In-situ synthesis of CdS/g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> hybrid nanocomposites with enhanced visible photocatalytic activity

A novel and simple in situ synthetic strategy was used to fabricate CdS/g-C₃N₄ hybrid nanocomposite catalysts with visible-light-driven photocatalytic activity from cadmium-containing carbon nitride compounds. X-ray diffraction measurements, high-resolution transmission electron microscopy images, and Fourier transform infrared spectra showed heterojunctions with a close interface between the g-C₃N₄ and the CdS nanoparticles and nanorods in the composite. Ultraviolet visible diffuse reflectance spectra exhibited a red shift that further presented the CdS in the polymer g-C₃N₄ skeleton, which allowed the efficient utilization of the solar spectrum for creating photogenerated electrons and holes. The photoluminescence spectra of the nanocomposites suggested charge transfer from g-C₃N₄ to CdS. The photocurrent intensity of hybrid nanocomposites was 2.3 times than that of pure g-C₃N₄ sample, and photocatalytic activity for the photodegradation of methyl orange was 2.5 times, and hydrogen evolution reaction was 2.8 times. Enhanced photocatalytic activity and photocurrent for the CdS/g-C₃N₄ hybrid nanocomposites were achieved.     

Novel Bi<Subscript>12</Subscript>TiO<Subscript>20</Subscript>/g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> composite with enhanced photocatalytic performance through Z-scheme mechanism

Novel Bi₁₂TiO₂₀/g-C₃N₄ composite was successfully prepared with Bi₁₂TiO₂₀ nanoparticles embedded within the fluffy crumpled g-C₃N₄ nanosheets. Bi₁₂TiO₂₀/g-C₃N₄ composites exhibit superior photoactivity and stability. As compared with g-C₃N₄ and Bi₁₂TiO₂₀, the photocatalytic efficiency of Bi₁₂TiO₂₀/g-C₃N₄ is effectively enhanced about 1.8- and 4.9-fold, respectively. Based on the trapping experiment, ^·OH and ^·O₂^? radicals are the dominant reactive oxygen species involved in the photocatalytic process. The proposed Z-scheme mechanism of charge transfer markedly promotes the carriers’ migration and separation, leading to the enhanced photocatalytic performance.     

Enhanced visible light photocatalytic activity for g-C<Subscript>3</Subscript>N<Subscript>4</Subscript>/SnO<Subscript>2</Subscript>:Sb composites induced by Sb doping

In this paper, g-C₃N₄/SnO₂:Sb composite photocatalysts were fabricated by in situ loading Sb-doped SnO₂ (SnO₂:Sb) nanoparticles on graphitic carbon nitride (g-C₃N₄) nanosheets via a facile hydrothermal method. The synthesized g-C₃N₄/SnO₂:Sb composites delivered enhanced visible light photocatalytic performance for degradation of rhodamine B in comparison with g-C₃N₄/SnO₂ composites without doping Sb. Various techniques including XRD, SEM, TEM, FTIR, XPS, PL and electrochemical method were employed to demonstrate the successful fabrication of g-C₃N₄/SnO₂:Sb composite and to investigate the enhanced mechanism of photocatalytic activity. The improvement of visible light absorption and the promotion of separation efficiency and interfacial transfer of photogenerated carriers induced by Sb doping were responsible for the enhancement of photocatalytic activity. This study provides a simple and convenient method to synthesize a visible light responsive catalyst with promising performance for the potential application in environmental protection.     

TiO<Subscript>2</Subscript>/g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> heterojunctions: <Emphasis Type="Italic">In situ</Emphasis> fabrication mechanism and enhanced photocatalytic activity

In situ fabrication of TiO₂/g-C₃N₄ (TCN) heterojunctions was achieved by a modified sol-gel method. TG analysis was employed to determine the content of TiO₂ in TCN composites. XRD, FTIR, TEM and HRTEM were used to analyze the phase composition, functional groups, morphology and microstructure of as-obtained products, respectively. Based on the measurement of surface Zeta potential of g-C₃N₄, a possible mechanism on in situ fabrication of TCN heterojunctions was concluded. The control experiments indicated that TCN heterojunctions exhibited better photocatalytic performance than either TiO₂ or g-C₃N₄, suggesting that the enchanced photocatalytic activity could be realized by TCN heterojunctions. Then, the evaluation of parameters affecting the photocatalytic performance of TCN heterojunctions was investigated. Even after five cycles, TCN heterojunctions still maintained high photocatalytic activity, exhibiting the good photocatalytic stability. UV-vis absorption spectra showed that almost all MB molecules were decomposed in the photocatalytic process. Finally, the possible mechanism on enhanced photocatalytic performance of TCN heterojunctions was discussed.     

