MOF Structure Research Articles

Integration of Metal‐Organic Frameworks into Hydrogels: Optimizing Their Properties and Applications

In recent years, MOFs hydrogels have attracted extensive attention due to their unique structure and excellent performance. MOF‐based hydrogels combine the highly ordered pore structure and tunability of MOF with the biocompatibility and flexibility of hydrogels, and are widely used in environmental governance, sensors, and biomedicine. In this review, we mainly summarize the synthesis methods, structural characteristics and mechanical properties of MOF‐based hydrogels, and the specific applications of MOF‐based hydrogels in different fields including adsorption of heavy metal ions and pollutant gases stress strain sensor and drug delivery. Finally, we analyze the existing problems, and provide suggestions for the development direction of MOF‐based hydrogels in the future. This paper aims to help readers quickly understand the current development of MOF‐based hydrogels.

Strategic Defect Engineering Enabled Efficient Oxygen Evolution Reaction in Reconstructed Metal‐Organic Frameworks

AbstractMetal‐organic frameworks (MOFs) have emerged as promising pre‐catalysts for oxygen evolution reaction (OER) due to their marvelous structural reconstruction process in strongly alkaline media. However, targeting design MOF structures to achieve excellent OER performance of reconstructed products is a challenge. Here, a strategic defect engineering is used to promote the OER performance of reconstructed products. Briefly, modified linkers with monocarboxylic acids (ferrocene carboxylic acid, FcCA) are incorporated into MOF (NiBDC‐FcCA), leading to its stepwise reconstruction into Fe‐doped Ni(OH)2 and NiOOH during the OER process, with the oxygen vacancy and strategic doping of metal Fe persisting throughout the multi‐step reconstruction. Benefiting from the synergistic interaction of oxygen vacancies and Fe doping, NiBDC‐FcCA delivers the extremely enhanced current density at 1.6 V versus reversible hydrogen electrode by ≈9 times compared with that of NiBDC. Moreover, the optimized NiBDC‐FcCA/Fe foam exhibits excellent OER catalytic activity and stability with a low overpotential of 250 mV at 200 mA cm−2 and negligible activity decay after 1200 h at 1 A cm−2. Density function theory calculations reveal that Fe doping weakens the interaction of oxygen intermediate with Ni sites, favoring the formation of OOH* to accelerate the OER process.

Ni‐MOF‐74 Derived Carbon‐Based Ni Catalysts for Efficient Catalytic Ammonia Synthesis via Pulsed DBD Plasma

ABSTRACTDesigning efficient noble metal‐free catalysts for plasma‐catalytic ammonia synthesis is significant and challenging. Carbon‐based metal catalysts were prepared at different pyrolysis temperatures using the Ni‐MOF‐74 precursor. The effects of Ni‐MOF‐74 and its derived carbon‐based metal catalysts on pulsed dielectric barrier discharge (DBD) plasma ammonia synthesis were investigated. The results showed that Ni‐MOF‐74‐300 with both the MOF structure and nickel metal particles exhibited the best catalytic performance for ammonia synthesis. The ammonia synthesis rate reached 41.38 mmol g−1 h−1, whereas the nitrogen conversion rate was as high as 1.54% with an energy yield of 3.04 g kWh−1. Compared to the situation of plasma only, the ammonia synthesis rate, nitrogen conversion rate, and energy yield were increased by 28.46 times, 5.7 times, and 5.5 times, respectively.

Fabrication of a novel non-enzymatic glucose sensor based on ruthenium supported by a combination of PBA nanocubes and MOF nanosheets

The development of novel catalysts with high catalytic activity is of high importance of electrochemical non-enzymatic glucose sensing. Herein, a sensitive non-enzymatic electrochemical sensor (Ru@NiCo-MOF/NiFe-PBA) has been synthesized using a fast, simple and eco-friendly method. The high stability of PBA and the large specific surface area (two-dimensional nanosheet structure) of MOF support the excellent electrochemical performance, while the incorporation of the highly active metal Ru enhances the electrochemical activity even more. The results reveal that the sensitivities of the sensor are 1070.77 and 487.62 μA mM−1 cm−2, corresponding to linear ranges of 0.01–0.67 mM and 0.67–5.07 mM, respectively. Meanwhile, the sensor has a low detection limit (0.446 μM) and a short response time (2 s), making it a strong candidate for non-enzymatic glucose sensors. The successful detection of glucose in saliva further demonstrates its potential for practical applications. Therefore, Ru@NiCo-MOF/NiFe-PBA will make an impact in the field of glucose monitoring and detection.

