Search Results (44)

To obtain an excellent electromagnetic wave (EMW) absorption material, a strategy was proposed in this study with the aid of in-situ growth of carbon nanotubes (CNTs) on the surface of a metal–organic framework (MOF)-derived FeCoNiMnMg high-entropy alloy (HEA). The HEA@CNT composite was successfully prepared via a solvothermal method combined with a one-step pyrolysis process. With the pyrolysis temperature increasing from 600 °C to 800 °C, the length of CNTs grew from 200 nm to about 600 nm approximately, while the defect density of CNTs was enhanced. This structural evolution significantly improved the dielectric properties and impedance matching. Consequently, the sample prepared at 800 °C (HEA@CNT-800) exhibited outstanding microwave absorption performances, achieving a minimum reflection loss (RL_min) of −57.52 dB at a matched thickness of 2.3 mm and an effective absorption bandwidth (EAB) of 4.4 GHz at a thinner thickness of 1.9 mm. This work provides a novel perspective for designing high-performance MOF-derived absorption materials. Full article

Metal–organic framework (MOF) materials were extensively studied in the removal of pollutants in wastewater. However, catalysts in the powder form usually suffered from the strong tendency to agglomerate and the intricate operation for recycling, which significantly limited their practical application. In comparison, monolithic catalysts with their high macroscopic operability and recoverability as well as impressive specific surface area have attracted tremendous attention in recent years. To address these issues, a monolithic Fe-based catalyst was prepared via in situ synthesis, using nickel–iron foam (NFF) as the substrate with cobalt (Co) incorporation. XPS analysis showed that Co doping enhanced the synergistic interaction among Fe, Ni, and Co, accelerating the redox cycle among species, thus improving electron transfer and laying a kinetic foundation for efficient peroxymonosulfate (PMS) activation. Quenching experiments and EPR indicated singlet oxygen (¹O₂) as the main reactive species; Co doping shifted the degradation pathway from radicals to non-radicals. Under optimized conditions (PMS: 0.08 mmol/L; catalyst: 1 cm²; initial Chlortetracycline (CTC): 50 mg/L), 95.7% CTC degradation was achieved within 60 min, and efficiency only dropped to 90.5% after 5 cycles. This catalyst provided theoretical and technical support for the application of monolithic MOF-derived catalysts and highly efficient PMS activators. Full article

Dry reforming of methane and ethanol is a promising catalytic process for the conversion of carbon dioxide and hydrocarbon feedstocks into synthesis gas (H₂/CO), which serves as a key platform for the production of fuels and chemicals. Over the past decade, substantial progress has been achieved in the design of catalysts with enhanced activity and stability under the demanding conditions of these strongly endothermic reactions. This review summarizes the latest developments in catalyst systems for DRM and EDR, including Ni-based catalysts, perovskite-type oxides, MOF-derived materials, and high-entropy alloys. Particular attention is given to strategies for suppressing carbon deposition and preventing metal sintering, such as oxygen vacancy engineering in oxide supports, rare earth and transition metal doping, strong metal–support interactions, and morphological control via core–shell and mesoporous architectures. These approaches have been shown to improve coke resistance, maintain metal dispersion, and extend catalyst lifetimes. The review also highlights emerging concepts such as multifunctional hybrid systems and innovative synthesis methods. By consolidating recent findings, this work provides a comprehensive overview of current progress and future perspectives in catalyst development for DRM and EDR, offering valuable guidelines for the rational design of advanced catalytic materials. Full article

The development of highly efficient catalysts for the hydrogenation of dicyclopentadiene (DCPD) remains a critical challenge. In this study, we designed a series of bimetallic Ce–Ni metal–organic framework (MOF)-derived nanocatalysts by precisely tuning the Ce/Ni ratio and calcination temperatures. The optimized catalyst, Ni–CeO_2(7:3) @C–400 °C, featuring highly dispersed carbon-coated Ni nanoparticles, achieved complete hydrogenation of DCPD to tetrahydrodicyclopentadiene (THDCPD) with 100% conversion and nearly 100% selectivity within 2 h under 100 °C and 2 MPa. The porous carbon framework significantly facilitated the diffusion and accessibility of DCPD molecules, combined with Ce species reconstructing the electronic structure of Ni active centers through electronic interactions, synergistically enhancing the hydrogenation efficiency. Furthermore, the catalyst demonstrated good structural stability. This work not only provides a robust strategy for the rational design of bimetallic MOF-derived catalysts but also highlights their potential for practical applications in industrial hydrogenation processes. Full article