Well-organized 3D urchin-like hierarchical TiO<Subscript>2</Subscript> microspheres with high photocatalytic activity

This article reported a well-organized 3D urchin-like hierarchical TiO₂ which was synthesized by a simple solvothermal method without using any template or surfactant. The results of scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and powder X-ray diffraction showed that the hierarchical morphology and size of TiO₂ could be effectively controlled by adjusting the precursor ratio of tetrabutyl titanate to TiCl₄ solution, the concentration of TiCl₄ solution, the solvothermal temperature, and the reaction time. It is believed that the formation of the urchin-like hierarchical TiO₂ followed a ‘nucleation–self-assembly–dissolution-recrystallization’ growth mechanism. In addition, the excellent photocatalytic activity of the urchin-like hierarchical TiO₂ was confirmed by photodegradation of methyl blue in water.     

Efficient visible-light driven photocatalysts: coupling TiO<Subscript>2</Subscript>(AB) nanotubes with g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> nanoflakes

The wide application of the titanium dioxide (TiO₂) as the photocatalysts is greatly hindered by its intrinsic large band gap and usually fast electron–hole recombination. Here, we reported the exploration of coupling g-C₃N₄ nanoflakes to TiO₂ nanotubes with the anatase and TiO₂(B) mixed phases (TiO₂(AB)) toward the efficient visible-light-driven hybrid photocatalyst. It is found that coupling TiO₂(AB) nanotubes with g-C₃N₄ nanoflakes could bring a profoundly extension the visible light adsorption capacity and enhanced photogenerated carrier separation. Accordingly, they exhibit much higher efficient photocatalytic activities toward the degradation of sulforhodamine B under the visible light irradiation, which is enhanced for nearly 15 times to those of the TiO₂(AB) and g-C₃N₄, suggesting their promising practical applications as novel and efficient semiconductor photocatalysts for the water purification.     

In<Subscript>2</Subscript>S<Subscript>3</Subscript> nanoparticles dispersed on g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> nanosheets: role of heterojunctions in photoinduced charge transfer and photoelectrochemical and photocatalytic performance

Fast recombination of photogenerated charge carriers is a major problem in the photoelectrochemical and photocatalytic processes. In this work, we report significantly improved PEC performance of a nanocomposite consists of In₂S₃ nanoparticles dispersed on g-C₃N₄ nanosheets synthesized by a simple and facile wet chemical route. The results of high-resolution TEM study show that the obtained In₂S₃ nanoparticles of size 10–20 nm exist in cubic phase and are uniformly dispersed on the surface of g-C₃N₄ nanosheets. The In₂S₃/g-C₃N₄ nanocomposite with 25 weight percentage of In₂S₃ exhibits 8.5 times higher photocurrent density than the single-phase g-C₃N₄ under visible light illumination. The enhanced photocurrent density exhibited by the In₂S₃/g-C₃N₄ nanocomposite is attributed to the efficient separation of photogenerated charge carriers. The charge transfer mechanism in In₂S₃/g-C₃N₄ heterojunction was studied by a series of experiments, such as electrochemical impedance spectroscopy, photoelectrochemical measurement and photoluminescence emission spectroscopy. The intimate interface promotes the charge transfer and inhibits the recombination rate of photogenerated electron–hole pairs, which significantly improves the photoelectrochemical performance. A detailed charge transfer mechanism is discussed based on the Mott–Schottky plot study. This heterojunction material is found to be an efficient photocatalyst for the degradation of both cationic rhodamine B dye and anionic methyl orange dye as the lifetime of photogenerated charge carriers is higher in the composite than in single-phase In₂S₃ and g-C₃N₄. A strong correlation between the photoelectrochemical and the photocatalytic performances is observed in this composite.     