Band Structure Engineering in 2D Metal-Organic Frameworks.

The design of 2D metal-organic frameworks (2D MOFs) takes advantage of the combination of the diverse electronic properties of simple organic ligands with different transition metal (TM) centers. The strong directional nature of the coordinative bonds is the basis for the structural stability and the periodic arrangement of the TM cores in these architectures. Here, direct and clear evidence that 2D MOFs exhibit intriguing energy-dispersive electronic bands with a hybrid character and distinct magnetic properties in the metal cores, resulting from the interactions between the TM electronic levels and the organic ligand π-molecular orbitals, is reported. Importantly, a method to effectively tune both the electronic structure of 2D MOFs and the magnetic properties of the metal cores by exploiting the electronic structure of distinct TMs is presented. Consequently, the ionization potential characteristic of selected TMs, particularly the relative energy position and symmetry of the 3d states, can be used to strategically engineer bands within specific metal-organic frameworks. These findings not only provide a rationale for band structure engineering in 2D MOFs but also offer promising opportunities for advanced material design.

Graphene oxide-containing chitosan@HKUST-1 beads with increased chemical stability for CO2 capture

HKUST-1 MOF was crystallized within chitosan matrix to form xerogel beads using an in-situ growth approach. Under mild conditions, CS@HKUST-1 xerogel beads exhibit high specific surface areas (SBET) up to 923 m2 g−1. By further incorporating graphene oxide (GO) to form ternary CS-GO@HKUST-1 xerogel beads, the HKUST-1 MOF structure remained stable for up to two days in a water solution at room temperature, whereas the MOF powder and CS@HKUST-1 xerogel beads underwent significant framework collapse within a day. CO2 adsorption measurements on these xerogel beads also show promising CO2 uptakes, surpassing 2.5 mmol g−1 at 298 K and 1 bar. Moreover, these composites could be regenerated for more than 10 cycles without any loss of quantity adsorbed.

Bimetallic Fe/Co-MOF dispersed in a PVA/chitosan multi-matrix hydrogel as a flexible sensor for the detection of lactic acid in sweat samples.

Anovel bimetallic Fe/Co-metal-organic framework (MOF) hydrogel-based wearable sweat sensorwas developed. Morphological and structural analysis of the hydrogel shows uniformly sized spines and spindle-shaped particles of the Fe/Co-MOF, and it has a high surface area (132.306 m2g-1) and porosity (0.059 cm3g-1) as confirmed by Brunauer-Emmett-Teller (BET) studies. The integration of the bimetallic MOF into a polyvinyl alcohol/chitosan (PVA/CS)-mixed matrix resulted in a multiple network hydrogel. The optimisation study investigated the effects of different pH of the PBS electrolyte, scan rates, and accumulation time in voltammetry. The electrochemical methods such as cyclic voltammetry (CV), square wave voltammetry (SWV), and electrochemical impedance spectroscopy (EIS) provided information on the redox behaviour, electrochemical stability, and catalytic activity of the hydrogel. The sensor demonstrates a wide linear detection range from 0.05µM to 100mM, a superior sensitivity of 0.02mAmM-1cm-2, and a lower limit of detection of 0.01µM . Active sites distributed over the hydrogel surface, specifically Fe2+ and Co2+ within the MOF structure, catalyse the oxidation of L-lactic acid, resulting in electron transfer and the formation of pyruvic acid. Notably, the fabricated sensor exhibits high selectivity, effectively discriminating against interfering species such as uric acid, ascorbic acid, glucose, urea, dopamine, NaCl, and CaCl2. Real-time analysis conducted in a simulated sweat sample via the standard addition method resulted in good recovery percentages of a minimum of 98%. The work presented here is a versatile and simple platform for point-of-care testing, especially for athletes and military personnel.

Full-Color Emissive Zirconium-Organic Frameworks Constructed via in situ "One-Pot" Single-Site Modification for Tryptophan Detection and Energy Transfer.

