Search Results (645)

Growing interest in sustainable, high-performance energy storage has driven extensive studies on advanced electrode materials for supercapacitor applications. In this study, a FeNiCo metal–organic framework/multiwalled carbon nanotube (MOF–MWCNT) composite was synthesized and employed as a modifying layer on a carbon felt electrode (CFE) via a drop-casting method. The electrochemical performance of the composite electrode was systematically evaluated in 1 M H₂SO₄ electrolyte. Structural and electrochemical studies demonstrate that the combined effect of the conductive CFE substrate, the electric double-layer capacitance of MWCNTs, and the pseudocapacitive properties of the trimetallic FeNiCo MOF markedly enhances the charge storage performance. Cyclic voltammetry and galvanostatic charge–discharge measurements demonstrate a maximum specific capacitance of approximately 180 F g⁻¹. The electrode delivers an energy density of 73.20 Wh kg⁻¹ at a power density of 3796.17 W kg⁻¹, demonstrating a favorable balance between energy and power performance. In addition, high coulombic efficiency confirms excellent charge–discharge reversibility. Notably, 71% of the initial capacitance is retained after 900 cycles in 1 M H₂SO₄, indicating stable electrochemical behavior even under strongly acidic conditions. These findings emphasize the promise of the FeNiCo MOF–MWCNT/CFE composite as a durable electrode design for next-generation supercapacitor devices. Full article

As a novel organic–inorganic hybrid porous crystalline material, metal–organic frameworks (MOFs) are ideal sensitive materials for detecting gases, antibiotics, and ions, owing to their ultra-high specific surface area, tunable pore structures, abundant active sites, and tailorable architectures. This review systematically summarizes the core structural features, preparation methods, and modification strategies of MOFs, elaborates on the adsorption and signal conversion mechanisms in target detection, and highlights typical applications, performance advantages, and practical scenarios of MOF-based sensors, clarifying their structure–activity relationships and performance differences from traditional semiconductor sensors. It further analyzes key challenges, including insufficient stability, poor conductivity, large-scale preparation difficulties, and real-sample interference, as well as industrialization bottlenecks such as batch-to-batch reproducibility, instrument integration, and high costs. Additionally, it supplements cross-field synergistic innovations and industrialization progress, and prospects future directions: function-oriented precise design, multifunctional composite optimization, portable intelligent devices, green large-scale synthesis, and standardization promotion. This review provides a comprehensive reference for advancing MOF-based detection research and applications in environmental monitoring, industrial safety, food safety, and healthcare. Full article

Benefiting from their outstanding porosity, considerable specific surface area, and natural flexibility, cellulose nanofibers (CNFs)/MOF materials have emerged as competitive candidates for advanced flexible energy storage devices. However, conventional CNFs/MOFs aerogels or films often suffer from poor recoverability under compression, bending, and folding, accompanied by severe plastic deformation that compromises the cycling and structural stability of devices. To address this issue, we report a rationally designed flexible PU/CNFs/ZIF-8/PANI composite foam with an interconnected micro-mesoporous structure. Using polyurethane foam as a soft substrate and CNFs/ZIF-8 as building blocks, the composite was fabricated through a combined strategy of impregnation, in situ ZIF-8 growth, hot-pressing, and in situ aniline polymerization with simultaneous etching of the ZIF-8. The incorporation of carboxylated CNFs enhances the hydrophilicity of the PU skeleton. This, in combination with the hot-pressed framework, establishes an interconnected 3D network, thereby effectively preventing the agglomeration of active materials. Meanwhile, the hierarchical pores derived from the sacrificial ZIF-8 template provide abundant electroactive sites, accelerate ion transport, and facilitate high PANI loading. By virtue of this synergistic architectural effect, the resultant electrode achieves a high specific capacitance of 449 F/g at 0.2 A/g, with 97% capacitance retention after 2000 cycles at 5 A/g. Furthermore, the composite foam demonstrates excellent mechanical flexibility, with a tensile strength of 0.87 MPa and an elongation at break of 230%. This work offers a feasible approach for developing high-performance flexible supercapacitors and provides novel perspectives for the rational design of portable energy storage devices. Full article