Fabrication of plate-on-plate Z-scheme SnS<Subscript>2</Subscript>/Bi<Subscript>2</Subscript>MoO<Subscript>6</Subscript> heterojunction photocatalysts with enhanced photocatalytic activity

A class of direct plate-on-plate Z-scheme heterojunction SnS₂/Bi₂MoO₆ photocatalysts was synthesized via a two-step hydrothermal method. The materials were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectra, Fourier transform infrared photoluminescence emission spectra, and UV–vis diffuse reflectance spectroscopy. The photocatalytic activity was estimated via the degradation of crystal violet (CV) and ciprofloxacin (CIP). The experimental results indicated that the 5 wt% SnS₂/Bi₂MoO₆ composites exhibited significantly enhanced performance in contrast to pure Bi₂MoO₆ or SnS₂ nanoflakes, and were also superior to the popular TiO₂ (P25). The degradation reaction accorded well with the first-order reaction kinetics equation; the rate constant of CV using a SnS₂ content of 5 wt% photocatalyst was ~?3.6 times that of the Bi₂MoO₆ and 2.4 times that of SnS₂. Furthermore, a SnS₂ content of 5 wt% exhibited a 1.7 times higher photocatalytic activity of CIP than that of pure Bi₂MoO₆, and 1.3 times that of pure SnS₂. Radical trapping experiments and an electron spin resonance technique indicated that h⁺ and ·OH were the dominant active species involved in the degradation process. A plasmonic Z-scheme photocatalytic mechanism was proposed to explain the superior photocatalytic activities and efficient separation of photogenerated electrons and holes.     

Si<Subscript>3</Subscript>N<Subscript>4</Subscript>/TiN composites produced from TiO<Subscript>2</Subscript>-Modified Si<Subscript>3</Subscript>N<Subscript>4</Subscript> powders

Si₃N₄/TiN composites have been produced by hot pressing at temperatures from 1600 to 1800°C in a nitrogen atmosphere, using silicon nitride powders prepared by self-propagating high-temperature synthesis and surface-modified with titanium dioxide nanoparticles. We examined the effect of TiO₂ content on the microstructure, phase composition, and mechanical strength of the ceramics. It is shown that titanium nitride can be formed by the reaction Si₃N₄ + TiO₂ → TiN + NO + N₂O + 3Si. The Si₃N₄/TiN composites containing 5–20% TiN have a low density, high porosity, and a bending strength of 60 MPa or lower. In Si₃N₄/TiN ceramics produced using calcium aluminates as sintering aids, the silicon nitride grains are densely packed, which ensures an increase in strength to 650 MPa.     

Multifunctional performance of gC<Subscript>3</Subscript>N<Subscript>4</Subscript>-BiFeO<Subscript>3</Subscript>-Cu<Subscript>2</Subscript>O hybrid nanocomposites for magnetic separable photocatalytic and antibacterial activity

Highly active gC₃N₄-BiFeO₃-Cu₂O nanocomposites were successfully prepared via a facile, cost effective and eco-friendly method of hydrothermally wet precipitation combined with ultrasonic dispersion process. The prepared samples were characterized by XRD, FTIR, HRSEM, EDS, TEM, UV–Vis DRS, PL, VSM, BET and electrochemical properties. By means of these analysis for examine the crystal phase, nanostructure, band gap and light-harvesting properties were carried out. UV-DRS spectra indicate that the bandgap of g-C₃N₄ (2.7 eV) reduced to 2.59 and 2.21 eV by mixed with corresponds to BiFeO₃ and BiFeO₃/Cu₂O nanomaterials. The ideal photocatalytic activity of the gC₃N₄-BiFeO₃-Cu₂O nanocomposites, where RhB dye under visible light irradiation which was up to 4.36 and 2.52 times as the higher photodegradation ability to compare pristine g-C₃N₄ and gC₃N₄-BiFeO₃ catalyst. The magnetization was confirmed by VSM studies, and hence, after the photocatalytic reaction, the magnetically separable catalyst can be quickly separated from the water by an external magnetic field. The superior photocatalytic performance is due to the synergistic effect on the interface of BiFeO₃/Cu₂O in the gC₃N₄-BiFeO₃-Cu₂O nanocomposites has reduced the bandgap which enables high separation efficiency of the charge carrier, suppressed recombination rate and their high surface area. Moreover, the chief gC₃N₄-BiFeO₃-Cu₂O catalyst can exhibited the lesser charge transfer resistance (impedance), enhances of photocurrent responses, whereas exposed to the development of photocatalytic appearance and more charge carrier ability. Also, the antibacterial activity of the gC₃N₄-BiFeO₃-Cu₂O nanocomposite has showing a well deactivation in both G⁺ (S. aureus) and G^? (E. coli) bacteria’s whereas compare to other prepared samples.     

