Efficient Photocatalytic Hydrogen Production Research Articles

Construction of 2D/2D S-scheme Bi2MoO6/Zn-TCPP heterojunction via in-situ self-assembly growth strategy to enhance interface effect for efficient photocatalytic hydrogen production

Two-dimensional/two-dimensional (2D/2D) heterojunctions are considered to be an effective strategy for forming strong interface effects and facilitating photogenerated carrier separation. However, it is usually limited by the size mismatch of the materials, even at the expense of its redox capability. Herein, 2D/2D S-scheme heterojunction photocatalyst Bi2MoO6/Zn-TCPP (BMO/ZTP) composed of 2D Bi2MoO6 and 2D Zn-TCPP (TCPP: tetrakis (4-carboxyphenyl) porphyrin) (MOFs) was constructed by in-situ self-assembly growth strategy. The size-compatible 2D/2D composites had abundant surface active sites and strong interactions. In addition, band bending and interfacial electric field (IEF) effect based on S-scheme heterojunction could accelerate the separation and migration of photogenerated carriers in BMO/ZTP. The best hydrogen precipitation rate of the BMO/ZTP was 10900.94 umol·g−1·h−1, which was 38.90 and 3.24 times higher than that of Bi2MoO6 (280.26 umol·g−1·h−1) and Zn-TCPP (3360.34 umol·g−1·h−1), respectively. The results indicated that 2D/2D BMO/ZTP S-scheme heterojunction could enhance the interface effect and retain strong reducing electrons to achieve efficient photocatalytic hydrogen production, which was confirmed by ultraviolet photoelectron spectroscopy (UPS), Tafel curve, electron spin resonance (ESR) and time-resolved photoluminescence (TRPL) characterization and density functional theory (DFT) calculations. This work provided a general strategy for constructing 2D Bi2MoO6 and 2D MOFs S-scheme heterojunctions to enhance interface effects for achieving efficient photocatalytic hydrogen production.

Designing delafossite CuAl1-xTMxO2 solid solutions: the role of 3d transition metal spin states in photo(electro)catalytic performance

This study delves into the effects of 3d transition metal (TM) spin states on the structural and electronic properties of CuAl1-xTMxO2 solid solutions, focusing on their implications for photo(electro)catalytic performance. The research reveals that the Jahn–Teller distortion, associated with TM3+, is a critical factor in determining the lattice parameters and photo(electro)catalytic performances. Solid solutions without Jahn–Teller distortion adhere to Vegard's law, whereas those with strong distortion exhibit deviations, indicating the influence of TMO6 octahedral distortion on solubility and lattice parameters. The electronic structure of solid solutions with weak Jahn–Teller distortion is governed by the O–Cu–O and TMO6 crystal fields, which leads to a narrowed bandgap and reduced conduction band minimum (CBM), impacting the hydrogen evolution potential. In particular, the CuAl0.5Cr0.5O2 shows a significant enhancement in photocurrent density and hydrogen production rate due to its balanced light absorption and effective charge carrier separation. In contrast, the weak Jahn–Teller distortion in CuAl1-xFexO2 results in localized electronic states at CBM, leading to diminished carrier mobility. Solid solutions with strong Jahn–Teller distortion, such as CuAl1-xTMxO2 (TM = Mn and Ni), display a range of electronic properties from semiconductor to semimetallic, with the semimetallic CuAl0.9Mn0.1O2 capable of infrared light absorption and efficient photocatalytic hydrogen and oxygen production.

Cu-doped ZnCdS-based photocatalyst for efficient photocatalytic hydrogen production by photothermal assistance

In solar energy utilization, photocatalytic hydrogen production has been widely researched. To address issues such as low efficiency of photocatalysts, Cu-doped Zn0.5Cd0.5S composite photocatalysts were prepared using a hydrothermal method for photocatalytic hydrogen production. The Cu/Zn0.5Cd0.5S photocatalyst was characterized using XRD, XPS, SEM, TEM, UV–vis-DRS, fluorescence spectrophotometer, and electrochemical workstation. The results indicate that Cu doping alters the crystal and band structures of Zn0.5Cd0.5S. Hydrogen production experiments were conducted under xenon lamp irradiation, and at 45 °C, the highest hydrogen production rate was 2.72 and 1.63 times that of single Zn0.5Cd0.5S and Cu-doped Zn0.5Cd0.5S at room temperature (25 °C), respectively. Cu doping imparted a photothermal effect to the photocatalytic hydrogen production experiment, enhancing its efficiency.Cu doping captured electrons by replacing some Zn, constructing an internal electric field, forming defect energy levels, which hindered electron-hole recombination. Additionally, Cu ions acted as a plasma, inducing a plasma effect during hydrogen production, accelerating the rate of solar energy conversion to thermal energy, thus improving hydrogen production efficiency. This research not only provides a photocatalyst for photocatalytic hydrogen production but also utilizes it for photothermal synergistic catalysis.

