97.48%, respectively. This study provides a reference for optimizing the synthesis of environmentally friendly, solar-responsive, photocatalytic sterilization materials from the perspective of preparation, raw materials and structure. Full article

The increasing global demand for clean water is driving the development of advanced wastewater treatment technologies. Graphitic carbon nitride (g-C₃N₄) has emerged as an efficient photocatalyst for degrading organic pollutants, such as synthetic dyes, due to its exceptional thermo-chemical stability. However, its application is limited by an insufficient specific surface area, low photocatalytic efficiency, and an unclear degradation mechanism. In this study, we aimed to enhance g-C₃N₄ by doping it with elemental chlorine, resulting in a series of Cl-C₃N₄ photocatalysts with varying doping ratios, prepared via thermal polymerization. The photocatalytic activity of g-C₃N₄ was assessed by measuring the degradation rate of RhB. A comprehensive characterization of the Cl-C₃N₄ composites was conducted using SEM, XRD, XPS, PL, DRS, BET, EPR, and electrochemical measurements. Our results indicated that the optimized 1:2 Cl-C₃N₄ photocatalyst exhibited exceptional performance, achieving 99.93% RhB removal within 80 min of irradiation. TOC mineralization reached 91.73% after 150 min, and 88.12% removal of antibiotics was maintained after four cycles, demonstrating the excellent stability of the 1:2 Cl-C₃N₄ photocatalyst. Mechanistic investigations revealed that superoxide radicals (·O₂⁻) and singlet oxygen (¹O₂) were the primary reactive oxygen species responsible for the degradation of RhB in the chlorine-doped g-C₃N₄ photocatalytic system. Full article

Graphitic phase carbon nitride (g-C₃N₄, abbreviated as CN) can be used as a photocatalyst to reduce the concentration of atmospheric carbon dioxide. However, there is still potential for improvement in the small band gap and carrier migration properties of intrinsic materials. K-B co-doped CN (KBCN) was investigated as a promising photocatalyst for carbon dioxide reduction via the Density Functional Theory (DFT) method. The electronic and optical properties of CN and KBCN indicate that doping K and B can improve the catalytic performance of CN by promoting charge migration and separation. In terms of the Gibbs free energy change, the CO₂ reduction reaction catalysed by KBCN results in CH₃OH, and its optimal pathway is CO₂ → *CO₂ → *COOH → CO → *OCH → HCHO → *OCH₃ → CH₃OH. Compared with CN, the doping elements K and B shift the rate-determining step from CO₂ → *CO₂ to *CO₂ → *COOH. The K and B elements co-doping tuned the charge distribution between the catalyst and the adsorbate and reduced the Gibbs free energy of the rate-determining step from 1.571 to 0.861 eV, suggesting that the CO₂ reduction activity of KBCN is superior to that of CN. Our work provides useful insights for the design of metallic–nonmetallic co-doped CN for photocatalytic CO₂ reduction (CO₂PR) reactions. Full article

The binary heterostructured semiconducting visible light photocatalyst of the iron-doped graphitic carbon nitride/bismuth molybdate (Fe-g-C₃N₄/Bi₂MoO₆) composite was prepared by coupling with Fe-doped g-C₃N₄ and Bi₂MoO₆ particles. In the present study, a comparison of structural characteristics, optical properties, and photocatalytic degradation efficiency and activity between Fe-doped g-C₃N₄ particles, Bi₂MoO₆ particles, and Fe-g-C₃N₄/Bi₂MoO₆ composite was investigated. The results of X-ray diffraction (XRD) examination indicate that the hydrothermal Bi₂MoO₆ particles have a single orthorhombic phase and Fourier transform infrared (FTIR) spectroscopy analysis confirms the formation of Fe-doped g-C₃N₄. The optical bandgaps of the Fe-doped g-C₃N₄ and Bi₂MoO₆ particles are 2.74 and 2.73 eV, respectively, as estimated from the Taut plots obtained from UV-Vis diffuse reflectance spectroscopy (DRS) spectra. This characteristic indicates that the two semiconductor materials are suitable for absorbing visible light. The transmission electron microscopy (TEM) micrograph reveals the formation of the heterojunction Fe-g-C₃N₄/Bi₂MoO₆ composite. The results of photocatalytic degradation revealed that the developed Fe-g-C₃N₄/Bi₂MoO₆ composite photocatalyst exhibited significantly better photodegradation performance than the other two single semiconductor photocatalysts. This property can be attributed to the heterostructured nanostructure, which could effectively prevent the recombination of photogenerated carriers (electron–hole pairs) and enhance photocatalytic activity. Furthermore, cycling test showed that the Fe-g-C₃N₄/Bi₂MoO₆ heterostructured photocatalyst exhibited good reproducibility and stability for organic dye photodegradation. Full article

