Cerium-based Metal-organic Framework Research Articles

Cerium-Based Metal–Organic Framework Nanocrystals for Colorimetric Screening of α-Glucosidase Inhibitors

Cerium-Based Metal–Organic Framework Nanocrystals for Colorimetric Screening of α-Glucosidase Inhibitors

Investigating replacement core-shell strategies for optimizing photocatalytic chromium reduction with MOF-on-MOF heterostructure on steel mesh

While cerium-based metal-organic frameworks (Ce-MOFs) exhibit inherent limitations in standalone photocatalytic efficacy, their potential amplifies when integrated into heterostructures with other semiconductors, leveraging the advantageous heterojunction effects. This study systematically explores the establishment of heterojunctions between Ce-MOFs and zirconium-based frameworks, delineating the performance variance based on the positioning of Ce-MOFs within the MOF-on-MOF architecture. When situated as the outer shell in these configurations, Ce-MOFs significantly enhance the photocatalytic capabilities compared to their placement in the core. Further, immobilizing these composite structures onto steel substrates demonstrates remarkable efficiency in the purification of hexavalent chromium from water under visible light exposure. Initially, Ce-MOF-801-on-Zr-MOF-801 and Zr-MOF-801-on-Ce-MOF-801 heterojunctions were synthesized to explore their combined and MOF-on-MOF effects. Subsequently, Ce-MOF-801-on-Zr-MOF-801 was applied onto a steel mesh substrate using the spraying method. The results demonstrated exceptional efficiency in Cr(VI) extraction and remarkable durability. Crucially, leaching tests and ICP-OES analysis confirmed the material's strong adhesion to the substrate, enabling repeated use. Impressively, even after multiple cycles, the material efficiently purified Cr(VI) from water within 120 min under visible light. With all these merits, the Cr(VI) removal efficiency of Ce-MOF-801-on-Zr-MOF-801/mesh with an initial Cr(VI) concentration of 5 ppm is near 100% for 2 h. This work presents a feasible and promising route to filter suitable photocatalyst materials by using mesh substrates for fixing environmental issues.

Cerium‐based metal–organic frameworks (MOFs) as a sustainable approach to mitigating environmental stress‐induced intestinal ulcers in earthworms

Exposure to environmental stresses such as heavy metal pollution, herbicides, and climate change may cause adverse effects on biological animals such as earthworms, leading to conditions including intestinal ulcers. This study outlines the potential of a cerium‐based metal–organic framework (Ce‐MOF) in healing alcohol‐induced ulcers in earthworms. The Ce‐MOF was synthesized via a solvothermal technique and analyzed using X‐ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. Ce‐MOF exhibited a one‐dimensional channel and demonstrated multi‐enzyme‐like activity. It was examined on earthworms suffering from ulcers caused by alcohol use. Examinations at a macroscopic level, histological analysis, and transmission electron microscopy images showed significant harm to the intestinal lining in ulcerated worms. The ulcer treatment with Ce‐MOF substantially enhanced intestinal morphology, repaired the epithelial lining, and facilitated ulcer healing. Furthermore, Ce‐MOF decreased the death rate and enhanced the weight of earthworms in comparison to untreated groups. This study emphasizes the potential of Ce‐MOF as an innovative therapeutic agent for alcohol‐induced ulcers, emphasizing its prospective uses in regenerative medicine and tissue regeneration.

Degradation of Levofloxacin by Electroactivated Sodium Persulfate on Carbon Cloth Cathode Modified with Cerium-Based Metal Organic Frameworks (Ce-MOF) Derivatives

Levofloxacin (LFX), which is difficult to degrade effectively due to its molecular stability, has become an problem that needs to be solved urgently. The advanced oxidation technology of persulfate has received increasing attention from researchers. In this study, a Ce-MOF derivative (Ce-MOF-T) was prepared by hydrothermal synthesis and calcination, which synergistically responded to electroactivation to generate sulfate radicals for the efficient degradation of LFX. It has been proven that electrical activation and the Ce-MOF derivatives work together to generate sulfate radicals and effectively degrade LFX. Ce-MOF-550-modified carbon cloth was used as the cathode and a platinum electrode as the anode, the concentration of LFX was 20 mg·L−1, the loading of Ce-MOF-550 was 15 mg, pH = 5, the concentration of sodium persulfate (PMS) was 0.3 g·L−1, the current density was 100 A·m−2, and the degradation rate was 82.05% after 1 h of reaction and 95% after 3 h of reaction. After five cycle tests, the degradation rate was still higher than 75.00%, indicating that the material had good stability. In addition, the degradation of LFX was consistent with a quasi-primary kinetic reaction with apparent rate constants of 2.26 × 10−2 min−1.

