Search Results (56)

Formic acid (FA) has emerged as a promising liquid hydrogen storage material, yet efficient photothermal dehydrogenation catalysts with high activity and H₂ selectivity remain challenging. Herein, a polymetallic synergistic PdCu/M-ZNC (where M represents the co-doped In, Sn and Mo species) is fabricated by molten-salt-assisted pyrolysis of ZIF-8 precursors followed by metal incorporation. The unique molten salt environment effectively preserves the porous architecture of ZIF-8, enabling the secure anchoring of PdCu alloy nanoparticles onto the carbonaceous matrix enriched with M-N_x coordination sites. Under light irradiation, the PdCu alloy sites kinetically accelerated the overall adsorption and activation of FA molecules. Based on empirical observations and corroborated by the established literature, this alloying effect was inferred to facilitate the C-H bond cleavage and HCOO* desorption processes. Concurrently, the M-N_x sites act as efficient electron transfer channels, facilitating the rapid coupling of photogenerated electrons with protons (H⁺) to evolve H₂. Consequently, the optimal catalyst exhibits an enhancement in gaseous product yield (404.46 mmol/g/h) and H₂ selectivity (67.49%) at 75 °C. This work offers a catalyst design that aligns with several principles of green chemistry: it maximizes the atom utilization of precious Pd, incorporates synergistic non-precious metals within MOF-derived frameworks to enhance stability, and leverages solar energy to drive hydrogen production under mild conditions, presenting a more sustainable pathway for hydrogen release from liquid carriers. 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

Gas sensors based on metal oxide semiconductors (MOS) have attracted significant attention in monitoring of methane emission and leakage monitoring due to their high sensitivity, fast response time, simple structure and low cost. However, the high power consumption caused by long-term high-temperature operation of MOS sensors restricts their application in mobile and portable devices. In this study, MOF-derived Co₃O₄ dodecahedrons for low-concentration methane detection at room temperature was prepared using Zeolitic Imidazolate Framework-67 (ZIF-67) as a template and with various calcination temperatures. Among them, the Co₃O₄-350 calcined at 350 °C exhibited the optimal CH₄ sensing performance at room temperature, with a response of R_g/R_a = 1.53 to 2000 ppm CH₄. This enhanced gas sensing performance is attributed to the highest Co³⁺ proportions and the largest specific surface area in Co₃O₄-350 nanomaterials, which provided more active sites for gas adsorption and reaction. To address the challenge of slow response speed and irrecoverability during CH₄ detection at room temperature, the Co₃O₄ nanomaterials were printed onto a micro-heater plate (MHP) to form a MEMS gas sensor. By introducing a pulse heating mode to the MEMS sensor, the response and recovery time were significantly reduced to 26 s and 21 s, respectively. This enhancement improves both the efficiency and reliability of the MEMS gas sensor for early-stage detection of CH₄ leaks in various industrial applications. Full article

The contamination of water resources by high concentrations of organic dyes poses severe threats to human health, making the removal of these pollutants critical. Metal–organic frameworks (MOFs) have shown promising potential in dye adsorption due to their high surface area and chemical stability. Zeolitic imidazolate framework-8 (ZIF-8), a typical MOF, is known for its thermal stability and is frequently used in removing organic dyes. To enhance its adsorption performance, ZIF-8 is often carbonized to form porous carbon-based materials. However, carbonized ZIF-8 (CZ) often demonstrates restricted adsorption capacity and sluggish kinetics. To address these limitations, we chemically modified low-temperature carbonized ZIF-8 (CZ-550) with polyethyleneimine (PEI) using cyanuric chloride (CC) as a crosslinking agent, producing a novel composite (CZ@PEI/CC-7) featuring abundant amine-rich active sites for adsorption. This study evaluated the adsorption performance of CZ@PEI/CC-7 in removing methyl orange (MO) dye. Our findings reveal that CZ@PEI/CC-7 exhibits accelerated adsorption kinetics aligning with the pseudo-second-order kinetic model, while its isotherms fit the Freundlich and Temkin models, highlighting a favorable multilayer adsorption. Significantly, CZ@PEI/CC-7 achieved an adsorption capacity of 3150 mg/g for MO, compared to 1100 mg/g for unmodified CZ-550. Furthermore, the composite demonstrated excellent acid-base stability across a broad pH range (2–12), retaining structural integrity and adsorption efficiency. These findings suggest that CZ@PEI/CC-7 is a promising candidate for efficient MO removal from water. Full article

