High Photocatalytic Efficiency Research Articles

Recent Progress on Piezoelectric Materials and Pyroelectric Materials for Photoelectrochemical Water Splitting.

Directly transforming solar energy into chemical compounds via photocatalytic water splitting can continually producing hydrogen, which is regarded as one of the ultimate sustainable energy sources. The key point of achieving a high photoelectrochemical (PEC) water splitting performance is the successful design and synthesis of high-efficient photocatalysis. However, the slow separation and fast recombination of photo generated charge carriers greatly limits the utilization of solar energy resulting in low PEC water splitting efficiency. Recently, piezoelectric/pyroelectric effect assisted PEC water splitting brings new sight on improving charger separate and transfer behaviors. In this review, the recent advancements and state-of-the-art progress in piezoelectric/pyroelectric effect assisted PEC water splitting are summarized and discussed. Different types of photocatalysts are classified according to their chemical constitutions and the corresponding advantages are also reviewed. Furthermore, the coupling of piezoelectric effect and pyroelectric effect is also introduced. Finally, the prospects, critical challenges and promising strategies for the application of piezoelectric/pyroelectric materials in PEC water splitting are highlighted.

Ultrafast hydrogen production in boron/oxygen-codoped graphitic carbon nitride revealed by nonadiabatic dynamics simulations.

Graphitic carbon nitride (g-C3N4 or GCN) shows promise in photocatalytic water splitting, despite facing the challenge of rapid electron-hole recombination. In this study, we investigated the influence of boron/oxygen codoping on the photocatalytic performance of GCN systems for hydrogen generation. First-principles calculations and nonadiabatic molecular dynamics (NAMD) simulations were employed to reveal that the recombination time of photogenerated carriers could be increased by 16% to 64% in the codoped systems compared to the pristine GCN. The time-dependent density functional theory (TDDFT) scheme was utilized to select energy windows and initiate dynamics in cluster models of B/O co-doped heptazine with water molecules. Notably, we observed efficient direct photodissociation of hydrogen atoms from water molecules within 60 fs and proton hops within the hydrogen-bonded network within 80 fs in the co-doped system, diverging from the previously proposed mechanism for pristine heptazine in NAMD simulations. This discovery underscores the significant role of faster proton-coupled electron transfer (PCET) reactions and rapid radiationless relaxation in achieving high photocatalytic efficiency in water splitting. Our work enhances the understanding of the internal mechanism of highly efficient photocatalysts for water splitting and provides a new design strategy for doped GCN.

EXPLORING THE IN‐SITU DEVELOPMENT OF A 1D/2D GADOLINIUM IRON OXIDE/TUNGSTEN DISULFIDE PHOTOCATALYST TO IMPROVE TETRACYCLINE DEGRADATION MEDIATED BY VISIBLE LIGHT

In the field of photocatalysis, heterojunction photocatalysts have garnered a lot of attention due to their high‐efficiency interfacial charge‐transfer property and their nanoarchitecture. Herein, GdFeO3/WS2is successfully synthesized by the in‐situ growth method and holds significant catalytic properties and efficient degradation for tetracycline. Using WS2 as a co‐catalyst could reduce e‐ and h+ recombination, improving GdFeO3's photocatalytic performance. The GdFeO3/WS2 possesses a bandgap of 1.9 eV, 178.9 m2 g−1 specific surface area, 0.2 nm pore size, and a lifespan of 6 ns. The optimal GdFeO3/WS2 photocatalyst exhibits a maximum removal of 96.2% at a tetracycline concentration of 10 mg/L, a pH of 3, and 40 mg of photocatalyst in an irradiation time of 90 min. Tetracycline has a higher photocatalytic efficiency in visible light (96.2%) than in sunlight (72.6%). Trapping tests revealed that the major reactive species for tetracycline removal in an aqueous solution are •OH, and •O2‐. The recycle experiment shows no deactivation of the GdFeO3/WS2 photocatalyst after 5 recycles. This study sheds light on the rational design of the GdFeO3/WS2 photocatalyst as a potential material for treating wastewater.

