Phase Carbon Nitride Research Articles

Preparation of High-Efficiency Fe/N-Doped Carbon Catalysts Derived from Graphite Phase Carbon Nitride for Reduction of Oxygen

Preparation of High-Efficiency Fe/N-Doped Carbon Catalysts Derived from Graphite Phase Carbon Nitride for Reduction of Oxygen

Efficient photocatalytic hydrogen peroxide production over S-scheme In2S3/molten salt modified C3N5 heterojunction

Graphitic phase carbon nitride (g-C3N5), as a novel n-type metal-free material, is employed as a visible light-receptive catalyst because of its narrow band gap and abundant nitrogen. To overcome the low carrier mobility efficiency of g-C3N5, its modification by K ions was adopted. In addition, In2S3 was selected to couple with modified g-C3N5 to overcome the recombination of photogenerated e−/h+. As a novel photocatalytic material, it was proven to possess a high visible light absorption capacity and a strong H2O2 production ability (up to 3.89 mmol⋅L-1 in 2 h). Moreover, a S-scheme heterojunction structure was successfully constructed between the two materials, which was tested and confirmed to be successful in raising the photogenerated e−/h+ separation efficiency. Ultimately, the primary processes of photocatalytic H2O2 production were summarized by superoxide radical and rotating disc electron measurements. This research provides a fresh perspective for the synthesis of C3N5-based S-scheme heterojunction photocatalysts for producing H2O2.

Bi, K co-doped graphitic phase carbon nitride for efficient photocatalytic H2O2 production

The emerging photocatalytic production of hydrogen peroxide (H2O2) using graphitic carbon nitride (g-C3N4) has attracted a lot of attention for its potential applications in various fields. However, However, the catalytic activity of pure g-C3N4 is still limited. Herein, Bi, K co-doped g-C3N4 (BixKy-CN) was prepared by co-thermal polymerization of a mixture of potassium nitrate, bismuth nitrate, melamine, and urea. The obtained Bi3.6K3-CN composite possesses more negative conduction and valence band positions that can, to some extent, enhance photocatalytic performance by lowering the energy barrier of redox reactions and by enhancing electron absorption capacity. Additionally, the pyrolysis process of the potassium nitrate and bismuth nitrate has a considerable impact on the formation of the morphology of g-C3N4, generating a porous lamellar-structure with nitrogen defects, resulting in increased oxygen adsorption and utilization capacity. These synergistic effects enable Bi3.6K3-CN to exhibit excellent photocatalytic activity and cycling stability for H2O2 production. After 3 hours of visible light irradiation, the production of H2O2 catalyzed by Bi3.6K3-CN can reach 1207.72 μmol L-1, which is 57 times higher than that of pure g-C3N4.

Dual elemental doping activated signaling pathway of angiogenesis and defective heterojunction engineering for effective therapy of MRSA-infected wounds

Multi-drug resistant bacterial infections pose a significant threat to human health. Thus, the development of effective bactericidal strategies is a pressing concern. In this study, a ternary heterostructure (Zn–CN/P-GO/BiS) comprised of Zn-doped graphite phase carbon nitride (g-C3N4), phosphorous-doped graphene oxide (GO) and bismuth sulphide (Bi2S3) is constructed for efficiently treating methicillin-resistant Staphylococcus aureus (MRSA)-infected wound. Zn doping-induced defect sites in g-C3N4 results in a reduced band gap (ΔE) and a smaller energy gap (ΔEST) between the singlet state S1 and triplet state T1, which favours two-photon excitation and accelerates electron transfer. Furthermore, the formation of an internal electric field at the ternary heterogeneous interface optimizes the charge transfer pathway, inhibits the recombination of electron-hole pairs, improves the photodynamic effect of g-C3N4, and enhances its catalytic performance. Therefore, the Zn–CN/P-GO/BiS significantly augments the production of reactive oxygen species and heat under 808 nm NIR (0.67 W cm−2) irradiation, leading to the elimination of 99.60% ± 0.07% MRSA within 20 min. Additionally, the release of essential trace elements (Zn and P) promotes wound healing by activating hypoxia-inducible factor-1 (HIF-1) and peroxisome proliferator-activated receptors (PPAR) signaling pathways. This work provides unique insight into the rapid antibacterial applications of trace element doping and two-photon excitation.

