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A membrane with a low methanol permeability and high proton conductivity (σ p) is essential for the effective operation of a direct methanol-based fuel cell. Herein, a bio-metal organic framework was prepared with natural α-amino acids as ligands and then combined with hydrolyzed polyacrylonitrile (PAN) nanofibers (AA-MOF@PAN). The resulting nanocomposite membranes were subsequently integrated into a Nafion matrix (AA-MOF@PAN/Nafion). The –NH 2 groups on AA-MOF@PAN interact with –SO 3 H groups on Nafion, forming long-range acid-base pairs along the interface between the matrix and nanofibers. This interaction creates abundant proton-conducting sites for proton exchange membrane. Notably, the AA-MOF@PAN-4h/Nafion membrane demonstrated an exceptional proton conductivity (σ p) of 0.25 S cm−1 and a higher power density of 117.61 mW cm−2 compared to the recast Nafion membrane. This study offers valuable insights into the three-dimensional ordered design of a natural α-amino acids as a proton transfer sites and highlighting their potential applications in proton exchange membranes. • In situ growth of uniformly distributed AA-MOF onto hydrolyzed PAN nanofiber. • AA-MOF@PAN were introduced as proton-conducting channels. • AA-MOF@PAN-4h/Nafion exhibited the highest proton conductivity of 0.25 S cm−1 at 80 °C. • Introduction of AA-MOF@PAN resulted in a reduced fuel crossover. [ABSTRACT FROM AUTHOR]

Electrosynthesis of urea from CO2 and NO3− is a sustainable alternative to energy‐intensive industrial processes. The main challenge hindering the progress of this technology lies in the development of advanced electrocatalysts that efficiently utilize abundant, low‐cost CO2 and nitrogen sources to yield urea with both high Faradaic efficiency (FE) and current density. In this work, we designed and prepared a new two‐dimensional metal–organic framework (MOF), namely PcNi−Fe−O, constructed by nickel‐phthalocyanine (NiPc) ligands and square‐planar FeO4 nodes, as the electrocatalyst for urea electrosynthesis. PcNi−Fe−O exhibits remarkable performance to yield urea at a high current density of 10.1 mA cm−2 with a high FE(urea) of 54.1 % in a neutral aqueous solution, surpassing those of most reported electrocatalysts. No obvious performance degradation was observed over 20 hours of continuous operation at the current density of 10.1 mA cm−2. By expanding the electrode area to 25 cm2 and operating for 8 hours, we obtained 0.164 g of high‐purity urea, underscoring its potential for industrial applications. Mechanism study unveiled the enhanced performance might be ascribed to the synergistic interaction between NiPc and FeO4 sites. Specifically, NH3 produced at the FeO4 site can efficiently migrate and couple with the *NHCOOH intermediate adsorbed on the urea‐producing site (NiPc). This synergistic effect results in a lower energy barrier for C−N bond formation than those of the reported catalysts with single active sites. [ABSTRACT FROM AUTHOR]

The wrinkles are pervasive in ultrathin two‐dimensional (2D) materials, but the regulation of wrinkles is rarely explored systematically. Here, we employed a series of carboxylic acids (from formic acid to octanoic acid) to control the wrinkles of Zr‐BTB (BTB=1, 3, 5‐(4‐carboxylphenyl)‐benzene) metal–organic framework (MOF) nanosheet. The wrinkles at the micrometer scale were observed with transmission electron microscopy. Furthermore, high‐angle annular dark‐field (HAADF) images showed lattice distortion in many nanoscale regions, which was precisely matched to the nano‐wrinkles. With the changes of hydrophilicity/hydrophobicity, MOF‐MOF and MOF‐solvent interactions were possibly synergistically regulated and wrinkles with different sizes were obtained, which was supported by HAADF, molecular dynamics, and density functional theory calculation. Different wrinkle sizes resulted in different pore sizes between the Zr‐BTB nanosheet interlayers, providing highly‐oriented thin films and the successive optimization of kinetic diffusion pathways, proved by grazing‐incidence wide‐angle X‐ray scattering and nitrogen adsorption. The most suitable wrinkle pore from Zr‐BTB‐C4 exhibited highly efficient chromatographic separation of the substituted benzene isomers. Our work provides a rational route for the modulation of nanoscale wrinkles and their stacked pores of MOF nanosheets and improves the separation abilities of MOFs. [ABSTRACT FROM AUTHOR]

ABSTRACT A copper‐based one‐dimensional framework compound [Cu2(L1)4(L2)]n (1) [L1 = 3‐(2‐thienyl)acrylic acid, L2 = 4,4′‐bipyridine] has been synthesized by slow diffusion of layers technique and characterized by spectroscopic methods and single‐crystal X‐ray crystallography. X‐ray diffraction analysis reveals that the compound is crystallized in the triclinic crystal system with space group Pī. Two neighboring Cu centers are bridged by four carboxylato groups from four different L1 ligands, leading to the formation of a paddle‐wheel [Cu2(COO−)4] secondary building unit (SBU). The paddle‐wheel units are interconnected by bidentate 4,4′‐bipyridine ligands to form a one‐dimensional infinite chain network. In [Cu2(L1)4(L2)]n (1), Cu(II) ion features a penta‐coordinated environment around it. Notably, [Cu2(L1)4(L2)]n (1) is capable of activating molecular oxygen to efficiently catalyze the oxidation of alcohols under base‐free conditions. [ABSTRACT FROM AUTHOR]

The slow kinetics of four-electron-transfer oxygen evolution reaction (OER) highly impedes the conversion efficiency of overall water splitting for green hydrogen production. Recently, metal-organic frameworks (MOFs) have attracted widespread attention due to their tunable morphologies, well-defined structures, and abundant metal sites. In this work, a series of cobalt-incorporated NiFe-MOF nanosheets were in-situ synthesized on nickel foam. Owing to the synergistic effect of exposed multi-metal sites, NiFeCo-BDC exhibits excellent OER activity, delivering an ultralow overpotential of 233 mV at the current density of 10 mA cm−2 with a small Tafel slope of 40.8 mV dec−1. In the continuous chronoamperometry test at 100 mA cm−2, almost no potential attenuation can be found over 200 h, demonstrating its remarkable stability. After OER, the amorphous metal oxyhydroxide layer is generated on surface, and the high-valent species are responsible for the superior OER performance. In-situ Raman spectra reveal that the organic ligands of NiFe-BDC and NiFeCo-BDC are etched and released during OER, and the Co incorporation facilitates the generation of amorphous layer. This work presents an effective strategy for design of multi-metal MOF-based electrocatalysts, and provides an insightful view on the structure evolution during OER. [Display omitted] • Construction of self-supported trimetallic NiFeCo-BDC nanoarrays. • Superior OER performance with ultra-low overpotential and excellent stability. • In-situ Raman studies on deciphering the self-reconstruction process. [ABSTRACT FROM AUTHOR]

We present the design of a novel functional metal-organic framework here, denoted as Co-sal–NH 2 –MOF@TiO 2 , featuring the comprise of controllably in-situ grown TiO 2 sheets from NH 2 -MOF(Ti) and [Co] catalytic sites stabilized by salicylaldimine moiety via site isolation for visible-light-driven hydrogen evolution from water. The hierarchical organization of TiO 2 and Co catalyst within NH 2 -MOF (Ti) leads to outstanding photocatalytic performance, as evidenced by a H 2 yield of 15,584 μmolg−1h−1 and turnover numbers (TON) reaching 5844 over 24 h. This catalyst also signifies distinctly enhanced activities of approximately 105-fold, 354-fold, 15-fold, and 100-fold, compared to the pristine NH 2 -MOF(Ti), MOF-derived TiO 2 , NH 2 -MOF(Ti)@TiO 2 and the combination of [Co catalyst + NH 2 -MOF(Ti) + TiO 2 ], respectively. EXAFs and XPS etc. analyses revealed a stable coordination environment for salicylaldimine-supported Co(II) catalytic unit, which integrated with in-situ grown TiO 2 sheets can not only guarantee catalyst stability, but also generate much more densely packed light-harvesting heterojunction units and thus promote separation and transfer of photogenerated carriers between TiO 2 and Co catalyst in NH 2 -MOF(Ti) under light through optimized band gap structure. This work outlines the in-situ construction of organic and inorganic hybrid heterojunction for H 2 production from water. The novel organic and inorganic hybrid heterojunction that [Co] catalytic sites stabilized by salicylaldimine moiety with in-situ derived TiO 2 sheets from MOF(Ti) to realize further promoted visible light-driven H 2 formation. [Display omitted] • Salicylaldimine-supported Co and in-situ derived TiO 2 were integrated into NH 2 -MOF(Ti). • Co-sal–NH 2 –MOF@TiO 2 represented 105-fold enhanced H 2 evolution rate over pristine MOF. • EXAFs and XPS revealed stable coordination environment of Sal-Co and charge transfer pathway. • Synergistic effect between TiO 2 and Co in MOF endow high stability and mobility of charge carriers. [ABSTRACT FROM AUTHOR]