Photo-Fenton-like degradation of tetracycline through peroxymonosulfate activation over 2D BiOBr/FeOOH nanosheets and membrane application

The selection of photosensitizer substrates with high photocatalytic efficiency is crucial for leveraging the advantages of metal-based materials in photo-Fenton-like process. Herein, we report a novel 2D layered BiOBr/FeOOH nanosheets equipped with a built-in electric field (BIEF) to activate peroxymonosulfate (PMS) for the degradation of tetracycline (TC). The photocatalytic efficiency of BiOBr is enhanced by fine-tuning the Br source quantity. Both experimental and theoretical analyses confirm that BIEF at the BiOBr/FeOOH heterointerface expedites the movement of photogenerated electrons, significantly boosting both photocatalytic and photo-Fenton-like activities. The BiOBr/FeOOH + PMS + Vis system exhibits a high TC removal rate of 96 % with only 0.24 mM of PMS and nearly 100 % of PMS utilization. Moreover, affixing BiOBr/FeOOH nanosheets onto a PVDF microfiltration membrane, we establish a continuous flow reactor system for antibiotic wastewater treatment. This system demonstrates a remarkable TC removal efficiency consistently above 97.5 % for 6 h of continuous injection, underscoring its practicality and potential for real-world applications.

Controllable construction of hollow Fe3O4/Ag particles for microwave absorption and photocatalysis

Hollow metallic composite particles are widely used in microwave absorption and catalysis due to their unique cavity structures, and favorable physical and electromagnetic properties. In this work, we propose an approach to prepare highly dispersed Fe3O4/Ag composite particles with a hollow structure using water-soluble green template method combined with in-situ growth process. The as-prepared cubic Fe3O4/Ag composite particles with an average size of 3.19 μm of hollow Ag and 11.65 nm of Fe3O4 coating on the surface were used as fillers for preparing microwave absorption epoxy resin films, showing a minimum reflection loss of −62.37 dB at 16.63 GHz with 7.5 mm thickness. An effective absorption bandwidth of 4.80 GHz can be observed in the frequency bands of 4.70–6.09 and 14.59–18.00 GHz. This mechanism is attributed to the internal cavity of the Fe3O4/Ag particles realizing multiple reflections of electromagnetic waves, and the synergistic effect of Fe3O4 and Ag. Moreover, this perspective is confirmed by their photocatalytic performance. The Fe3O4/Ag particles achieve a high photocatalytic degradation efficiency of 99.84 % for Congo red dye within 30 min of light exposure and maintain a value of 96.62 % after 6 cycles, demonstrating an outstanding reusability.

Construction of TiO2@Cu2O-CuS heterostructures integrating RGO for enhanced full-spectrum photocatalytic degradation of organic pollutants

This study presents the development and optimization of TiO2@Cu2O-CuS heterostructures, enhanced with reduced graphene oxide (RGO), for efficient photocatalytic degradation of organic pollutants, focusing on imidacloprid. Two configurations, TiO2/RGO/Cu2O-CuS and Cu2O-CuS/RGO/TiO2, are explored to highlight the impact of material layering on photocatalytic efficiency. The strategic integration of RGO optimizes charge transfer, crucial for photocatalysis. Comprehensive characterization techniques, such as X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS), Raman spectroscopy, and Nitrogen adsorption-desorption isotherms, provide insights into the crystalline structure, morphology, surface chemistry, and textural properties of the heterostructures. The TiO2/RGO/Cu2O-CuS configuration significantly outperforms its counterpart in photocatalytic activity under full-spectrum (UV–VIS–IR) illumination, due to improved charge carrier dynamics and synergistic interactions between the composite materials. Remarkably, the TiO2/RGO/Cu2O-CuS assembly achieved over 95 % degradation of imidacloprid under simulated solar irradiation, marking a breakthrough in solar spectrum utilization for photocatalysis and exhibits promising recyclability, maintaining its high photocatalytic efficiency even after multiple degradation cycles, highlighting its potential for sustainable pollutant removal applications. Additionally, this configuration demonstrates a twofold increase in degradation efficiency compared to separate UV and VIS irradiations, emphasizing its rapid pollutant removal capability. This research underscores the critical role of material layer sequencing in developing high-efficiency photocatalytic systems and marks a significant advancement in environmental remediation technologies that harness renewable energy sources.

