Search Results (16)

In this study, AgI/Ag₃PO₄/WO₃ ternary composite photocatalysts with dual Z-scheme heterojunction were fabricated via the in situ loading of Ag₃PO₄ onto WO₃ followed by anion exchange. Compared to single photocatalysts and binary composites, the AgI/Ag₃PO₄/WO₃ composites exhibited enhanced photocatalytic activity in the photodegradation of chlortetracycline hydrochloride (CTC) under visible-light irradiation. Notably, the AAW-40 photocatalyst, which contained an AgI/Ag₃PO₄ molar ratio of 40%, degraded 75.7% of the CTC within 75 min. Moreover, AAW-40 demonstrated an excellent performance in the cyclic degradation of CTC over four cyclic degradation experiments. The separation and transfer kinetics of the AgI/Ag₃PO₄/WO₃ composite were investigated with photoluminescence spectroscopy, time-resolved photoluminescence spectroscopy, and electrochemical measurements. The improved photocatalytic performance was primarily due to the creation of a silver-bridged dual Z-scheme heterojunction, which facilitated the efficient separation of photoinduced electron–hole pairs, retained the strong reducing capability of electrons in AgI, and ensured the strongly oxidizing nature of the photoexcited holes in WO₃. The dual Z-scheme charge-transfer mechanism was further validated using in situ X-ray photoelectron spectroscopy. This study provides a foundation for developing innovative dual Z-scheme photocatalytic systems aimed at the efficient degradation of antibiotics in wastewater. Full article

Food spoilage caused by microbial contamination remains a global challenge, driving demand for sustainable antibacterial packaging. Conventional photocatalytic materials suffer from limited spectral response, rapid charge recombination, and insufficient reactive oxygen species (ROS) generation under visible light. Here, a Z-scheme heterojunction was constructed by coupling zeolitic imidazolate framework-8 (ZIF-8) with Ag₃PO₄, achieving dual-spectral absorption and spatial charge separation. The directional electron transfer from Ag₃PO₄’s conduction band to ZIF-8 effectively suppresses electron-hole recombination, prolonging carrier lifetimes and amplifying ROS production (·O₂⁻/·OH). Synergy with Ag⁺ release further enhances bactericidal efficacy. Incorporated into a cellulose acetate matrix (CAM), the ZIF-8/Ag₃PO₄/CAM film demonstrates 99.06% antibacterial efficiency against meat surface microbiota under simulated sunlight, alongside high transparency. This study proposes a Z-scheme heterojunction strategy to maximize ROS generation efficiency and demonstrates a scalable fabrication approach for active food packaging materials, effectively targeting microbial contamination control and shelf-life prolongation. Full article

In this work, a novel dual Z-scheme CdS/Ag₂MoO₄/β-Bi₂O₃ (CAB) composite heterojunction was synthesized, with the ultrafine CdS nanoparticles decorating two different-sized particles. In the beginning, the synergistic effect between BO and AMO makes the 10% Ag₂MoO₄/β-Bi₂O₃ (10AB) photocatalyst exhibit an optimal degradation efficiency of 87.1% for methylene blue (MB) of 10 mg·L⁻¹ within 60 min; furthermore, its photocatalytic activity was enhanced by incorporating CdS nanoparticles on the surface of the AB heterojunction. The results showed that the 25% CdS/10% AMO/BO (25C10AB) composite achieved a maximum MB degradation efficiency of 99%. Optical and photoluminescence measurements showed that the dual Z-scheme CAB heterojunction has high crystallinity and efficient charge carrier migration and separation, which makes the samples more efficient for removing pollutants. Theoretical studies (DFT/FEM calculations) were performed to better understand the migration direction of e⁻ and h⁺ in the photocatalytic degradation mechanism. This work provides a feasible approach to obtaining an efficient heterojunction composite photodegradation catalyst. Full article