In this work, a series of Ni‐WxC/carbon materials have been prepared from a MOF precursor, DUT‐8(Ni), following different tungsten deposition routes. After pyrolysis, nickel‐tungsten alloys and tungsten carbide phases over nitrogen‐doped carbons were obtained. These materials were applied to cellulose hydrogenolysis, where molar yields of up to 46 % in ethylene glycol (EG) and 9 % in propylene glycol (PG) were obtained at 245 °C after 1 hour of reaction time. The best performing catalyst demonstrated promising stability, as the EG yield remained constant over 3 recycling tests and very little nanoparticles sintering was observed. [ABSTRACT FROM AUTHOR]

Separating propylene (C3H6) from propylene/propane (C3H6/C3H8) mixture using energy‐efficient adsorption is industrially important, but due to the lack of universal pore features, the rational selection of a suitable adsorbent in the ocean of porous materials is a tough task. In this study, a comprehensive work on the discovery of high‐performance C3H6/C3H8 separation adsorbents is carried out by utilizing the advantages of high‐throughput computational screening (HTCS). First, based on the HTCS data mining in the CoRE MOF 2019 and Tobacco 3.0 database, the target material, Cd‐HFDPA, is screened out. Second, the pore electrostatic potential (ESP) analysis shows that Cd‐HFDPA has obvious pore characteristics and high affinity for C3H6 according to ESP matching, which is further confirmed by adsorption isotherms, Ideal Adsorbed Solution Theory selectivity, adsorption enthalpy analyses, and breakthrough experiments. Finally, an industrial two‐bed pressure swing adsorption process for Cd‐HFDPA adsorbent is proposed and its productivity and energy consumption are compared with other benchmark materials. [ABSTRACT FROM AUTHOR]

A sensitive analytical procedure for simultaneous extraction and determination of bisphenol A and alkyl phenols, namely, 4‐sec‐butylphenol, 4‐tert‐butylphenol, and 4‐tert‐amylphenol from aqueous samples with metal–organic framework (MOF)‐based dispersive micro‐solid‐phase extraction (D‐µSPE) and high‐performance liquid chromatography (HPLC) technique is developed. Sample contaminants were preconcentrated with amino‐functionalized aluminum MOF and later eluted with acetonitrile. The reconstituted sample was subjected to HPLC analysis. Various procedural parameters related to D‐µSPE were optimized. Under optimized preconcentration and chromatographic conditions, calibration curves with excellent linearity (R2 > 0.9986) in the working range of 0.25–100 ng mL−1 were prepared. Limit of detection (S/N = 3) for every analyte within the range of 0.020–0.022 ng mL−1 was obtained. Analyte's recovery 91.16%–97.01% (RSD = 1.02–3.01) for intraday and 89.86%–95.83% (RSD = 1.15–3.13) for inter‐day analysis was obtained from real water samples. [ABSTRACT FROM AUTHOR]

Research concerning coordination polymers has been intense due to their significant variability and structural stability. With this in mind, an ionic neodymium coordination polymer was synthesized, composed of an anionic one‐dimensional polymer interconnected to a cationic three‐dimensional porous polymer, poly[dodecaaquabis(μ‐pyridine‐4‐carbohydrazide‐κ2N:O)bis(μ2‐4‐sulfobenzoato‐κ2O:O′)bis(μ3‐4‐sulfobenzoato‐κ3O:O′:O′′)trineodymium(III)] catena‐poly[aquabis(μ‐pyridine‐4‐carbohydrazide‐κ2N:O)bis(μ2‐4‐sulfobenzoato‐κ2O:O′)neodymium(III)] 4.33‐hydrate, {[Nd3(C7H4O5S)4(C6H7N3O)2(H2O)12][Nd(C7H4O5S)2(C6H7N3O)2(H2O)]·4.33H2O}n. The ligands used were 4‐sulfobenzoate (PSB) and pyridine‐4‐carbohydrazide, popularly known as isoniazid (INH), an antibiotic drug. The compound crystallizes in the monoclinic space group C2/c, with Z = 4. Solid‐state calculations suggest that the crystal structure is mainly stabilized by hydrogen bonds, i.e. O—H...O and N—H...O interactions among the polymers, and by van der Waals interactions involving the organic side chains. This net is tetragonal, 2‐nodal 3,4‐connected, and can be described as the dmd (sqc 528) type. [ABSTRACT FROM AUTHOR]

Although metal‐organic frameworks (MOFs) show promise as electrocatalysts due to their unique intrinsic features, their activity and stability often fall short. Herein, NiFe‐MOFs is used as a model to introduce group VIB metalates (Na2WO4, Na2CrO4, and Na2MoO4) into the topological conversion process of layer double hydroxide (LDHs)/MOFs, creating a series of interstitial VIB element‐doped LDHs/MOFs catalysts. The metalates engage in the alkaline hydrolysis process of MOF, generating LDHs on the MOF surface. Furthermore, altering the pH value in the reaction environment can modify the catalysts' morphology, dopant/LDHs content, and electronic structure. Consequently, the prepared interstitial W‐doped NiFe‐LDHs/MOFs catalyst displays superior catalytic performance, with overpotentials of only 250 mV at 500 mA cm−2. Moreover, a homemade anion‐exchange membrane water electrolysis (AEMWE) system featuring the fabricated electrocatalyst as the anode can operate stably for 500 hours at 1 A cm−2. The exceptional catalytic activity and stability stem from optimized intermediate adsorption/desorption behavior and the unique LDHs/MOFs nanostructure. This work not only highlights the potential of the catalysts for practical applications but also offers a new design approach for modulating MOFs using an alkaline hydrolysis strategy. [ABSTRACT FROM AUTHOR]

The dissolution/shuttling of sodium polysulfides, coupled with sodium dendrites growth, severely compromises the lifespan and stability of room temperature sodium–sulfur (RT Na–S) batteries. Herein, it proposes employing a functionalized porous ZIF‐based membrane (PZM) to address these two challenges. First, the metal ions embedded within the zeolitic imidazolate framework chemically bind with polysulfide anions, curtailing their detrimental shuttling. Second, the tailored porous structure of the membrane ensures a selective and uniform pathway for sodium ions, significantly reducing non‐uniform deposition and curbing dendritic sodium growth. Third, the intrinsically non‐combustible nature of the ZIF‐based membrane acts as a fortification against thermal outbursts and electrolyte decomposition. Implementing this polysulfide‐resistant, dendrite‐inhibiting and flame‐retardant PZM with a standard S/C cathode leads to the creation of a robust separator with lean electrolyte RT Na–S battery. This configuration may impart a novel perspective for the advancement and enhancement of RT Na–S battery systems. [ABSTRACT FROM AUTHOR]

