Search Results (348)

Novel solid strong base catalysts have attracted considerable attention in fine chemical synthesis owing to their unique advantages. In this work, a magnetic solid strong base catalyst with controlled morphology and porous carbon shell structure was successfully fabricated using low-cost carbon sources combined with Fe₃O₄ nanoparticles. KOH was used to introduce strong basic sites through ultrasonic-assisted impregnation. The carbon shell acted as a protective barrier to suppress detrimental interactions between basic species and the support while maintaining structural integrity after high-temperature activation without morphology degradation. The obtained K/C/Fe₃O₄ catalyst exhibits excellent catalytic performance and near-ideal superparamagnetic behavior. In the transesterification reaction for dimethyl carbonate (DMC) synthesis, the K/C/Fe₃O₄ catalyst provides superior performance than conventional solid base catalysts and maintains stable activity over six consecutive cycles. Notably, efficient solid–liquid separation was achieved successfully via magnetic separation, demonstrating practical applicability for the K/C/Fe₃O₄ catalyst. Full article

Graphitic carbon nitride (g-C₃N₄) is emerging as one of the most promising non-metallic semiconductors for the degradation of pollutants in water by photocatalytic processes. Its exceptional reduction–oxidation (redox) potentials and adequate band gap of approximately 2.7 eV give it the ability to absorb in the visible light range. However, the characteristic sensitivity to light absorption is limited, leading to rapid recombination of electron–hole pairs. Therefore, different strategies have been explored to optimize this charge separation, among which the formation of heterostructures based on g-C₃N₄ is highlighted. This review addresses recent advances in photocatalysis mediated by g-C₃N₄ heterostructures, considering the synthesis methods enabling the optimization of the morphology and active interface of these materials. Next, the mechanisms of charge transfer are discussed in detail, with special emphasis on type II, type S, and type Z classifications and their influence on the efficiency of photodegradation. Subsequently, the progress in the application of these photocatalysts for the degradation of water pollutants, such as toxic organic dyes, pharmaceutical pollutants, pesticides, and per- and polyfluoroalkyl substances (PFAS), are analyzed, highlighting both experimental advances and remaining challenges. Finally, future perspectives oriented towards the optimization of heterostructures, the efficiency of synthesis methods, and the practical application of these in photocatalytic processes for environmental remediation. Full article

The simultaneous generation of hydrogen fuel and wastewater remediation via electrocatalytic urea oxidation has emerged as a promising approach for sustainable energy and environmental solutions. However, the practical application of this process is hindered by the limited active sites and high charge-transfer resistance of conventional anode materials. In this work, we introduce a novel CoP@P, N-CNTs/NF electrocatalyst, fabricated through a facile one-step thermal annealing technique. Comprehensive characterizations confirm the successful integration of CoP nanoparticles and phosphorus/nitrogen co-doped carbon nanotubes (P, N-CNTs) onto nickel foam, yielding a unique hierarchical structure that offers abundant active sites and accelerated electron transport. As a result, the CoP@P, N-CNTs/NF electrode achieves outstanding urea oxidation reaction (UOR) performance, delivering current densities of 158.5 mA cm⁻² at 1.5 V and 232.95 mA cm⁻² at 1.6 V versus RHE, along with exceptional operational stability exceeding 50 h with negligible performance loss. This innovative, multi-element-doped electrode design marks a significant advancement in the field, enabling highly efficient UOR and energy-efficient hydrogen production. Our approach paves the way for scalable, cost-effective solutions that couple renewable energy generation with effective wastewater treatment. Full article

This research systematically investigates the influence of high-energy ball-milling (BM) parameters on the acidic and textural properties of zeolite Y. Among the BM parameters, the milling time (MT) exerted a more significant influence on the zeolite degradation than milling speed (MS), primarily affecting particle size and crystallinity. Milling produced nanozeolites with particle sizes ranging from 210 to 430 nm, and their activity was tested in the catalytic cracking of vacuum gas oil (VGO). The highest catalytic activity was observed for the zeolite with a particle size of 397 nm and a crystallinity of 75.9%: the VGO conversion was 69.0%, and the gasoline fraction yield was 33.9%, compared to the parent zeolite’s 62.7% and 22.1%, respectively. It was found that the activity of milled zeolites in catalytic cracking is determined by the accessibility of acid sites, which can be controlled by forming an optimal micro-mesoporous structure. Full article