A double-layer core–shell photocatalytic coating was engineered on carbon fibers (CFb) derived from bamboo pulp precursors, employing a sequential process involving seed pre-loading, solvothermal treatment, and impregnation. XRD, SEM, and SEM-EDS analyses revealed that g-C₃N₄ and Bi₂O₃ nanosheets were co-assembled on the carbon fiber skeleton, and 50 nm MoS₂ particles were successfully loaded, resulting in the fabrication of MoS₂/g-C₃N₄/Bi₂O₃/CFb photocatalytic fibers. UV–vis spectroscopy, transient photocurrent response, and EIS tests demonstrated that the introduction of narrow-bandgap visible-light photocatalysts (g-C₃N₄ and MoS₂) enhanced light absorption and improved the separation and migration efficiency of photogenerated electron hole pairs. Photocatalytic degradation experiments of MB showed that MoS₂/g-C₃N₄/Bi₂O₃/CFb significantly outperformed g-C₃N₄/Bi₂O₃/CFb and Bi₂O₃/CFb, achieving a degradation efficiency of 92% within 60 min. Band structure calculations and analysis confirmed the formation of Z-scheme heterojunctions between g-C₃N₄ and Bi₂O₃, as well as between MoS₂ and Bi₂O₃. This dual Z-scheme heterojunction endowed MoS₂/g-C₃N₄/Bi₂O₃/CFb with enhanced redox capabilities, providing a novel strategy for developing efficient photocatalytic materials. Full article

This study focused on the preparation and investigation of g-C₃N₄/TiO₂ photocatalysts using different TiO₂ morphologies (anatase nanoparticles (TPs), poorly crystalline nanotubes (aTTs), and well-crystalline anatase nanorods (TRs)) and self-synthesized g-C₃N₄ (CN). The synthesis of the g-C₃N₄/TiO₂ composites was carried out using a mortar mixing technique and a g-C₃N₄ to TiO₂ weight ratio of 1:1. In addition, the g-C₃N₄/TiO₂ composites were annealed in a muffle furnace at 350 °C for 2 h in air. The successful formation of a g-C₃N₄/TiO₂ composite with a mesoporous structure was confirmed using the results of XRD, N2 physisorption, and FTIR analyses, while the results of microscopic analysis techniques confirmed the preservation of TiO₂ morphology in all g-C₃N₄/TiO₂ composites investigated. UV-Vis DR measurements showed that the investigated g-C₃N₄/TiO₂ composites exhibited visible-light absorption due to the presence of CN. The results of solid-state photoluminescence and electrochemical impedance spectroscopy showed that the composites exhibited a lower charge recombination compared to pure TiO₂ and CN. For example, the charge transfer resistance (RCT) of the CNTR/2 composite of TR and CN calcined in air for 2 h was significantly reduced to 0.4 MΩ, compared to 0.9 MΩ for pure TR and 1.0 MΩ for pure CN. The CNTR/2 composite showed the highest photocatalytic performance of the materials tested, achieving 30.3% degradation and 25.4% mineralization of bisphenol A (BPA) dissolved in water under visible-light illumination. In comparison, the pure TiO₂ and CN components achieved significantly lower BPA degradation rates (between 2.4 and 11.4%) and mineralization levels (between 0.6 and 7.8%). This was due to (i) the presence of Ti³⁺ and O-vacancies in the TR, (ii) enhanced heterojunction formation, and (iii) charge transfer dynamics enabled by a dual mixed type-II/Z scheme mechanism. Full article

A novel dual Z-scheme heterojunction photocatalyst was constructed by introducing the narrow-bandgap semiconductor CuInS₂ (CIS) into the dual metal-organic framework (MOF) system of UiO-66(Zr) and NH₂-MIL-101(Fe). This structure effectively overcomes the limitations of conventional photocatalysts in terms of light absorption range and the separation efficiency of photogenerated charge carriers. The prepared ternary catalyst, (UiO-66(Zr))-(NH₂-MIL-101(Fe))/CuInS₂, exhibited excellent photocatalytic performance under visible light irradiation, achieving a hydrogen production rate of 888 μmol g⁻¹ h⁻¹ and a methylene blue (MB) degradation efficiency of up to 95.03%. The significant enhancement in performance is attributed to the material’s porous structure, extended light absorption range, and optimized electron transfer pathways. Additionally, the construction of the dual Z-scheme heterojunction further promotes the separation and migration of photogenerated charge carriers, suppressing electron–hole recombination. This study demonstrates the great potential of dual Z-scheme heterojunctions in improving photocatalytic efficiency and provides an important theoretical foundation and design strategy for the development of efficient photocatalysts. Full article