The stainless steel mesh was covered by MOF-199 and applied in the four-component synthesis of 2-aminospiro[indeno[1,2-b]quinoxalin-11,4-pyran]-3-carbonitriles as a novel and efficient heterogeneous catalyst. The preparation of MOF-199-covered stainless steel mesh (MOF-199@SSM) was confirmed by FT-IR, FE-SEM and DEX analyses. MOF-199@SSM catalyst can be easily separated from the reaction mixture by simple forceps and reused. The stability of the catalyst was examined using a hot filtration test and no leaching occurred during the reaction. The reactions conditions were mild and the reaction times were relatively short. No by-product was produced, so, high purity and high yields of products were obtained. [ABSTRACT FROM AUTHOR]

An interseting Cu(II)-based organic framework containing a Cu2O5 cluster, [Cu (TBA)(CH3OH)]n (1) has been hydrothermally synthesized with tetrabromoterephthalate (H2TBA) ligand, and characterized through infrared spectroscopy (IR), elemental and thermal analysis (EA), power X-ray diffraction (PXRD), and single-crystal X-ray diffraction (SCXRD) analyses. The X-ray single-crystal diffraction analysis shows that the CuII center is hexa-coordinated and situated on perfect octahedral geometry formed by four carboxyl oxygen atoms of four symmetry-related TBA2− anions and two O-donors of two reverse µ2-CH3OH bridges. Each TBA2− ligand plays as a µ4 tetra-monodentate linker and connect four Cu2+ cations together to form the three dimensional structure of 1. Surprisingly, there are no significant hydrogen bonds and π-stack interactions in 1, but the Br···Br halogen bonds interactions. Detailed topology analysis found that the 3D cluster-based metal-organic framework of 1 can be simplified to 4 topological types: a 4-c 1-nodal net dia with point symbol {66}, a 6,6-c 2-nodal net htp with point symbol {413·62}{48·66·8}, a 4,6-c 2-nodal net bpq with point symbol {32·62·72}{34·42·64·75}, and a 6,8-c 2-nodal net 6,8T902 with point symbol {34·44·54·63}{38·414·54·62}, respectively. Moreover, 1 exhibits intense solid-state luminescence emissions centered at 478 nm at room temperature, which mainly originates from the intraligand π→ π* transitions of TBA2−. The CCDC number of 1 is 2,355,788. [ABSTRACT FROM AUTHOR]

A portable sensing platform with excellent performance was constructed using CoNi-MOF-based chitosan-polyacrylamide hydrogel as a signal amplifier for the detection of adrenaline. [Display omitted] The development of a portable smartphone-based electrochemical sensor for analyzing adrenaline levels in real samples can make a great contribution to the research community worldwide. In order to achieve this goal, the key challenge is to build sensing interfaces with excellent electrocatalytic properties. In this work, microspherical bimetallic metal–organic frameworks (CoNi-MOF) consisting of nanoclusters were first synthesized using a hydrothermal method. On this basis, the catalytic activity of pure chitosan-polyacrylamide hydrogel (CS-PAM) was modulated by adding different amounts of CoNi-MOF during the in-situ synthesis of CS-PAM. Finally, a portable electrochemical detection system based on CS-PAM was established for the detection of adrenaline. A series of resulting composite hydrogels with a large specific surface area, abundant active sites, and unique network structure facilitate the enrichment and catalysis of adrenaline molecules. Under optimal conditions, the analytical platform constructed by using CoNi-MOF-based CS-PAM has the advantages of a wide detection range (0.5–10 and 10–2500 μM), a low detection limit (0.167 μM), and high sensitivity (0.182 and 0.133 μA·μM·cm−2). In addition, the sensor maintains selective detection of the target in the presence of many different types of interferences, and the current response is not significantly reduced even after 60 cycles of testing. We strongly believe that the designed smart portable sensing can realize the accurate determination of adrenaline in complex systems, and this study can provide new ideas for the research of MOFs-based hydrogels in electrochemical analysis. [ABSTRACT FROM AUTHOR]

A MOF-derived low Ru-loaded high entropy alloy self-supporting electrode is proposed for ZABs. This work provides a good guide for improving catalytic performance. [Display omitted] Exploiting the high-entropy alloy (HEA) electrocatalysts with the synergistic effect of multi-metal components is an effective approach to address the slow kinetics and undesirable stability of the oxygen evolution reaction (OER) in Zn-air batteries (ZABs), but still faces many challenges. In this study, a multimetallic Metal-organic framework (MOF)-derived HEA catalyst was successfully fabricated on carbon fiber as a flexible self-supporting electrode (denoted as CC@FeCoNiMoRu-HEA/C) for high-performance liquid/flexible ZABs using a facile and cost-effective strategy. The three-dimensional (3D) highly open network framework and hierarchical porous structure accelerate the mass transport of OH−/O 2 and charge transfer. The electronic structure adjustment, lattice defects and high entropy effects enable the CC@FeCoNiMoRu-HEA/C catalysts to perform high OER catalytic activity and strong durability while reducing the Ru content and lowering the economic cost. In situ Raman spectra and XPS results reveal the generation of metal-OOH intermediates on the HEA surface during the OER process. In a practical demonstration, the liquid ZAB assembled with CC@FeCoNiMoRu-HEA/C + Pt/C as the air electrode offers stable open-circuit voltage, large power density, excellent specific capacity and satisfactory cycle life, outperforming the commercial RuO 2 + Pt/C-based reference ZAB. More attractively, the flexible solid-state ZAB also achieves fast dynamic response, high peak power density, robust cycling stability as well as favorable mechanical flexibility, indicating a promising application prospect in future flexible electronics and wearable devices. This work provides a viable pathway to develop low precious metal-loaded HEAs as advanced OER self-supporting electrocatalysts and realize high-performance flexible energy storage devices. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) have emerged as a class of highly promising materials for wastewater dye removal due to their unique properties. However, the existing body of research has primarily concentrated on the removal of organic dyes. To address this gap and contribute to advancements in water treatment technologies, this study investigates the efficacy of a zirconiumterephthalate-based MOF for the adsorptive removal of hematite, an inorganic dye, from aqueous environments. This investigation explored the influence of key parameters, including initial dye concentration, pH, adsorbent dosage, and adsorption temperature, on the adsorption capacity of NH2-UiO-66 for hematite. The findings revealed that elevated temperatures and initial dye concentrations promoted hematite adsorption onto NH2-UiO-66. Furthermore, the analysis of experimental data demonstrated concordance with the theoretical predictions of both the linearized Freundlich and Langmuir isotherm models. The study of kinetic models reveals that the pseudo-first-order model can adequately describe experimentally obtained data. The adsorption thermodynamic parameter ΔG0 was found to be approximately -3.70, -3.94, and -4.19 kJ.mol-1 at 298, 313, and 328 K, respectively. Furthermore, the ΔH0 and ΔS0 parameters were 5.15 kJ.mol-1 and 54.3 J.mol-1, respectively, indicating an endothermic adsorption mechanism. Further investigation found that the regeneration effectiveness is greater than 92% even after three adsorption cycles. [ABSTRACT FROM AUTHOR]

Increased energy consumption, driven by climate change and the rise of new industries, has spurred a demand for alternative cooling technologies to replace energy‐intensive systems and mitigate environmental pollution. Radiative cooling, leveraging the optical properties of materials to cool without emitting pollutants or consuming energy, is considered a suitable solution. Among the various form of radiative cooling devices, paint stands out as a practical application for radiative cooling. Hence, a passive daytime radiative cooling (PDRC) paint is developed using a polyurethane binder and zeolitic imidazolate framework (ZIF)‐8. ZIF‐8 is synthesized in an environmentally friendly manner using deionized water as the solvent, resulting in paint with a reflectance of 94.9%, emissivity of 94%, and cooling power of 113 W m−2. Temperature measurements reveal that the paint reduced ambient temperatures by an average of 5.7 °C, reaching up to 8.1 °C during the day. Additionally, with a self‐assembly monolayer coating, the PDRC surface exhibited super‐hydrophobicity and self‐cleaning capabilities. Therefore, the proposed ZIF‐8‐based PDRC paint offers sub‐room temperature cooling potential and is anticipated to reduce energy consumption for cooling, thereby alleviating environmental pollution in various applications, particularly in building exteriors. [ABSTRACT FROM AUTHOR]