The recalcitrance and biological toxicity of phenolic pollutants pose a serious threat to the safety of aquatic environments, and developing efficient and stable catalytic degradation technologies is a key research focus in the current environmental field. In this study, a composite material (MSN) of NH₂-MIL-101(Fe) modified by MoSe₂ nanosheets was constructed via a one-step composite strategy, aiming to address the bottlenecks of low Fe³⁺/Fe²⁺ cycling efficiency and iron ion leaching in traditional Fe-based MOFs when activating peroxymonosulfate (PMS). Characterization results showed that MoSe₂ nanosheets were uniformly dispersed on the surface of NH₂-MIL-101(Fe), and strong electronic interactions existed between them, which significantly optimized the electronic environment of active sites. MSN-3 exhibited excellent performance in activating PMS for phenol degradation: the degradation rate reached 90% within 30 min, with a k = 0.073 min⁻¹, which was much higher than that of other systems. It also showed good structural stability and cyclic regeneration ability. Mechanistic studies confirmed that the core active species in the MSN-3/PMS system are ¹O₂, •SO₄⁻ and •OH. The two-dimensional layered structure of MoSe₂ can serve as an efficient electron transport bridge to promote Fe³⁺/Fe²⁺ cycling; amino modification further optimizes the electron density of Fe active centers. The two synergistically construct a dual redox cycle of Fe³⁺/Fe²⁺ and Mo⁴⁺/Mo⁶⁺, significantly enhancing PMS activation efficiency and ¹O₂ production. This study provides a new strategy for designing Fe-MOFs-based PMS activation catalysts and also offers technical support for the practical treatment of recalcitrant organic pollutants in water. Full article

Four different MIL-68(Al) catalysts were synthesized and characterized by XPS, SEM, TEM, XRD, DLS, Nitrogen adsorption removal, and other methods. An aluminum-based MOF (Metal Organic Framework) (MIL-68(Al))/graphite oxide (GO) composite with TiO₂ showed the largest BET specific area with best adsorption performance. Representation demonstrated that MIL-68(Al) and TiO₂ nanoparticles are uniformly dispersed on the surface of the GO lamellar, and a tight heterojunction structure is formed between them. The MIL-68(Al)/GO/TiO₂ exhibits good pore characteristics, structural morphology, and catalytic performance. Adsorption experiments of methyl orange can reach 99.7% with the effect of MIL-68(Al)/GO/TiO₂ in water for 20 min. Moreover, the pH range can be applied to 1–13 and a high concentration of 200 mg/L methyl orange solution also worked well. In addition, this kind of catalyst can also be used for rhodamine B, methylene blue, congo red, and tetracycline in 20 min with good adsorption. Meanwhile, simple filtration can quickly recover MIL-68(Al)/GO/TiO₂ and effectively reuse it. Free radical capture experiments showed a large number of •OH radicals during the adsorption of MO (Methyl Orange) solution by MIL-68(Al)/GO/TiO₂. Meanwhile, the electrostatic interaction, π-π packing and hydrogen bonding make MIL-68(Al)/GO/TiO₂ have a higher adsorption capacity for MO. Therefore, co-doping optimized the structure of MIL-68(Al), enhancing its stability in strong acids and bases while improving adsorption performance across a broader pH range than previously reported. This work addresses the instability of MIL-68(Al) under extreme conditions, demonstrating its significant potential for wastewater treatment applications. Full article