Organic linker-based luminescent metal-organic frameworks (LMOFs) have received extensive studies due to the unlimited species of emissive organic linkers and tunable structure of MOFs. However, the multiple-step organic synthesis is always a great challenge for the development of LMOFs. As an alternative strategy, in situ "one-pot" strategy, in which the generation of emissive organic linkers and sequential construction of LMOFs happen in one reaction condition, can avoid time-consuming pre-synthesis of organic linkers. In the present work, we demonstrate the successful utilization of in situ "one-pot" strategy to construct a series of LMOFs via the single-site modification between the reaction of aldehydes and o-phenylenediamine-based tetratopic carboxylic acid. The resultant MOFs possess csq topology with emission covering blue to near-infrared. The nanosized LMOFs exhibit excellent sensitivity and selectivity for tryptophan detection. In addition, two component-based LMOFs can also be prepared via the in situ "one-pot" strategy and used to study energy transfer. This work not only reports the construction of LMOFs with full-color emissions, which can be utilized for various applications, but also indicates that in situ "one-pot" strategy indeed is a useful and powerful method to complement the traditional MOFs construction method for preparing porous materials with tunable functionalities and properties.

3D Printed Metal Organic Framework Hydrogel for Dye Adsorption and Gas Sensing

AbstractMetal organic frameworks (MOFs) have tunable chemical structures, orderly pore structures, and modifiable surface functional groups making them a promising material for environmental remediation. However, their rigid powder morphology poses significant challenges for customizing MOF structures with adjustable mechanical properties. Here, we synthesis the stretchable UV‐curable MOF hydrogels through high‐resolution digital light processing 3D printing, and evaluated its adsorption effect on seven common dyesand.The results showed that it had selective adsorption effect on methylene blue (MB), and the adsorption effect increased with the increase of the initial concentration of MB: its adsorption capacity on 6 mgL−1, 12 mgL−1 and 24 mgL−1 MB solution reached 13.55 mgg−1, 26.31 mgg−1 and 50.70 mgg−1 respectively. Compared to powdered MOFs, the 3D‐printed MOF (Cu‐BTC) exhibited superior adsorption for dye and radioactive pollution, with methylene blue adsorption increasing from 8.93 mgg−1 to 25.05 mgg−1 and I2 adsorption from 141.56 mgg−1 to 792.65 mgg−1. Furthermore, the 3D‐printed MOF structure proved easily cleanable with dilute HCl and reusable over five times without degradation. In addition, our study highlighted the suitability of the 3D‐printed MOF for CO2‐sensing devices, demonstrating its broad applicability in environmental remediation and sensing technology.

Photothermal Catalytic Removal of 1,2-DCE with High HCl Selectivity over the Brønsted Acid-Enriched Sulfur-Doped MOFs.

Chlorinated volatile organic compounds come from a wide range of sources and are highly toxic, posing a serious threat to biological health and the environment. Herein, a high-efficiency and energy-saving photothermal synergistic catalytic oxidation method was developed for the removal of 1,2-dichloroethane (1,2-DCE). Compared to traditional thermocatalysis, the 1,2-DCE conversion over Ru-U6S in photothermal synergistic catalysis at 340 °C increased by approximately 44% not only reducing energy consumption but also avoiding the instability of MOF structure caused by high reaction temperature. The excellent photothermal catalytic oxidation activity was derived from the synergistic effect of photo- and thermocatalysis. Ru-U6S demonstrated excellent 1,2-DCE adsorption capacity and stronger light utilization and could produce more reactive oxygen species (•OH and •O2-) after light illumination, which participated in the oxidation reaction, promoting the release of the active site of the catalyst. The results of H2O-TPD and NH3-DRIFTS exhibited that the use of S-containing ligands in the synthesis process increased the hydroxyl groups and Brønsted acid sites, significantly improved the selectivity of CO2 and HCl in the oxidation process, and reduced the release of chlorine-containing byproducts. This work provides a high-efficiency and energy-saving strategy for removing chlorinated volatile organic compounds and increasing the selectivity of ideal products directly with MOFs directly.