The metal–organic framework (MOF) incorporation in sulfonated poly(ether ketone) (SPEEK) membranes improves the performance of proton exchange membrane fuel cells (PEMFC) that use this filler in the electrolyte. Mesoporous ZrO2/C and ZnO/C nanocomposites derived from the respective MOFs, Zr-BDC-MOF and Zn-BDC-MOF, were used as fillers in SPEEK to determine the influence of the metal (Zr or Zn) and ligand (terephthalic acid (BDC) or carbon (C)) on the proton conductivity and oxidative stability of proton exchange membranes (PEMs). At a temperature of 100 °C, the results show that adding 7 wt% of Zr-BDC-MOF to SPEEK resulted in 2.5-fold higher proton conductivity than pristine SPEEK. However, water uptake and oxidative stability studies reveal that this membrane loses its chemical stability. The data set shows that the inclusion of 7 wt% ZrO2/C to SZrC(7) membrane resulted in the best proton conductivity, ca. 2.2-fold higher than SPEEK at 100 °C, making it attractive for application in PEMFC at high temperatures. Our findings show that the influence of the metal used as a filler (Zr or Zn) is lower than that of the ligand (BDC or C) on the oxidative stability and proton conductivity of PEMFC. [ABSTRACT FROM AUTHOR]

Per- and polyfluoroalkyl substances (PFAS), a pressing environmental and public health concern due to their persistence and toxicity, especially affecting aquatic environments. Short-chain PFAS, with their high solubility and mobility in aquatic medium, have become more concentrated in water bodies. However, removing these short-chain PFAS from water is challenging and requires effective, sustainable solutions. This study evaluates MIP-202, an eco-friendly, cost-effective adsorbent, for removing PFBS, PFPeS, PFBA, and PFPeA from water. MIP-202 demonstrates exceptional performance in removing these PFAS at trace concentrations, with values of 620.5 mg/g, 603.2 mg/g, 573.9 mg/g, and 525.7 mg/g for PFBS, PFPeS, PFBA, and PFPeA, respectively. The adsorption of PFAS molecules onto MIP-202 was found to be described by Langmuir isotherm model. Also, pseudo-second-order model better described the kinetic information. Solution pH significantly influences MIP-202's efficiency, with an optimal pH of 3 for all PFAS. The removal mechanism involves electrostatic interactions between PFAS and protonated amine groups in MIP-202, along with the participation of Zr clusters in the adsorption. Remarkably, MIP-202 retains its adsorption capacity even after undergoing eight regeneration cycles. In conclusion, MIP-202 shows promise as an effective and sustainable solution for eliminating short-chain PFAS from water environments. Its exceptional performance at trace concentrations, high adsorption capacity, rapid recovery, and reusability make it an appealing choice for addressing the challenges posed by short-chain PFAS in practical applications. [ABSTRACT FROM AUTHOR]

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In this study, a new metal–organic framework (MOF) based on copper (II) functionalized with graphene oxide (MOF-Cu@GO) was successfully synthesized and applied as an efficient sorbent for dispersive micro-solid phase extraction (D-μSPE) of losartan potassium (LP) from water. The MOF-Cu@GO sorbent was characterized using DRX, FTIR, XPS, TGA, RAMAN, BET, SEM, EDX, and potential Z. The influence of different parameters in the D-μSPE method was studied and optimized using the fractional factorial design 25–1 and central composite design. The results indicated that the adsorption process was spontaneous and endothermic followed the pseudo-second order model kinetics and the Freundlich isotherm. The maximum adsorption capacity of MOF-Cu@GO sorbent was 415 mg g−1. The adsorption mechanism proposed of LP onto MOF-Cu@GO proceeded via electrostatic interaction, hydrogen bonds, unsaturated sites of the ligand, and π-π interactions. The microextraction procedure was followed by determination of LP with high performance liquid chromatography (HPLC–UV-Vis). Under optimized conditions, the limits of detection and quantitation were found to be 25 and 80 ng ml−1 respectively, the method exhibited a linear response (r = 0.998) in the concentration range of 0.1–50 µg ml−1 of LP, with a relative standard deviation less than 2% (n = 5). The D-μSPE method showed preconcentration factor of 684.9 and high percentage of LP extraction of 99.78% ± 2.62, the accuracy of the method was demonstrated by studying the recovery of LP from water samples of 100.3 ± 1.06. The material obtained can be used up to 3 cycles with time for the sorption and determination of 30 min indicating good stability and reusability. The MOF-Cu@GO proposed is an efficient and fast sorbent in the D-μSPE for determination of LP from aqueous solutions. [ABSTRACT FROM AUTHOR]

Oral ulcers are a common oral mucosal disease that seriously affect the quality of life. Traditional drug treatments have shown unsatisfactory efficacy and potential adverse reactions. In this study, curcumin-loaded multifunctional magnesium metal–organic framework-embedded hyaluronic acid-soluble microneedles patches were developed to optimize treatment strategies for oral ulcers. This microneedles patch achieves efficient release of curcumin and Mg2+ in the ulcer through precisely targeted delivery and controllable release mechanism, significantly regulates inflammation, promotes cell migration and angiogenesis, and accelerates the ulcer healing process. At the same time, the synergistic effect of curcumin and gallic acid effectively alleviated oxidative stress, while the backplate ε-poly-l-lysine and needle tip Mg2+ jointly constructed an antibacterial barrier to effectively inhibit pathogens. Verification using an oral ulcer rat model showed that the microneedles patch exhibited excellent therapeutic effects. This not only opens up a new avenue for clinical oral treatment but also marks a breakthrough in nanobiomaterials science and drug delivery technology and heralds a broad prospect in the field of oral ulcer treatment in the future. [ABSTRACT FROM AUTHOR]

This research commenced with an exploration of how metal nodes in metal‐organic frameworks (MOFs) influence photodynamic therapy (PDT) outcomes. Ultimately, it is revealed that intermolecular interactions are the core mechanism determining the optical properties and PDT efficacy of MOFs. An advanced system of MOFs based on the integration of twelve rare earth ions (RE3+) with boron dipyrromethene (BODIPY)‐derived ligands is reported. Intriguingly, this series of MOFs exhibits a reverse relationship between the radius of RE3+ and PDT efficacy. Single‐crystal X‐ray diffraction analyses along with theoretical calculations indicate that varying RE3+ results in a spatial displacement of the ligands along the dipole direction, diminishing electrostatic (dipole–dipole) interactions while enhancing dispersion (π–π) interactions, thereby enhancing the generation of triplet excitons. Consequently, a novel parameter, Ae‐v = EvdW / Eint × 100%, is proposed to quantify the interplay between non‐radiative energy dissipation via electrostatic interactions and efficient energy utilization in generating singlet oxygen through dispersion interactions. Furthermore, with consistent acoustic sensitivity aligned with the sonoluminescence mechanism, RE‐DCBs are employed in sono‐photodynamic cancer therapy, attaining significant therapeutic results in tumor treatment during in vivo experiments. [ABSTRACT FROM AUTHOR]