Utilizing isomeric monomers to construct covalent organic frameworks (COFs) could easily and precisely regulate their structure in order to raise the photocatalytic performance towards two-step single-electron oxygen reduction reaction (ORR) to hydrogen peroxide (H₂O₂). Herein, isomeric anthraquinone (AQ)-based COFs (designated as 1,4-DQTP and 2,6-DQTP) were successfully fabricated through a simple yet effective one-step solvothermal synthesis approach, only utilizing isomeric monomers with alterations in the catalysts. Specifically, the black 1,4-DQTP displayed a high photocatalytic H₂O₂ production rate of 865.4 µmol g⁻¹ h⁻¹, with 2.44-fold enhancement compared to 2,6-DQTP (354.7 µmol g⁻¹ h⁻¹). Through a series of experiments such as electron paramagnetic resonance (EPR) spectroscopy and the free radical quenching experiments, as well as density functional theory (DFT) calculations, the photocatalytic mechanism revealed that compared with 2,6-DQTP, 1,4-DQTP possessed a stronger and broader visible light absorption capacity, and thus generated more photogenerated e⁻-h⁺ pairs. Ultimately, more photogenerated electrons were enriched on the AQ motif via a more apparent electron push–pull effect, which provided a stable transfer channel for e⁻ and thus facilitated the generation of superoxide anion radical intermediates (•O₂⁻). On the other hand, the negative charge region of AQ’s carbonyl group evidently overlapped with that of TP, indicating that 1,4-DQTP had a higher chemical affinity for the uptake of protons, and thus afforded a more favorable hydrogen donation for H⁺. As a consequence, the rational design of COFs utilizing isomeric monomers could synergistically raise the proton-coupled electron transfer (PCET) kinetics for two-step single-electron ORR to H₂O₂ under visible light illumination. This work provides some insights for the design and fabrication of COFs through rational isomer engineering to modulate their photocatalytic activities. Full article

This study proposes a co-hydrothermal method for the dechlorination of polyvinyl chloride (PVC) and the preparation of hydrothermal carbon. During the co-hydrothermal process, lignin was mixed with PVC, with ammonium carbonate serving as a supplementary additive. The effects of hydrothermal temperature, reaction time, and ammonium carbonate concentration on the dechlorination efficiency of PVC and the pH value of the system are discussed. The experimental results showed that the incorporation of lignin and ammonium nitrate manifested a remarkable synergistic effect, which substantially augmented the dechlorination process of polyvinyl chloride (PVC). Under optimal conditions (220 °C, 240 min), the dechlorination efficiency of PVC reached 99.43%. The hydrothermal carbon derived from the co-hydrothermal process exhibited a 73.9% higher calorific value (31.07 MJ/kg) compared with that obtained from pure PVC (17.87 MJ/kg). A physicochemical characterization demonstrated that lignin effectively enhanced the uniform dispersion of PVC particles during hydrothermal treatment. Concurrently, ammonium carbonate increased the solution’s alkalinity, facilitating a nucleophilic attack by OH⁻ on C-Cl bonds and accelerating dechlorination through intensified substitution reactions. Full article

Recently, aquatic life and human health are seriously threatened by the release of pharmaceutical drugs. For a sustainable ecosystem, emerging contaminants like antibiotics must be removed from drinking water and wastewater. To address this issue pure and cerium-doped titanium dioxide (CeT) nanoparticles were produced with stable tetragonal (anatase) lattices by room temperature sol–gel method and employing the inorganic titanium oxysulfate (TiOSO₄) as titanium precursor. The structural analysis by X-ray diffraction (XRD) revealed that at calcination temperature of 600 °C all (un and doped) powders were composed of crystalline anatase TiO₂ with the crystallite sizes in the range of 13.5–11.3 nm. UV–vis DRS spectroscopy revealed that the most narrowed bandgap value of 2.75 eV was calculated for the 0.5CeT sample containing the optimum dopant content of 0.5 weight ratio. X-ray spectroscopy (XPS) confirmed the presence of the impurity level Ce³⁺/Ce⁴⁺, which became responsible for the decrease in bandgap as well as for the photoinduced carriers recombination rate. Photocatalytic tests showed that the maximum decomposition of the model spiramycin (SPR) antibiotic pollutant was 88.0% and 77.0%, under UV and visible light, respectively. According to the reaction kinetics, SPR decomposition adhered to the Langmuir–Hinshelwood (L–H) model and via ROS experiments mainly hydroxyl radicals (OH^•) followed by photogenerated holes (h⁺s) become responsible for the pollutant degradation. In summary, this study elaborates on the role of xCeT nanoparticles as an efficient photocatalyst for the elimination of organic contaminants in wastewater. Full article