Herein, an electrochemical sensor is reported for the first time based on an ordered macro–microporous composite derived from metal–organic frameworks (MOFs) for the highly sensitive detection of auramine O (AO), a Group 2B carcinogen. The hierarchical pore architecture, integrating an ordered macroporous network with a microporous ZIF-8 framework, enables the uniform dispersion of a high density of catalytically active sites. The interconnected macroporous channels facilitate efficient mass transport and rapid removal of reaction byproducts, effectively preventing pore blockage and ensuring stable sensing performance during repeated measurements. Owing to these structural advantages, the proposed sensor exhibits outstanding analytical performance toward AO detection, with a sensitivity of 0.4843 μA μM⁻¹, a detection limit of 0.168 μM (S/N = 3), and a wide linear range from 0.5 to 50 μM. Moreover, the sensor demonstrates excellent selectivity and reproducibility, maintaining reliable responses even in the presence of 100-fold excess common food constituents such as tartrazine and glucose. Real sample analysis further confirms its high accuracy and operational stability. Overall, the electrochemical sensor based on silver nanoparticle-decorated ordered macro–microporous ZIF-8 synthesized via in situ reduction shows great potential as a portable and on-site tool for rapid AO detection in food. More broadly, ordered macro–microporous MOF-derived materials represent a promising platform for advanced electrochemical sensor applications. Full article

Aqueous zinc-ion batteries (AZIBs) are promising for large-scale grid storage due to inherent safety, low cost, environmental compatibility, high theoretical capacity (820 mAhg⁻¹), and suitable redox potential (−0.763 V vs. SHE). However, practical deployment is hindered by coupled challenges at the zinc anode–hydrogen evolution, dendrite growth, and corrosion/passivation, which severely limit cycle life and coulombic efficiency. This review systematically summarizes key advances in AZIB research. It first elucidates working principles and four cathode energy storage mechanisms: Zn²⁺ insertion/extraction, H⁺/Zn²⁺ co-insertion, chemical conversion, and dissolution/deposition. Second, it examines four mainstream cathodes (manganese-based, vanadium-based, Prussian blue analogs, and organic compounds), analyzing performance bottlenecks and corresponding optimization via structural modification. Third, it explores functional mechanisms of advanced separators (polymer, inorganic/ceramic composite, MOF-based, and cellulose-based) in regulating uniform Zn²⁺ deposition and suppressing dendrites. Fourth, it summarizes anode optimization strategies: artificial protective layers for interface stabilization, electrolyte additives to modulate Zn²⁺ solvation/deposition, and 3D porous structures to reduce local current density and provide nucleation sites. Finally, key scientific challenges and future directions are discussed—multi-strategy synergy, in situ characterization, practical battery construction, and sustainable technological development, offering theoretical guidance for advancing AZIBs toward large-scale applications. This review aims to provide a comprehensive perspective spanning from materials to systems, and from mechanisms to applications. Its core objective is not merely to list the types of cathode materials, but to establish a logical bridge directly connecting “key challenges” to “optimization strategies,” with a particular emphasis on the issues and solutions related to the cathode side. Full article