Electrochemical water splitting offers a promising route to sustainable hydrogen production. Metal-Organic Frameworks (MOFs) have emerged as potential electrocatalysts due to their tunable structure and composition. We investigated the electrocatalytic activity of ZIF-67 for the hydrogen evolution reaction (HER) in alkaline media. Synthesis parameters, including temperature, reaction time, acidity, molar ratio of 2-methylimidazole (2-MIM) to cobalt source, cobalt source type, addition method of 2-MIM, and solvent type, were systematically varied to optimize the electrocatalytic properties of ZIF-67. The synthesized ZIF-67 electrocatalysts were characterized using BET, FESEM, EDS, TEM, XRD, FTIR, and UV–vis spectroscopy. The electrocatalytic properties were evaluated by cyclic voltammetry (CV), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and chronoamperometry methods. The optimized ZIF-67 electrocatalyst exhibited remarkable performance, with a low overpotential of 171 mV, a small Tafel slope of 82 mV.dec−1, a low charge transfer resistance of 97 Ω, a high double-layer capacitance of 13.5 mF cm−2, and high stability for 15 h at the current density of 10 mA cm−2. The enhanced electrocatalytic activity of the optimized ZIF-67 was attributed to its high surface area, tunable pore structure, and the presence of active cobalt sites. [Display omitted] • ZIF-67 electrocatalyst with superior performance (S16) is synthesized under optimized conditions (80–120 °C, 1 h, CoSO 4 ·7H 2 O precursor, dropwise 2-MIM addition, 2-MIM/Co ratio 16:1, pH 11). • The optimized ZIF-67 electrocatalyst exhibits a well-defined rhombic dodecahedral morphology with high surface area (1370 m2gr−1.), pore volume (1.02 cm³.gr−1), and narrow band gap (1.97 eV). • The cobalt-based electrocatalyst achieves exceptional HER activity in 1 M KOH: low overpotential (ƞ 10 = 171 mV), fast kinetics (β = 82 mV.dec−1), high C dl (13.5 mF cm−2), and remarkable stability (15 h). [ABSTRACT FROM AUTHOR]

In this paper, the Co/Zn-based zeolite imidazole framework (Co/Zn-ZIF) was synthesized by an etching method. Then, a certain amount of sulfur powder was doped into it and annealed to synthesize ZnS/Co9S8 composites with a core–shell structure mechanism (CS-ZnS/Co9S8). Compared with the single-metal ZIF, which is more studied at present, the application of a bimetallic ZIF shows remarkable excellent performance in gas sensing. The test results show that the sensor with a CS-ZnS/Co9S8 film has ultrahigh sensitivity to ammonia. At its optimal operating temperature of 240 °C, the detection limit of ammonia concentration can be detected to be 0.2 ppm. At the same time, the response of the CS-ZnS/Co9S8 thin-film sensor to 5 ppm concentration of ammonia is 4.56, which is 2.85 times and 3.26 times that of the single ZnS and Co9S8 thin-film sensors. In addition, the CS-ZnS/Co9S8 thin-film sensor has a response/recovery time of 7 s/9 s and has excellent repeatability, long-term stability, selectivity, and antihumidity interference. In addition to the polyhedral core–shell mechanism formed by ZnS/Co9S8, the p–n heterojunction directly formed by ZnS and Co9S8 is also a very important factor for the substantial improvement of its sensing performance. [ABSTRACT FROM AUTHOR]

Efficient and environmentally friendly synthesis methods for metal‐organic frameworks (MOFs) have emerged as a compelling topic in the organometallic field. In this study, we successfully electro‐synthesized a MOF based on mixed ligands, benzene‐1,4‐dicarboxylate (BDC) and 4,4′‐bipyridine (Bpy), denoted as MOF‐508b, and investigated its CO2 adsorption capacity, comparing it with that of Zn‐BDC and Zn‐Bpy coordination polymers. Unlike the circular shapes of Zn‐BDC and Zn‐Bpy, MOF‐508 adopts a three‐dimensional structure upon binding with the pillar ligand, featuring mesoporous pore sizes. MOF‐508b demonstrates superior stability at room temperature, exhibiting a thermal stability of 400 °C. The CO2 capture potential of the materials was assessed under low‐pressure conditions at room temperature. The pillared layer of MOF‐508b results in the reduction of open metal sites, facilitating the binding of active CO2 through coordination, thereby influencing its optimum CO2 adsorption capacity (2.51 mmol g−1), which was found to be lower than that of Zn‐Bpy (3.83 mmol g−1) and Zn‐BDC (4.46 mmol g−1). The adsorption mechanism on MOF‐508b follows the Weber‐Morris model, emphasizing diffusion within particles over direct attachment to the material surface. [ABSTRACT FROM AUTHOR]

ABSTRACT Venturello‐structured polyoxometalates (POMs) are effective homogeneous catalysts and confining POMs to size‐matched metal‐organic frameworks (MOFs) as heterogeneous catalyst is an effective way to improve their practical application. The appropriate pore and narrow window of pristine UiO‐67 can not only enclose POMs in single molecule but also limit their leaching and can provide a suitable platform for the oxidation of most sulfur‐containing organic compound. The composite (CTA)3PW4@UiO‐67 was prepared by a facile in situ synthesis method, characterized by a variety of means and tested for desulfurization of multicomponent simulated diesel. The results prove that the active component (CTA)3PW4 is effectively encapsulated, and the composite (CTA)3PW4@UiO‐67 show remarkable desulfurization activity and excellent reusability. In addition, the kinetics and possible mechanism of the reaction were investigated. This work opens up a new idea for the design of “host‐guest adapted” catalyst suitable for fuel desulfurization technology. [ABSTRACT FROM AUTHOR]

This work introduces a robust acid‐base catalytic system based on the zirconium‐based metal‐organic framework (Zr‐MOF) MOF‐808, selected for its open structure, high stability, and low presence of structural defects compared to other Zr‐MOFs. Four bifunctional benzoate ligands bearing free carboxylic acid (‐COOH) and nitrogen‐containing groups were introduced into the MOF‐808 using solvent‐assisted ligand exchange methods. Unlike other materials, the acid and base sites in the bifunctional MOF‐808 materials are situated in the same capping ligand, leading to a bifunctional behavior between the two neighboring sites. The system was tested for Knoevenagel condensation and deacetylation‐Knoevenagel tandem reactions, demonstrating high catalytic activity and excellent yields. Additionally, computational modeling provided insights into the catalytic mechanism and the role of the acid‐base sites. The study provides a better understanding of the unique behavior of the bifunctional MOF‐808 catalyst and offers prospects for designing new and efficient catalytic systems for organocatalysis. [ABSTRACT FROM AUTHOR]

ABSTRACT A novel 3D magnesium‐based metal organic framework (Mg‐MOF) has been solvothermally synthesized using 5‐(pyridin‐4‐yl)isophthalic acid. The ligand has demonstrated to preserve two types of coordination modes depending on the connection mode of the pyridine group. The uncoordinated pyridine groups provide Lewis base sites (LBSs), whereas the coordinated ones promote to form a rarely reported eight‐connected tetranuclear Mg clusters. Benefiting from the multinuclearity with high number of connections, the framework keeps good performance of high thermal stability until 500°C. Furthermore, the framework exhibits potential open metal sites (OMSs) benefiting from the terminal coordinated water groups of the metal clusters. Owing to the abundant active sites, the Mg‐MOF exhibits good sensitivity to nitrofuran antibiotics and Cr2O72−, with high KSV (at 104 M−1 level) and low limit of detection (LOD) values (∼10−6 M). Density functional theory (DFT) investigation reveals that the interchange of the HOMO–LUMO energy levels of the framework and antibiotics is responsible for the sensing activity. In addition, the Mg‐MOF is greatly recyclable in five cycles while maintaining the structural rigidity and sensing activity, making it a promising luminescence probe material. [ABSTRACT FROM AUTHOR]

While the ambient N2 reduction to ammonia (NH3) using H2O as hydrogen source (2N2+6H2O=4NH3+3O2) is known as a promising alternative to the Haber–Bosch process, the high bond energy of N≡N bond leads to the extremely low NH3 yield. Herein, we report a highly efficient catalytic system for ammonia synthesis using the low‐temperature dielectric barrier discharge plasma to activate inert N2 molecules into the excited nitrogen species, which can efficiently react with the confined and concentrated H2O molecules in porous metal–organic framework (MOF) reactors with V3+, Cr3+, Mn3+, Fe3+, Co2+, Ni2+ and Cu2+ ions. Specially, the Fe‐based catalyst MIL‐100(Fe) causes a superhigh NH3 yield of 22.4 mmol g−1 h−1. The investigation of catalytic performance and systematic characterizations of MIL‐100(Fe) during the plasma‐driven catalytic reaction unveils that the in situ generated defective Fe−O clusters are the highly active sites and NH3 molecules indeed form inside the MIL‐100(Fe) reactor. The theoretical calculation reveals that the porous MOF catalysts have different adsorption capacity for nitrogen species on different catalytic metal sites, where the optimal MIL‐100(Fe) has the lowest energy barrier for the rate‐limiting *NNH formation step, significantly enhancing efficiency of nitrogen fixation. [ABSTRACT FROM AUTHOR]