Crystalline–amorphous core–shell-like heterostructures have attracted considerable attention in electrocatalysis due to their unique electronic and structural properties; however, tuning the surface composition of the amorphous shell remains a major challenge. In this work, we report a simple, low-cost, one-pot hydrazine-assisted chemical deposition method for synthesizing a series of Co-doped Ni@Ni(OH)₂ catalysts with a crystalline Ni core and an amorphous Ni(OH)₂ shell. Among the prepared catalysts, the sample containing 10 wt.% cobalt (denoted as b-Co-doped Ni@Ni(OH)₂) exhibited the highest electrocatalytic activity toward both the oxygen evolution reaction (OER) and the urea oxidation reaction (UOR). In 1.0 M KOH, the b-Co-doped Ni@Ni(OH)₂ catalyst achieved a 40 mV lower overpotential at 50 mA·cm⁻² compared to undoped Ni@Ni(OH)₂ for the OER. For the UOR in 0.33 M urea/1.0 M KOH, it delivered approximately twice the anodic current density relative to the undoped sample, along with improved reaction kinetics as evidenced by a Tafel slope of 70.7 mV·dec⁻¹. This performance enhancement is attributed to the optimized core–shell-like architecture, cobalt doping-induced electronic modulation, increased electrochemically active surface area, and improved charge transfer efficiency. Overall, this study demonstrates a promising and scalable strategy for designing advanced Ni-based bifunctional catalysts for sustainable energy conversion and wastewater treatment applications. Full article

With the advancement of industrialization and urbanization, the arbitrary emission of sewage containing TC-tetracycline and hexavalent chromium (Cr(VI)) possesses a serious threat to both ecological–environment and public health. However, developing a low-toxicity and cost-effective photocatalyst for the simultaneous elimination of these two pollutants remains a formidable task. This study devised a photocatalytic sample (CSMX-X) comprised of Copper(I) sulfide (Cu₂S) and Titanium carbide (Ti₃C₂) through a simple solvothermal method and applied it to remove TC-tetracycline and Cr(VI). The CSMX-X not only increases the specific surface area from 2.7 m²·g⁻¹ for pure Cu₂S to 30.65 m²·g⁻¹, but also effectively addresses the problems of insufficient separation efficiency of photogenerated holes and electrons and low carrier density. The photocatalytic efficiency for an individual pollutant (10 mg·L⁻¹ Cr(VI) or 20 mg·L⁻¹ TC-tetracycline) can reach more than 90%, while the removal efficiency for mixed Cr(VI) and TC-tetracycline pollutants only decreases by 12%. Meanwhile, copper leaching levels under different pH conditions (0.032–0.676 mg·L⁻¹) are considerably lower than the 2 mg·L⁻¹ safety standard set by the World Health Organization. This study provides valuable perspectives for constructing Cu₂S-based composite photocatalysts to remove multiple contaminants in real aquatic environments. Full article

This study employed an in-situ displacement technique to eliminate the oxide layer present on the surface of micron aluminum (μAl). Utilizing the exposed metallic aluminum, we facilitated the displacement of copper and nickel nanoparticles. These nanoparticles, approximately 90 nanometers in size, were densely adhered to the surface of the μAl particles. The elemental composition and structural characteristics of the composite particles were meticulously analyzed using Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Energy Dispersive Spectroscopy (EDS), Vibrating Sample Magnetometry (VSM), and X-Ray Photoelectron Spectroscopy (XPS). Subsequently, thermal analysis and combustion performance assessments were conducted to elucidate the catalytic effects of the composite particles ([nCu+nNi]/μAl) on the thermal decomposition and combustion efficiency of ammonium perchlorate (AP). The results elucidate that the nanoparticles immobilized on the surface of μAl are unequivocally metallic copper (nCu) and metallic nickel (nNi). Following the application of nCu and nNi, the oxidation reaction of μAl accelerated by nearly 400 °C; furthermore, the incorporation of [nCu+nNi]/μAl raised the thermal decomposition peak temperature of AP by approximately 130 °C. Notably, the thermal decomposition activation energy of raw AP reached as high as 241.7 kJ/mol; however, upon doping with [nCu+nNi]/μAl, this activation energy significantly diminished to 161.4 kJ/mol. The findings of the combustion experiments revealed that both the raw AP and the AP modified solely with μAl were impervious to ignition via the hot wire method. In contrast, the AP doped with [nCu+nNi]/μAl demonstrated pronounced combustion characteristics, achieving an impressive peak flame temperature of 1851 °C. These results substantiate that the nCu and nNi, when deposited on the surface of μAl, not only facilitate the oxidation and combustion of μAl but also significantly enhance the thermal decomposition and combustion dynamics of ammonium perchlorate. Consequently, the [nCu+nNi]/μAl composite shows considerable promise for application in high-burn-rate hydroxyl-terminated polybutadiene (HTPB) propellants. Full article