In situ Construction of Single-Atom Electronic Bridge on COF to Enhance Photocatalytic H2 Production.

Photocatalytic hydrogen production is one of the most valuable technologies in the future energy system. Here, we designed a metal-covalent organic frameworks (MCOFs) with both small-sized metal clusters and nitrogen-rich ligands, named COF-Cu3TG. Based on our design, small-sized metal clusters were selected to increase the density of active sites and shorten the distance of electron transport to active sites. While another building block containing nitrogen-rich organic ligands acted as a node that could in situ anchor metal atoms during photocatalysis and form interlayer single-atom electron bridges (SAEB) to accelerate electron transport. Together, they promoted photocatalytic performance. This represented the further utilization of Ru atoms and was an additional application of the photosensitizer. N2-Ru-N2 electron bridge (Ru-SAEB) was created in situ between the layers, resulting in a considerable enhancement in the hydrogen production rate of the photocatalyst to 10.47 mmol g-1 h-1. Through theoretical calculation and EXAFS, the existence position and action mechanism of Ru-SAEB were reasonably inferred, further confirming the rationality of the Ru-SAEB configuration. A sufficiently proximity between the small-sized Cu3 cluster and the Ru-SAEB was found to expedite electron transfer. This work demonstrated the synergistic impact of small molecular clusters with Ru-SAEB for efficient photocatalytic hydrogen production.

Thermal Exfoliation and Phosphorus Doping in Graphitic Carbon Nitride for Efficient Photocatalytic Hydrogen Production.

Photocatalytic H2 evolution has been regarded as a promising technology to alleviate the energy crisis. Designing graphitic carbon nitride materials with a large surface area, short diffusion paths for electrons, and more exposed reactive sites are beneficial for hydrogen evolution. In this study, a facile method was proposed to dope P into a graphitic carbon nitride framework by calcining melamine with 2-aminoethylphosphonic acid. Meanwhile, PCN nanosheets (PCNSs) were obtained through a thermal exfoliation strategy. Under visible light, the PCNS sample displayed a hydrogen evolution rate of 700 μmol·g-1·h-1, which was 43.8-fold higher than that of pure g-C3N4. In addition, the PCNS photocatalyst also displayed good photostability for four consecutive cycles, with a total reaction time of 12 h. Its outstanding photocatalytic performance was attributed to the higher surface area exposing more reactive sites and the enlarged band edge for photoreduction potentials. This work provides a facile strategy to regulate catalytic structures, which may attract great research interest in the field of catalysis.

Rare earth oxide Y2O3 modified g-C3N4 for efficient photocatalytic hydrogen production: photocatalytic performance and electron transfer channels

This work used a one-step calcination process to prepare g-C3N4 composites with varying Y2O3 loading. XRD, TEM, and XPS verified the structure and morphology of the composite photocatalyst, and its photoelectrochemical and hydrogen production performance were studied. According to the experimental results, it is found that the composite structure between Y2O3 and g-C3N4 effectively suppresses the photoelectron–hole complex and enhances the photocatalytic hydrogen production properties of g-C3N4. Under the irradiation of a 300 W xenon lamp, YCN-3 had superior photocatalytic hydrogen generation performance, achieving a rate of 1079.61 μmol g−1 h−1, which was 2.3 times greater than that of g-C3N4 in its unmodified state. After three consecutive photocatalytic operations, satisfactory stability and reusability were obtained. Finally, the possibility of a mechanism for the photocatalytic charge transfer pathway is discussed, which provides an effective way for g-C3N4 photocatalytic hydrogen production.