Controlled preparation of bamboo charcoal/BiOCl with efficient visible-light-driven photocatalytic activity for organic pollutant degradation using the residues of bamboo processing

In this research, bamboo charcoal (BC)/BiOCl composites were successfully prepared by a simple hydrothermal method, where the BC was derived from the residues of bamboo processing. The BC/BiOCl composites displayed nanosheet structures with tight combination between bamboo charcoal and BiOCl. The oxygen vacancies (OVs) concentration and photoelectric properties of BC/BiOCl composites were boosted with the doped bamboo charcoal. The photocatalytic performance of the composites was evaluated by the degradation of RhB and TCH. Meanwhile, the possible intermediates, degradation pathways and toxicity of the pollutants in the photocatalytic process were elucidated. When the additive dosage of BC and hydrothermal temperature were 5% and 140°C, the 5BC-140 has highest photocatalytic efficiency under visible light irradiation, and the degradation rates of RhB and TCH over the 5BC-140 composite were 97.9% and 69% at 36 min and 120 min, with the kinetic constants of 6.2 times and 2.0 times as high as those of pure BiOCl, respectively. The establishment of Bi-O-C bonds in the BC/BiOCl played a pivotal role in constructing atomic-level interfacial channels to boost the charge carriers’ separation. The enhanced photocatalytic activity was originated from the robust interaction between bamboo charcoal and BiOCl, promoting the rapid transfer of electrons and suppressing the combination of photogenerated electron-hole pairs through the increased oxygen vacancies. In addition, incubation experiments on green beans demonstrated the nontoxicity of contaminant solution degraded by the BC/BiOCl composites.

Metasurface-enhanced photochemical activity in visible light absorbing semiconductors.

Heterogeneous photocatalysis is an important research problem relevant to a variety of sustainable energy technologies. However, obtaining high photocatalytic efficiency from visible light absorbing semiconductors is challenging due to a combination of weak absorption, transport losses, and low activity. Aspects of this problem have been addressed by multilayer approaches, which provide a general scheme for engineering surface reactivity and stability independent of electronic considerations. However, an analogous broad framework for optimizing light-matter interactions has not yet been demonstrated. Here, we establish a photonic approach using semiconductor metasurfaces that is highly effective in enhancing the photocatalytic activity of GaAs, a high-performance semiconductor with a near-infrared bandgap. Our engineered pillar arrays with heights of ∼150nm exhibit Mie resonances near 700nm that result in near-unity absorption and exhibit a field profile that maximizes charge carrier generation near the solid-liquid interface, enabling short transport distances. Our hybrid metasurface photoanodes facilitate oxygen evolution and exhibit enhanced incident photon-to-current efficiencies that are ∼22× larger than a corresponding thin film for resonant excitation and 3× larger for white light illumination. Key to these improvements is the preferential generation of photogenerated carriers near the semiconductor interface that results from the field enhancement profile of magnetic dipolar-type modes.

The Solvent Role for the Decomposition of Paracetamol in Distilled and Drinking Water by Pure and Ag-Modified TiO2 Sol-Gel Powders.