Highly sustainable water mist-responsive superwetting sponge (DTMO/FS-50/Hollow-CuCo-ZIF@Sponge) for speedy pollutants removal and solvent-free regeneration

Smart solvent-responsive superwetting materials are particularly favored due to their ability to handle different types of pollutants. However, most of them rely on organic solvent vapors, and neglect the desorption efficiency of pollutants, especially using the solvent-free desorption method. A responsive sponge was fabricated by coating hollow MOFs particles with different sizes, greatly enhancing roughness and porosity, and followed by modification with short-chain fluorinated surfactants, long-chain siloxanes, tannic acid, and polydopamine. There are several advantages in this paper: (I) a hollow MOFs structure was achieved, greatly enhancing specific surface area, porosity, and active sites, which acted as a superior container for responsive modifiers network. (II) the reactions among biomass dopamine hydrochloride (PDA), tannic acid (TA), long-chain siloxanes, short-chain fluorinated surfactants and PU substrate, formed smart responsive biomass macromolecular networks, not only greatly improved adhesion between hollow MOFs and sponge substrate, but also showed enhanced synergistic effects for smart wettability transition. (III) the coated sponge showed smart responsive superwetting behaviors under environmentally friendly water mist rather than organic vapors or unfriendly vapors. (IV) the coated sponge could handle various kinds of pollutants based on polarity selection, and also quickly desorb the pollutants after change the polarity under water mist activation. The intelligent sponge can quickly and selectively adsorbed various microplastics and efficiently deal with oil-in-water and oil-in-water emulsions. It has good mechanical durability, maintaining a separation capacity of more than 88 % after repeated adsorption and desorption of MPs180 times.

Synthesis, characterization, and catalytic activity of zinc-isonicotinic acid MOF

The synthesis and characterization of Zn (INA) microcrystalline MOF was conducted, revealing its high catalytic activity in the production of substituted benzyl alcohol (BzOH) to substituted benzaldehyde (BzA). The MOF was found to be cost-effective and efficient, with a short synthesis time and moderate reaction conditions. The MOF's structure was confirmed through XRD, SEM, and TEM imaging, and its purity was confirmed through EDS analysis. The TGA investigation revealed significant thermal stability with minimal weight loss and BET studies shows the substantial surface area and pore volume, suggesting potential for various industrial uses. The MOF's efficiency under mild reaction conditions, low cost, and absence of noble metals makes it a promising candidate for sustainable catalytic applications.

Understanding pore features of pillar-layered MOFs on one-step C2H4 purification from C2H6/C2H4 mixtures

Purification of ethylene from ethane through adsorption separation is a key industrial process in present chemical field, since the similar physical properties of both C2H4 and C2H6 that makes them difficult to separate. Therefore, constructing C2H6-selective adsorbents and clarifying its structure–activity relationship is a very difficult undertaking. In this study, 3D pillar-layered metal organic frameworks (MMOF-kgm (M = Zn, Co, Ni) and NiMOF-sql) with different topologies, kagome and square lattice, were constructed by using the cheap ligands (1,4-benzenedicarboxylic acid and triethylenediamine). The effect of pore features on C2H6/C2H4 separation performance and the separation mechanism were systematically investigated by the above two isomeric MOFs. In particular, NiMOF-kgm with kagome topology provides narrower triangular pore shows notably adsorption of C2H6 over C2H4, which is validated by gas adsorption, IAST selectivity and breakthrough measurements. The selective adsorption mechanisms of MOF with kagome topology were further revealed through DFT calculations. This study provides in-depth insights into optimizing the pore structure of MOFs to enhance C2H6/C2H4 separation performance, offering new design strategies for developing efficient materials for ethane-selective adsorbent for one-step ethylene purification.

Rare earth europium recovery using selective metal-organic framework incorporated mixed-matrix membrane

Rare-earth elements (REEs) play a crucial role in state-of-the-art technologies and sustainable energy generation. However, conventional production methods of REE often instigate detrimental impacts on environment. Hence, the development of efficient and sustainable hydrometallurgical methods for REE recovery from complex solution has become a crucial research focus. This study investigates a mixed-matrix membrane composed of a highly europium selective metal-organic framework-based adsorbent, Cr-MIL-PMIDA, embedded in sulfonated poly(ether ketone) (SPEK) polymer membrane matrix to preferentially concentrate europium (Eu3+) ions in the presence of other competing cations. The activated membrane notably reduced ionic conductivity for Eu3+ compared to other multivalent ions. Membrane extraction experiments further confirmed the selective behavior, demonstrating slower diffusion for Eu3+ compared to Mg2+ and Zn2+ cations. Especially, at pH 5, Mg2⁺ and Zn2⁺ recovery was greater than 30%, whereas Eu³⁺ recovery remained lower than 4%. We propose that the strong chemical affinity between the phosphate group and Eu3+ help partition of the Eu3+ ions in the membrane phase and inhibit the diffusion and further partitioning of the Eu3+ ion from bulk solution. Furthermore, we demonstrate the stability of the composite membrane and the embedded MOF particles in aqueous solution for up to 12 days without degradation, attributing it to the robust chemical stability of the MOF structure.