Highlights Corrosion of steel is one of the challenging issues that researchers has focused on it. Among corrosion control methods, organic coatings with suitable lifetime and efficiency are a great of interest. In the present research, polyaniline‐ copper‐based metal organic framework (PANI‐Cu‐MOF) is synthesized using in‐situ oxidation polymerization method and successfully characterized with different techniques. Then, 0.5, 1, and 1.5 wt. % of PANI‐Cu‐MOF composite are added to vinyl ester (VE) resin based on bisphenol A and coated on ST37 steel. The performance of the as‐prepared coatings on ST37 is evaluated using electrochemical impedance spectroscopy (EIS) for 360 h. The EIS results showed that loading of PANI‐Cu‐MOF (0.5 wt. %) in VE led to the highest protective properties against aggressive species with |Z|0.01 Hz = 6.76 × 107 Ωcm2 after 360 h. The uniform distribution of PANI‐Cu‐MOF composite in VE and its hydrophobic property causes a delay in the penetration of the corrosive species into the coating, thus increasing the corrosion resistance. PANI‐Cu‐MOF composite is embedded to VE resin as novel anti‐corrosive pigment. The highest Rcoat are achieved for VE‐PANI‐Cu‐MOF 0.5 wt. %. In the presence of PANI‐Cu‐MOF, the corrosive species penetrations decreased. [ABSTRACT FROM AUTHOR]

The rational utilization of hydrogen is crucial for addressing the challenges of resource depletion and environmental pollution resulting from rapid industrialization. However, the development of the hydrogen industry is significantly hindered by inadequate hydrogen storage technologies and materials. As a new type of porous crystalline materials with ultra-high specific surface area, tunable pore sizes and structure as well as tailorable chemical functionality, metal-organic framework materials (MOFs) hold great promise for efficient hydrogen storage. In this review, we summarize the recent and important progress of MOFs for hydrogen storage, and provide a comprehensive understanding by exploring the influencing factors, mechanisms, and strategies for improving hydrogen storage capacity. Special emphasis is given to the influence of pore structure, isosteric enthalpy of hydrogen adsorption and synthesis parameters on the hydrogen storage capacity of MOFs. And the strategies for enhancing hydrogen storage performance of MOFs are also systematically introduced and discussed. Finally, we present a short conclusion give a brief outlook on the future development of MOFs as hydrogen storage materials, providing guidance for the rational design and synthesis of advanced MOFs suitable for hydrogen storage. • Recent and important progress of MOFs for H 2 storage is summarized. • Factors, mechanisms, and strategies for improving H 2 storage capacity in MOFs are analyzed. • Pore structure, adsorption enthalpy, synthesis parameter of MOFs are emphasized. • Challenges and new trends of MOFs for H 2 storage are prospected. [ABSTRACT FROM AUTHOR]

Photocatalytic nitrate reduction reaction (NitRR) is a promising route for environment remediation and sustainable ammonia synthesis. To design efficient photocatalysts, the recently emerged nanoarchitectonics approach holds great promise. Here, we report a nanohouse‐like S‐scheme heterjunction photocatalyst with high photocatalytic NitRR performance. The nano‐house has a floor of plate‐like metal organic framework‐based photocatalyst (NH2‐MIL‐125), on which another photocatalyst Co(OH)2 nanosheet is grown while ZIF‐8 hollow cages are also constructed as the surrounding wall/roof. Experimental and simulation results indicate that the positively charged, highly porous and hydrophobic ZIF‐8 wall can modulate the environment in the nanohouse by (i) NO3− enrichment/NH4+ discharge and (ii) suppression of the competitive hydrogen evolution reaction. In combination with the enhanced electron‐hole separation and strong redox capability in the NH2‐MIL‐125@Co(OH)2 S‐scheme heterjunction confined in the nano‐house, the designed photocatalyst delivers an ammonia yield of 2454.9 μmol g−1 h−1 and an apparent quantum yield of 8.02 % at 400 nm in pure water. Our work provides new insights into the design principles of advanced photocatalytic NitRR photocatalyst. [ABSTRACT FROM AUTHOR]

Noble gas xenon (Xe) is an excellent anesthetic gas, but its rarity, high cost and constrained production prohibits wide use in medicine. Here, we have developed a closed‐circuit anesthetic Xe recovery and reusage process with highly effective CO2‐specific adsorbent CUPMOF‐5 that is promising to solve the anesthetic Xe supply problem. CUPMOF‐5 possesses spacious cage cavities interconnected in four directions by confinement throat apertures of ~3.4 Å, which makes it an ideal molecular sieving of CO2 from Xe, O2, N2 with the benchmark selectivity and high uptake capacity of CO2. In situ single‐crystal X‐ray diffraction (SCXRD) and computational simulation solidly revealed the vital sieving role of the confined throat and the sorbent‐sorbate induced‐fit strengthening binding interaction to CO2. CUPMOF‐5 can remove 5 % CO2 even from actual moist exhaled anesthetic gases, and achieves the highest Xe recovery rate (99.8 %) so far, as verified by breakthrough experiments. This endows CUPMOF‐5 great potential for the on‐line CO2 removal and Xe recovery from anesthetic closed‐circuits. [ABSTRACT FROM AUTHOR]

[Display omitted] • Plastics waster derived defective d -UiO-66 was synthesized by solvent-free routine. • d -UiO-66 possesses higher surface areas and pore volume than pristine UiO-66. • The LOM adsorption capacity of d -UiO-66 is 3.5 times of UiO-66. • d -UiO-66 exhibits the record LOM adsorption capacity of 588 g mg−1. • Defects in d -UiO-66 promote the mass transfer and create more active sites. Large amount of polyethylene terephthalate (PET) plastics waster and emerging contaminants in water, including fluoroquinolone antibiotics, pose challenges to human survival. In this work, a green synthesis scheme is proposed in which the defective UiO-66 (d -UiO-66) is fabricated via a solvent-free routine by using PET plastics waster as raw materials for lomefloxacin (LOM) removal. In comparison with defect-free UiO-66, the created defect imparts d -UiO-66 with higher porosity and abundant defective Zr sites, which are beneficial to boost LOM adsorption. As expected, d -UiO-66 exhibited excellent LOM adsorption performances, showcasing a saturation adsorption capacity of 588 mg g−1 and a kinetic rate constant of 0.204 g mg−1 h−1, which are 3.5 and 2.0 times higher than those of the pristine UiO-66, respectively. Remarkably, the LOM saturation adsorption capacity of d -UiO-66 surpasses that of all reported adsorbents. Mechanism study reveals that this outstanding adsorption performance of d -UiO-66 is mainly ascribed to the abundant defective sites, high porosity, together with the strong hydrogen bonding interaction and π-π stacking interaction between d -UiO-66 and LOM. Therefore, the d -UiO-66 obtained by the solvent-free method can not only effectively upcycle PET plastic waster, but also efficiently remove LOM, demonstrating a potential routine to simultaneous address the solid PET waster and wastewater. [ABSTRACT FROM AUTHOR]

Gases are essential for various applications relevant to human health, including in medicine, biomedical imaging, and pharmaceutical synthesis. However, gases are significantly more challenging to safely handle than liquids and solids. Herein, we review the use of porous materials, such as metal‐organic frameworks (MOFs), zeolites, and silicas, to adsorb medicinally relevant gases and facilitate their handling as solids. Specific topics include the use of MOFs and zeolites to deliver H2S for therapeutic applications, 129Xe for magnetic resonance imaging, O2 for the treatment of cancer and hypoxia, and various gases for use in organic synthesis. This Perspective aims to bring together the organic, inorganic, medicinal, and materials chemistry communities to inspire the design of next‐generation porous materials for the storage and delivery of medicinally relevant gases. [ABSTRACT FROM AUTHOR]