Composite catalysts combining a metal–organic framework (MOF) with its derivatives have attracted significant attention in electrocatalysis due to their unique properties. In this study, we report the synthesis of a Ni-doped Co-1,4-benzenedicarboxylate (defined as Co₃Ni₁BDC) metal–organic framework via a straightforward solvothermal method, aiming to enhance oxygen evolution reaction (OER) activity. The introduction of Ni modulated the electronic structure, yielding high catalytic activity with an overpotential (η₁₀₀) of 300 mV and excellent stability for the OER. The Co₃Ni₁BDC material was further encapsulated with Co₂P nanoparticles via a controlled phosphating annealing process, forming a hybrid electrocatalyst (Co₃Ni₁BDC@Co₂P) to boost hydrogen evolution reaction (HER) performance. The Co₃Ni₁BDC@ Co₂P catalysts exhibited superior HER performance with low overpotentials of η₁₀ = 20 mV and η₁₀₀ = 127 mV, outperforming the Co₃Ni₁BDC precursor. An alkaline electrolyzer assembled with Co₃Ni₁BDC//Co₃Ni₁BDC@Co₂P achieved a cell voltage of 1.70 V at a current density of 20 mA cm⁻². This work provides a valuable idea for designing efficient electrocatalysts for overall water splitting. Full article

Developing efficient bifunctional oxygen reduction (ORR) and oxygen evolution (OER) electrocatalysts is critical for renewable energy technologies. Noble metal catalysts face limitations in cost, scarcity, and bifunctional compatibility. Herein, we report the synthesis of nickel nanoparticles encapsulated in nitrogen-doped carbon nanosheets (Ni@NC-T) via a solvothermal polymerization and pyrolysis process using a Ni-hexamine coordination framework (NiHMT) as a precursor. The Ni@NC-900 catalyst exhibits superior ORR and OER activity under alkaline conditions, with an ORR performance (half-wave potential = 0.86 V) comparable to commercial Pt/C and an OER overpotential of only 430 mV at 10 mA cm⁻². Structural analysis indicates that the hierarchical porous structure and high specific surface area (409 m² g⁻¹) of Ni@NC-900 facilitate the exposure of active sites and enhance mass transport. The surface-doped nitrogen species, predominantly in the form of pyridinic N and graphitic N, promote electron transfer during the ORR. Furthermore, its application as a bifunctional cathode in rechargeable zinc-air batteries results in a high power density of 137 mW cm⁻², surpassing the performance levels of many existing carbon-based bifunctional catalysts. This work highlights a facile strategy for the fabrication of transition metal-based catalysts encapsulated in MOF-derived carbon matrices, with promising potential for energy storage and conversion devices. Full article

Heavy metal pollution has posed a serious threat to the ecological environment and human health. Thus, the development of accurate and effective methods for their detection is crucial. In this study, a novel electrochemical sensor was fabricated to detect Cu²⁺ and Hg²⁺, based on N-doped carbon nanotube-wrapped Ni nanoparticle (Ni@N-CNT) sensing material, which was derived from the pyrolysis of Ni²⁺ doped ZIF-8. For electrode material design, the packaging structure not only protected the encapsulated Ni nanoparticles from electrochemical corrosion in the acid electrolyte but also provided excellent electro-catalytic activity and electrical conductivity by controlling their size. Thanks to the overall performance of the Ni@N-CNT composite, the proposed sensor exhibited excellent analytical performance for Cu²⁺ and Hg²⁺ detection, with ultra-low detection limits of 33.3 ng⋅L⁻¹ and 33.3 ng⋅L⁻¹, respectively. The sensor also demonstrated good repeatability, reproducibility and selectivity. In addition, the method was successfully applied to the electrochemical analysis of Cu²⁺ and Hg²⁺ in actual Chinese cabbage samples with satisfactory recovery, confirming its practical applicability. Full article