This current study assessed the impacts of morphology adjustment of perovskite BiFeO₃ (BFO) on the construction and photocatalytic activity of P-infused g-C₃N₄/U-BiFeO₃ (U-BFO/PCN) heterostructured composite photocatalysts. Favorable formation of U-BFO/PCN composites was attained via urea-aided morphology-controlled hydrothermal synthesis of BFO followed by solvosonication-mediated fusion with already synthesized P-g-C₃N₄ to form U-BFO/PCN composites. The prepared bare and composite photocatalysts’ morphological, textural, structural, optical, and photocatalytic performance were meticulously examined through various analytical characterization techniques and photodegradation of aqueous rhodamine B (RhB). Ellipsoids and flakes morphological structures were obtained for U-BFO and BFO, and their effects on the successful fabrication of the heterojunctions were also established. The U-BFO/PCN composite exhibits 99.2% efficiency within 20 min of visible-light irradiation, surpassing BFO/PCN (88.5%), PCN (66.8%), and U-BFO (26.1%). The pseudo-first-order kinetics of U-BFO/PCN composites is 2.41 × 10⁻¹ min⁻¹, equivalent to 2.2 times, 57 times, and 4.3 times of BFO/PCN (1.08 × 10⁻¹ min⁻¹), U-BFO, (4.20 × 10⁻³ min⁻¹), and PCN, (5.60 × 10⁻² min⁻¹), respectively. The recyclability test demonstrates an outstanding photostability for U-BFO/PCN after four cyclic runs. This improved photocatalytic activity exhibited by the composites can be attributed to enhanced visible-light utilization and additional accessible active sites due to surface and electronic band modification of CN via P-doping and effective charge separation achieved via successful composites formation. Full article

Fluorescent graphitic carbon nitride (g-C₃N₄) doped with various heteroatoms, such as B, P, and S, named ^Bg-C₃N₄, ^Pg-C₃N₄, and ^Sg-C₃N₄, were synthesized with variable band-gap values as diagnostic materials. Furthermore, they were embedded within hyaluronic acid (HA) microgels as g-C₃N₄@HA microgel composites. The g-C₃N₄@HA microgels had a 0.5–20 μm size range that is suitable for intravenous administration. Bare g-C₃N₄ showed excellent fluorescence ability with 360 nm excitation wavelength and 410–460 emission wavelengths for possible cell imaging application of g-C₃N₄@HA microgel composites as diagnostic agents. The g-C₃N₄@HA-based microgels were non-hemolytic, and no clotting effects on blood cells or cell toxicity on fibroblasts were observed at 1000 μg/mL concentration. In addition, approximately 70% cell viability for SKMEL-30 melanoma cells was seen with ^Sg-C₃N₄ and its HA microgel composites. The prepared g-C₃N₄@HA and ^Sg-C₃N₄@HA microgels were used in cell imaging because of their excellent penetration capability for healthy fibroblasts. Furthermore, g-C₃N₄-based materials did not interact with malignant cells, but their HA microgel composites had significant penetration capability linked to the binding function of HA with the cancerous cells. Flow cytometry analysis revealed that g-C₃N₄ and g-C₃N₄@HA microgel composites did not interfere with the viability of healthy fibroblast cells and provided fluorescence imaging without any staining while significantly decreasing the viability of cancerous cells. Overall, heteroatom-doped g-C₃N₄@HA microgel composites, especially ^Sg-C₃N₄@HA microgels, can be safely used as multifunctional theragnostic agents for both diagnostic as well as target and treatment purposes in cancer therapy because of their fluorescent nature. Full article

In this investigation, we employ a numerical simulation approach to model a hydrogenated lead-free ${\mathrm{C}\mathrm{s}}_2\mathrm{A}\mathrm{g}\mathrm{B}\mathrm{i}{\mathrm{B}\mathrm{r}}_6$ double perovskite solar cell with a p-i-n inverted structure, utilizing SCAPS-1D. Contrary to traditional lead-based perovskite solar cells, the ${\mathrm{C}\mathrm{s}}_2\mathrm{A}\mathrm{g}\mathrm{B}\mathrm{i}{\mathrm{B}\mathrm{r}}_6$ double perovskite exhibits reduced toxicity and enhanced stability, boasting a maximum power conversion efficiency of $\mathrm{6.37\%}$. Given its potential for improved environmental compatibility, achieving higher efficiency is imperative for its practical implementation in solar cells. This paper offers a comprehensive quantitative analysis of the hydrogenated lead-free ${\mathrm{C}\mathrm{s}}_2\mathrm{A}\mathrm{g}\mathrm{B}\mathrm{i}{\mathrm{B}\mathrm{r}}_6$ double perovskite solar cell, aiming to optimize its structural parameters. Our exploration involves an in-depth investigation of various electron transport layer materials to augment efficiency. Variables that affect the photovoltaic efficiency of the perovskite solar cell are closely examined, including the absorber layer’s thickness and doping concentration, the hole transport layer, and the absorber defect density. We also investigate the impact of the doping concentration of the electron transport layer and the energy level alignment between the absorber and the interface on the photovoltaic output of the cell. After careful consideration, zinc oxide is chosen to serve as the electron transport layer. This optimized configuration surpasses the original structure by over four times, resulting in an impressive power conversion efficiency of $\mathrm{26.3\%}$, an open-circuit voltage of $1.278 \mathrm{V}$, a fill factor of $\mathrm{88.21\%}$, and a short-circuit current density of $23.30 \mathrm{m}\mathrm{A}.{\mathrm{c}\mathrm{m}}^{-2}$. This study highlights the critical role that numerical simulations play in improving the chances of commercializing Cs₂AgBiBr₆ double perovskite solar cells through increased structural optimization and efficiency. Full article