The high risk of CO poisoning justifies the need for indoor air quality control and warning systems based on the detection of low concentrations (ppm‐ppb) of CO. Cobalt corrole complexes selectively bind CO vs. O2, CO2, N2, opening new fields of applications. By combining the CO chemisorption properties of cobalt corroles with the known sorption capacity of MOFs, we hope to obtain high performance sensing materials for CO detection. In addition, the exposed metal sites of MOFs lead to CO2 physisorption, allowing the co‐detection of CO and CO2. In this work, PCN‐222, a stable Zr‐based MOF made from Ni(TCPP) with natural vacancies, has been used as a porous matrix for the grafting of electron‐poor metallocorroles. The materials were characterized by powder XRD, SEM and optical microscopy, BET analyses and gas adsorption measurements at 298 K. No degradation of the crystalline structure of PCN‐222 was observed. At 1 atm, the adsorbed CO(g) volumes measured for the best materials were 12.15 cm3 g−1 and 14.01 cm3 g−1 for CoCorr2@PCN‐222 and CoCorr3@PCN‐222 respectively, and both materials exhibited high CO chemisorption and selectivity against O2, N2, and CO2 at low pressure due to the highest energy of the chemisorption process vs physisorption. [ABSTRACT FROM AUTHOR]

Solar‐driven interfacial evaporation (SIE) of brine may solve the fresh water shortage issue but suffers from salt‐fouling. Meanwhile, adsorption can extract valuable lithium (Li) from brine but is hampered by low adsorption capacity/rate, additional energy input and low selectivity, etc. Here, as a proof‐of‐concept, the design of a separated solar evaporator (S‐evaporator) is reported for simultaneously efficient fresh water collection and Li+ selective adsorption by SIE of brine, accomplishing their complementation using only sunlight. The S‐evaporator consists of a tilted n‐shaped H2TiO3‐modified fabric and a photothermal sheet on it. The superhydrophilic fabric transports brine to the photothermal sheet and provides affluent sites for Li+ adsorption. The photothermal sheet promotes SIE and enhances Li+ adsorption by significantly increasing the fabric's temperature. Consequently, simultaneous fresh water collection and Li+ selective adsorption are realized by the S‐evaporator. Under 1 kW m−2 illumination, the S‐evaporator shows long‐term stable evaporation rate (1.51 kg m−2 h−1) for 20 wt% brine, high Li+ adsorption capacity (20.09 mg g−1), good Li+ adsorption selectivity from real brine and good cycle stability. The S‐evaporator has great application potential for efficiently extracting fresh water and Li+ from brine as demonstrated by the large SIE setup in real outdoor conditions. [ABSTRACT FROM AUTHOR]

Metal‐organic frameworks (MOFs) can effectively remove methylene blue (MB) from wastewater due to their abundant adsorption sites and multi‐level pores. In this paper, a copper‐based MOF: {[Cu ⋅ (L) ⋅ (H2O)] ⋅ (DMF)}n (1) (H2L=2‐hydroxyterephthalic acid; DMF=N,N‐dimethylformamide), was synthesized by hydrothermal synthesis method. X‐ray single crystal diffraction showed that a two‐dimensional structure was formed by the carboxyl group of L2− in 1 took μ2‐η1 : η1 bridged two adjacent Cu(II). In this two‐dimensional structure, the coordinated water molecules and hydroxyl group on L2− were distributed on the surface of 1. Thus, it had abundant adsorption sites. The transmission electron microscopy (TEM) of copper‐based MOF nano adsorbent showed that the particle diameter of the nano adsorbent prepared by a cell fragmentation apparatus was about 50 nm. The performance of the copper‐based MOF nano adsorbent in adsorbing MB indicated that the optimal adsorbent dosage was 0.20 g/L and the solution pH was 6. Under the optimal experimental conditions, its maximum adsorption capacity for MB was 143.3 mg/g, which was superior to most MOFs adsorbents. The adsorption thermodynamic analysis showed that the copper‐based MOF nano adsorbent at 25–45 °C was an exothermic (ΔH<0), and spontaneous (ΔG<0) process. [ABSTRACT FROM AUTHOR]

Polypyrrole (PPy) is favoured in energy storage for its high pseudo-capacitive performance, notably as polypyrrole nanotubes (PPyNTs) due to their easy synthesis, cost-effectiveness and electrochemical solid properties. Metal-organic frameworks (MOFs) have also gained attention for enhancing supercapacitors (SCs). In this study, we fabricated aerogel composites with PPyNTs, MOFs and reduced graphene oxide (rGO) as SC electrode materials. Varying concentrations of PPyNTs and rGO were explored, with MOFs added to assess their impact. Electrochemical tests revealed that the composite with PPyNTs and Zn-MOF achieved the highest specific capacitance of approximately 270 F/g at 0.5 A/g. [ABSTRACT FROM AUTHOR]

A multifunctional, multiphase-supported photocatalyst was fabricated via the combination of LCD three-dimensional (3D) printing, cold plasma discharge (CPD) technology, and surface chemistry to be used for the degradation of organic pollutants in water and for the generation of hydrogen gas. BiOBr was chosen as the main catalytic phase and was used in association with a phosphor, SrAl2O4:Eu2+,Dy3+ (SAED), and a metal–organic framework, Ni-BDC. Their immobilization was realized thanks to polydopamine (PDA), which is used as a coupling agent. While BiOBr was the most active photocatalytic phase, the phosphor acted as a light-storing component for photodegradation in the dark and overall, as a boost for photoactivity. PDA also boosted the photoactivity, in parallel with its crucial role in the immobilization of the SAED/Ni-MOF/BiOBr catalyst on fractal polymer support. An in situ complexation-assisted precipitation (ISCAP) process was used, allowing the formation of the catalytic phases with nano features. The resulting hybrid photocatalysts were tested through rhodamine B (RhB) dye photodegradation upon visible light irradiation or light/dark alternating conditions to simulate more realistic variable light illumination. We found that, although used in a very small amount, the Ni-MOF had a significant impact on the photoactivity, forming a Z-scheme heterojunction with BiOBr. Finally, H2 evolution testing further established the photocatalytic activity and versatility of the supported catalysts. [ABSTRACT FROM AUTHOR]

Small molecule organic materials are widely used as anode materials for lithium‐ion batteries (LIBs) due to their high reversible capacity, designable structure, and environmental friendliness. However, they suffer from poor intrinsic electronic conductivity, severe dissolution, and low initial coulombic efficiency. Recently, metal–organic frameworks (MOFs) have demonstrated in metal‐ion batteries, outperforming some small molecule organic materials in terms of both cycling stability and rate capability. Herein, the first rational design and synthesis of a new cobalt‐based MOF (CoBPDCA), are reported employing cobalt(II) nitrate as the metal source and small organic molecules (2,2‐bipyridyl‐4,4‐dicarboxylic acid, BPDCA) as the ligands, which shows exceptional chemical stability and impressive electron conductivity. Most importantly, CoBPDCA electrodes deliver a high reversible capacity of 1112.9 mAh g−1 at 0.05 C (1 C = 1000 mA g−1) and outstanding high‐rate durability (166.3 mAh g−1 after 2500 cycles at 10 C). Employing a series of spectroscopic and morphological characterizations and density functional theory (DFT) calculations, it is revealed that these impressively electrochemical performances are contributed to the dual active redox centers of Co cations and BPDCA ligands (CN and CO groups), and the superb electron conductivity. This work might provide a new strategy and a deeper understanding of the other MOFs' development for LIBs. [ABSTRACT FROM AUTHOR]