To achieve the “double carbon” goal, it is urgent to reform the energy system. The oxygen evolution reaction (OER) is a vital semi-reaction for many new energy-storage and conversion devices. Metal nanoparticles embedded in heteroatom-doped carbon materials prepared by the pyrolyzing of metal–organic frameworks (MOFs) have been a key route to obtain high-performance electrochemical catalysts. Herein, a nanocatalyst embedding Ni nanoparticles into S- and N-co-doped carbon nanoplate (Ni NPs@SN-CNP) has been synthesized by pyrolysis of a Ni-MOF precursor. The prepared Ni NPs@SN-CNP exhibits superior oxygen evolution performance with an overpotential of 256 mV to attain 10 mA cm⁻² and a low Tafel slope value of 95 mV dec⁻¹. Moreover, a self-assembled overall-water-splitting cell with Ni NPs@SN-CNP/NF||Pt-C/NF achieves a low potential of 1.56 V at 10 mA cm⁻² and a high cycling stability for at least 10 h. The improvement in this performance is benefit from its large surface area, unique morphology, and the nanostructure of the electrocatalyst. This study presents a novel and simple approach to designing high-performance OER catalysts. Full article

This study explores the electrochemical properties of additive-free NiCo₂O₄ derived from NiCo–metal–organic frameworks (MOFs) as a high-performance anode material for lithium-ion batteries (LIBs), excluding the effect of additives. NiCo-MOF was synthesized via an ultrasonic-assisted method and deposited on stainless steel foils using alternating current electrophoretic deposition (AC-EPD). The resulting thin films exhibited outstanding cycling stability and rate performance, maintaining a specific capacity of ~1200 mAh/g over 250 cycles at a high current density of 2.35 A/g, with nearly 100% Coulombic efficiency. Differential capacity analysis revealed enhanced redox activity at 0.8 V and 1.7 V during lithiation and delithiation, attributed to the decomposition of NiCo₂O₄ into metallic Ni and Co, followed by their oxidation to Ni²⁺ and Co³⁺, respectively. The gradual activation of electroactive sites, coupled with improved electrode kinetics and structural adjustments, contributed to the observed capacity increase over cycles. These findings underscore the potential of NiCo₂O₄ as a robust and efficient anode material for next-generation LIBs. Full article

Mixed-metal nickel-iron, Ni_xFe materials draw attention as affordable earth-abundant electrocatalysts for the oxygen evolution reaction (OER). Here, nickel and mixed-metal nickel-iron metal–organic framework (MOF) composites with the carbon materials ketjenblack (KB) or carbon nanotubes (CNT) were synthesized in situ in a one-pot solvothermal reaction. As a direct comparison to these in situ synthesized composites, the neat MOFs were postsynthetically mixed by grinding with KB or CNT, to generate physical mixture composites. The in situ and postsynthetic MOF/carbon samples were comparatively tested as (pre-)catalysts for the OER, and most of them outperformed the RuO₂ benchmark. Depending on the carbon material and metal ratio, the in situ or postsynthetic composites performed better, showing that the method to generate the composite can influence the OER activity. The best material Ni₅Fe-CNT was synthesized in situ and achieved an overpotential (η) of 301 mV (RuO₂ η = 354 mV), a Tafel slope (b) of 58 mV/dec (RuO₂ b = 91 mV/dec), a charge transfer resistance (R_ct) of 7 Ω (RuO₂ R_ct = 39 Ω), and a faradaic efficiency (FE) of 95% (RuO₂ FE = 91%). Structural changes in the materials could be seen through a stability test in the alkaline electrolyte, and chronopotentiometry over 12 h showed that the derived electrocatalysts and RuO₂ have good stability. Full article

Metal–organic framework (MOF)-derived transition metal compounds and their composites have attracted great interest for applications in energy conversion and storage. In this work, hexagonal micro-prisms of Ni-doped CoTiO₃ composited with amorphous carbon (Ni_xCTO/C) were synthesized using Ti-Co-based MOFs as precursors. The experimental results indicate the substitutional doping of Ni²⁺ for Co²⁺ in CoTiO₃ (CTO), leading to improved conductivity, as further confirmed by density functional theory calculations. Thus, the carbon-free sample of Ni-doped CTO exhibits improved lithium storage properties compared to the pristine one. Furthermore, when coupled with in situ-formed carbon, the dually modified Ni_0.05CTO/C micro-prisms demonstrated a significantly increased reversible capacity of 584.8 mA h g⁻¹, excellent rate capability, and superior cycling stability at a high current density of 500 mA g⁻¹. This enhanced electrochemical performance can be attributed to the synergistic effect of Ni doping and carbon coating. Full article