In this study, pure TiO2 gels were synthesized by applying the sol-gel method, using Ti(IV) butoxide with the addition of two different solvents, namely ethylene glycol (EG) and isopropanol (isop), with only air moisture present. It was established using XRD that the gel prepared with the addition of EG was amorphous even at 400 °C, while the other gel was amorphous up to 300 °C. It was found that TiO2 (anatase) had a dominant crystalline phase during heating to 600 °C, while at 700 °C, TiO2 (rutile) appeared. The as-obtained powdered materials were annealed at 500 °C and subsequently underwent photocatalytic tests with paracetamol. Additionally, the TiO2 samples were modified with Ag+ co-catalysts (10-2 M), using photofixation by UV illumination. The photocatalytic activity of the Ag-modified powders was also tested in the photodegradation of a commonly used paracetamol in aqueous solution under UV light illumination. The obtained data exhibited that the annealed samples had better photocatalytic efficiency and decomposed paracetamol faster in comparison to the non-annealed sol-gel powders. The highest degradation efficiency was observed for the TBT/isop/Ag material, with degradation efficiencies average values of 65.59% and 75.61% paracetamol achieved after the third cycle of photocatalytic treatment. The co-catalytically modified powders had higher photocatalytic efficiency in comparison to the pure nanosized powders. Moreover, the sol-gel powders of TBT/EG, TBT/EG/Ag (10-2 M), TBT/isop, and TBT/isop/Ag (10-2 M) demonstrated the ability to retain their photocatalytic activity even after three cycles of use, suggesting that they could find practical use in the treatment of pharmaceutical wastewater. The observed photocatalytic efficiency and positive impact of silver make the prepared powders a desirable choice for pharmaceutical drug degradation, helping to promote environmentally friendly and effective wastewater treatment technology.

Rare-Earth Metal-Organic Framework with Nonplanar Porphyrin Groups for High-Efficiency Photocatalysis.

Nonplanar porphyrins play crucial roles in many biological processes and chemical reactions as catalysts. However, the preparation of artificial nonplanar porphyrins suffers from complicated organic syntheses. Herein, we present a new rare-earth porphyrinic metal-organic framework (RE-PMOF), BUT-233, which is a three-dimensional (3D) framework structure with the flu topology consisting of 4-connected BBCPPP-Ph ligands H4BBCPPP-Ph = 5',5⁗-(10,20-diphenylporphyrin-5,15-diyl)bis([1,1':3',1″-terphenyl]-4,4'' dicarboxylic acid) and 8-connected Eu6 clusters. Noteworthily, the porphyrin cores of the BBCPPP-Ph ligands in BUT-233 are nonplanar with a ruffle-like conformation. In contrast, the porphyrin core in the free ligand H4BBCPPP-Ph is in a nearly ideally planar conformation, as confirmed by its single-crystal structure. BUT-233 is microporous with 6-8 Å pores and a Brunauer-Emmett-Teller (BET) surface area of 649 m2/g, as well as high stability in common solvents. The MOF was used as a photocatalyst for the oxidation degradation of a chemical warfare agent model molecule CEES (CEES = 2-chloroethyl ethyl sulfide) under the light-emitting diode (LED) irradiation and an O2 atmosphere at room temperature. CEES was almost completely converted into its nontoxic light-oxidized product CEESO (CEESO = 2-chloroethyl ethyl sulfoxide) in only 5 min with t1/2 = 2 min (t1/2: half-life). Moreover, the toxic deep-oxidized product 2-chloroethyl ethyl sulfone (CEESO2) was not detected. The catalytic activity of BUT-233 was high in comparison with those of some previously reported MOF catalysts. The results of photo/electrochemical property studies suggested that the high catalytic activity of BUT-233 was benefited from the presence of nonplanar porphyrin rings on its pore surface.

Photocatalysis and irradiative TL defect center analysis studies of Cu2+ ionic ZnO nano lattice

The objective of the study is to create a series of ZnO nano powders doped with CuO using sol–gel technology in order to look into their photocatalytic activity for the photodegradation and cleaning process. XRD, BET surface area, surface morphology, chemical analysis, and FT-IR measurements have all been used to look at the nano powders' structure from this point of view. The results suggest that the materials were made at the nanoscale level, and their hexagonal shape makes them good as catalytic nano resources. Photoluminescence and UV–visible diffusion reflection spectroscopy were also used to test the nano powders. The results show that the nano powders that were made are visually active. To find out how photocatalytic the nanoparticles are, they were used to break down CR (10 ppm) and MV (10 ppm) dyes when exposed to light. The nano powder with 1.0 mol% of CuO doped ZnO nanoparticles had the highest photocatalytic efficiency (86 %). It had a band gap energy of 3.15 eV and reacted with both dyes for 90 min. Researchers looked at radical scavengers and the effect of catalyst dose on how well they broke down substances. The reaction that broke down had pseudo-first-order kinetics, and the rate of the reaction was four times faster when 1.0 mol% Cu was added to the ZnO catalyst. The degradation efficiency only dropped by 1 % after three rounds of the process. Because of this, the 1.0 mol% Cu-ZnO was used as a photocatalyst that broke down textile dyes well and had a lot of promise to be used again. The samples were also checked for thermoluminescence while they were exposed to 25 kGy of gamma radiation. Samples were tested for their trap depth characteristics, indicating the test samples' potential for TL activity.