The complex system of high-entropy materials makes it challenging to reveal the specific function of each site for oxygen evolution reaction (OER). Here, with nickel foam (NF) as the substrate, FeCoNiCrMo/NF is designed to be prepared by metal–organic frameworks (MOF) as a precursor under an argon atmosphere. XRD analysis confirms that it retains a partial MOF crystal structure (characteristic peak at 2θ = 11.8°) with amorphous carbon (peaks at 22° and 48°). SEM-EDS mapping and XPS demonstrate uniform distribution of Fe, Co, Ni, Cr, and Mo with a molar ratio of 27:24:30:11:9. Electrochemical test results show that FeCoNiCrMo/NF has excellent OER characteristics compared with other reference prepared samples. FeCoNiCrMo/NF has an overpotential of 285 mV at 100 mA cm⁻² and performs continuously for 100 h without significant decline. The OER mechanism of FeCoNiCrMo/NF further reveal that Co and Ni are true active sites, and the dissolution of Cr and Mo promote the conversion of active sites into MOOH following the lattice oxygen mechanism (LOM). The precipitation–dissolution equilibrium of Fe also plays an important role in the OER process. The study of different reaction sites in complex systems points the way to designing efficient and robust catalysts. Full article

Aerogel sponges of bio-based polymers loaded with metal–organic frameworks (MOFs) are highly promising for environmental applications, but a central challenge is to improve their stability and efficiency for removal processes. Here, the effective incorporation of the MOFs MIL-100(Fe) and ZIF-8 in composite aerogels of chitosan–pectin–lactic acid is reported. The presence of pectin was critical to loading the MOFs efficiently and homogeneously, while the incorporation of lactic acid induced a large increase in the Young’s modulus and provided structural preservation in aqueous solutions. The presence of MOFs enhanced the removal of two dyes, methyl orange (MO) and methylene blue (MB), under batch and flow conditions, with removal efficiencies of methyl orange of about 85% and 90% when loaded with ZIF-8 and MIL-100(Fe), respectively. Bentonite, celite 545, and two ionenes were loaded for comparison. Factors beyond charge-to-charge electrostatic interactions influenced the removal, since no correlations were obtained between the electrical charges of dyes, fillers, and polymers. The kinetic data were analyzed by adapting the Langmuir kinetic model, incorporating absorption and desorption processes, which allowed the recovery of the respective rate constants. Full article

This study examined the effect of build orientation on the surface finish of micro-optofludic (MoF) devices fabricated via a polydimethylsiloxane (PDMS)-based 3D-printing primary–secondary fabrication protocol, where an inkjet 3D-printing technique was implemented. The molds (i.e., primaries) for fabricating the MoF devices were 3D-printed in two orientations: along $XY$ (Dev-1) and across $YX$ (Dev-2) the printhead direction. Next, the surface finish was characterized using a profilometer to acquire the primary profile of the surface along the microchannel’s edge. The results indicated that the build orientation had a strong influence on the latter, since Dev-1 displayed a tall and narrow Gaussian distribution for a channel width of 398.43 ± 0.29 µm; Dev-2 presented a slightly lower value of 393.74 ± 1.67 µm, characterized by a flat and broader distribution, highlighting greater variability due to more disruptive, orthogonally oriented, and striated patterns. These results were also confirmed by hydrodynamically testing the two MoF devices with an air–water slug flow process. A large experimental study was conducted by analyzing the mean period trend in the slug flow with respect to the imposed flow rate and build orientation. Dev-1 showed greater sensitivity to flow rate changes, attributed to its smoother, more consistent microchannel geometry. The slightly narrower average channel width in Dev-2 contributed to increased flow velocity at the expense of having worse discrimination capability at different flow rates. This study is relevant for optimizing 3D-printing strategies for the fabrication of high-performance microfluidic devices, where precise flow control is essential for applications in biomedical engineering, chemical processing, and lab-on-a-chip systems. These findings highlight the effect of microchannel morphology in tuning a system’s sensitivity to flow rate modulation. Full article