Designing and fabricating a highly sensitive non-enzymatic glucose sensor is crucial for the early detection and management of diabetes. Meanwhile, the development of innovative electrode substrates has become a key focus for addressing the growing demand for constructing flexible sensors. Here, a simple one-step laser engraving method is applied for preparing laser-induced graphene (LIG) on polyimide (PI) film, which serves as the sensor substrate. NiCo-layered double hydroxides (NiCo-LDH) are synthesized on LIG as a precursor, utilizing the zeolitic imidazolate framework (ZIF-67), and then reacted with Ni(NO₃)₂ via solvent-thermal methods. The sensitivity of the non-enzymatic electrochemical glucose sensor is significantly improved by employing NiCo-LDH/LIG as the sensing material. The porous and interconnected structure of NiCo-LDH, derived from ZIF-67, enhances the accessibility of electrochemically active sites, while the incorporation of LIG ensures exceptional conductivity. The combination of NiCo-LDH with LIG enables efficient electron transport, leading to an increased electrochemically active surface area and enhanced catalytic efficiency. The fabricated electrode achieves a low glucose detection limit of 0.437 μM and demonstrates a high sensitivity of 1141.2 and 631.1 μA mM⁻² cm⁻² within the linear ranges of 0–770 μM and 770–1970 μM, respectively. Furthermore, the NiCo-LDH/LIG glucose sensor demonstrates superior reliability and little impact from other substances. A flexible integrated LIG-based non-enzymatic glucose sensor has been developed, demonstrating high sensitivity and suggesting a promising application for LIG-based chemical sensors. Full article

Carbon fiber, with its strong mechanical properties and electrical conductivity, is ideal as a fiber electrode in wearable or structural energy storage devices. However, its energy storage capacity is limited, and coatings like transition metal oxides (TMOs) enhance its electrochemical performance. Metal–organic frameworks (MOFs) are commonly used to grow TMOs on carbon fibers, increasing the surface area for better energy storage. Despite this, TMOs have limited electrical conductivity, so ion exchange is often used to dope them with additional cations, improving both conductivity and energy storage capacity. This study compares different ion-exchange cations in ZIF-L-derived TMO coatings on carbon fiber. Testing both supercapacitor and Li-ion battery applications, Ni-doped samples showed superior results, attributed to their higher exchange ratio with cobalt. As a supercapacitor electrode, the Ni-doped material achieved 13.3 F/g at 50 mA/g—66% higher than undoped samples. For Li-ion battery anodes, it reached a specific capacity of 410.5 mAh/g at 25 mA/g, outperforming undoped samples by 21.4%. Full article

Oxygen evolution reaction (OER) is a critical half-reaction in electrochemical overall water splitting and metal–air battery fields; however, the exploitation of the high activity of non-noble metal electrocatalysts to promote the intrinsic slow kinetics of OER is a vital and urgent research topic. Herein, Fe-doped Ni₃S₂ arrays were derived from MOF precursors and directly grown on nickel foam via the traditional solvothermal way. The arrays integrated into nickel foam can be used as self-supported electrodes directly without any adhesive. Due to the synergistic effect of Fe and Ni elements in the Ni₃S₂ structure, the optimized Fe_2.3%-Ni₃S₂/NF electrode delivers excellent OER activity in an alkaline medium. The optimized electrode only requires a small overpotential of 233 mV to reach the current density of 10 mA cm⁻², and the catalytic activity of the electrode can surpass several related electrodes reported in the literature. In addition, the long-term stability of the Fe_2.3%-Ni₃S₂/NF electrode showed no significant attenuation after 12 h of testing at a current density of 50 mA cm⁻². The introduction of Fe ions could modulate the electrical conductivity and morphology of the Ni₃S₂ structure and thus provide a high electrochemically active area, fast reaction sites, and charge transfer rate for OER activity. Full article

Binary transition metal selenides (BTMSs) are more promising than single transition metal selenides (TMS) as anode materials of sodium-ion batteries (SIBs). However, it is still very challenging to prepare high-performance BTMSs in the pure phase, instead of a mixture of two TMSs. In this study, a binary metal center-based MOF derived selenization strategy was developed to prepare iron–cobalt selenide (Fe₂CoSe₄@NC) and iron–nickel selenide (Fe₂NiSe₄@NC) nanocomposites in the single phase and when wrapped with carbon layers. As the anode material of SIBs, Fe₂CoSe₄@NC exhibits higher long-term cycling performance than Fe₂NiSe₄@NC, maintaining a capacity of 352 mAh g⁻¹ after 2100 cycles at 1.0 A g⁻¹, which is ascribed to the higher percentage of the nanopores, larger lattice spacing, and faster Na+ diffusion rate in the electrode materials of the former rather than the latter. Full article