One-Step Synthesis of Alkali Metal-Hydroxyl Double Modified Graphite Phase Carbon Nitride and Photocatalytic Degradation of Phenolic Compounds

In this work, potassium ion-hydroxyl double modified graphite phase carbon nitride (KCN–OH) was synthesized in one step by alkali hydrothermal (AH) method. The as-prepared catalysts were characterized by XRD, FT-IR, UV–Vis, N2 adsorption, SEM, XPS, PL, ESR, TPD and EIS. The introduction of potassium ion causes the reduced crystal size, increased specific surface area and promoted electron–hole separation efficiency of as-prepared catalyst. The hydroxyl group not only further improves the electron–hole separation efficiency but, as the electron donor group, can also make stronger interaction between catalyst and acidic phenolic compounds. The photocatalytic degradation of phenol was investigated under visible light. The results show that the phenol degradation rate constant of KCN–OH is 0.22 h[Formula: see text] under visible light, which is over 3.7 and 2.0 times higher than that of neat g-C3N4 and single hydroxyl-modified g-C3N4. KCN–OH also displays outstanding catalytic and structural stability. The possible reaction mechanism is discussed in this paper.

Defect‐Repaired g‐C3N4 Nanosheets: Elevating the Efficacy of Sonodynamic Cancer Therapy Through Enhanced Charge Carrier Migration

AbstractSonodynamic therapy (SDT) has garnered growing interest owing to its high tissue penetration depth and minimal side effects. However, the lack of efficient sonosensitizers remains the primary limiting factor for the clinical application of this treatment method. Here, defect‐repaired graphene phase carbon nitride (g‐C3N4) nanosheets are prepared and utilized for enhanced SDT in anti‐tumor treatment. After defect engineering optimization, the bulk defects of g‐C3N4 are significantly reduced, resulting in higher crystallinity and exhibiting a polyheptazine imide (PHI) structure. Due to the more extended conjugated structure of PHI, facilitating faster charge transfer on the surface, it exhibits superior SDT performance for inducing apoptosis in tumor cells. This work focuses on introducing a novel carbon nitride nanomaterial as a sonosensitizer and a strategy for optimizing sonosensitizer performance by reducing bulk defects.

Defect-Repaired g-C3N4 Nanosheets: Elevating the Efficacy of Sonodynamic Cancer Therapy Through Enhanced Charge Carrier Migration.

Sonodynamic therapy (SDT) has garnered growing interest owing to its high tissue penetration depth and minimal side effects. However, the lack of efficient sonosensitizers remains the primary limiting factor for the clinical application of this treatment method. Here, defect-repaired graphene phase carbon nitride (g-C3N4) nanosheets are prepared and utilized for enhanced SDT in anti-tumor treatment. After defect engineering optimization, the bulk defects of g-C3N4 are significantly reduced, resulting in higher crystallinity and exhibiting a polyheptazine imide (PHI) structure. Due to the more extended conjugated structure of PHI, facilitating faster charge transfer on the surface, it exhibits superior SDT performance for inducing apoptosis in tumor cells. This work focuses on introducing a novel carbon nitride nanomaterial as a sonosensitizer and a strategy for optimizing sonosensitizer performance by reducing bulk defects.

Interface engineered 2D-2D-g-C3N4/SnWO4 S-scheme heterojunction: Clioquinol degradation and dopamine sensing properties

A convenient and walkable protocol has been established to simplify the fabrication of surface-engineered heterojunctions between 2D/2D g-C3N4-β-SnWO4. The method involves a one-step, simultaneous thermal exfoliation-deposition technique that utilizes bulk carbon nitride and stannous tungstate in a thermal spreading process. The prepared catalysts demonstrate excellent performance in the photocatalytic decomposition of Clioquinol (a neurotoxic drug) and dopamine sensing. The results indicate that the optimal loading of carbon nitride is 12 %, with this catalyst completely decomposing clioquinol within 80 min. Lower and higher loadings result in inferior performance due to ineffective interfacial contact, the formation of a bulk-like carbon nitride phase, and the encapsulation of stannous tungstate particles, respectively. A plausible mechanism has been proposed based on scavenger studies. The 12 % g-C3N4-SnWO4 sample exhibits the lowest charge transfer resistance and demonstrates good dopamine sensing properties. The selective sensing performance has been confirmed in the presence of glucose, ascorbic acid, and urea. The limit of detection (LOD) for the 12 % g-C3N4-SnWO4 sensor system is determined to be 1.78 μM.