A highly versatile Z-scheme heterostructure, Ho₂SmSbO₇/YbDyBiNbO₇ (HYO), was synthesized using an ultrasonic-assisted solvent thermal method. The HYO heterojunction, composed of dual A₂B₂O₇ compounds, exhibits superior separation of photogenerated carriers due to its efficient Z-scheme mechanism. The synergistic properties of Ho₂SmSbO₇ and YbDyBiNbO₇, particularly the excellent visible light absorption, enable HYO to achieve exceptional photocatalytic performance in the degradation of fenitrothion (FNT). Specifically, HYO demonstrated an outstanding removal efficiency of 99.83% for FNT and a mineralization rate of 98.77% for total organic carbon (TOC) during the degradation process. Comparative analyses revealed that HYO significantly outperformed other photocatalysts, including Ho₂SmSbO₇, YbDyBiNbO₇, and N-doped TiO₂, achieving removal rates that were 1.10, 1.20, and 2.97 times higher for FNT, respectively. For TOC mineralization, HYO exhibited even greater enhancements, with rates 1.13, 1.26, and 3.37 times higher than those of the aforementioned catalysts. Additionally, the stability and durability of HYO were systematically evaluated, confirming its potential applicability in practical scenarios. Trapping experiments and electron paramagnetic resonance analyses were conducted to identify the active species generated by HYO, specifically hydroxyl radicals (•OH), superoxide anions (•O₂⁻), and holes (h⁺). This facilitated a comprehensive understanding of the degradation mechanisms and pathways associated with FNT. In conclusion, this study represents a substantial contribution to the advancement of efficient Z-scheme heterostructure and offers critical insights for the development of sustainable remediation approaches aimed at mitigating FNT contamination. Full article

As photoelectrochemical catalyst material, Z-scheme heterojunction 3D WO₃@Co₂SnO₄ composites were designed through a hydrothermal-calcination method. The morphology and structure were characterized by SEM, EDS, XRD, XPS, DRS, and Mott–Schottky analysis, and the photoelectrochemical properties were explored with the transient photocurrent and electrochemical impedance. The construction of Z-scheme heterojunction markedly heightened the separation efficiency of photogenerated electron-hole pairs of WO₃ and enhanced the light absorption intensity, retaining the strong redox ability of the photocatalyst. The 3D WO₃@Co₂SnO₄ was used as a photocathode for production of H₂O₂. Under the optimal reaction conditions, the yield of H₂O₂ can reach 1335 μmol·L⁻¹·h⁻¹. The results of free radial capture and rotating disc test revealed the existence of direct one-step two-electron and indirect two-step one-electron oxygen reduction to produce H₂O₂. Based on the excellent H₂O₂ production performance of the Z-scheme heterojunction photoelectrocatalytic material, 3D WO₃@Co₂SnO₄ and stainless-steel mesh were used to construct a dual-cathode photoelectric-Fenton system for in-situ degradation of a variety of pollutants in water, such as dye (Methyl orange, Rhodamine B), Tetracycline, sulfamethazine, and ciprofloxacin. The fluorescence spectrophotometry was used to detect hydroxyl radicals with terephthalic acid as a probe. Also, the photocatalytic degradation mechanism was revealed, indicating the dual-cathode photoelectron-Fenton system displayed satisfactory potential on degradation of different types of environmental pollutants. This work provided insights for designing high-activity photoelectrocatalytic materials to produce H₂O₂ and provided possibility for construction of a photoelectric-Fenton system without extra additions. Full article

