Layered Double Hydroxide Composites Research Articles

Layered Double Hydroxides as Systems for Capturing Small-Molecule Air Pollutants: A Density Functional Theory Study

Air pollutants are usually formed by easily spreading small molecules, representing a severe problem for human health, especially in urban centers. Despite the efforts to stem their diffusion, many diseases are still associated with exposure to these molecules. The present study focuses on modeling and designing two-dimensional systems called Layered Double Hydroxides (LDHs), which can potentially trap these molecules. For this purpose, a Density Functional Theory (DFT) approach has been used to study the role of the elemental composition of LDHs, the type of counterion, and the ability of these systems to intercalate NO2 and SO2 between the LDH layers. The results demonstrated how the counterion determines the different possible spacing between the layers, modulating the internalization capacity of pollutants and determining the stability degree of the system for a long-lasting effect. The variations in structural properties, the density of states (DOS), and the description of the charge transfer have been reported, thus allowing the investigation of aspects that are difficult to observe from an experimental point of view and, at the same time, providing essential details for the effective development of systems that can counteract the spread of air pollutants.

Synergistic Effects of ZnO@NiM′-Layered Double Hydroxide (M′ = Mn, Co, and Fe) Composites on Supercapacitor Performance: A Comparative Evaluation

Synergistic Effects of ZnO@NiM′-Layered Double Hydroxide (M′ = Mn, Co, and Fe) Composites on Supercapacitor Performance: A Comparative Evaluation

Design of Selective Nanoparticles of Layered Double Hydroxide (Mg/Al-LDH) for the Analysis of Anti-Inflammatory Non-Steroidal Agents in Environmental Samples, Coupled with Solid-Phase Extraction and Capillary Electrophoresis

A simple, fast, and low-cost pre-concentration methodology based on the application of solid-phase extraction coupled to layered double hydroxides (LDHs) and capillary electrophoresis was developed for the determination of naproxen (NPX), diclofenac (DFC), and ibuprofen (IBP) in environmental sample waters. A systematic study of the LDH composition was designed, including the effects of interlayer anions (NO3−, Cl−, CO32−, BenO−, and SDS−) and the effect of molar ratio (Mg:Al). The optimal composition of MgAl/Cl−-LDH (Mg:Al; 1.5:1.0) was coupled to an SPE system: pH (neutral pH), LDH amount (15 mg), and extraction capacity ranged from 79.71 to 83.11% for the three anti-inflammatory non-steroidal agents analyzed. A recovery rate of up to 80.87% was obtained when 0.01 M chloride acid in methanol was used as the eluent and 50 mL of sample was used. Under optimal conditions, the linear range of the calibration curve ranges from 18.02 to 200 μg L−1, with limits of detection ranging from 6.03 to 18.02 μg L−1 for the three NSAIDs. The precision of the methodology was evaluated in terms of inter- and intra-day repeatability, with %RSD < 10% in all cases. The proposed method was applied to analyze environmental water samples (bottle, tap, cistern, well, and river water samples). The developed method is a robust technique capable of combining with other analytical methods to quantitatively determine anti-inflammatory non-steroidal agents.

Green fabrication and efficiency of activated biochar-layered double hydroxide (LDH) nanocomposites against toxic Pink-XFG dye

Removal of dyes has been a matter of great interest for researchers because of health and toxicity issues. In this research work, green biochar was produced using precipitation technique, and by the adsorption process, it was supported on layered double hydroxide (LDH). Biochar/LDH composites were synthesized from Neem, Amaltas, and Keekar stems, eggshells, and Eucalyptus (N, A, K, Egg, and Eu’s biochar/LDH-composite). These composites were employed to remove synthetic dyes from an aqueous solution. Recent studies have identified optimal conditions for LDH-composites under various parameters: pH 9 or 10 with a dosage of 0.05 g/50 mL yields higher adsorption capacities across different LDH composites, ranging from 40.74 to 48.30 mg/g at a reaction time of 90 min using a Pink-XFG dye concentration of 10 ppm, which is favorable. Temperatures of 303–308 K are suitable. Second-order kinetics, along with the Langmuir and Freundlich adsorption isotherms, along with exothermic reactions, presented good-fit results on adsorption kinetics and equilibrium data. The adsorption potential was significantly affected by various concentrations of electrolytes, surfactants, detergents, and heavy metal ions. 0.5 N hydrochloric acid was determined to be the most efficient agent for the process of desorption. These methods are very cost-effective, eco-friendly, and easy to manufacture.