In this study, the in situ solvothermal synthesis of a copper-based metal–organic framework (Cu-BTC MOF) into two porous ceramic substrates with a 10 cm diameter and 2 cm thickness was reported. X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, diffuse reflectance spectroscopy (DRS), Tauc plot analysis, optical microscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were the techniques that were utilized to verify the formation and incorporation of the MOF into ceramics (two samples, with different SiO₂ particles; 500 µm (Ceramic 1), and 150 µm (Ceramic 2)). The synthesized Cu-MOF exhibited a crystalline structure. Both the composites and the Cu-MOF exhibited visible-light absorption, with optical band gaps of 2.5 eV and 2.4 eV, respectively, as determined by DRS. TEM images demonstrated that crystalline MOF domains were successfully included inside the ceramics. Methyl orange (MO), Congo red (CR), and methylene blue (MB) were used to assess the composites’ ability to remove dyes. Catalytic hydrogenation, powered by in situ hydrogen production from NaBH₄ hydrolysis, demonstrated high removal efficiencies of 91–97% after 60 min. Adsorption, on the other hand, was ineffective. Despite undergoing four consecutive cycles without performance degradation, the materials demonstrated remarkable recyclability. Cu-MOF@ceramic composites are effective, durable, and practically applicable for improved wastewater treatment. Full article

In recent decades, the requirement for materials with excellent electromagnetic wave (EMW) absorption properties has been steadily expanding. Developing and designing multifunctional hybrid absorbers featuring diverse components and synergistic loss mechanisms have become a significant research field. MOF materials feature abundant heterogeneous interfaces and high porosity, and their derivatives exhibit superior magnetic effects. They can enhance EMW absorption through multiple scattering and reflection. These merits enable them to satisfy the demands of diverse EMW absorption applications. Therefore, this work summarizes the investigations and applications of MOF derivatives in EMW absorption. The EMW absorption mechanisms of MOF derivatives are thoroughly investigated from the aspects of precursor design, framework construction, and compounding with reinforcing phases. Meanwhile, the research progress of related materials is summarized, including multi-component MOF-derived EMW absorbers, MOF-derived biomass composite absorbing materials, and MOF-derived conductive polymer composite absorbers. In addition, the subsequent progress of EMW absorbers shows promising prospects. The various deficiencies of MOF-derived absorbers in current research are also analyzed. It is expected to provide more systematic and thorough guidance for the future investigations in related fields. Full article

Core–shell metal–organic framework (MOF) composites, owing to their unique structural advantages, have emerged as a prominent research focus in the field of chemistry, advanced materials and chemical engineering. By integrating MOFs with other functional components such as MOFs, covalent organic frameworks (COFs), metal oxides, carbon materials, ionic liquids or polymers into synergistic heterogeneous architectures, coreshell MOFs can markedly enhance physicochemical stability and enable diversified functional performances. This work provides a systematic overview of the major construction strategies for these materials, including in situ growth, self-templating, seed-mediated methods, one-pot synthesis and post-synthetic modification. It also summarizes recent applications in catalysis (thermal, electrocatalytic and photocatalytic processes) as well as gas adsorption and separation (such as CO₂ capture from flue gas, natural gas purification and acetylene separation). The final section discusses future research directions, including a deeper understanding of interfacial growth mechanisms, the development of green and scalable synthesis routes, the validation of engineering-oriented applications, and the integration of machine learning with high-throughput computation for structural prediction and accelerated materials screening, thereby providing important guidance for the development of high-performance core–shell MOFs. Full article

Metal–organic frameworks (MOFs) possess ordered pore structure, high surface area, tunable composition and tailorable functionality, and thus present promising prospect in many applications. Among them, titanium-based MOFs (Ti-MOFs) composed of organic ligands and titanium–oxygen clusters exhibit great potential in photocatalysis, owing to their diverse topological configurations, outstanding photocatalytic activity, low toxicity, and easy production. The latest developments in Ti-MOFs, including the synthetic strategies, structural features, methods for enhancing catalytic performance, and typical applications, were reviewed in this paper. The application in CO₂ reduction, hydrogen evolution, organic pollutant removal, and photocatalytic sensing were emphasized. Moreover, we present a distinctive perspective on the relationship between the structure and their applications of Ti-MOFs, and provide new information in the design and construction of advanced Ti-MOFs for high-efficiency photocatalytic conversion. Full article