Polypyrrole nanoclips-coated Co/C nanostructures with enhanced microwave absorption

There is a challenge to boost the electromagnetic wave absorption performance of magnetic carbon-based materials by rationally adjusting the structure of MOF. In this paper, nanoclip-shaped polypyrrole (PPy) was wrapped on the surface of the Co/C nanoparticle derived from Co-MOF via in-situ polymerization of pyrrole with the help of cetylammonium bromide. The electromagnetic parameters of prepared Co/C@PPy can be easily tuned by adjusting the feed ratio of PPy to Co/C. The optimum value of reflection loss (RL) for Co/C@PPy is −45.49 dB at 2.4 mm and 15.12 GHz when the feed ratio of pyrrole to Co/C is 200 μL to 80 mg, and the effective absorption bandwidth (EAB, RL ≤ −10 dB) reaches 5.97 GHz (11.76–17.73 GHz) at the matching thickness of 2.5 mm. This study paves the way for further design and preparation of the nanocomposites based on MOF-derived nanostructures with excellent EMW absorption performance.

Conducting Composite Polymer-Based Solid-State Electrolyte with High Ion Conductivity via Amorphous Condensed Structure and Multiple Li+ Transport Channels.

Traditional PEOelectrolyte has high crystallinity which hinders the transmission of Li+, resulting in poor ion conductivity and complicated processing technology. Herein, a polymer electrolyte (p-electrolyte) with a wide electrochemical window and high ionic conductivity is designed, which possesses an amorphous condensed structure. The amorphous structure provides fast transport channels for Li+, so the p-electrolyte possesses an electrochemical window of 4.2V, and high ionic conductivity of 1.58 × 10-5Scm-1 at room temperature, which is 1-2 orders of magnitude higher than that of traditional PEO electrolyte. By using the designed polymer electrolyte as the foundation, an in situ curable composite polymer electrolyte (CPE-L) with multiple Li+ transport channels is elaborately constructed. The Cu-BTC MOF stores abundant Li+, which is introduced into the p-electrolyte. The rich unsaturated Cu2+ coordination sites of Cu-BTC can anchor TFSI- to release Li+, and the pore structure of Cu-BTC MOF cooperates with LLZTO nanoparticles to provide multiple fast transport channel for Li+, resulting in remarkable ionic conductivity (1.02 × 10-3Scm-1) and Li+ transference number (0.58). The Li||CPE-L||Li symmetric battery cycles stably for more than 700h at 0.1mAcm-2, while the specific capacity of full battery is ≈153mAhg-1 (RT, 0.2C).

Module-based machine learning models using sigma profiles of organic linkers to predict gaseous adsorption in metal-organic frameworks

BackgroundMetal-organic frameworks (MOFs) have drawn considerable attention for their potential in adsorption applications, such as gas separation and storage. Machine learning (ML) augmented high-throughput screening approaches have emerged as an effective strategy to expedite the materials search. Traditionally, ML models developed to predict the adsorption properties of MOFs rely on various geometrical and chemical descriptors. While these descriptors are effective, they tend to be specific to each MOF's unique structure, completely omitting the modular nature of MOFs. MethodsA new approach is proposed in this study: a modular descriptor based on the sigma profile of MOF organic linkers. These sigma profiles effectively represent the chemical environment of organic linkers. With these profiles as input features, we train extreme gradient boosting (XGBoost) models to predict the Henry's coefficient (KH) of adsorption for hydrocarbons and acid gases in MOFs. FindingsThe results show that sigma profiles enhance the prediction accuracy and emerge as the most important features for hydrocarbon gases. This study highlights the potential of sigma profiles in developing accurate ML models for identifying optimal MOF adsorbents. Such an approach could also facilitate an inverse design of MOFs with targeted properties.