In Situ Fabrication of Hierarchical CuO@CoNi-LDH Composite Structures for High-Performance Supercapacitors.

Layered double hydroxide (LDH) materials, despite their high theoretical capacity, exhibit significant performance degradation with increasing load due to their low conductivity. Simultaneously achieving both high capacity and high rate performance is challenging. Herein, we fabricated vertically aligned CuO nanowires in situ on the copper foam (CF) substrate by alkali-etching combined with the annealing process. Using this as a skeleton, electrochemical deposition technology was used to grow the amorphous α-phase CoNi-LDH nanosheets on its surface. Thanks to the high specific surface area of the CuO skeleton, ultrahigh loading (̃16.36 mg cm-2) was obtained in the fabricated CF/CuO@CoNi-LDH electrode with the cactus-like hierarchical structure, which enhanced the charge transfer and ion diffusion dynamics. The CF/CuO@CoNi-LDH electrode achieved a good combination of high areal capacitance (33.5 F cm-2) and high rate performance (61% capacitance retention as the current density increases 50 times). The assembled asymmetric supercapacitor device demonstrated a maximum potential window of 0-1.6 V and an energy density of 1.7 mWh cm-2 at a power density of 4 mW cm-2. This work provides a feasible strategy for the design and fabrication of high-mass-loading LDH composites for electrochemical energy storage applications.

EDTA-interlayer modified Mg/Fe layered double hydroxides for enhanced adsorption of methyl orange: Adsorption performance and mechanism study

Herein, we explored the efficacy of ethylenediaminetetraacetic acid (EDTA) intercalation modified layered double hydroxides (LDHs) composites for removing the anionic dye methyl orange (MO) from aqueous solutions. EDTA intercalated layered hydroxides (EDTA-Mg/Fe LDHs) with a 4:1 Mg/Fe molar ratio have been successfully prepared and thoroughly characterized using SEM-EDS, FTIR, XRD, XPS, UV-Vis and Zeta potential analysis. Batch adsorption experiments were conducted to evaluate the adsorption performance of the innovative adsorbent on MO. The results indicated successful EDTA loading into Mg/Fe LDHs, exhibiting excellent adsorption performance for MO. At pH 6.0, with a 0.03 g adsorbent dose, MO removal exceeded 91.10% within 90 min, following a pseudo second order kinetic model. The maximum adsorption capacity reached 1207.43 mg/g, fitting well with the Redlich Peterson model. Thermodynamic parameters suggested a spontaneous and favorable adsorption process. Furthermore, we assessed the desorption and regeneration effectiveness of EDTA-Mg/Fe LDHs, emphasizing the importance of developing cost-effective and environmentally friendly adsorbents with practical applications and scientific significance.

Three-dimensional honeycomb composites consist of metal carbides and layered double hydroxides for high-performance supercapacitor electrode materials

To achieve excellent electrochemical performance and stability, a composite material based on metal carbides (MXene) and CoNiZn layered double hydroxides (LDHs) has been synthesized, which synergistically combines the high electrical conductivity of MXene with the high theoretical specific capacity of LDHs. The as-prepared three-dimensional honeycomb-structural MXene/CoNiZn LDH composites have excellent cycle stability with a capacitance retention rate of 87.8% after 100,000 cycles and outstanding electrochemical activity with a specific capacitance of 2044.9 F g−1 at a scan rate of 5 mV s−1. Furthermore, electrochemical impedance spectroscopy also shows a reduced internal resistance indicating that the honeycomb-porous structure facilitates electron transfer and ion diffusion. This study provides a feasible route to develop high-performance supercapacitor electrode materials.

Synthesis of 3D CC/NCNF/NiFe LDH composites as highly active oxygen evolution reaction electrocatalysts

Nitrogen doped carbon nanofibers (NCNFs), which are grown on carbon cloth (CC) and loaded with NiFe layered double hydroxide (LDH) nanosheets, are synthesized by chemical vapor deposition, ammonia annealing and electrodeposition. The obtained three dimensional CC/NCNF/NiFe LDH composites demonstrate an overpotential of 220 mV at current density of 10 mA cm−2 and a small Tafel slope of 30 mV dec−1 for oxygen evolution reaction (OER), both of which are superior to those of the state-of-the-art iridium oxide catalysts. The excellent OER performances of the CC/NCNF/NiFe LDH composites may be attributed to collective contributions of large surface areas of CNFs, nitrogen doping and synergy between NCNFs and NiFe LDHs.