To address the inherent limitations of Cu₂Se as a lithium-ion battery (LIB) anode, a Cu₂Se/MnSe@C composite was rationally designed and synthesized via selenization of a CuMn bimetallic metal–organic framework (MOF) precursor. This synthesis strategy integrates carbon composite engineering and heterogeneous structure construction, achieving in situ formation of Cu₂Se/MnSe heterogeneous nanoparticles anchored on amorphous carbon nanosheets. Structural characterizations confirm the successful construction of well-defined Cu₂Se/MnSe interfaces and uniform dispersion of selenide components, with Mn introduction inducing regulated electron transfer between Cu₂Se and MnSe. Electrochemical evaluations demonstrate that the Cu₂Se/MnSe@C composite exhibits a significantly enhanced lithium storage performance compared to single-component Cu₂Se@C, including higher specific capacity and superior rate capability. Mechanistic studies reveal that the synergistic effects of the carbon matrix (enhancing electrical conductivity and mitigating volume expansion) and the Cu₂Se/MnSe heterogeneous interface (lowering charge transfer resistance, accelerating Li⁺ diffusion, and boosting pseudocapacitive contribution) are responsible for the performance enhancement. Moreover, Cu₂Se/MnSe@C||LiFePO₄ full cells deliver a stable average operating voltage and reliable cycling stability, validating the composite’s practical application potential. Full article

Transition metal oxides (TMOs) have been recognized as highly prospective anode materials for lithium-ion batteries (LIBs) due to their low cost, high capacity, and distinctive lithiation mechanisms. Nevertheless, their practical adoption is constrained by significant volume changes during lithiation/delithiation, inferior electrical conductivity, severe particle agglomeration, unsatisfactory cycling stability, and limited rate performance. In an effort to mitigate these flaws, we developed a tactic employing a zeolitic imidazolate framework (ZIF) as the self-sacrificing template and tuning the Co/Fe/Ni ratio with a ZIF framework to prepare an innovative trimetallic metal–organic framework (MOF)-derived CoNiO₂/NiCo₂O₄/NiFe₂O₄ compound (CFNO422) with nano/micro hierarchical architecture. The nano/micro hierarchical structure effectively accommodates volume changes, alleviates structural stress, and offers copious active sites for lithium storage. More importantly, the synergistic interaction among multiple component oxides promotes richer redox reactions and enhances electronic conductivity. Benefiting from the structural compatibility and composition, CFNO422 delivers an outstanding reversible capacity (1301.3 mAh g⁻¹ up to 120 cycles at 0.2 A g⁻¹), enhanced rate capability (614.3 mAh g⁻¹ even at 2.0 A g⁻¹), and exceptional cycling stability (527.4 mAh g⁻¹ over 600 cycles at 1.0 A g⁻¹). This research proposes a versatile synthesis for MOF-derived polymetallic oxides as anode materials, opening a new avenue for advanced energy storage. Full article

During the refining processes, when catalyst activity falls below acceptable levels and it is not possible to regenerate it for its reuse, the catalyst is disposed of as solid waste; however, the spent catalysts could be a promising source of metals for manufacturing new products due to their high content of heavy metals, such as nickel. In this research, nickel recovered from a spent hydrodesulfurization catalyst by ultrasonication-assisted leaching was used as a metal source for the synthesis of Ni-MOF-74 material (Ni-MOF-74E), and its properties and CO₂ adsorption capture capacity were compared with a Ni-MOF-74 prepared with commercial salt nickel nitrate (Ni-MOF-74C). The MOF-74 structure was confirmed by analytical techniques such as FT-IR and powder X-ray diffraction. By SEM and EDX, the fusiform morphology and the elemental composition were found. The CO₂ capture capacity, evaluated at 298 K, 288 K and 273 K, showed that the Ni-MOF-74E material presented an adsorption capacity higher than 2.2 mmol g⁻¹ and a heat adsorption of 44 kJ mol⁻¹. Full article