Doping undermines fairness in sports and threatens athlete health, while conventional detection methods like LC-MS and GC-MS face challenges such as complex procedures, matrix interferences, and lengthy processing times, limiting on-site applications. Two-dimensional (2D) materials, including graphene, MoS₂, and metal–organic frameworks (MOFs), offer promising solutions due to their large surface areas, tunable electronic structures, and special interactions with doping agents, such as hydrogen bonding, π-π stacking, and electrostatic forces. These materials enable signal transduction through changes in conductivity or fluorescence quenching. This review highlights the use of 2D materials in doping detection. For example, reduced graphene oxide–MOF composites show high sensitivity for detecting anabolic steroids like testosterone, while NiO/NGO nanocomposites exhibit strong selectivity for stimulants like ephedrine. However, challenges such as environmental instability and high production costs hinder their widespread application. Future efforts should focus on improving material stability through chemical modifications, reducing production costs, and integrating these materials into advanced systems like machine learning. Such advancements could revolutionize doping detection, ensuring fairness in sports and protecting athlete health. Full article

This study successfully prepared MIL-101(Fe)@MoS₂ composite photocatalysts via hydrothermal methods to address the efficient removal of refractory organic dyes in dye wastewater. Characterization using X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) confirmed that molybdenum disulfide (MoS₂) was uniformly loaded onto the surface of MIL-101(Fe), forming a heterojunction that significantly enhanced light absorption capacity and charge separation efficiency. In a visible-light-driven photo-Fenton system, this material exhibited excellent degradation performance for Congo red (CR). At an initial CR concentration of 50 mg/L, a catalyst dosage of 0.2 g/L, 4 mL of added H₂O₂, and pH 7, CR was completely degraded within 30 min, with the total organic carbon (TOC) removal reaching 72.5%. The material maintained high degradation efficiency (>90%) across a pH range of 3–9, overcoming the traditional Fenton system’s dependency on acidic media. Radical-trapping experiments indicated that superoxide radicals (·O₂⁻) and photogenerated holes (·h⁺) were the primary active species responsible for degradation, revealing a synergistic catalytic mechanism at the heterojunction interface. Recyclability tests showed that the material retained 90.8% degradation efficiency after five cycles, and an X-ray photoelectron spectroscopy (XPS) analysis demonstrated the stable binding of Fe and Mo, preventing secondary pollution. This study provides a scientific basis for developing efficient, stable, and wide-pH adaptable photo-Fenton catalytic systems, contributing significantly to the advancement of green water treatment technologies. Full article

Multi-object tracking (MOT) in satellite videos is a challenging task due to the small size and blurry features of objects, which often lead to intermittent detection and tracking instability. Many existing object detection and tracking models often struggle with these issues, as they are not designed to effectively handle the unique characteristics of satellite videos. To address these challenges, we propose LocaLock, a joint detection and tracking framework for MOT that incorporates feature matching concepts from single object tracking (SOT) to enhance tracking stability and reduce intermittent tracking results. Specifically, LocaLock utilizes an anchor-free detection backbone for efficiency and employs a local cost volume (LCV) module to perform precise feature matching in the local area. This provides valuable object priors to the detection head, enabling the model to “lock” onto objects with greater accuracy and mitigate the instability associated with small object detection. Additionally, the local computation within the LCV module ensures low computational complexity and memory usage. Furthermore, LocaLock incorporates a novel motion flow (MoF) module to accumulate and exploit temporal information, further enhancing feature robustness and consistency across frames. Rigorous evaluations on the VISO dataset demonstrate the superior performance of LocaLock, surpassing existing methods in tracking accuracy and precision within the demanding satellite video analysis domain. Notably, LocaLock achieved state-of-the-art performance on the VISO benchmark, achieving a multi-object tracking accuracy (MOTA) of 62.6 while ensuring fast running speed. Full article