Effective Detection of Cu(II) Ions Based on Carbon Dots@Exfoliated Layered Double Hydroxides Composites Fluorescence Probe.

A series of carbon dots@exfoliated layered double hydroxides (CDs@LDH) composites were hydrothermally fabricated by Mg/Al LDH and formamide. The results of FTIR, UV-vis, and XPS spectra in company with HRTEM images showed that crystalline nano CDs formed on the single layer of LDH by Mg-C bond. With the increase of solvothermal reaction time from 2 to 6h, the band gap and the binding energy of aminic and graphitic N species of CDs@LDH composites decreased, whereas the crystallinity increased. The fluorescence peaks of CDs@LDH composites could be deconvoluted into short-wavelength (416nm) and large-wavelength (443nm) components by Gaussian function, and the fluorescence intensities of both components enhanced with the extension of the solvothermal reaction time. The simultaneous enhancements of fluorescence lifetime and quantum yield resulted from the relatively high electron density in graphitic nitrogen of CDs@LDH, whereas the reduction of nonradiative rate was due to the high crystallinity in the carbon core of CDs@LDH. A strong exciton-lattice interaction also has been validated based on the excitation and emission spectra of CDs@LDH, so the fluorescence emission of CDs@LDH composite was heavily related to its crystalline carbon core and nitrogen-containing groups. CDs@LDH with high nitrogen-containing exhibited a superior detection property for Cu2+ ion sensing with the linear range of 26.90 ~ 192.20μM and a limit of detection of 0.1957μM. The photo-induced electron transfer (PET) process dominated the fluorescence quenching of CDs@LDH by Cu2+ ion since the fluorescence lifetime decreased with the increase of Cu2+ ion concentration.

The preparation of layered double hydroxide wrapped with triazine-based organic framework to enhance the flame retardancy for polypropylene

Layered double hydroxide (LDH) can be used as a flame retardant (FR) for polypropylene (PP) because of its excellent flame retardancy and smoke-suppression effects. However, the agglomeration of LDH seriously affects its dispersity in the PP matrix, thus limiting its application as a FR polymer. This study aimed to enhance the dispersion of LDH in the PP matrix for improving its flame retardancy performance. Herein, a reactive triazine-based organic framework (TOF) was designed and formed by the in situ polymerisation of cyanuric chloride and melamine, and then the LDH surface was covered with TOF to obtain a novel core–shell FR (LDH@TOF), with TOF as the ‘shell’ and LDH as the ‘core’. Subsequently, LDH@TOF was melted into the PP matrix as nanofillers to prepare PP and LDH@TOF composites (PP/LDH@TOF). As expected, the PP/LDH@TOF composites exhibited superior flame-retarding performance (limiting oxygen index of 29.2% and UL-94 V-0 rating) and favourable smoke-suppression performance at 20 wt% of LDH@TOF loading. Moreover, the peak heat release rate, total heat release and total smoke production of PP/LDH@TOF composites decreased by 29.9%, 12.1% and 12.4%, respectively, compared with those of PP and LDH composites. The outstanding flame retardancy properties of the PP/LDH@TOF composites were attributed to the better dispersibility of LDH@TOF in the PP matrix, the synergy of the physical barrier effect of nanosheets and the dense carbonisation acceleration of LDH@TOF. The findings of this study provide a highly efficient approach for functionalising LDH for expanding its application value of PP composites.

Mangifera indica stone-assisted layered double hydroxide biocomposites: efficient contenders for reactive dye adsorption from aqueous sources

Layered double hydroxide composites were synthesized from Mangifera indica stones for enhanced reactive green 5 dye removal from wastewater.

Layered double hydroxide-based electrode materials derived from metal-organic frameworks: synthesis and applications in supercapacitors.