Controllable synthesis of NiCoMo-LDH with nanofloral structure assisted by monodisperse spherical silica for asymmetric supercapacitor

Traditional layered double hydroxides (LDH) have disadvantages such as small layer spacing, insufficient active sites and poor electrical conductivity, which seriously restricts their future utilization in the realm of energy storage. In this paper, a controlled synthesis strategy of tercomponent metal NiCoMo-LDH is proposed by using the structural advantages of metal-organic skeleton (MOF) templates, combining structural regulation and atom doping. On the basis of the synthesis of Ni-MOF 74, Co and Mo atoms are introduced for a small amount of doping, and the monodisperse spherical SiO2 is inserted to adjust the pore structure of NiCoMo-MOF, expand the lamellar spacing, and effectively avoid the accumulation and agglomeration of lamella. Finally, NiCoMo-LDH cathode material with loose porous and coarsely curled nanosphere structure was synthesized through the chemical reaction of OH− with SiO2 and the destruction of the skeleton structure of MOF. The specific capacitance of the material is 1423.3 F·g−1 at 0.5 A·g−1, and after 5000 cycles of charging and discharging, 80.0% of the original specific capacitance is sustained. Moreover, NiCoMo-LDH//AC ASC possesses a high energy density of 39.1 Wh·kg−1 at the power density 400 W·kg−1. Combined with density functional theory (DFT) calculation, the fact that metal doping can not only effectively improve the conductivity of electrode materials has been further proved, but also accelerate the electron/ion migration rate, which successfully reveal the synergistic enhancement mechanism of electrochemical properties of materials.

In Situ growth of high-crystallinity MOF@CTF core-shell hybrid heterostructures and their application in photoelectrochemical sensing of vancomycin

Vancomycin is a first-line drug for the treatment of methicillin-resistant Staphylococcus aureus (MRSA) and multidrug-resistant bacterial infections. It is of great significance to develop rapid detection methods for vancomycin in different matrices. In this work, a novel method for the in-situ preparation of MOF@CTF core-shell hybrid heterogeneous structures was proposed and applied to the photoelectrochemical detection of vancomycin. The insolubility of the imine precursor structure in homogeneous solvents and the Lewis acidic centers in the MOF structure induced the initial arrangement of CTF on the surface of PCN-224. By encapsulating a layer of highly crystalline CTF structure onto the initial morphology of PCN-224, a MOF@CTF heterogeneous structure was formed. Importantly, the introduction of anthracene-based electron-donating groups into the CTF structure and the formation of a donor-acceptor system with triazine rings enhanced the photoconversion efficiency of the heterogeneous structure by establishing a continuous separated built-in electric field within the core-shell structure. The successful in-situ synthesis of the core-shell hybrid heterogeneous structure was confirmed through microscopic morphology, PXRD, XPS, and FT-IR. Furthermore, investigations into the semiconductor properties of the heterogeneous structure, including semiconductor type, bandgap, and photo-voltage, were conducted. Results showed that the heterogeneous structure exhibited a doubled photocurrent density compared to the original PCN-224. Additionally, a molecularly imprinted photoelectrochemical sensor (MIPECS) for vancomycin was constructed. Under optimized conditions, the sensor demonstrated a superior concentration response range (0.1 nM - 1 μM) and detection limit (0.031 nM, 3σ/S, n = 11). Simultaneously, the potential applicability of the sensor in animal-derived foods, serum, and environmental water samples was evaluated, yielding satisfactory results.

Innovative Si@MOF-5@CNT hybrid: Tailoring energy storage and catalysis in batteries, supercapacitors, and hydrogen evolution

This work presents the silicon-doped metal-organic framework with carbon nanotube additive (Si@MOF-5/CNT) composite as a versatile and cutting-edge foundation for advanced energy storage devices. This novel work highlights the doping impact of silicon and CNT to MOF-5 structure, which improves the stability and electrochemical performance. Regarding battery applications, the Si@MOF-5/CNT composite delivers a specific capacity of 1642C/g. The asymmetric structure with Si@MOF-5/CNT and activated carbon is built for supercapacitor applications. This hybrid system (Si@MOF-5/CNT//AC) provides the specific capacity of 132C/g, an energy density of 46 Wh/kg, and a power density of 1100 W/kg. In Hydrogen Evolution Reaction (HER) applications, the Si@MOF-5/CNT composite showed a minimum overpotential of 158 mV and a Tafel slope of 59.28 mV/dec. Our findings place this composite at the forefront, demonstrating improved performance and versatility in dealing with the ever-changing environment of energy storage difficulties.