One-dimension carbon self-doping g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> nanotubes: Synthesis and application in dye-sensitized solar cells

One-dimension carbon self-doping g-C₃N₄ nanotubes (CNT) with abundant communicating pores were synthesized via thermal polymerization of saturated or supersaturated urea inside the framework of a melamine sponge for the first time. A ～16% improvement in photoelectric conversion efficiency (η) is observed for the devices fabricated with a binary hybrid composite of the obtained CNT and TiO₂ compared to pure TiO₂ device. The result of EIS analysis reveals that the interfacial resistance of the TiO₂-dye|I₃^?/I^? electrolyte interface of TiO₂-CNT composite cell is much lower than that of pure TiO₂ cell. In addition, the TiO₂-CNT composite cell exhibits longer electron recombination time, shorter electron transport time, and higher charge collection efficiency than those of pure TiO₂ cell. Systematic investigations reveal that the CNT boosts the light harvesting ability of the photovoltaic devices by enhancing not only the visible light absorption but also the charge separation and transfer.

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Unravelling charge carrier dynamics in protonated g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> interfaced with carbon nanodots as co-catalysts toward enhanced photocatalytic CO<Subscript>2</Subscript> reduction: A combined experimental and first-principles DFT study

In this work,we demonstrated the successful construction of metal-free zerodimensional/two-dimensional carbon nanodot (CND)-hybridized protonated g-C3N4 (pCN) (CND/pCN) heterojunction photocatalysts by means of electrostatic attraction.We experimentally found that CNDs with an average diameter of 4.4 nm were uniformly distributed on the surface of pCN using electron microscopy analysis.The CND/pCN-3 sample with a CND content of 3 wt.％ showed the highest catalytic activity in the CO2 photoreduction process under visible and simulated solar light.Thisprocess results in the evolution of CH4 and CO.The total amounts of CH4 and CO generated by the CND/pCN-3 photocatalyst after 10 h of visible-light activity were found to be 29.23 and 58.82 μmol·gcatalyst-1,respectively.These values were 3.6 and 2.28 times higher,respectively,than the amounts generated when using pCN alone.The corresponding apparent quantum efficiency (AQE) was calculated to be 0.076％.Furthermore,the CND/pCN-3 sample demonstrated high stability and durability after four consecutive photoreaction cycles,with no significant decrease in the catalytic activity.The significant improvement in the photoactivity using CND/pCN-3 was attributed to the synergistic interaction between pCN and CNDs.This synergy allows the effective migration of photoexcited electrons from pCN to CNDs via wellcontacted heterojunction interfaces,which retards the charge recombination.This was confirmed by photoelectrochemical measurements,and steady-state and time-resolved photoluminescence analyses.The first-principles density functional theory (DFT) calculations were consistent with our experimental results,and showed that the work function of CNDs (5.56 eV) was larger than that of pCN (4.66 eV).This suggests that the efficient shuttling of electrons from the conduction band of pCN to CNDs hampers the recombination of electron-hole pairs.This significantly increased the probability of free charge carriers reducing CO2 to CH4 and CO.Overall,this study underlines the importance of understanding the charge carrier dynamics of the CND/pCN hybrid nanocomposites,in order to enhance solar energy conversion.     