The recalcitrant nature of emerging contaminants (ECs) in aquatic environments necessitates the development of effective strategies for their remediation, given the considerable impacts they pose on both human health and the delicate balance of the ecosystem. Semiconductor-based photocatalytic technology is recognized for its dual benefits in effectively addressing both ECs and energy-related challenges simultaneously. Among the plethora of photocatalysts, black phosphorus (BP) stands as a promising nonmetallic candidate, offering a host of advantages including its tunable direct band gap, broad-spectrum light absorption capabilities, and exceptional charge mobility. Nevertheless, pristine BP frequently underperforms, primarily due to issues related to its limited ambient stability and the rapid recombination of photogenerated electron–hole pairs. To overcome these challenges, substantial research efforts have been devoted to the creation of BP-based photocatalysts in recent years. However, there is a noticeable absence of reviews regarding the advancement of BP-based materials for the degradation of ECs in aqueous solutions. Therefore, to fill this gap, a comprehensive review is undertaken. In this review, we first present an in-depth examination of the fabrication processes for bulk BP and BP nanosheets (BPNS). The review conducts a thorough analysis and comparison of the merits and limitations inherent in each method, thereby delineating the most auspicious avenues for future research. Then, in line with the pathways followed by photogenerated electron–hole pairs at the interface, BP-based photocatalysts are systematically categorized into heterojunctions (Type I, Type II, Z-scheme, and S-scheme) and hybrids, and their photocatalytic performances against various ECs and the corresponding degradation mechanisms are comprehensively summarized. Finally, this review presents personal insights into the prospective avenues for advancing the field of BP-based photocatalysts for ECs remediation. Full article

The design of highly efficient organic/inorganic photocatalysts with visible-light response has attracted great attention for the removal of organic pollutants. In this work, the polyacrylonitrile (PAN) worked as the matrix polymer, while polyaniline (PANI) and Sb₂S₃–ZnO were used as organic/inorganic photocatalysts. The heterojunction PAN/PANI–Sb₂S₃–ZnO photocatalyst was prepared using electrospinning and surface ultrasound. PAN/PANI–Sb₂S₃–ZnO exhibited an excellent visible-light absorption intensity in the wavelength range of 400–700 nm. The maximum removal efficiencies of PAN/PANI–Sb₂S₃–ZnO for four organic dyes were all greater than 99%. The mechanism study showed that a dual Z-scheme could be constructed ingeniously because of the well-matched bandgaps between organic and inorganic components in the photocatalyst, which achieved efficient separation of photogenerated carriers and reserved photogenerated electrons (e⁻) and holes (h⁺) with strong redox ability. The active species •OH and •O₂⁻ played an important role in the photocatalytic process. The composite photocatalyst also had excellent stability and reusability. This work suggested a pathway for designing novel organic/inorganic composite photocatalysts with visible-light response. Full article

The dual Z-scheme heterojunction CuBi₂O₄/Bi₂Sn₂O₇/Sn₃O₄(CBS) was successfully constructed through in situ growth methods, and its photocatalytic performance was evaluated via degradation of tetracycline hydrochloride under visible light. Out of all samples, CBS-2 exhibited the highest photocatalytic activity, with an apparent rate constant of 2.34, 20.16, and 44.17 times that of Bi₂Sn₂O₇, CuBi₂O₄, and Sn₃O₄, respectively. Even after four cycles, the photocatalytic efficiency remained above 85%. The improvement can be attributed to the construction of the Z-scheme heterojunction, which effectively promotes the separation and migration of photogenerated carriers. The possible photocatalytic degradation mechanism of dual Z-scheme heterojunction CBS was deduced based on the theory of free radical capture and energy band. Full article

A facile two-step synthesis of ternary hetero-composites of ZnO, CuO, and single-walled carbon nanotubes (SWCNTs) was developed through a recrystallization process followed by annealing. A series of nanocomposites were prepared by varying the weight ratio of copper(II) acetate hydrate and zinc(II) acetate dihydrate and keeping the weight ratio of SWCNTs constant. The results revealed the formation of heterojunctions (ZnO–SWCNT–CuO, ZSC) of three crystal structures adjacent to each other, forming a ternary wurtzite-structured nanoparticles along with defects. Enhanced charge separation (electron-hole pairs), reduced band gap, defect-enhanced specific surface area, and promoted oxidation potential were key factors for the enhanced photocatalytic activity of the ternary nanocomposites. OH^• radicals were the main active species during dye degradation, and O₂^−• and h⁺ were also involved to a lesser extent. A type II heterojunction mechanism approach is proposed based on the charge carrier migration pattern. Among the synthesized nanocomposites, the sample prepared using copper(II) acetate hydrate and zinc(II) acetate dihydrate in a 1: 9 ratio (designated a ZSC3) showed the highest photocatalytic activity. ZSC3 achieved 99.2% photodecomposition of methylene blue in 20 min, 94.1% photodecomposition of Congo red in 60 min, and 99.6% photodecomposition of Rhodamine B in 40 min under simulated sunlight. Additionally, ZSC3 showed excellent reusability and stability, maintaining 96.7% of its activity even after five successive uses. Based on overall results, the ZSC sample was proposed as an excellent candidate for water purification applications. Full article

