Search Results (288)

This article systematically reviews the structural characteristics of layered double hydroxides and biochar (LDHs/biochar) composites, summarizes the features and optimization strategies of preparation methods such as coprecipitation, hydrothermal synthesis, ball milling, and calcination–reconstruction, analyzes their adsorption performance and mechanisms in controlling various water pollutants including organic contaminants, heavy metals, and nutrients, and provides insights into future research trends and practical applications, aiming to offer references for improving material performance and promoting practical use. The existing research results show that LDHs/biochar composites exhibit good application potential for various pollutants, such as dyes, antibiotics, heavy metal ions, and phosphates. The coprecipitation method is simple and easy to operate, and the LDHs/biochar composites prepared by this method exhibit favorable adsorption performance, with potential for industrial-scale production. The mechanisms of pollutant removal by LDHs/biochar composites primarily include electrostatic attraction, ion exchange, hydrogen bonding, complexation, and π–π electron interactions. Both the biomass type and the LDH type influence the adsorption performance of the composites. Therefore, designing LDHs/biochar composites based on pollutant characteristics and adsorption mechanisms is key to achieving effective pollution control. Currently, research on target pollutant-oriented material design and material regeneration remains underdeveloped and requires further breakthroughs. Full article

Mg–La mixed metal oxides derived from layered double hydroxide (LDH) precursors were synthesized via coprecipitation and evaluated as heterogeneous catalysts for solventless glycerol etherification to short-chain polyglycerols. The influence of Mg/La molar ratio on the structural, textural, and catalytic properties of the catalysts was systematically investigated using XRD, BET, SEM-EDX, FTIR, TPD-CO₂, TPD-NH₃ and ICP-OES analyses. XRD confirmed the formation of La₂O₂CO₃ phases, while CO₂-TPD analysis revealed the presence of abundant medium-to-strong basic sites. Among the synthesized catalysts, Mg_0.25La_0.75O₂ exhibited the highest basic site concentration (6830 µmol g⁻¹) and superior catalytic performance due to the possible cooperative interaction between Mg- and La-derived sites. Under optimum reaction conditions of 220 °C, 8 h, and 2 wt% catalyst loading, the catalyst achieved 90% glycerol conversion with 70% diglycerol selectivity, 23% triglycerol selectivity, and 84% combined diglycerol and triglycerol yield. Reaction temperature, catalyst loading, and reaction duration significantly influenced oligomer distribution and catalyst performance. Reusability studies demonstrated acceptable catalyst stability for up to four cycles before gradual deactivation caused by oligomer deposition and metal leaching. The results highlight Mg–La mixed oxides as promising catalysts for sustainable solvent-free glycerol valorization, while demonstrating a scalable and environmentally benign strategy for maximizing lower-degree polyglycerol production within shorter reaction durations and reduced processing cost. Full article

Nickel–iron layered double hydroxide (Ni_1−xFe_x-LDH) with different Ni/Fe ratios was prepared by a simple hydrothermal method and evaluated for ozone decomposition under various humidity conditions. In particular, Ni_0.8Fe_0.2-LDH showed outstanding activity and stability across a wide humidity range and maintained complete ozone conversion for 10 h even at 90% relative humidity. The combined characterization and catalytic results indicate that the cooperative effect of Ni and Fe increases the specific surface area, tunes the metal valence states, and optimizes the humidity-dependent reaction pathway. More importantly, the catalyst shows clear self-healing behavior after ozone exposure, suggesting that the ozone-induced surface reconstruction is at least partly reversible rather than fully destructive. These results identify an efficient Ni_1−xFe_x-LDH catalyst for ozone abatement and provide insight into the dynamic behavior of hydroxyl-rich layered catalysts under oxidizing atmospheres. Full article