Designing multifunctional materials that mimic the light‐dark decoupling of natural photosynthesis is a key challenge in the field of energy conversion. Herein, we introduce MnBr‐253, a precious metal‐free metal–organic framework (MOF) built on Al nodes, bipyridine linkers and MnBr(CO)3(bipyridine) complexes. Upon irradiation, MnBr‐253 colloids demonstrate an electron photocharging capacity of ~42 C ⋅ g−1MOF, with state‐of‐the‐art photocharging rate (1.28 C ⋅ s−1 ⋅ g−1MOF) and incident photon‐to‐electron conversion efficiency of ~9.4 % at 450 nm. Spectroscopic and computational studies support effective electron accumulation at the Mn complex while high porosity and Mn loading account for the notable electron storage performance. The charged MnBr‐253 powders were successfully applied for hydrogen evolution under dark conditions thus emulating the light‐decoupled reactivity of photosynthesis. [ABSTRACT FROM AUTHOR]

In nature, catechol oxidase catalyzes the oxidation of o‐diphenol to o‐quinone to produce a series of highly important polyphenolic natural products. Although mimicking the functionality of natural enzyme using a nanozyme was found to be beneficial, attaining a high specificity is challenging. Herein, we have explored the thickness‐dependent oxidase activity and specificity of Cu‐metal‐organic framework (MOF) nanosheets. The unique synthetic method offers control over the thickness of the Cu‐MOF nanosheets. The ultrathin (4 nm) Cu‐MOF (Cu‐UMOF) nanosheets as an oxidase nanozyme exhibit high specificity for catechol oxidation without having any peroxidase activity. Interestingly, the thicker (20–30 nm) Cu‐MOF nanosheets showed poor catechol oxidase and peroxidase activity. The binuclear Cu‐center, coordinative, and electronic unsaturation tuned electronic structure in Cu‐UMOF, resulting in higher specificity for catechol oxidation than thicker Cu‐MOF. [ABSTRACT FROM AUTHOR]

Novel antimicrobial strategies are urgently needed to treat extensively drug‐resistant (XDR) bacterial infections due to the high mortality rate and lack of effective therapeutic agents. Herein, nanoengineered human umbilical cord mesenchymal stem cells (hUC‐MSCs), named PMZMU, are designed as a sonosensitizer for synergistic sonodynamic‐nano‐antimicrobial therapy against gram‐negative XDR bacteria. PMZMU is composed of a bacterial targeting peptide (UBI29‐41) modified hUC‐MSCs membrane (MSCm), a sonosensitizer meso‐tetra(4‐car‐boxyphenyl) porphine doped mesoporous organo‐silica nanoparticle and an acidity‐responsive metal–organic framework ZIF‐8. This innovative formulation enables efficient loading of polymyxin B, reduces off‐target drug release, increases circulation and targeting efficacy, and generates reactive oxygen species upon ultrasound irradiation. PMZMU exhibits remarkable in vitro inhibitory activity against four XDR bacteria: Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa (PA), and Escherichia coli. Taking advantage of the bacterial targeting ability of UBI29‐41 and the inflammatory chemotaxis of hUC‐MSC, PMZMU can be precisely delivered to lung infection sites thereby augmenting polymyxin B concentration. PMZMU‐mediated sonodynamic therapy significantly reduces bacterial burden, relieves inflammatory damage by promoting the polarization of macrophages toward M2 phenotype, and improves survival rates without introducing adverse events. Overall, this study offers promising strategies for treating deep‐tissue XDR bacterial infections, and guides the design and optimization of biomimetic nanomedicine. [ABSTRACT FROM AUTHOR]

Developing films of chiral metal–organic frameworks (MOFs) with high circular polarization luminescence (CPL) is facing a great challenge for chiral sensing applications. Herein, a layer‐by‐layer chiral induction method is first reported to prepare enantiopure MOF films for CPL sensing. By layer‐by‐layer induction with the chiral inductor camphorsulfonic acid, fluorene‐based chiral MOF D/L‐ZnHF‐SO2 film (HF‐SO2 = 3,7‐Dibenzothiophenedicarboxylate, 5,5‐dioxide) with preferential growth orientation and homogeneous surface are prepared, which shows strong chiral feature and CPL with higher asymmetry factor of ±0.073. In addition, by mixed ligand approach, the isostructural fluorene ligand 9‐fluororenone‐2,7‐dicarboxylate is chosen to replace part of HF‐SO2 for preparing a series of chiral MOF films with tunable CPL emission. Furthermore, the prepared chiral MOF films with strong CPL performance are further utilized for enantiomers sensing. The CPL changes consisted with enantioselective adsorption results showed that D/L‐ZnHF‐SO2 film has good discrimination against chiral R/S‐phenylethylamine enantiomers, first reporting chiral MOF‐based candidates for the application in CPL sensing of enantiomers. This work provides a facile and effective approach for preparing chiral MOF films materials with high and tunable CPL performance, and also gives a new way to achieve CPL sensing of chiral enantiomers. [ABSTRACT FROM AUTHOR]

In a project to preserve photographic archives in Southeast Asia, the authors sought to develop sustainable solutions with low environmental impact, avoiding air conditioning and using locally available materials. Dry cabinets were tested and implemented to store a glass plate negative collection that was rehoused in envelopes and boxes made locally. The project took just over a year to complete, and two years of monitoring environmental conditions have shown that relative humidity can be stabilized at low levels. However, the dry cabinets are airtight to limit the introduction of moisture and dust, preventing air exchange. In order to avoid the build-up of degradation by-products released by the stored materials, and in particular off-gassing of acetic acid from the cellulose acetate-based photographs, the use of an adsorbent is necessary. To achieve this, a cellulose-based composite with particles of a porous hybrid inorganic/ organic solid, denoted as a metal–organic framework (MOF), at a very high loading over 70% by weight and shaped as a sheet of paper, has been prepared and tested. This special paper maintains acetic acid-free air in the cabinets and also helps to reduce the energy consumption by reducing the need for cool storage. This MOF paper composite traps small carboxylic acids and was found to be an appropriate solution for maintaining clean air in the dry cabinets or any other confined space or enclosure. Additionally, it can also be designed to trap other noxious pollutants such as hydrogen sulfide or formaldehyde, by choosing other MOFs. [ABSTRACT FROM AUTHOR]

In the present era, a significant amount of research work is focused on eco‐friendly technologies and advanced liquid waste management strategies. Notably, industries primarily textile chemical processing sectors which are inherently involved with a wide array of dye usage, are integral focal points for these transformative endeavors. Against this backdrop, we have successfully synthesized an innovative photocatalyst with a remarkable capability to rapidly neutralize deleterious dyes within an astonishingly brief span of 4–6 minutes, facilitated by exposure to UV‐visible irradiation. Briefly, our approach entails the hydrothermal synthesis of a composite material based on zinc stannate (ZnSnO3) nanoparticles integrated with the copper‐decorated metal‐organic framework (ZnSnO3@H3BTC‐Cu MOF). The resulting material is endowed with a crystalline and porous architecture that confers a specific surface area measuring 437.25 m2 g−1, a value surpassing that of unadorned nano‐ZnSnO3 by a factor of approximately 15 (29.11 m2 g−1). Noteworthy beyond its enhanced surface features, the newly synthesized ZnSnO3@H3BTC−Cu MOF exhibits remarkable antibacterial efficacy against gram‐positive S. aureus and gram‐negative E. coli bacterial strains. It might also be considered a stable photocatalyst to be used in wastewater treatment, as evidenced by the photoelectrochemical and photocatalytic investigation. [ABSTRACT FROM AUTHOR]

ABSTRACT In this study, a Fe‐MOF was synthesized via a coprecipitation procedure and then used as support for stabilizing Ag ions and producing three‐dimensional cluster bud Ag2O@Fe‐MOF nanoflower composite (3D CB Ag2O@Fe‐MOF NFC) by microwave irradiation. The synthesized 3D CB Ag2O@Fe‐MOF NFC was applied as a heterogeneous nano‐organocatalyst in green and new preparation of naphthopyranopyrimidines via three‐component condensation of aryl aldehydes, β‐naphthol, and barbituric acids in the solvent‐free conditions at 100°C. Convenience, solvent‐free conditions, good yield, and short reaction time make this strategy a promising candidate compared to other methods. The reusability and high efficiency of this catalyst four times without any notable loss of its activity makes this strategy attractive for large‐scale eco‐friendly applications. [ABSTRACT FROM AUTHOR]