Metal-organic frameworks (MOFs) have emerged as promising electrode materials for supercapacitors (SCs) due to their highly porous structures, tunable chemical compositions, and diverse morphologies. However, their applications are hindered by low conductivity and poor cycling performance. A novel approach for resolving this issue involves the growth of layered double hydroxides (LDHs) using MOFs as efficient templates or precursors for electrode material preparation. This method effectively enhances the stability, electrical conductivity, and mass transport ability of MOFs. The MOF-derived LDH exhibits a well-defined porous micro-/nano-structure, facilitating the dispersion of active sites and preventing the aggregation of LDHs. Firstly, this paper introduces synthesis strategies for converting MOFs into LDHs. Subsequently, recent research progress in MOF-derived LDHs encompassing pristine LDH powders, LDH composites, and LDH-based arrays, along with their applications in SCs, is overviewed. Finally, the challenges associated with MOF-derived LDH electrode materials and potential solutions are discussed.

Insight into the synthesis of LDH using the urea method: morphology and intercalated anion control.

Layered double hydroxides (LDHs) are a class of layered solids applied in many application fields. The study of synthetic methods able to control the interlayer composition and morphology of LDH is an open issue. The urea method, which exploits the thermal decomposition of urea, is known for yielding highly crystalline LDH in the carbonate form. This form is highly stable and, to replace carbonate ions with more easily exchangeable anions, a second step is required. In this work, we modified the urea method to obtain MgAl and ZnAl LDH in the chloride or nitrate form through a one-step synthesis. The effects of the urea/(Al + M(II)) molar ratio (R), reaction time and metal salt concentrations were deeply investigated. We found that LDH in chloride and nitrate forms can be prepared from solutions of metal salts not exceeding 1 M by adjusting R and maintaining the reaction time at 48 hours. The morphology of these products was found to depend on the R value and on the metal salts used in the synthesis. A high R value and nitrate salts favoured the formation of sand-rose crystals, while chloride salts induced the formation of plate-like crystals. The crystal growth mechanism and the parameters influencing the morphology are discussed with reference to ZnAl LDH by monitoring the synthesis over time.

Synthesis and characterization of new composite from modified silica-coated MnFe2O4 nanoparticles for removal of tetracycline from aqueous solution.

In this study, a new composite from silica coated MnFe2O4 nanoparticles, diethylenetriamine, 3-chloropropyl trimethoxysilane and Mg-Al Layered Double Hydroxide (Mg-Al LDH/DETA/CPTMS/SCNPs) composite was synthesized. The Mg-Al LDH/DETA/CPTMS/SCNPs composite was examined by Fourier transform infrared spectrometer (FT-IR), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDS), X-ray diffraction (XRD), Thermogravimetric Analysis (TGA) and Vibrating Sample Magnetometry (VSM). The synthesized composite exhibited magnetic property with a saturation magnetization of 0.40 emu g-1. The Mg-Al LDH/DETA/CPTMS/SCNPs composite was utilized as a successful adsorbent for removal of tetracycline from aqueous solutions. The effect of various operation factors such as initial drug concentration, adsorbent dosage, pH and contact time were investigated. The optimized variable conditions such as adsorbent dose of 60 mg L-1, drug concentration of 100 mg L-1, pH = 7 and contact time 30 min were obtained. For describing the adsorption isotherms, the Langmuir, Freundlich and Temkin adsorption models were utilized. The results indicated that the adsorption isotherm is in good agreement with Langmuir model. According to the Langmuir analysis, the maximum adsorption capacity (qm) of the Mg-Al LDH/DETA/CPTMS/SCNPs composite for tetracycline was obtained to be 40.16 mg g-1. The kinetic studies revealed that the adsorption in all cases to be a pseudo second-order process. The negative value of ΔG° and the positive value of ΔH° showed the adsorption process to be spontaneous and endothermic.

Insight into the flame-retardant mechanism of different organic-modified layered double hydroxide for epoxy resin

Aiming to enhance the flame-retardant efficiency of layered double hydroxide (LDH) in epoxy resin (EP), positively charged LDH was modified by incorporating various anionic modifiers, resulting in a series of organically modified LDH. These modifiers were selected based on the length of nonpolar tails with and without aromatic ring such as sodium dodecylbenzene sulfonate (SDBS), sodium dodecyl sulfate (SDS) and sodium benzene sulfonate (SBS). The chemical composition, structure and hydrophobicity of organic-modified LDH were characterized and the flame-retardant efficiency of organic-modified LDH in EP were investigated. The incorporation of organic-modified LDH into EP resulted in improved Tg and flame retardancy, which depended on the type of modifiers used as well as the structure and loading amount of LDH. Particularly, LDH@DBS exhibited higher improvement efficiency in flame retardancy and Tg than that of LDH@BS and LDH@DS due to the enlarged interlayer spacing, which facilitated the homogeneous dispersion and compatibility in the epoxy matrix. These results demonstrated that good compatibility between organic-modified LDH and polymer was advantageous to enhance the flame-retardancy efficiency and thermal mechanical properties of polymer.