In this study, both vanadium and copper elements were anchored on graphitic carbon nitride (gCN) (denoted as V/Cu/gCN) via a thermal decomposition process as a novel nanosheet photocatalyst for the removal of monocrotophos (MCP). The prepared nanosheet features were studied by utilizing XRD, UV–Visible absorption spectrometry, PL, FE-SEM, TEM, and XPS techniques. These analytical techniques revealed the successful formation of direct Z-scheme heterojunctions of V/Cu/gCN nanosheets. The dopant materials significantly enhanced the electron–hole separation and enhanced the removal rate of MCP as compared with bulk gCN. The investigation of effective operating conditions confirmed that a higher removal of MCP could be obtained at a doping concentration of 0.3 wt% and a catalytic dosage of 8 mg with 80 min of visible-light irradiation. The generation of various reactive radicals during the degradation process of the photocatalyst was observed using a scavenging treatment process. Additionally, the scavenging process confirmed that e⁻, OH•, h⁺, and O₂^•− played a major role in MCP degradation. The direct Z-scheme dual-heterojunction mechanism, as well as the possible pathway for the fragmentation of MCP by the V/Cu/gCN nanosheet photocatalyst, was derived in detail. This research article provides a novel perspective on the formation of excellent semiconductor photocatalysts, which exhibit enormous potential for environmental treatments. Full article

Graphitic carbon nitride (g-C₃N₄) with a porous nano-structure, nitrogen vacancies, and oxygen-doping was prepared by the calcination method. Then, it was combined with ZnIn₂S₄ nanosheets containing zinc vacancies to construct a three-dimensional (3D) flower-like Z-scheme heterojunction (pCN-N/ZIS-Z), which was used for photocatalytic hydrogen evolution and the degradation of mixed pollutants. The constructed Z-scheme heterojunction improved the efficiency of photogenerated charges separation and migration, and the large surface area and porous characteristics provided more active sites. Doping and defect engineering can change the bandgap structure to improve the utilization of visible light, and can also capture photogenerated electrons to inhibit recombination, so as to promote the use of photogenerated electron-hole pairs in the photocatalytic redox process. Heterojunction and defect engineering synergized to form a continuous and efficient conductive operation framework, which achieves the hydrogen production of pCN-N/ZIS-Z (9189.8 µmol·h⁻¹·g⁻¹) at 58.9 times that of g-C₃N₄ (155.9 µmol·h⁻¹·g⁻¹), and the degradation rates of methyl orange and metronidazole in the mixed solution were 98.7% and 92.5%, respectively. Our research provides potential ideas for constructing a green and environmentally friendly Z-scheme heterojunction catalyst based on defect engineering to address the energy crisis and environmental restoration. Full article

The novel ternary-component Ag/AgI/α-MoO₃ (AAM) photocatalyst was successfully fabricated by a facile hydrothermal method combined with a charge-induced physical adsorption and photo-reduced deposition technique. X-ray diffraction, scanning/transmission electron microscope, X-ray photoelectron, UV-vis diffuse reflectance, photoluminescence and electrochemical impedance spectroscopy were employed to characterize the composition, morphology, light-harvesting properties and charge transfer character of the as-synthesized catalysts. The ternary-component AAM heterojunctions exhibited an excellent visible-light photocatalytic oxidative desulfurization activity, in which the AAM-35 (35 represents weight percent of AgI in AAM sample) possessed the highest photocatalytic activity of the conversion of 97.5% in 2 h. On the basis of band structure analysis, radical trapping experiments and electron spin resonance (ESR) spectra results, two different catalytic mechanisms were suggested to elucidate how the photogenerated electron-hole pairs can be effectively separated for the enhancement of photocatalytic performance for dual composites AM-35 and ternary composites AAM-35 during the photocatalytic oxidative desulfurization (PODS) of thiophene. This investigation demonstrates that Z-scheme Ag/AgI/α-MoO₃ will be a promising candidate material for refractory sulfur aromatic pollutant’s removal in fossil fuel. Full article