In this study, a novel, highly efficient, environment friendly, and low-cost nanocatalyst, denoted as Ni(x)@Co−N−C, was successfully developed by encapsulating Ni nanoparticles into N-doped porous carbon derived from ZIF-67. A variety of techniques including powder X-ray diffraction (XRD), nitrogen adsorption/desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectrometer (XPS) were used to characterize the prepared materials. The TEM images reveal that the nanoparticles were distributed homogeneously in the carbon support. The N atoms in the carbon support serve as the sites for the nucleation and uniform growth of Ni nanoparticles. The catalyst was used for the degradation of environmentally harmful 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Among all the catalysts investigated, Ni(10)@Co-N-C exhibited the highest catalytic activity for the hydrogenation of 4-NP, with a specific reaction rate of 6.1 × 10⁻³ s⁻¹, activity parameter of 31 s⁻¹g⁻¹, and turn over frequency (TOF) of 1.78 × 10¹⁹ molecules g_metal⁻¹s⁻¹. On the other hand, the specific reaction rate and TOF value were 1.7 × 10⁻³ s⁻¹ and 6.96 × 10¹⁸ molecules g_metal⁻¹s⁻¹, respectively, for Co−N−C. This suggests that Ni(10)@Co−N−C is about three times more catalytically active than the Co−N−C catalyst. The superb activity of Ni(10)@Co−N−C in comparison to Co−N−C can be ascribed to the homogeneous dispersion of small-sized Ni nanoparticles, the interconnected three-dimensional porous arrangement of the support Co−N−C, the presence of N atoms in the carbon framework that stabilize metal nanoparticles, and the synergistic electronic effect between Ni and Co. The Ni(10)@Co−N−C catalyst maintained consistent catalytic activity over multiple cycles, which suggests that porous N-containing carbon support can effectively prevent aggregation and leaching of metal nanoparticles. The ICP-AES analysis of the recycled Ni(10)@Co−N−C revealed a slight reduction in metal content compared to the fresh sample, suggesting almost negligible leaching of metal nanoparticles. Full article

This study reports the synthesis, characterization, and catalytic performance of a series of catalysts of Ru supported on CeO₂-Y₂O₃ composites (Ru/CeYX; X = 0, 33, 66, and 100 wt.% Y₂O₃) for CO₂ hydrogenation. Supported material modification (Y₂O₃-CeO₂), by the Y₂O₃ incorporation, allowed a change in selectivity from methane to RWGS of the CO₂ hydrogenation reaction. This change in selectivity is correlated with the variation in the physicochemical properties caused by Y₂O₃ addition. X-ray diffraction (XRD) analysis confirmed the formation of crystalline fluorite-phase CeO₂ and α-Y₂O₃. High-resolution transmission electron microscopy (HR-TEM) and energy-dispersive X-ray spectroscopy (EDS) elemental mapping revealed the formation of a homogeneous CeO₂-Y₂O₃ nanocomposite. As the Y₂O₃ content increased, the specific surface area, measured by BET, showed a decreasing trend from 106.3 to 51.7 m² g⁻¹. X-ray photoelectron spectroscopy (XPS) of Ce3d indicated a similar Ce³⁺/Ce⁴⁺ ratio across all CeO₂-containing materials, while the O1s spectra showed a reduction in oxygen vacancies with increasing Y₂O₃ content, which is attributed to the decreased surface area upon composite formation. Catalytically, the addition of Y₂O₃ influenced both conversion and selectivity. CO₂ conversion decreased with increasing Y₂O₃ content, with the lowest conversion observed for Ru/CeY100. Regarding selectivity, methane was the dominant product for Ru/CeY0 (pure CeO₂), while CO was the main product for Ru/CeY33, Ru/CeY66, and Ru/CeY100, indicating a shift towards the reverse water–gas shift (RWGS) reaction. The highest RWGS reaction rate was observed with the Ru/CeY33 catalyst under all tested conditions. The observed differences in conversion and selectivity are attributed to a reduction in active sites due to the decrease in surface area and oxygen vacancies, both of which are important for CO₂ adsorption. In order to verify the surface species catalytically active for RWGS, the samples were characterized by FTIR spectroscopy under reaction conditions. Full article