Multifunctional Biocompatible Nanoparticles: Surface Modification and Synthesis of Layered Double Hydroxides for Biomedical Applications

Layered Double Hydroxides (LDHs) are considered versatile materials owing to their distinctive features resulting from the isomorphous substitution of metal cations, namely M(II) and M(III), inside their octahedral locations. The LDH layer structure is characterized by a balanced arrangement of exchangeable hydrated or solvated anions within the interlayer and outer regions. This arrangement gives rise to a two-dimensional heterostructure with an ABAB pattern. Various metal cations have a role in LDHs composition, leading to their classification as hydrocalumites and hydrotalcite. Pristine-LDHs that include diverse inorganic anions have shown significant potential in biological applications. These substances have been investigated for their potential use in many applications, including but not limited to antacids, vaccination adjuvants, etc. The attainment of monodispersity in the size of LDHs is of utmost importance for their efficacy in biomedicine. This research emphasizes that the potential of LDHs is contingent upon effectively resolving difficulties, including those associated with size polydispersity. This study suggests using Surface Modified and Synthesized Layered Double Hydroxides for Biomedical Applications (SMS-LDH-BMA). The present study presents a novel approach that incorporates various enhancements, such as a decreased hydrodynamic diameter of 44.6 nm, a zeta potential of -23.86 mV, a high encapsulation efficiency of 91.2%, a substantial drug loading capacity of 14.6%, a favorable cell viability of 96.44%, and a controlled release rate of GLIB at 3.73 μg/mL/min. These findings demonstrate the efficacy of SMS-LDH-BMA in tackling these obstacles and augmenting the drug delivery capabilities and biomedical applications of LDHs.

Core-shell Cu2O@CuS@NiCo layered double hydroxide composites as supercapacitor electrode materials

A facile multi-step strategy was designed to synthesize core-shell Cu2O@CuS @NiCo-LDH (LDH, layered double hydroxide) composites. Initially, the Cu2O@CuS matrix material was synthesized by heat treatment and vulcanization at 25 °C, and subsequently, the desired Cu2O@CuS@NiCo-LDH composites were obtained using a hydrothermal method. A core-shell structure consisting of nanosheets uniformly grown on the cubic surface of the core–shell unit was achieved. The states and properties of nanosheet loading with different ratios of Ni and Co were investigated. and Cu2O@CuS @NiCo-LDH in supercapacitors, and a specific capacitance of 970.5 F g−1 was obtained at 1 A g−1. Density functional theory simulations provided additional confirmation of the beneficial synergistic interaction between Cu2O@CuS and NiCo-LDH. The constructed Cu2O@CuS@NiCo-LDH//activated carbon asymmetric supercapacitor (ASC) also attained an energy density of 53.3 Wh kg−1 at a power density of 820 W kh−1. Additionally, the assembled ASC demonstrated extremely high stability with a capacitance retention of 85.5 % after 25,000 cycles of testing thanks to its distinct structure design. These results indicate that the Cu2O@CuS@NiCo-LDH electrode shows promise for application as an energy-storage electrode material.

Multiple oxyanions modification on nickel–iron layered double hydroxides for enhanced oxygen evolution reaction