Dichloromethane, as a widely used highly volatile industrial solvent, has neurotoxicity and hepatotoxicity and is suspected of being a carcinogen to humans. Therefore, it is necessary to develop a detection method that is more convenient for users, responds faster and is more efficient than traditional analytical techniques. In cataluminescence (CTL) technology, as a promising alternative, the performance of CTL sensors critically depends on the design of high-performance sensitive materials. In this study, by rationally designing two typical metal–organic frameworks (MOFs), UIO-66 (zirconium-based) and HKUST-1 (copper-based), UIO-66/HKUST-1 nanocomposites for dichloromethane CTL detection were prepared by using a simple hydrothermal method. The experimental results show that when the composition ratio of UIO-66 is 2%, this composite exhibits the strongest CTL response to dichloromethane. Under optimized conditions, this sensor exhibits high selectivity, excellent stability (RSD = 3.98%), and a rapid response advantage for dichloromethane. The response time and recovery time are 5 and 19 s, respectively. It shows a good linear relationship within the concentration range of 8.4–84 ppm, along with a detection limit as low as 1.71 ppm. Analysis indicates that the enhanced performance stems from the formation of high-concentration oxygen vacancies and significantly strengthened synergistic effects at the UIO-66/HKUST-1 composite. This increases the concentration of surface reactive oxygen species, thereby providing more active sites for catalytic reactions. This work provides a robust and efficient sensing strategy for dichloromethane detection. Full article

One of the many applications of metal–organic frameworks (MOFs) is their use as adsorbents for removing emerging contaminants, such as ciprofloxacin (CIP), a fluoroquinolone-class antibiotic, from aqueous environments. We selected the copper-based MOF HKUST-1 and coupled it with TiO₂, then immobilized the composite on glass beads (TiO₂/HKUST-1@GB) to produce a reusable photocatalyst. The immobilization of the composite on glass beads improved the structural strength as well as the reusability of the photocatalyst. Together, these properties pave the way for scale-up for commercial applications in continuous-flow water treatment systems. Herein, we used XRD, FTIR, and SEM to characterize the immobilized catalyst and assess its structural, morphological, and optical properties. Photocatalytic experiments showed 98% degradation in 45 min under UV irradiation at pH 6 and a CIP concentration of 200 μgL⁻¹. The TiO₂/HKUST-1@GB composite showed higher degradation compared to pristine TiO₂ and HKUST-1 due to enhanced charge–carrier separation and synergistic interfacial effects. The reusability of the composite over five cycles was observed, with high stability and negligible Cu and Ti leaching, indicating promising environmental performance. Thus, TiO₂/HKUST-1@GB provides an efficient and sustainable approach for removing ciprofloxacin from aqueous solutions. The degradation performance, reusability, and ability to work simultaneously in adsorption and photocatalytic processes make TiO₂/HKUST-1@GB a promising candidate for the advanced treatment of aqueous-phase antimicrobial compounds such as ciprofloxacin. Full article

Catalytic systems that couple pollutant degradation with hydrogen evolution have attracted significant attention due to their potential to simultaneously address environmental and energy issues. In this study, an S-scheme heterojunction composed of lamellar polymeric carbon nitride (PCN) anchored with a rod-like cerium metal–organic framework (Ce-MOF) was successfully synthesized via a facile one-step oxidation method, enabling efficient visible-light-driven photocatalytic hydrogen evolution and simultaneous tetracycline degradation. The optimized PCN/Ce-MOF composite delivers a hydrogen production rate of 495.7 μmol g⁻¹ h⁻¹ and achieves a tetracycline removal efficiency of 78%. Such excellent performance is attributed to the charge transfer mechanism of the S-scheme heterojunction in the PCN-Ce-MOF composite during the reaction process, while retaining the intrinsic redox capabilities of both materials. Meanwhile, mechanistic studies reveal that tetracycline can effectively capture holes during its efficient degradation, inhibit electron–hole recombination, and promote proton reduction to generate hydrogen. This investigation provides valuable insights for the rational design of S-scheme heterojunction photocatalysts, aiming to achieve efficient and stable photocatalytic hydrogen production and synergistic degradation of organic pollutants. Full article