Implanting pyrazine ring into g-C3N4 for accelerating photocatalytic hydrogen evolution

It is of great significance to develop an efficient and stable photocatalyst for the photocatalytic decomposition of water to produce hydrogen. Within this paper, an effective and simple strategy was adopted to introduce pyrazine ring into graphite-like carbon nitride framework to realize efficient and stable hydrogen production process. After evaluation, the hydrogen production efficiency of the modified semiconductor material is 3.05 folds higher than the unmodified graphite-like phase carbon nitride, and an excellent stability performance was also achieved. It is proved that the light absorption ability of doped semiconductor composite nanomaterials was enhanced markedly by introducing 2-aminopyrazine into the carbon nitride structure. Meanwhile, the segregation efficiency of photo-induced carriers was obviously accelerated because the amino groups can work as hole trapping agents. Additionally, the introduced amino groups own Lewis alkalinity, which is in favour of the photoreduction. This work expands a new perspective of stable photocatalysts in the water split to produce hydrogen.

Polylactic acid-based dressing with oxygen generation and enzyme-like activity for accelerating both light-driven biofilm elimination and wound healing.

Photodynamic therapy (PDT) is a widely used therapeutic approach for eradicating bacterial biofilms in infected wound, but its effectiveness is limited by the hypoxic environment within the biofilm. This study aimed to investigate whether the efficiency of photodynamic removing biofilm is improving by providing oxygen (O2), as well as the expression of cytokines involved in infected wound healing. Manganese dioxide (MnO2) nanoparticles with catalase-like activity were grown in situ on graphitic phase carbon nitride (g-C3N4, CN) nanosheets to construct an all-in-one CN-MnO2 nanozyme, which was then incorporated into poly-L-lactic acid (PLLA) to prepare CN-MnO2/PLLA wound dressing by electrospinning. Subsequently, the in vitro antibacterial biofilm ratio and antibacterial ratio of CN-MnO2/PLLA wound dressing were examined by spread plate and crystal violet staining under irradiation with 808nm near-infrared light and 660nm visible light. Meanwhile, the rat skin injury model was established, and hematoxylin and eosin (H&E), Masson's, tumor necrosis factor-α (TNF-α), Arginase 1 (Arg-1), vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (BFGF) were evaluated in vivo to assess the effect of CN-MnO2/PLLA wound dressing on wound healing. Biofilm density caused by Staphylococcus aureus and Pseudomonas aeruginosa had elimination rates of 83 and 62%, respectively, when treated with CN-MnO2/PLLA dressing. Additionally, the dressing exhibited high antibacterial efficacy against both bacteria, achieving 99 and 98.7% elimination of Staphylococcus aureus and Pseudomonas aeruginosa, respectively. Furthermore, in vivo experiments showed that the CN-MnO2/PLLA wound dressing achieved complete healing of infected wounds on Day 14, with a wound healing rate of >99% by increasing collagen deposition, expression of anti-inflammatory cytokine Arg-1, vascularization cytokine VEGF, and epithelial cell BFGF, and inhibiting the expression of inflammatory cytokine TNF-α. The CN-MnO2/PLLA wound dressing exhibited excellent antibacterial properties in vitro and in vivo. In addition, CN-MnO2/PLLA wound dressing accelerated rapid wound healing through an anti-inflammatory, pro-vascular regeneration and skin tissue remodeling mechanism.

Analysis of degradation effect of carbon nitride nanomaterials in pollutant treatment

Abstract Photocatalytic technology is known as a green technology in solving energy problems and pollution problems, which can generate clean energy and degrade pollutants. In order to study the degradation performance of carbon nitride and its composites on air pollutants and water pollutants, this paper constructs TiO2/g-C3N4 composite photocatalysts by compositing graphite-like phase carbon nitride (g-C3N4) with titanium dioxide (TiO2) using titanium tetrachloride and melamine as raw materials in a water bath method. The physicochemical properties of the prepared complexes were analytically characterized by X-ray diffraction, UV-Vis diffuse reflectance, and X-ray photoelectron spectroscopy, and their degradation activities were examined and compared. The results of all the tests showed that the prepared 5 wt% TiO2/g-C3N4 nanocomposites performed better compared to other mass percentages of nanomaterials. The degradation of pollutants also resulted in better photocatalytic performance of the 5 wt% nanomaterials, with catalytic efficiencies of 54.2% and 99.5% for NO and methylene blue, respectively, at 30 min, and the good photocatalytic activity remained after five cycles.