The electrochemical oxygen evolution reaction (OER) holds paramount significance as a pivotal stage within electrochemical water-splitting processes, particularly in hydrogen production. Highly efficient OER electrocatalysts with inherent capability to effectively lower the energy barrier and promote fast kinetics are in high demand. In this research, we have introduced a novel strategy of modifying the non-precious metal benchmark catalyst, NiFe layered double hydroxide (LDH), through multiple oxyanions. Our approach involved incorporating MoS42− as a source of modified anions to enhance the performance of LDH in OER. Under specific conditions of the hydrothermal reaction, a majority of the sulfur (S) within the MoS42− anions underwent oxidization, resulting in the formation of SO42− and MoOxS4-x2- groups. As a result, NiFe LDH composites that were modified with multiple oxyanionic moieties, were successfully fabricated. Thanks to the synergistic effects of these oxyanions, which accelerate the generation of active NiOOH species, the optimized NiFe LDH-MoS4-0.1/NF sample exhibited a significantly low overpotential of 228 and 270 mV at current densities of 10 and 100 mA cm−2, respectively, along with a low Tafel slope of 35.5 mVdec−1 in 1 M KOH electrolyte solution. Our study underscored the importance of embracing diverse oxyanions modification strategy to amplify the performance of OER, opening up numerous opportunities for energy conversion and storage applications.

CeO2@LDH decorated 3D porous module with mortise-tenon structure: Activation of peroxymonosulfate for ultrafast removal of tetracycline

Constructing a robust catalytic module with lower energy consumption, fast liquid transport, and simultaneous highly catalytic oxidizability presents an enticing alternative for industrialized water treatment. Herein, a kind of cerium oxide (CeO2) loaded layered double hydroxide (LDH) composites that was fabricated by seeds embedded epitaxial growth based on hydrothermal method anchored on a three-dimensional porous polyvinylidene fluoride (PVDF) framework (denoted as CeO2@LDH-PVDF) and function as an efficient catalytic activator for peroxymonosulfate (PMS) activation. This module features as lamellar LDH nano-flowers not only in situ anchoring onto both sides of the PVDF surface but also along the wall of the pores in an ab-plane vertically interlaced growth pattern. A packed tower device suitable for the catalytic module is also proposed as proof of concept for consecutive pollutants disposal. This module exhibits dual functions of filtration and oxidation, demonstrating a promising removal efficiency for tetracycline (95.8%, 30 mg/L) in conjunction with PMS. Accurate operation parameters are obtained by using the response surface methodology to further reduce the energy consumption (CeO2 containing: 9.03%, PMS concentration: 0.798 mM; pH: 6.513). Encouragingly, the CeO2@LDH-PVDF is not only capable of achieving ultrafast removal in flowing various contaminants, but also reveals wide practical applicability in tap water and reservoir. Moreover, it provides evidence that the binding force between LDH and PVDF is enhanced by virtue of the unique “Mortise-Tenon” structure, which is conducive to maintaining the catalytic activity. Furthermore, the formation of a complex of M−(HO)OSO3− and the succeeding redox cycle of Ni2+/Ni3+, Fe2+/Fe3+, Co2+/Co3+ explain the generation of reactive radicals in PMS activation. Moreover, a new redox cycle of Ce3+/Ce4+ promotes the utilization efficiency of PMS. Three possible tetracycline degradation pathways are proposed and the toxicity of the by-products is reduced. Finally, the module possesses an ideal universality, good cycling stability, favorable antifouling performance, and superior renewability. It is predicted to be integrated with multiple mature technologies to conduct industrial water treatment due to its changeable shape and durability.

Modulation Engineering of Electromagnetic Wave Absorption Performance of Layered Double Hydroxides Derived Hollow Metal Carbides Integrating Corrosion Protection.

Layered double hydroxides (LDHs) with unique layered structure and atomic composition are limited in the field of electromagnetic wave absorption (EMA) due to their poor electrical conductivity and lack of dielectric properties. In this study, the EMA performance and anticorrosion of hollow derived LDH composites are improved by temperature control and composition design using ZIF-8 as a sacrifice template. Diverse regulation modes result in different mechanisms for EMA. In the temperature control process, chemical reactions tune the composition of the products and construct a refined structure to optimize the LDHs conductivity loss. Additionally, the different phase interfaces generated by the control components optimize the impedance matching and enhance the interfacial polarization. The results show that the prepared NCZ (Ni3ZnC0.7/Co3ZnC@C) has a minimum reflection loss (RLmin ) of -58.92dB with a thickness of 2.4mm and a maximum effective absorption bandwidth (EABmax ) of 7.36GHz with a thickness of 2.4mm. Finally, due to its special structure and composition, the sample exhibits excellent anticorrosion properties. This work offers essential knowledge for designing engineering materials derived from metal organic framework (MOF) with cutting-edge components and nanostructures.