Enhanced Fenton-like process over Z-scheme MoO3 surface decorated with Fe2O3 under visible light

Photocatalysts consisting of Z-scheme heterojunctions are commonly used in wastewater treatment due to their exceptional reactivity in photocatalysis and highly efficient visible-light utilization. In this work, Fe2O3-decorated MoO3 rods were synthesized through a two-step method and their photodegradation of methylene blue (MB) was evaluated. The Fe2O3/MoO3 rods were characterized by XRD, SEM, micro-Raman, XPS, UV–Vis DRS, and PL to investigate their structural, morphological, and optical properties. The results indicate that the photodegradation efficiency of Fe2O3/MoO3 improved through a reduction in the gap energy and persistence of a 1D hexagonal prism structure. The degradation rate of MB was enhanced from 31.7 to 91.5% after irradiation for 180 min owing to electron–hole separation and Fenton-like process. Formation of the OH radical is a key factor in the photodegradation reaction and with the addition of H2O2 the efficiency can further improve via a Fenton-like mechanism. Furthermore, the Z-scheme mechanism concurrently delineated. The Fe2O3/MoO3 rod composites were also found to retain high photocatalytic efficiency after being reused five times, which may be useful for future applications.

CTAC-assisted monoclinic BiVO4 with oxygen defects for efficient photocatalytic performances: A combined experimental and DFT study

Developing a photocatalyst with high photocatalytic efficiency, chemical stability, and self-degradation capability is essential for optimizing photodegradation processes in environmental applications. In this study, we synthesized a monoclinic BiVO4 photocatalyst whose surface morphology was modulated by hexadecyltrimethylammonium chloride (CTAC) using a facile hydrothermal method. Experimental results demonstrated a substantial increase in the degradation rate (99%) for the CTAC-modified monoclinic BV/CT25 photocatalyst (with an initial CTAC concentration of 25 g/L) compared to the CTAC-free tetragonal BiVO4 photocatalyst (73%). This highlights the effective enhancement of photocatalytic degradation performance through CTAC modification. Furthermore, density functional theory (DFT) calculations revealed that the band gap of BV/CT25 remained unchanged, suggesting that changes in oxygen vacancies (OVs) and density of states, along with the porous lattice structure, contributed to the improved performance. These findings were further supported by FESEM, as well as EPR and XPS characterizations. In addition, photodegradation tests at various pH conditions and cyclic tests suggested that the modification enhanced the morphological stability and reusability of the modified BiVO4 photocatalysts. Overall, this study provides valuable insights into the design of next-generation photocatalysts, leveraging surfactants to control surface properties and emphasizing the key attributes of high photocatalytic efficiency, chemical stability, and improved reusability.

Sunlight driven photocatalytic degradation of organic pollutants by solvothermally synthesized rGO-BiVO4 nanohybrids