Neuron specific enolase assay based on the perovskite CoSn(OH)6 for enhancing the anodic electrochemiluminescence of luminol

Electrochemiluminescence (ECL) is a widely applied technique for trace detection and analysis, but the stability of luminophores and external environmental factors strongly influence the analysis results. Herein, a low-potential ECL sensing platform based on enhanced nanomaterial catalysis for the traditional system luminol-H2O2 is proposed for the detection of neuron specific enolase (NSE). In this strategy, Au nanoparticles modified with three-dimensional graphitic phase carbon nitride (3DCNA) were used as a solid platform for antibodies (Ab2), which not only solved the problem of accumulation between traditional two-dimensional nanosheets but also had good biocompatibility, ensuring the accuracy of the analysis results. CoSn(OH)6, benefiting from its inherently higher catalytic activity and greater number of adsorption sites on perovskite hydroxide, can catalyze the oxidationreduction reaction of H2O2 to improve the ECL behavior of luminol and lower the applied voltage to reduce damage to biological activity. Owing to these exceptional properties, this proposed sandwich ECL immunosensor was explored for the primary diagnosis of SCLC by detecting NSE with a detection limit of 0.18 pg mL–1. It exhibited satisfactory linearity in the range of 0.0005 ng mL–1 to 100 ng mL–1 with favorable stability, excellent specificity, and good reproducibility. This study provides an important reference for low-potential ECL with promising application prospects in actual clinical analysis and detection.

Investigation into the degradation of air and runoff pollutants using nano g-C3N4 photocatalytic road surfaces

Exhaust emissions and road runoff pollution pose significant environmental challenges, leading to severe air pollution and irreversible soil damage, respectively. The adoption of self-cleaning road surfaces with photocatalytic properties has emerged as an effective approach to combat both types of pollution. Currently, nano titanium dioxide (TiO2) stands as the most widely used semiconductor for photocatalytic pavements. However, its limited light/radiation utilization remains a concern. To address this, the present study focuses on the use of the green nanomaterial graphene-like phase carbon nitride (g-C3N4), which has a smaller band gap to improve its light utilization. Comprehensive characterizations were performed to elucidate its physical/chemical properties. Subsequently, photocatalytic road coatings with various active substance contents were prepared by incorporating g-C3N4 into epoxy resin, and the functional pavement's performances were evaluated. A laboratory assessing method for the degradation of runoff pollution and NO contaminant was devised, enabling the evaluation of the redox capacity of semiconductive photocatalysts. Experimental results demonstrate that the nano g-C3N4 photocatalytic coating exhibits significant enhancement in degradation efficiency for a typical water pollutant, methylene blue (MB), being 2.76 times that of the nano TiO2 photocatalytic coating. Additionally, its ability to degrade NO gaseous contaminant under visible-light irradiation is 7 times more than the control sample of TiO2 coating. Moreover, the photocatalytic coating has good anti-slip property and long-term performance. Thus, nano g-C3N4 proves to be a more suitable semiconductor material for self-cleaning road surfaces, holding tremendous potential to mitigate diverse pollution arising from transportation under natural light conditions.

Nickel-decorated graphite phase carbon nitride photocatalysts coupled with carbazole-based calixarene dyes for high-efficiency visible light-driven hydrogen evolution

The development of artificial devices that mimic the highly efficient and sophisticated photosystems found in nature is a subject worthy of in-depth study. Two calixarene D-π-A dyes, C4-CZSTP and C4-CZBTP, containing an N-methylcarbazole group as a secondary auxiliary electron donor, are synthesized on the basis of our previously reported calixarene dye C4-BTP. These dyes are then cooperated with Ni-deposited g-C3N4 to prepare ternary photocatalysts, denoted as C4-CZSTP/Ni/g-C3N4, C4-CZBTP/Ni/g-C3N4 and C4-BTP/Ni/g-C3N4, and their photocatalytic performances are evaluated under visible light irradiation. The optimized 4.0 wt% C4-CZSTP/Ni/g-C3N4 sample gives a remarkable H2 evolution rate of 5552 μmol g−1 h−1, representing one of the highest records among the reported analogous systems based on g-C3N4. And after an extended test of 49 h, a total H2 yield of 63.57 mmol g−1 is obtained, corresponding to a turnover number (TON) based on C4-CZSTP moles (TONC4-CZSTP) of 3180. This performance can be attributed to the enhanced light-harvesting and photoelectron conversion of the as-prepared calixarene dyes, the adjusted energy levels and the effective cooperation of the three components. The optimal performance of C4-CZSTP/Ni/g-C3N4 among the three dye-sensitized systems is due to its higher lowest unoccupied molecular orbital (LUMO) value, i.e. stronger electronic driving force from the excited dye to g-C3N4. This study provides an interesting example for the design and preparation of a low-cost, high-efficiency and noble metal-free photocatalytic system for solar fuel production.