There is increasing interest in structured layered double hydroxide (LDH)-based catalysts because they combine tunable acid–base/redox chemistry with reactor architectures that can reduce diffusion lengths, improve heat management, and lower pressure-drop penalties. This review evaluates LDH, LDH-derived oxide (LDO/MMO), reduced metal/LDO, reconstructed hydroxide-rich, and mixed dynamic states integrated into honeycomb monoliths, open-cell foams, meshes/felts, thin films, washcoats, coated plates, microchannels, capillaries, and additively manufactured lattices. To move beyond descriptive comparison, the literature is assessed using unified evaluation dimensions: operative active state, support architecture, coating/integration route, active-phase loading, coating thickness and uniformity, reactor-volume-normalized productivity or STY, ΔP/L, axial/radial thermal gradients, time-on-stream, coating loss, regeneration recovery, and pilot-readiness. Representative benchmarks illustrate both the promise and reporting gaps of the field: NiFe-LDH-derived monoliths for CO₂ methanation have reached ~70% CO₂ conversion at 300 °C with >90% CH₄ selectivity and only 0.7% post-test mass loss; NiFe-LDH/iron-foam monoliths retained 85% ozone conversion after 168 h; high-entropy LDH-derived oxides showed T50/T90 values of 246/254 °C for toluene oxidation; and Au/LDH capillary films achieved 31.9% glycerol carbonate yield and 3.78 g h⁻¹ g⁻¹ productivity. The strongest current cases are pollution abatement and CO₂ methanation, whereas biomass upgrading, fine-chemical flow, high-entropy coatings, and photo/electrocatalytic films require deeper module-level validation. Overall, structured LDH catalysts should be treated as coupled chemistry–coating–reactor systems whose performance must be judged simultaneously by activity, accessible catalyst inventory, transport efficiency, pressure drop, thermal profile, durability, regeneration, and manufacturability. Full article

Transition-metal oxide/layered double hydroxide (LDH) electrodes often suffer from insufficient utilization of active sites, sluggish electron/ion transport, and limited cycling stability at high rates. Here, La-doped ZnCo₂O₄/MnCo-LDH nanoflowers serve as the positive electrode and Ti-supported Sb-doped SnO₂ (Ti/Sb-SnO₂) serves as the negative electrode for constructing an asymmetric supercapacitor. A stepwise hydrothermal route, La-doping regulation, and ethylenediamine-assisted morphology control transform stacked nanosheets into open porous nanoflowers with a specific surface area of 382.5 m² g⁻¹, thereby exposing more electroactive sites and shortening OH⁻ diffusion pathways. La³⁺-induced lattice distortion and defect-related oxygen species further tune the electronic structure and improve interfacial charge-transfer kinetics. The optimized La-ZnCo₂O₄/MnCo-LDH electrode delivers 2130 F g⁻¹ at 1 A g⁻¹ and retains 1993 F g⁻¹ after 10,000 cycles at 3 A g⁻¹. The Ti/Sb-SnO₂ negative electrode provides 673 F g⁻¹ at 1 A g⁻¹ and 302 F g⁻¹ at 15 A g⁻¹. The assembled device operates stably from 0 to 1.8 V in 2 M KOH and achieves 69 Wh kg⁻¹ and 13,500 W kg⁻¹. Full article

Municipal solid waste incineration fly ash (MSWI FA) represents a significant environmental challenge due to its high content of toxic heavy metal (HM) and large-scale generation. This study demonstrates the feasibility pathway for converting hazardous MSWI FA into well-crystallized layered double hydroxide nanosheets (LDH-FA). Sodium dimethyl dithiocarbamate (SDD) was incorporated as a chelating stabilizer to enable synergistic HM immobilization during acid leaching and crystallization. High-resolution transmission electron microscopy (HRTEM) confirmed the characteristic two-dimensional nanosheet morphology with interlayer spacings consistent with LDH structures, while elemental mapping revealed homogeneous distribution of Pb and Zn within the nanosheet matrix. SDD dosages higher than 1.0 wt% effectively suppressed HM leaching, and Pb concentrations were controlled below 0.1 mg/L and Zn maintained at minimal levels. BCR sequential extraction analysis further demonstrated that SDD treatment effectively transformed HMs from bioavailable acid-soluble fractions to stable forms. This investigation establishes an innovative approach to MSWI FA resource utilization and provides mechanistic insights into HM stabilization within LDH nanostructures, offering a scientific basis for safer applications of waste-derived nanomaterials. Full article