This study reports photocatalytic degradation of organic dyes by rGO-BiVO4 nanohybrids. rGO- BiVO4 nanohybrids were solvothermally prepared with different rGO loading (1.5, 3 and 6 %) and their structural, optical and photocatalytic properties were investigated. Effect of rGO loading on photocatalytic dye degradation was studied and the factors responsible were analyzed. Structural analysis was done using XRD and Raman analyses which clearly showed monoclinic phase of the BiVO4. FESEM images showed sub-micron spheres of BiVO4 along with sheet-like structures corresponding to rGO. A slight change in the band gap was observed from 2.2 eV for BiVO4 to around 2 eV for the rGO-BiVO4 nanohybrids. Band to band transitions as well as the transitions from the defect bands were observed from the PL spectra. Photocatalytic degradation studies of organic pollutant MB under natural sunlight showed 3 % rGO-BiVO4 to be the best photocatalyst which degraded 88.4 % of MB in 80 min with rate constant of 0.0244 min−1. It was observed that for obtaining a maximum catalytic efficiency an optimum loading of rGO proved to be best. In either case of higher or lower loading of rGO showed a lower degradation performance. Amongst the samples synthesized 3 % rGO loading was found to be the optimum rGO loading to have the lowest band gap (2 eV) as well as the reduced recombination that has resulted in highest photocatalytic efficiency under solar irradiation.

Developed Photocatalytic Cotton Fabric with Agricultural By-Products Tea Saponins for Accelerating Aqueous Chromium(VI) Reductive Removal

ABSTRACT In order to achieve the goal of preparing functional textiles using tea saponin, in this work, carboxymethylated tea saponin (CTS) was used to modify cotton fabrics by an industrial rolling and baking process, and then functional textiles could be obtained after coordination with Fe3+, which could remove Cr species from water by photocatalytic reduction and adsorption processes. High CTS concentrations and higher treatment temperatures led to an increase in the carboxyl group content (QCOOH) and Fe content (QFe) of the obtained Fe-CTS-Cotton. The increase in the QFe value of the functional textiles favored the photocatalytic reduction of Cr(VI). Fe-CTS-Cotton with high QCOOH values showed excellent adsorption performance for the generated Cr(III) ions during the adsorption process. Therefore, the high photocatalytic reduction efficiency and strong Cr(III) ion trapping ability were the reasons for the recycling of Fe-CTS-cotton as a hybrid photocatalyst for enhanced removal of Cr(VI).

Hollow Cu2-xS@NiFe Layered Double Hydroxide Core-Shell S-Scheme Heterojunctions with Broad-Spectrum Response and Enhanced Photothermal-Photocatalytic Performance.

Designing a reasonable heterojunction is an efficient path to improve the separation of photogenerated charges and enhance photocatalytic activity. In this study, Cu2-xS@NiFe-LDH hollow nanoboxes with core-shell structure are successfully prepared. The results show that Cu2-xS@NiFe-LDH with broad-spectrum response has good photothermal and photocatalytic activity, and the photocatalytic activity and stability of the catalyst are enhanced by the establishment of unique hollow structure and core-shell heterojunction structure. Transient PL spectra (TRPL) indicates that constructing Cu2-xS@NiFe-LDH heterojunction can prolong carrier lifetime obviously. Cu2-xS@NiFe-LDH shows a high photocatalytic hydrogen production efficiency (5176.93µmolh-1g-1), and tetracycline degradation efficiency (98.3%), and its hydrogen production rate is ≈10-12 times that of pure Cu2-xS and NiFe-LDH. In situ X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) provide proofs of the S-scheme electron transfer path. The S-scheme heterojunction achieves high spatial charge separation and exhibits strong photoredox ability, thus improving the photocatalytic performance.

Rapid Thermal Processing and Improved Photocatalysis of Bi2O3-BaTiO3 Heterojunction

Bi2O3-BaTiO3 heterojunction with high photocatalysis efficiency was directly synthesized by rapid thermal processing (RTP). Bi2O3 and BaTiO3 were mixed in ratio and treated by RTP and conventional thermal processing (CTP), respectively. RTP samples have obvious Bi2O3 diffraction peaks, while CTP samples show pure BaTiO3 tetragonal perovskite. More small particles and layered existed in RTP samples. Photodegradation of MB solutions shows that RTP can promote photocatalytic efficiency. Its main lies in the following points: RTP can remove grain boundary defects by strengthening the bond grains; RTP can limit the solution region of the two substances to a certain range to get the best built-in electric field width; and RTP can strengthen the tetragonal BaTiO3 phase to hasten ion movement. Therefore, RTP can achieve much higher photocatalytic efficiency by improving the build heterojunction. This work provides a direct and efficient route to get improvement and high performance of heterojunction.