Vesicular BiVO4 nanostructures modified by g-C3N4 quantum dots for enhanced photocatalytic activity

Photocatalysis technology has been an available method to alleviate the improper discharge of dye wastewater by employing light energy to degrade the dye pollutants. Here, the vesicular BiVO4 hollow structures were modified by graphite phase carbon nitride quantum dots (CNQDs) to construct the BiVO4-based photocatalyst (BiVO4/CNQDs) for the enhanced removal of dye molecules. The CNQDs with a diameter of 2–5 nm evenly decorate on BiVO4 vesicles to construct the close interface of the BiVO4/CNQDs heterojunctions. Compared with vesicular BiVO4, the enhanced visible-light decomposition of methyl orange (MO) comes down to the coordination of different components, the C and/or N doping and hollow structure. This is helpful to increase surface area of bulk BiVO4, broaden light response, narrow band gap and obstruct charge combination. Especially, the up-conversion luminescence of the CNQDs can induce BiVO4 to generate more photo-excited electrons to participate in the MO photo-degradation reaction. The BiVO4/CNQDs heterojunctions with the unique hollow structure and excellent photocatalytic activity display the promising utilization in wastewater treatment.

Metal-free catalysts with local fluorination regulation for peroxymonosulfate activation: Nearly 100 % singlet oxygen production for selective degradation of aqueous organic pollutants

Generating singlet oxygen (1O2) via activating peroxymonosulfate (PMS) is crucial for the selective removal of organic pollutants in aquatic environments. However, achieving efficient and selective conversion of PMS into 1O2 without consuming energy or metals remains a significant challenge. In this study, graphite phase carbon nitride (g-C3N4) was locally fluorinated via a simple polymerization method. The local fluorinated g-C3N4 (FCN) was used as a metal-free catalyst to activate PMS, enabling highly efficient degradation of 4-chlorophenol (100 %) and detoxification. The FCN/PMS system demonstrates exceptional selectivity for electron-rich pollutants, functions effectively across a broad pH range (2–10), and exhibits remarkable interference resistances to background scavenging ions and natural organic compounds. Furthermore, quenching experiments, probe tests, electron paramagnetic spin resonance measurements, electrochemical characterizations, and theoretical calculations demonstrated that 1O2 was the only reactive species in the catalytic process. Local fluorination regulated the electronic structure of g-C3N4, juxtaposing electron-rich fluorine with electron-deficient carbon dual active sites. This modification alters the electron transfer direction between PMS and g-C3N4, allowing for nearly 100 % selective generation of 1O2via dual electron transfer channels without the need for energy or metals. This study provides a new strategy for designing metal-free heterogeneous catalysts to selectively generate 1O2 in a green way and can facilitate the wider applications of advanced oxidation processes for water purification.

Effective degradation of phenol by activating PMS with bimetallic Mo and Ni Co-doped g C3N4 composite catalyst: A Fenton-like degradation process promoted by non-free radical 1O2

The application of bimetal supported graphite phase carbon nitride in activated peroxymonosulfate (PMS) process has become a research hotspot in recent years. In this study, 8-g C3N4/Mo/Ni composite catalyst material was successfully prepared by doping Mo and Ni in graphite phase carbon nitride. The bimetallic active sites were formed in the catalyst, and PMS was activated by the metal valence Mo6+/Mo4+ and Ni2+/Ni(0) through redox double cycle to effectively degrade phenol. When pH was neutral, the degradation rate of 20 mg/L phenol solution with 8-g C3N4/Mo/Ni (0.35 g/L) and PMS (0.6 mM) could reach 95% within 20 min. The degradation rate of 8-g C3N4/Mo/Ni/PMS catalytic system could reach more than 90% within 20min under the condition of pH range of 3–11 and different anions. Meanwhile, the degradation effects of RhB, MB and OFX on different pollutants within 30min were 99%, 100% and 82%, respectively. Electron spin resonance and quenching experiments showed that in 8-g C3N4/Mo/Ni/PMS system, the degradation mechanism was mainly non-free radicals, and the main active species in the degradation process was 1O2. This study provides a new idea for the study of bimetal supported graphite phase carbon nitride activation of PMS and the theoretical study of degradation mechanism.