Hf2CO2-based heterojunctions for efficient photocatalytic hydrogen production and highly responsive self-powered flexible photodetector

The heterojunctions based transition metal carbide (MXenes) provides new possibilities for achieving high-performance photodetector. The electronic, mechanical, optical, and photocatalytic properties of the Hf2CO2-based heterojunctions are calculated based on first-principles calculations, and the photocurrent (Iph) and extinction ratio (ER) are calculated based on quantum transport simulations. The Hf2CO2/Sc2CF2, Hf2CO2/Zr2CO2, and Hf2CO2/Sc2CCl2 heterojunctions are ionic semiconductors with indirect bandgap. The Hf2CO2/Sc2CF2 heterojunction exhibits high solar to hydrogen efficiency (ηSTH) of 40.14 % and applying biaxial strain can effectively modulate the ηSTH of the Hf2CO2/Zr2CO2 heterojunction. The Hf2CO2/Zr2CO2 heterojunction has low overpotentials (ηHER) of 0.19 V and exhibits high electron mobility. The photodetector based on the Hf2CO2/Zr2CO2 heterojunction exhibits high Iph, and the photodetector based on the Hf2CO2/Sc2CF2 heterojunction has large ER and sensitivity to infrared and ultraviolet polarized light. The Iph and ER are significant increase by bending the photodetector. Our research indicates the potential applications of the Hf2CO2-based heterojunctions in photocatalytic water splitting and photodetector.

InP/PtS2 heterojunctions: Z-scheme photocatalysts with enhanced light absorption for high solar-to-hydrogen conversion efficiency

In this paper, the structure and electronic properties of InP/PtS2 heterojunction as well as the photocatalytic and solar hydrogen production efficiency are studied by first principles. Studies have shown that InP/PtS2 heterojunction is type II band alignment, typical Z heterostructure, has strong light absorption coefficient in the absorption spectrumand, InP/PtS2 heterojunction with an indirect bandgap of 1.97 eV，the band edge positions that meet the energy band prerequisites for water splitting across different pH levels，The band edge positions and light absorption capabilities have been modified through biaxial strain, with tensile strain enhancing the absorption capacity within the visible light spectrum ranging from 450 to 800 nm(nm). The InP/PtS2 heterojunction achieves a solar-to-hydrogen conversion efficiency (ηSTH) of 32.5%, which is higher than that of most heterojunctions. The InP/PtS2 heterojunction is anticipated to emerge as a promising contender for the next generation of photocatalysts.

Construction of schottky-assisted Z-scheme heterojunction Cd0.3Zn0.7S@Ti3C2/Ag/CeO2 boosted carriers charge separation for efficient photocatalytic hydrogen production

The purposeful modulation of interfacial charge transfer pathways in heterogeneous structures is an innovative and feasible strategy to improve photocatalysis efficiency. However, it is often characterized by difficulties in charge separation and transport and the high charge recombination limits its applications. Herein, a Cd0.3Zn0.7S-based heterostructure of Cd0.3Zn0.7S@Ti3C2/Ag/CeO2 was fabricated in which the efficient electron transfer route was designed by synergistic action of Z-scheme and Schottky junction. Serial characterizations and Density-Functional Theory calculations identify the Schottky junction promoted the electrons in Cd0.3Zn0.7S to transfer to Ti3C2, whereas the Z-scheme heterojunction accelerated the electrons transfer from CeO2 to Cd0.3Zn0.7S@Ti3C2 with Ag acting as the electronic intermediary. Significantly, the optimized Cd0.3Zn0.7S@Ti3C2/Ag/CeO2 exhibited stronger photocatalytic H2 evolution of 16.3 mmol·g−1·h−1 with an apparent quantum efficiency of 29.8 % at 420 nm, which was 4.2 times higher than the pristine Cd0.3Zn0.7S material. This work offers valuable insights into realizing the desired charge transfer route through artificial heterointerface and a new possibility for applying Cd1-xZnxS materials in photocatalytic hydrogen production.

Ferroelectric polarization-electric field promoted S-scheme CdSe/BaxSr1-xTiO3 for highly efficient solar hydrogen evolution

Coupling the ferroelectric polarization and internal electric field to realize effective separation and migration of photogenerated charges is highly attractive for accomplishing efficient photocatalytic hydrogen production. In this work, an internal electric field modulated S-scheme heterostructure was fabricated by depositing CdSe on ferroelectric BaxSr1-xTiO3 (BxST) through an in-situ growth method. Because of the oriented powerful electron transport driven by the strong spontaneous polarization and internal electric field, the as-synthesized CdSe/BxST heterojunctions demonstrated excellent solar to H2 performance. Without the addition of noble metal cocatalyst, 7% CdSe/B0.8ST exhibited a H2 evolution rate of 1971.8 µmol g-1 h−1 with an apparent quantum yield of 12.1% at 365 nm. Moreover, the obtained heterojunction catalysts exhibit good stability after 12 h continuous irradiation. This work provides a viable strategy on the utilization of ferroelectric polarization and internal electric field strategy to promote charge transfer and separation of S-scheme photocatalysts.