Faced with a global energy crisis and ecological degradation, overall water splitting (OWS) is a pivotal approach for renewable energy conversion and storage. However, its industrial application is hindered by the high energy barriers/sluggish kinetics of the anodic oxygen evolution reaction (OER), as well as the scarcity of precious metal catalysts limiting large-scale deployment. Herein, a cobalt-based layered double hydroxide (Co-LDH) was used as the precursor, and a multi-strategy synergistic modification (hydrothermal synthesis, Fe doping, sulfurization, and external magnetic field magnetization) was applied to fabricate the Fe-Co₃S₄-MS-20 min electrocatalyst. This strategy establishes Fe-Co bimetallic synergistic active centers, and magnetic treatment modulates the electron configuration of Fe 3d orbitals without changing the material’s lattice spacing or morphology. Structural characterizations and electrochemical measurements were used to investigate the effects of combined modifications on the catalyst’s phase structure, morphology, electronic structure, and trifunctional catalytic performance toward the hydrogen evolution reaction (HER), OER, and urea oxidation reaction (UOR). The Fe-Co₃S₄-MS-20 min catalyst exhibits a larger electrochemical active surface area, lower charge transfer resistance, and smaller Tafel slope in 1 M KOH, it achieves overpotentials of 165 mV for HER (10 mA·cm⁻²) and 310 mV for OER (100 mA·cm⁻²), along with superior UOR performance and long-term stability. In situ impedance and Raman spectroscopy confirm that magnetization accelerates charge transfer and promotes in situ reconstruction. Synergistic multi-strategy regulation optimizes the electronic structure of active centers, reducing electrocatalytic energy barriers. This work provides new insights into designing high-performance non-precious metal electrocatalysts and offers experimental support for external magnetic field regulation in electrocatalyst modification. Full article

Electrochemical water splitting stands as a feasible approach for sustainable hydrogen production, but its industrial implementation is restricted by sluggish oxygen evolution reaction (OER) kinetics and excessive dependence on freshwater resources. As a widely existing alternative, seawater contains a high concentration of chloride ions (Cl⁻), which give rise to serious electrode corrosion and catalyst deactivation, bringing great challenges to actual electrolysis applications. Herein, we report a facile room-temperature two-step soaking strategy to fabricate sulfur-modified NiFe layered double hydroxide (S-NiFe-LDH) catalysts for efficient OER in both alkaline freshwater and seawater electrolytes. The introduction of sulfur not only optimizes the electronic structure of NiFe-LDH to strengthen intrinsic catalytic activity and speed up charge transfer, but also promotes the formation of a Cl⁻-resistant layer, thus significantly improving corrosion resistance. In addition, DFT calculations show sulfur modification in NiFe layered double hydroxide upshifts the O 2p-band center to activate lattice oxygen, switches the oxygen evolution reaction pathway to the lattice oxygen mechanism with reduced thermodynamic barriers, and realizes the selective adsorption of OH⁻ over Cl⁻. As a result, the as-prepared S-NiFe-LDH catalyst exhibits exceptional OER performance, requiring overpotentials (η) of 250, 270, and 290 mV to reach current densities of 50, 100, and 200 mA·cm⁻² in 1 M KOH, respectively, with a Tafel slope of 22.3 mV·dec⁻¹. Moreover, it maintains remarkable stability for more than 200 h in alkaline seawater electrolytes and achieves nearly 100% Faradaic efficiency for water splitting, effectively avoiding the parasitic chlorine evolution reaction (CER). This work provides a scalable and energy-efficient synthetic route for designing advanced non-noble metal catalysts, paving the way for industrial-scale hydrogen production from seawater. Full article

This study investigates the structure–performance relationship of Fe³⁺- and Zr⁴⁺-modified layered double hydroxides (LDHs) for fluoride removal from water. Mg–Al LDHs with different metal loadings (Zr0.05, Zr0.1, Fe0.8, and Fe1) were synthesized via ultrasound-assisted coprecipitation and characterized using XRD, SEM–EDS, FTIR, XPS, and N₂ physisorption. Among the synthesized materials, Zr0.05-LDH exhibited the highest adsorption performance. Response surface methodology identified adsorbent dosage as the most influential parameter, achieving a maximum fluoride removal efficiency of 98.17% under optimal conditions (pH ≈ 5, adsorbent dose of 0.88 g/L, and initial fluoride concentration of 12.6 mg/L). Zr0.05-LDH showed the largest specific surface area (261 m²/g) and a maximum adsorption capacity of 137 mg/g, as described by the Langmuir isotherm model. Kinetic studies indicated rapid adsorption, with equilibrium reached at approximately 180 min. Fluoride removal was governed primarily by inner-sphere complexation at Zr⁴⁺ and Fe³⁺ sites, accompanied by anion exchange and electrostatic interactions. The adsorbent retained 89% of its capacity after five regeneration cycles. Groundwater tests from Durango, Mexico, demonstrated effective fluoride reduction below Mexican and WHO guideline limits despite competing anions. These results demonstrate the potential of modified LDHs for fluoride-contaminated groundwater treatment. Full article