Nanofilaments of Si<Subscript>3</Subscript>N<Subscript>4</Subscript>

Silicon nitride nanofilaments were synthesized at 1600°C in nitrogen on the surface of a ceramic substrate made of amorphous silicon oxynitride obtained by hexamethyl disilasane pyrolysis. The diameter of filaments represented by different morphological types (filaments, ribbons, needles) was 100–500 nm, and the length was several millimeters.     

N-TiO<Subscript>2</Subscript>/g-C<Subscript>3</Subscript>N<Subscript>4</Subscript>/Up-conversion phosphor composites for the full-spectrum light-responsive deNO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> photocatalysis

The ternary composites consisted of nitrogen-doped titanium dioxide, carbon nitride and up-conversion phosphors (UP) were successfully prepared by a solvothermal method. The heterojunction could be formed when N-TiO₂ and g-C₃N₄ were combined together. The composite of N-TiO₂/g-C₃N₄@UP had excellent ultraviolet, visible and infrared light absorption, indicating the possibility for the utilization of full spectrum of solar light. When N-TiO₂ was coupled with g-C₃N₄ and up-conversion phosphors to form a composite, the visible light and NIR light absorption of the samples increased. The ternary composite N-TiO₂/g-C₃N₄@G-UP presented reasonable deNO _x performance of about 8.0% under the irradiation of IR light of 980 nm. The intensification of the photocatalysis might be realized by utilizing up-conversion phosphors, which could convert low-energy NIR light into high-energy photons (visible light) and increase the efficient irradiation on the surface of photocatalyst.     

Fabrication of Ag<Subscript>3</Subscript>PO<Subscript>4</Subscript>-AgBr-PTh composite loaded on Na<Subscript>2</Subscript>SiO<Subscript>3</Subscript> with enhanced visible-light photocatalytic activity

A novel Ag₃PO₄-AgBr-PTh composite loaded on Na₂SiO₃ was synthesized for enhanced visible-light photocatalytic activity. The photocatalytic activity of the samples was evaluated by photodegrading rhodamine B (RhB) under visible light irradiation. The main reactive species and possible photocatalytic mechanism were also discussed. As a result, the Ag₃PO₄-AgBr-PTh composite loaded on Na₂SiO₃ exhibited enhanced photocatalytic activity for RhB compared with Ag₃PO₄ under visible-light irradiation. Additionally, it was demonstrated that the hole (h⁺) and superoxide radical (?O ₂ ^? ) were the major reactive species involving in the RhB degradation. PTh played vital role for the enhanced photocatalytic activity of Ag₃PO₄-AgBr-PTh-Na₂SiO₃ composite, which offered an electron transfer expressway and accelerated the transfer of the electrons from the CB of AgBr into Ag₃PO₄. This work could provide a new perspective for the synthesis of Ag₃PO₄-based composites and the improvement of photocatalytic activity of Ag₃PO₄.     

Magnetically separable Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@TiO<Subscript>2</Subscript> nanospheres: preparation and photocatalytic activity

A facile and efficient approach for the fabrication of Fe₃O₄@TiO₂ nanospheres with a good core–shell structure has been demonstrated. Products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). The results showed that Fe₃O₄@TiO₂ nanocomposites exhibited high degree of crystallinity, excellent magnetic properties at room temperature. Furthermore, the as-prepared Fe₃O₄@TiO₂ nanocomposites exhibited good photocatalytic activity toward the degradation of Rhodamine B (RhB) solution. Additionally, the recycling experiment of Fe₃O₄@TiO₂ nanocomposites had been done, demonstrating that Fe₃O₄@TiO₂ nanocomposites have high efficiency and stability.     

Microstructure characterization of in situ synthesized porous Si<Subscript>3</Subscript>N<Subscript>4</Subscript>–Si<Subscript>2</Subscript>N<Subscript>2</Subscript>O composites using feldspar additive

Porous Si₃N₄–Si₂N₂O bodies fabricated by multi-pass extrusion process were investigated depending on the feldspar addition content (4–8 wt% Si) in the raw silicon powder. The diameter of the continuous pores was about 250 μm. The polycrystalline Si₂N₂O fibers observed in the continuous pores as well as in the matrix regions of the nitrided bodies can increase the filtration efficiency. In the 4 wt% feldspar addition, the diameter of the Si₂N₂O fibers in the continuous pores of the nitrided bodies was about 90–150 nm. A few number of rope typed Si₂N₂O fibers (∼4 μm) was found in the case of 8 wt% feldspar addition. However, in the 8 wt% feldspar addition, the matrix showed highly porous structure composed of large number of the Si₂N₂O fibers (∼60 nm). The relative densities of the Si₃N₄–Si₂N₂O bodies with 4 wt% and 8 wt% feldspar additions were about 65% and 61%, respectively.     