MOF-derived hollow octahedral CoxP/MOF-801 p-n heterojunction for efficient photocatalytic hydrogen production

Hydrogen energy produced through photocatalytic water splitting is widely recognized as a viable solution to the depletion of non-renewable energy resources and ecological contamination concerns. This work designed and synthesized the MOF-derived hollow octahedral CoxP/MOF-801 p-n heterojunction photocatalyst. According to the result of hydrogen production test, the hydrogen production amount of CoxP/MOF-801-2 could reach 25.31 mmol g−1 under light irradiation for 5 h. The hollow octahedral structure and p-n heterojunction of the photocatalyst helped to enhance the light trapping ability and promote carrier transfer, resulting in improved performance of photocatalytic hydrogen production. To sum up, the design of hollow octahedral CoxP/MOF-801 photocatalyst effectively improved the photocatalytic hydrogen production performance.

Efficient solar utilization: Multifunctional solar absorber devices realize self-driven hydrogen production

Considered as one of the effective approaches to address the energy crisis and develop green and sustainable energy, the application of solar energy in multiple stages was investigated in this study. By designing a WS2/ZnIn2S4 heterojunction, a multifunctional coupling system based on interfacial water evaporation technology was constructed. In this system, the water evaporation rate was 1.67 kgꞏm−2ꞏh−1, and the photocatalytic degradation efficiency of rhodamine B reached 96.5 %. Moreover, the electric energy output from thermoelectric conversion was innovatively in situ applied for photocatalytic hydrogen production, which increased the photocatalytic hydrogen production efficiency by five times, with a hydrogen production rate of 40.3 μmolꞏcm−2ꞏh−1. This study successfully integrated thermoelectric power generation, photocatalytic hydrogen production, and photocatalytic degradation of dye wastewater into an advanced solar-driven interface evaporation system, enabling the simultaneous conversion of solar energy into multiple forms of energy, improving solar energy utilization efficiency, which was of great significance for promoting the practical application of solar energy.

Thienyl-fused dibenzothiophene-S,S-dioxide based conjugated polymer toward highly efficient photocatalytic hydrogen production

Dibenzothiophene-S,S-dioxide (BTDO) is one of the cutting-edge electron-acceptor monomers for designing conjugated polymer based organic materials toward photocatalytic H2 production from water. Normally, structure design of BTDO containing donor-acceptor (D-A) polymer photocatalyst mainly focuses on screening electron-donor motifs, the importance of modification on BTDO molecular toward improving charge carrier separation and photocatalytic performance is always ignored. Herein, a novel thienyl-fused BTDO building block (BTDO-DT) is prepared and utilized to synthesize B-BTDO-DT polymer photocatalyst by Sonogashira-Hagihara cross-coupling polycondensation using 1,4-Diethynylbenzene (B) and BTDO-DT as monomers. Experimental and density functional theory (DFT) calculation results demonstrate that modification of BTDO by thiophene not only enlarges light absorption region and promotes photogenerated e−/h+ separation, but also decreases H atom adsorption free energy (ΔGH*) on oxygen atom in the OSO group. As a result, B-BTDO-DT exhibits an outstanding visible light induced photocatalytic H2 production rate of 156.6 μmol h−1 using 30 mg catalyst without Pt cocatalyst, which is 4.5 times higher than that of B-BTDO. And the H2 production rate of B-BTDO-DT is further improved to be 259.8 μmol h−1 with 2.0 wt% Pt as co-catalyst. The present work may open a new direction for the design of conjugated polymer based photocatalysts with high photocatalytic activities.