In this study, we have proposed an electrochemiluminescence (ECL) signal amplification system which is based on two-dimensional (2D) flower-like CdS@Co/Mo-MOF composites as a co-reaction accelerator of the g-C₃N₄/S₂O₈²⁻ system for ultrasensitive detection of chlorpromazine hydrochloride (CPH). Specifically, the 2D flower-like Co/Mo-MOF with mesoporous alleviated the aggregation of CdS NPs while simultaneously fostering reactant-active site contact and improving the reactant–product transport rate. This allowed the material to act as a novel co-reaction accelerator, speeding up the transformation of the S₂O₈²⁻ into SO₄^•− and enhancing the cathodic ECL emission of g-C₃N₄. Moreover, the signal probe which was synthesized by coupling the 2D CdS@Co/Mo-MOF and graphitic carbon nitride (g-C₃N₄) achieved the generation of SO₄^•− in situ and reduced energy loss. The results confirmed that the ECL signal was enhanced 6.2-fold and stabilized by CdS@Co/Mo-MOF. Based on the extremely strong quenching effect of chlorpromazine hydrochloride (CPH) on this system, a “signal-off” type sensor was constructed. The sensor demonstrated excellent sensitivity and linear response to CPH concentrations ranging from 1 pmol L⁻¹ to 100 μmol L⁻¹, with a low detection limit of 0.4 pmol L⁻¹ (S/N = 3). Full article

Aqueous-phase reforming (APR) is an alternative method for treating and utilizing biogas slurry (BS) to produce renewable hydrogen from organic oxygen-containing wastewater. Considering the fluctuating characteristics of BS with changes in the degree of fermentation, developing an efficient catalyst is a major concern for the APR of BS. The novel catalyst based on molybdenum-based metal–organic-framework-derived oxides (Mo-MOF-derived α-MoO₃) was reported in this study. The results indicated that the variables (e.g., pH, organic load, and salinity) of BS corresponded to the fermentation times and exhibited decreasing trends after APR under the reaction conditions of 225 °C and 30 min. Decarboxylation was identified as the main side reaction in the APR of BS over the catalyst. An optimal yield of 2.17 mL_hydrogen/mL_BS was achieved when BS was obtained from 6 days of fermentation. Finally, the Mo-MOF-derived α-MoO₃ catalyst was obtained from the greater specific surface area of MOFs. The catalyst had a weaker acidity than the initial α-MoO₃, making it more preferred for facilitating the APR of BS. Full article

The photocatalytic conversion of ethanol and the simultaneous development of hydrogen technology play a role in solving the energy crisis and reducing environmental pollution. In this research, rod-like M-MoS₂ serves as a channel for charge transfer, leading to superior photocatalytic activity compared to H-MoS₂. Further, two-dimensional (2D) B-doped C₃N₄ (BCN) nanosheets were anchored on the one-dimensional (1D) rod-like M-MoS₂ surface to form a 1D/2D heterojunction, with M-MoS₂/BCN-0.08 (mass ratio of M-MoS₂:BCN of 0.08:1) exhibiting the highest photocatalytic performance. Under visible light irradiation, the ethanol conversion rate reached 1.79% after 5 h of photocatalytic reaction per gram of catalyst, while generating 421 μmol of 2,3-butanediol (2,3-BDO), 5460 μmol of acetaldehyde (AA), and 5410 μmol of hydrogen gas (H₂). This different characterization provides evidence that a significant amount of photoinduced electrons generated in BCN under illumination conditions rapidly transfer to the conduction band (CB) of M-MoS₂ through the rod-like structure of M-MoS₂, and finally transfer to Pt to promote the production of hydrogen gas. The photoinduced holes in the valence band (VB) of M-MoS₂ are rapidly consumed by ethanol upon transferring to BCN, effectively separating the photoinduced electron–hole pairs and resulting in superior photocatalytic performance. Full article