The key to selectively cleaving C–O bonds in lignin to produce high-value aromatic chemicals lies in the development of efficient and stable catalysts. In this study, a heterostructured catalyst with N-doped carbon-supported Co and dual-phase Mo_xC nanoparticles was prepared via the in situ pyrolysis of a Co–Mo–N precursor. The dual-phase α-MoC/β-Mo₂C heterostructure is adjusted by varying the Co:Mo ratio to affect the structure and electronic properties of the catalyst. The heterostructures bring about enhanced electron transfer from Co to Mo, which promotes hydrogen dissociation over the Co sites, significantly improving the catalyst’s hydrogenolysis activity and stability. The optimal catalyst with Co₁Mo_xC@NC exhibits excellent hydrogenolysis activity; under the optimal reaction conditions (260 °C, 1 MPa H₂, 3 h), the yield of aromatic monomers reaches 28.5%. Such prominent performance not only benefits from the numerous α-MoC/β-Mo₂C hetero-interfaces that offer abundant active sites for hydrogen dissociation, but also should be ascribed to the strong synergistic effect between Co and Mo. Full article

Electrochemical water splitting is a feasible and effective method for attaining hydrogen, offering a mechanism for renewable energy solutions to combat the world’s energy crises due to the scarcity of fossil fuels. Evidently, the viability and stability of the electrocatalysts are fundamental to the electrochemical water-splitting process. However, the net efficiency of this process is noticeably hindered by the kinetic drawbacks related to the OER. Hence, NiFe LDH has been widely used as a highly efficient OER and HER catalyst material due to its unique nanostructure, tunable composition, and favorable electronic structure. This review offers a systematic analysis of the latest progress in the fabrication of functional NiFe LDH catalysts and associated fabrication strategies, structure optimizations, and performance improvements. Special emphasis is given to understanding the role of nanostructure engineering in increasing active site accessibility, enhancing the effectiveness of subsequent electron transfer, and boosting the intrinsic catalytic activity for HER and OER. Moreover, we discuss the influence of doping, defects, and the formation of heterostructures with other materials on the OER and HER activities of NiFe LDHs. Additional accounts of basic structures and the OER and HER catalytic activities are provided, along with an enhanced theoretical understanding based on DFT studies on the NiFe LDH. Moreover, the limitations and potential developments of the work focus on the need for existing synthesis approaches, the stability of the NiFe LDH catalysts, and their insertion into working electrochemical processes. This review is a comprehensive analysis of the current state of research and developments in the use of NiFe LDH catalysts for the electrochemical water-splitting process to foster improved development of sustainable hydrogen sources in the future. Full article

In this study, a sulfur-doped cobalt–iron catalyst (CoFeS/NF) was synthesized on a nickel foam (NF) substrate via a facile one-step electrodeposition method, and its performance in urea electrolysis for hydrogen production was systematically investigated. Sulfur doping induced significant morphology optimization, forming a highly dispersed nanosheet structure, which enhanced the specific surface area increase by 1.9 times compared with the undoped sample, exposing abundant active sites. Meanwhile, the introduction of sulfur facilitated electron redistribution at the surface modulated the valence states of nickel and cobalt, promoted the formation of high-valence Ni³⁺/Co³⁺, optimized the adsorption energy of the reaction intermediates, and reduced the charge transfer resistance. Electrochemical evaluations revealed that CoFeS/NF achieves a current density of 10 mA cm⁻² at a remarkably low potential of 1.18 V for the urea oxidation reaction (UOR), outperforming both the undoped catalyst (1.24 V) and commercial RuO₂ (1.35 V). In addition, the catalyst also exhibited excellent catalytic activity and long-term stability in the total urea decomposition process, which was attributed to the amorphous structure and the synergistic enhancement of corrosion resistance by sulfur doping. This study provides a new idea for the application of sulfur doping strategy in the design of multifunctional electrocatalysts, which promotes the coupled development of urea wastewater treatment and efficient hydrogen production technology. Full article