Protonated Z-scheme CdS-covalent organic framework heterojunction with highly efficient photocatalytic hydrogen evolution

The low efficiency of photocatalytic hydrogen production from water is mainly suffer from limited light absorption, charge separation and water delivery to the active centers. Herein, an inorganic–organic Z-scheme heterojunction (CdS-COF-Ni) is constructed by in-situ growth of CdS nanosheets on the porphyrin-based covalent organic framework with nickel ions (COF-Ni) in the porphyrin centers. A built-in electric field is formed at the interface, which accelerates the separation and transfer of photogenerated charges. Moreover, through the surface protonation treatment in ascorbic acid (AC) solution, the hydrophilicity of the obtained composite is obviously increased and facilitates the transport of water molecules to the photocatalytic centers. Under the synergistic effect of the interfacial interaction and surface protonation treatment, the photocatalytic hydrogen production rate is optimized to be 18.23 mmol h−1 g−1 without adding any cocatalysts, which is 21 times that of CdS. After a series of photoelectrochemical measurements, in situ X-ray photoelectron spectroscopy (XPS) analysis, and density functional theory (DFT) calculations, it is found that the photocatalytic charge transfer pathway conforms to the Z-scheme mechanism, which not only greatly accelerates the separation and transfer of photogenerated charges, but also retains a high reduction capacity for water splitting. This work offers a good strategy for constructing highly efficient organic–inorganic heterojunctions for water splitting.

Construction of Covalent organic frameworks with bex topology for efficient photocatalytic hydrogen production

Covalent organic frameworks (COFs) have become effective platforms for solar energy conversion and utilization. The rational design of the COF topology provides an effective strategy to expand the π-conjugation system and improve the photocatalytic activity. Herein, we have prepared two sub-stoichiometric pyrene-based 2D-COFs with the bex topology, HITMS-COF-10 and HITMS-COF-11, with high crystallinity and specific surface area. The HITMS-COF-11 exhibits an outstanding photocatalytic hydrogen evolution reaction (HER) rate of 25000 μmol g−1 h−1 in water under visible illumination (λ > 420 nm), demonstrating that the bex topological COFs could be one of the state-of-the-art photocatalyst candidates for hydrogen evolution and the importance of tuning the topological diversity at molecular levels for solar energy conversion and utilization.

Conjugated diacetylene polymers with intrachain D-A block heterostructure for efficient photocatalytic hydrogen production

Solar-driven photocatalytic hydrogen production has been considered as a promising candidate technology for supplying green and sustainable energy source alternative to fossils. But its low solar-to-hydrogen conversion efficiency level hampers its practical application, and lack of effective structure for promoting charge separation is one of the accounts. Herein, intrachain heterojunction structure comprised of donor-acceptor (D-A) blocks has been proved to be one of effective structures for addressing such an issue. Utilizing the facile oxidative coupling polymerization reactions of diacetylene monomers and oligomers, a block heterojunction polymeric photocatalyst named PDTPDPA-BP bearing D-A blocked heterostructure was synthesized by first separative oligomerizations of diacetylene-functionalized dibenzothiophene sulfone (DTP) and triphenylamine (TPA) monomers and then mixed together and undergoing further polymerization. In photocatalytic hydrogen production, PDTPDPA-BP displayed a hydrogen evolution rate of 2164 μmol g−1 h−1, which is much larger than those of PDTP (1270 μmol g−1 h−1) and PTPA (57 μmol g−1 h−1) synthesized by homopolymerization of DTP and TPA monomers, respectively, and their 1:1 molar ratio physical blend (363 μmol g−1 h−1). By means of Fluorescence spectroscopy and photo-responsive measurements, it was found PDTPDPA-BP has narrower bandgap and more efficient charge separation than the other polymers. Therefore, the work highlights intrachain heterojunction structure promotes exciton dissociation into free charge carries, and thus deserves the consideration in the design of high performance organic photocatalysts.

Materials Advances in Photocatalytic Solar Hydrogen Production: Integrating Systems and Economics for a Sustainable Future.

Photocatalytic solar hydrogen generation, encompassing both overall water splitting and organic reforming, presents a promising avenue for green hydrogen production. This technology holds the potential for reduced capital costs in comparison to competing methods like photovoltaic-electrocatalysis and photoelectrocatalysis, owing to its simplicity and fewer auxiliary components. However, the current solar-to-hydrogen efficiency of photocatalytic solar hydrogen production has predominantly remained low at ≈1-2% or lower, mainly due to curtailed access to the entire solar spectrum, thus impeding practical application of photocatalytic solar hydrogen production. This review offers an integrated, multidisciplinary perspective on photocatalytic solar hydrogen production. Specifically, the review presents the existing approaches in photocatalyst and system designs aimed at significantly boosting the solar-to-hydrogen efficiency, while also considering factors of cost and scalability of each approach. In-depth discussions extending beyond the efficacy of material and system design strategies are particularly vital to identify potential hurdles in translating photocatalysis research to large-scale applications. Ultimately, this review aims to provide understanding and perspective of feasible pathways for commercializing photocatalytic solar hydrogen production technology, considering both engineering and economic standpoints.