Mass spectrometry of carbon nitride C<Subscript>3</Subscript>N<Subscript>4</Subscript>

Carbon nitride has been synthesized in macroscopic amounts by means of the original method based on an ecologically safe technology using inorganic initial compounds. The product has been characterized by mass spectrometry (MS), X-ray diffraction, and quantitative chemical analysis. The MS and thermochemical data show that stoichiometry of the samples of carbon nitride obtained using the proposed method corresponds to the empirical formula C₃N₄.     

Ultrasonic-assisted synthesis of amorphous Bi<Subscript>2</Subscript>S<Subscript>3</Subscript> coupled (BiO)<Subscript>2</Subscript>CO<Subscript>3</Subscript> catalyst with improved visible light-responsive photocatalytic activity

A series of Bi₂S₃/(BiO)₂CO₃ composite photocatalysts with different loadings of amorphous Bi₂S₃ were successfully synthesized through an ultrasonic-assisted ion-exchange reaction between thioacetamide (CH₃CSNH₂) and (BiO)₂CO₃, and characterized by XRD, XPS, BET, EELS, EDX, SEM, TEM/HRTEM, UV–Vis, and photoluminescence (PL) techniques. The results of TEM/HRTEM, EELS, and EDX indicate that the composite catalyst Bi₂S₃/(BiO)₂CO₃ has been successfully synthesized with the deposited Bi₂S₃ present in amorphous state on the surface of (BiO)₂CO₃. The activities of the catalysts for RhB degradation under visible light show that the catalyst prepared under ultrasonic is more active than the one synthesized without ultrasonic. The optimized sample Bi₂S₃/(BiO)₂CO₃ (U5.0) exhibits a much higher activity, about 4.8 times to that of pure (BiO)₂CO₃. Based upon the band structures of Bi₂S₃/(BiO)₂CO₃, it is deduced that the migration of the visible light-induced electrons from the conduction band of Bi₂S₃ to that of (BiO)₂CO₃ should have facilitated the separation of photogenerated carriers, as confirmed by the suppressed photoluminescence spectra. Using different scavengers, the ·O₂ ^? and holes are clearly identified as the main oxidative species for RhB photodegradation. In light of these observations, a potential photocatalytic mechanism of RhB degradation over Bi₂S₃/(BiO)₂CO₃ is proposed.     

Synthesis of graphene oxide/Ag<Subscript>3</Subscript>PO<Subscript>4</Subscript> composite with enhanced visible-light photocatalytic activity

The nano-scale Ag₃PO₄ was successfully synthesized by the silver ammonia complexing precipitation method at room temperature. And the Graphene oxide (GO)/Ag₃PO₄ nanocomposites with different contents of GO were successfully synthesized using the electrostatic driving method. The as-prepared GO/Ag₃PO₄ nanocomposites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV–visible diffuse reflectance spectroscopy (UV–Vis DRS), confirming that Ag₃PO₄ were highly dispersed to GO sheet. The photocatalytic properties of GO/Ag₃PO₄ were evaluated by the degradation of Methyl Orange (MO) under visible light irradiation and solar irradiation respectively. The results showed that the photocatalytic efficiencies of GO/Ag₃PO₄ nanocomposites had enhanced largely and the kinetics reaction models were followed first-order. Furthermore, 5% GO/Ag₃PO₄ exhibited the highest photocatalytic activity on degradation of MO under visible-light irradiation. The improved photocatalytic performances of the GO/Ag₃PO₄ nanocomposites mainly attributed to the introducing of GO, which benefit for electron transfer and inhibit the recombination of electron–hole pairs, promoting the practical application of Ag₃PO₄ in water purification.