The selective oxidative transformation of 5-hydroxymethylfurfural (HMF) is a key route toward producing a wide variety of chemicals in the biorefinery industry. Herein, we report a NiAl layered double hydroxide (NiAl-LDH) catalyst as a highly effective electrocatalytic oxidation catalyst for the transformation of HMF into 2,5-diformylfuran (DFF), a valuable furan-based chemical, with about 75.53% DFF selectivity under neutral conditions. It demonstrated good stability without deactivation after 9 cycles of repeated electrolysis. The NiAl-LDH electrocatalyst was deposited on a nickel foam support via a hydrothermal method, and its structural properties and surface morphology were extensively investigated. Systematic studies of reaction temperature, current intensity, and electrolyte concentration revealed that the neutral electrolyte plays a critical role in achieving high DFF selectivity by suppressing aldehyde over-oxidation. Mechanistic investigations with electrochemically active surface area (ECSA), electrochemical impedance spectroscopy (EIS), Tafel slope and density functional theory (DFT) calculations revealed that the reversible transformation between Ni(OH)₂ and active NiOOH species in the NiAl-LDH electrocatalyst was the main reason for the oxidation of HMF, while the incorporation of Al provided structural support to the electrode, enabling the catalyst to exhibit excellent stability during electrolysis. Overall, this work demonstrates an active, earth-abundant metal electrocatalyst for the valorization of biomass-derived 5-HMF to DFF. Full article

The uncontrolled discharge of synthetic azo dyes such as methyl orange (MO) into water bodies has become a major environmental concern because of their strong chemical stability, limited biodegradability, and harmful effects on aquatic ecosystems. In this study, MgNiFe layered double hydroxides (LDHs) were synthesized through a co-precipitation route using a molar ratio of (Mg + Ni)/Fe equal to 3, and their adsorption ability toward MO in aqueous media was investigated. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDX), Fourier-transform infrared spectroscopy (FTIR), and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The characterization results revealed the successful formation of a hydrotalcite-like layered structure with good crystallinity, a relatively uniform distribution of metallic species, and the incorporation of carbonate anions within the interlayer galleries. In addition, the adsorption performance was evaluated by studying the effects of several operational factors, namely adsorbent dosage, initial pH, and contact time. To better understand the interaction between these parameters and identify the optimum operating conditions, a Box–Behnken response surface design was applied. The results indicate solution pH is the most influential parameter in the adsorption process. Under optimized conditions, a maximum removal efficiency of 86.86% was obtained, corresponding to an adsorption capacity of approximately ~86.86 mg·g⁻¹ (based on 100 mL solution volume). The enhanced adsorption performance may be attributed to the combined effect of the multivalent metal cations (Mg²⁺, Ni²⁺, and Fe³⁺), likely increases the surface positive charge density of the LDH and promotes interactions with anionic dye molecules. These interactions are suggested to involve electrostatic attraction and possible surface adsorption processes. However, in the absence of post-adsorption characterization, the exact adsorption mechanism remains hypothetical. Overall, the results demonstrate the promising potential of MgNiFe LDHs as efficient adsorbent materials for the treatment of dye-contaminated wastewater. Full article

Electrochemical water splitting for hydrogen production is a key technological route toward the large-scale generation of green hydrogen. However, the anodic oxygen evolution reaction (OER) suffers from sluggish kinetics and high overpotential, necessitating the development of non-noble metal catalysts that simultaneously possess low cost, high activity, and excellent stability. In this work, a nitrogen-doped graphene quantum dots@nickel–iron layered double hydroxide (N-GQDs@NiFe-LDH) composite catalyst was in situ constructed via a facile hydrothermal strategy. Benefiting from the electronic modulation and structural confinement effects of N-GQDs, the intrinsic catalytic activity and structural stability of the catalyst were simultaneously enhanced. The as-prepared catalyst requires an overpotential of only 320 mV to deliver a current density of 500 mA cm⁻² and maintains 98% of its initial activity after 100 h of chronoamperometric stability testing, demonstrating promising potential for practical applications. Multiscale characterizations revealed that N-GQDs formed strong electronic interactions with Ni/Fe active sites at the interface, significantly enhanced interfacial electron transport, and accelerated the OER kinetics. This study demonstrates that the N-GQDs@NiFe-LDH catalytic system constructed via an interfacial heterostructure engineering strategy provides a new insight for the rational design and development of efficient non-noble-metal OER electrocatalysts. Full article