Facile synthesis of Ag2S cocatalyst modified Zn0·6Cd0·4S for efficient photocatalytic hydrogen production

The investigation and development of straightforward methods for fabricating efficient photocatalysts are critical for converting solar energy to fuel. This study reports the successful synthesis of Ag2S/Zn0·6Cd0·4S (AZC) composites featuring zinc vacancies using a simple, two-step hydrothermal approach. These composites, characterized by nanoparticle morphologies, demonstrated strong visible light absorption, high photocurrent density and exceptional charge-transfer efficiency. Notably, the 0.5% AZC composite showcased outstanding hydrogen production (18.77 mmol g−1 h−1) and stability, achieving an apparent quantum yield (AQY) of 23.8%. The remarkable photocatalytic activity of this composite is attributed to the inclusion of Ag2S serving as an electron trapping cocatalyst, and the presence of zinc vacancies. Furthermore, the study elucidates the underlying photocatalytic mechanism of the 0.5% AZC composite.

The photocatalytic wastewater hydrogen production process with superior performance to the overall water splitting

The utilization of a cost-free sacrificial agent is a novel approach to significantly enhance the efficiency of photocatalytic hydrogen (H2) production by water splitting. Wastewater contains various organic pollutants, which have the potential to be used as hole sacrificial agents to promote H2 production. Our studies on different pollutants reveals that not all pollutants can effectively promote H2 production. However, when using the same pollutants, not all photocatalysts achieved a higher H2 evolution rate than pure water. Only when the primary oxidizing active species of the photocatalyst are •OH radicals, which are generated by photogenerated holes, and when the pollutants are easily attacked and degraded by •OH radicals, can the production of H2 be effectively promoted. It is noteworthy that the porous brookite TiO2 photocatalyst exhibits a significantly higher H2 evolution rate in Reactive Red X-3B and Congo Red, reaching as high as 26.46 mmol⋅g−1⋅h−1 and 32.85 mmol⋅g−1 ⋅h−1, respectively, which is 2–3 times greater than that observed in pure water and is 10 times greater than most reported studies. The great significance of this work lies in the potential for efficient H2 production through the utilization of wastewater.

The Preparation of g-C3N4/ZnIn2S4 Nano-Heterojunctions and Their Enhanced Efficient Photocatalytic Hydrogen Production.

Hydrogen production technology has triggered a research boom in order to alleviate the problems of environmental pollution and the pressure on non-renewable energy sources. The key factor of this technology is the use of an efficient photocatalyst. g-C3N4 is a typical semiconductor photocatalytic material that is non-toxic and environmentally friendly and does not cause any serious harm to human beings. Therefore, it can be applied to drug degradation and the photocatalytic production of H2. Combined with ZnIn2S4, this semiconductor photocatalytic material, with a typical lamellar structure, has become one of the most promising catalysts for research due to its suitable bandgap structure and excellent photoelectric properties. In this study, 10% g-C3N4/ZnIn2S4 nano-heterojunction composite photocatalytic materials were successfully prepared by compounding ZnIn2S4 and g-C3N4 semiconductor materials with good visible-light-trapping ability. Under visible light irradiation, the photocatalytic activity of the composites was significantly better than that of pure g-C3N4 and ZnIn2S4. This is attributed to the formation of a heterojunction structure, which effectively inhibited the recombination of photogenerated carriers through the interfacial contact between the two semiconducting materials, and then improved the separation efficiency of the photogenerated electron-hole pairs, thus enhancing the catalytic activity. In this study, pure g-C3N4 and ZnIn2S4 were prepared using calcination and hydrothermal methods, and then, the composites were synthesized using ultrasonic and hydrothermal means. The differences in the structure, morphology, and hydrogen production performance of the materials before and after recombination were analyzed in detail using XRD, SEM, and FTIR characterization, which further verified that the 10% g-C3N4/ZnIn2S4 nano-heterojunction composites possessed excellent photocatalytic activity and stability, providing new possibilities for the optimization and application of photocatalytic hydrogen production technology.