3D-printed Al2O3 framework supported carbon-bridged tri-s-triazine of g-C3N4 for photocatalytic tetracycline oxidation

Powder-like g-C3N4 has been widely used as a photocatalyst but exhibits several drawbacks, including unrecyclable, high charge recombination, and limited light absorption. In this study, carbon-bridged g-C3N4 was successfully prepared and coated on a 3D-printed Al2O3 substrate for the photocatalytic oxidation of tetracycline. Oxamide (OD), malonamide (MD), and succinamide (SD) were used as carbon-containing linkers to react with precursors (melamine and urea) and produce carbon-bridged g-C3N4. Carbon substitution at the bridged N atoms of g-C3N4 improved light absorption, reduced charge recombination, and resulted in high photocatalytic tetracycline removal efficiency. Computational calculations were also employed, and Bader charge analysis supported the charge redistribution and charge transfer of the carbon-bridged g-C3N4 samples. Our results indicated that the degradation of tetracycline followed step-by-step oxidation, deamination, and mineralization to form CO2 and H2O. The 3D-printed Al2O3-supported carbon-bridged g-C3N4 exhibited a high removal rate of 85–90 % and stability for photocatalytic reactions and can be reused for at least 10 cycles. This study demonstrates that the 3D-printed Al2O3-supported carbon-bridged g-C3N4 catalyst is an efficient and effective catalyst support system for photocatalytic reactions.

Synthesis of highly efficient ternary phase graphene/Bi/SnO2 photocatalyst for degradation of organic dye pollutants

In this work, graphene nanosheets (GNs) are prepared from graphite rods obtained from waste dry-cell batteries using the electrochemical exfoliation (ECE) method. Then GNs used as a matrix to modify tin oxide (SnO2) and Bismuth (Bi) nanoparticles to prepare a binary phase SnO2@G and ternary-phase Bi@SnO2@G nanocomposite materials by wet-chemical method and used as a photocatalysts for degradation of organic dye pollutants. XRD diffraction pattern clearly confirmed the presence of tetragonal crystal system of SnO2 which was maintaining its structure in SnO2@G and G/Bi/SnO2. The stretching and bending vibrations of the functional groups were analyzed using FTIR analysis. FESEM images demonstrated the surface morphology and the texture of the as synthesized sample. Raman Spectroscopic investigation was carried out to confirm the in-plane blending of SnO2 and graphene inside the composite matrix. The as-prepared ternary-phase Bi@SnO2@G-based photocatalyst showed high degradation efficiency of 99.6% and 94.5% for direct blue (DB) and methyl blue (MB) dyes, respectively, under visible light irradiation by (i) minimizing the hole and electron recombination, (ii) providing a high surface area, and (iii) reducing the band gap energy. This study provides an effective, low-cost, and smart approach for producing GNs on a wide scale from battery waste along with nanohybrid composites with high photocatalytic efficiency.

Photoelectron Migration Boosted by Hollow Double-Shell Dyads Based on Covalent Organic Frameworks for Highly Efficient Photocatalytic Hydrogen Generation.

Photocatalytic hydrogen production based on noble metal-free systems is a promising technology for the conversion of solar energy into green hydrogen, it is pivotal and challenging to tailor-make photocatalysts for achieving high photocatalytic efficiency. Herein, we reported a hollow double-shell dyad through uniformly coating covalent organic frameworks (COFs) on the surface of hollow Co9S8. The double shell architecture enhances the scattering and refraction efficiency of incident light, shortens the transmission distance of the photogenerated charge carriers, and exposes more active sites for photocatalytic conversion. The hydrogen evolution rate is as high as 23.15 mmol g-1 h-1, which is significantly enhanced when compared with that of their physical mixture (0.30 mmol g-1 h-1) and Pt-based counterpart (11.84 mmol g-1 h-1). This work provides a rational approach to the construction of noble-metal-free photocatalytic systems based on COFs to enhance hydrogen evolution performance.