This study presents the production of isoamyl, n-butyl and cyclohexyl esters of levulinic acid with an excellent yield under solvent-free conditions. The catalysts used were MgAlO and M²⁺MgAlO-mixed oxides containing the transition metals (M²⁺ = Co²⁺, Ni²⁺, Zn²⁺), obtained from calcined layered double hydroxides (LDH). They are easily accessible, low-cost, and environmentally friendly and possess the requisite acid–base properties for esterification reactions. The effect of reaction time and the molar ratio of levulinic acid to the alcohols used on the esterification reaction was investigated. The catalysts were characterized by X-ray diffraction (XRD), XRF, SEM and temperature-programmed desorption of CO₂ (TPD-CO₂). Gas chromatography–mass spectroscopy (GC/MS) was used for the identification and quantification of the product mixtures. Mixed oxides containing transition metals exhibited significantly higher activity than MgAlO. Under the selected reaction conditions, the conversion of levulinic acid and the yield of isoamyl ester reached 100% at a reagent ratio of 1:1. As a by-product of esterification, only dicyclohexyl ether was found at a reactant ratio of 1:1.5. Full article

Layered double hydroxides (LDH) demonstrate significant potential in flexible superca-pacitors due to their high energy storage capability and adjustable architectures. Never-theless, the practical specific capacitance exhibited by current LDH remains below expec-tations, which is attributed to suboptimal electrode performance and limited active sites. Herein, a novel Fe-doped NiFeCo-LDH/NiFeCoO nanosheet composite supported on car-bon cloth was designed and fabricated as a flexible electrode. In this composite, the Ni-FeCo-LDH supplies numerous reactive centers and accelerates electrochemical kinetics, while the NiFeCoO and carbon cloth significantly improve electrical conductivity and cy-cling stability. Moreover, the heterointerface formed between the LDH and the metal oxide phase further facilitates charge transfer. Owing to such synergistic interactions, the pre-pared NiFeCo-LDH/NiFeCoO@CC electrode demonstrates an excellent areal specific ca-pacitance of 3.282 F cm⁻² at a current density of 1 mA cm⁻², while maintaining a high ca-pacity preservation reaching 88.09% following 5000 cycles. Furthermore, the assembled NiFeCo-LDH/NiFeCoO@CC//AC asymmetric supercapacitor delivers an outstanding en-ergy density reaching 0.302 mWh cm⁻² under a power density of 0.776 mW cm⁻², coupled with an excellent capacitance preservation of 85.29% over 5000 cycles. Meanwhile, it can maintain its initial capacitance under varying bending degrees, rendering it widely ap-plicable for future advanced flexible and wearable electronic devices. Full article

The global energy transition and the implementation of carbon capture, utilization, and storage (CCUS) strategies require energy-efficient and scalable CO₂ separation technologies. Mixed-matrix membranes (MMMs), combining polymer matrices with functional inorganic or hybrid nanofillers, have emerged as advanced separation platforms capable of surpassing the conventional permeability–selectivity trade-off observed in neat polymer membranes. This review critically evaluates recent developments in modern hybrid membranes for CO₂ separation from synthetic and industrial gas mixtures, including CO₂/N₂ (flue gas), CO₂/CH₄ (natural gas and biogas upgrading), and syngas systems. Particular emphasis is placed on MMMs incorporating covalent organic frameworks (COFs), metal–organic frameworks (MOFs), graphene oxide (GO), MXenes, transition metal dichalcogenides (TMDs), carbon nanotubes (CNTs), g-C₃N₄, layered double hydroxides (LDH), zeolites, metal oxides, and magnetic nanoparticles. Reported performance ranges include CO₂ permeability (P_CO2) typically between 100 and 800 Barrer, CO₂/N₂ selectivity up to 319, and CO₂/CH₄ selectivity up to 249, depending on filler chemistry, loading, and interfacial compatibility. The mechanisms governing gas transport—molecular sieving, selective adsorption, facilitated transport, and diffusion-pathway engineering—are systematically discussed. Key challenges addressed include filler dispersion, polymer–filler interfacial defects, physical aging, moisture sensitivity, oxidation (particularly in MXenes), and scalability toward industrial membrane modules. Future perspectives focus on sub-nanometer pore engineering, surface functionalization to enhance CO₂ affinity, controlled alignment of 2D nanosheets to promote directional transport, multifunctional core–shell and hollow structures, and the integration of computational modeling and machine learning for accelerated material design. Modern hybrid MMMs are identified as strategically important materials enabling high-efficiency CO₂ separation processes aligned with decarbonization and energy transition objectives. Full article