Synergistic silver doping and N vacancy promoting photocatalytic performances of carbon nitride for pollutant oxidation and hydrogen production

Carbon nitride (C3N4) has attracted immense interest as a low-cost, non-toxic and naturally abundant raw material. However, graphite-like phase carbon nitride (g-C3N4) still suffers from poor visible light absorption, fast charge carrier recombination, slow electron mobility and relatively fewer surface-active sites. In this work, we synthesized silver-doped N vacancy-rich carbon nitride (AgCN) with convoluted ultra-thin lamellar layers from Ag precursors and melamine-cyanuric acid monomers using a self-assembly supramolecular strategy. AgCN exhibited excellent photocatalytic performance and stability. The introduction of N vacancies disrupted the off-domain π-bonds and weakened the conjugation effect of the triazine ring elements. The large specific surface area of the convoluted ultra-thin lamellar structure helps suppress the aggregation of active silver centers, and the Ag-N2C2 bond acts as a bridge for photoexcited charge transfer to promote the separation and transfer of photogenerated electron/hole pairs for surface redox reactions. As a result, AgCN exhibited excellent photocatalytic performance for photodegradation of rhodamine B (RhB) and hydrogen production (1.69 mmol g-1h−1), well outperforming the pristine CN. Density flooding theory (DFT) calculations revealed the improved conductivity and efficient separation of electron-hole pairs in AgCN at the excited state, generating superoxide radicals, singlet oxygen and holes.

Comparison of Modification Methods of Photocatalyst G-C3N4 in Hydrogen Production Performance

Non-metallic polymer semiconductor graphite phase carbon nitride (g-C3N4) is a low-cost, environmentally friendly raw material with suitable bandgap width and stable chemical properties. However, there are still problems such as lower surface area, higher recombination rate of photo-excited charge carriers, and lower utilization rate of visible light. This paper introduces the structure, physicochemical properties, preparation methods, and modification ideas of graphite phase carbon nitride, focusing on several popular modification achievements in recent years, as well as a horizontal comparison of their respective production methods, mechanisms, and hydrogen production efficiency. Finally, the challenges and prospects in the modification of carbon nitride are discussed.

Accelerated bone defect repairment by carbon nitride photoelectric conversion material in core–shell nanofibrous depended on neurogenesis

Highly efficient bone repair materials are essential for the clinical treatment of large bone defects. This study aimed to develop nanofibrous scaffolds for bone defect repairment. Here, we reported that insulin like growth factor (IGF) adsorbed into phosphorus doped graphite phase carbon nitride (C3N4(P)) as core, and nerve growth factor (NGF) adsorbed into silk fibroin (SF) as shell to prepare nanofibrous scaffolds (IGF@C3N4(P)/NGF@SF) by coaxial electrospining for accelerating bone formation. Additionally, C3N4(P) was employed as a photoelectric conversion material capable of achieving the mutual conversion of light and electricity. Remarkably, we found that red light + IGF@C3N4(P)/NGF@SF scaffold may enhance osteogenesis in bone mesenchymal stem cells (BMSCs) by activating the extracellular regulated protein kinases1/2 (Erk1/2), which subsequently activated runt-related transcription factor 2 (Runx2) and the mammalian target of rapamycin (mTOR) pathway. Consequently, the mRNA expression levels of downstream osteogenic related genes were increased. Furthermore, we observed that red light + IGF@C3N4(P)/NGF@SF scaffold promoted BMSCs induced neural differentiation cells differentiated into neuron and upregulated the mRNA expression levels of neuron specific related genes. Interestingly, we also demonstrated the formation of new neurons in the Haversian canal within the cranial defect area in mice, indicating that red light + IGF@C3N4(P)/NGF@SF scaffold promoted osteogenesis with neurogenesis. Moreover, our RNA sequencing results supported the activation of neurogenesis along with osteogenesis. Based on these novel findings, we conclude that red light + IGF@C3N4(P)/NGF@SF scaffold exhibits great potential as a prospective biomaterial for promoting bone defect repairment with neurogenesis, and the utilization of red light is crucial in facilitating this process.