Porous CePO4@carbon composite derived from cerium-based metal–organic framework for the simultaneous detection of dopamine, uric acid, and acetaminophen

Cerium phosphate (CePO4) has attracted increasing attention in the field of electrochemistry. In this work, a mesoporous CePO4@carbon composite was successfully prepared via the high-temperature calcination method using cerium-based metal–organic framework (Ce-MOF) as a precursor. The obtained samples were characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), N2 adsorption–desorption technique, and X-ray photoelectron spectroscopy (XPS). The findings revealed that the in-situ pyrolysis of Ce-MOF generated uniform composite, which showed high electrical conductivity and plenty of catalytic active sites. These structural advantages of the composite were conductive to the electron transfer, substrate diffusion, and redox reactions. Thereafter, CePO4@carbon was developed to modify the commercially purchased glass carbon electrode (GCE: CHI 104) for simultaneous detection of dopamine (DA), uric acid (UA), and acetaminophen (APAP). The linear detection ranges for DA, UA, and APAP were 2.5–310.0 μM, 3.0–305.0 μM, and 2.5–617.0 μM, respectively. The detection limits (LOD) for DA, UA, and APAP were 0.009 μM, 0.016 μM, and 0.014 μM, respectively. Furthermore, the constructed electrode can be employed to detect the concentration of DA, UA, and APAP in real-samples. This work provides a method for manufacturing highly efficient CePO4 based materials for electrochemical sensing.

Synthesis, Structure and (Photo)Catalytic Behavior of Ce-MOFs Containing Perfluoroalkylcarboxylate Linkers: Experimental and Theoretical Insights.

Cerium-based Metal-Organic frameworks (Ce-MOFs) are attracting increasing interest due to their similar structural features to zirconium MOFs. The redox behavior of Ce(III/IV) adds a range of properties to the compounds. Recently, perfluorinated linkers have been used in the synthesis of MOFs to introduce new characteristic into the structure. We report the synthesis and structural characterization of Ce(IV)-based MOFs constructed using two perfluorinated alkyl linkers. Their structure, based on hexanuclear Ce6O4(OH)4 12+ clusters linked to each other by the dicarboxylate ions, has been solved ab-initio from X-ray powder diffraction data and refined by the Rietveld method. The crystallization kinetics and the MOF formation mechanism was also invesitigated by Synchrotron radiation with XAS spectroscopies (EXAFS and XANES). The MOFs present the same fcu cubic topology as observed in MOF-801 and UiO-66, and they showed good stability in water at different pH conditions. The electronic structure of these MOFs has been studied by DFT calculations in order to obtain insights into the density of states structure of the reported compounds, resulting in band gaps in the range of 2.8-3.1 eV. Their catalytic properties were tested both thermally and under visible light irradiation for the degradation of methyl orange (MO) dye.

Mechanisms of metabolic regulation and enhanced methane production by hydrolytic nanozyme in sludge anaerobic digestion

Artificial nanozymes have demonstrated potential as natural enzyme substitutes due to their efficient biomacromolecule hydrolysis. However, the metabolic and catalytic mechanisms of nanozyme during the biodegradation of complex organics remain inadequately understood. This study evaluated the effect of the hydrolytic mechanism of cerium-based metal–organic frameworks (Ce-MOFs) hydrolytic nanozyme on shaping microbiome and metabolic functions. Biochemical methane potential test revealed that Ce-MOF-based hydrolytic nanozyme increased methane production by 7.8 − 22.2% as the hydrolytic nanozyme dosage increased from 50 to 150 mg/g VS. The highest methane production observed in 150 mg/g VS dosage of Ce-MOF (Ce-MOF-150) could be attributed to the enhanced sludge hydrolysis, acidogenesis, and methanogenesis processes, proven by the increased relative abundance of dominant acidogens and methanogens. Furthermore, 150 mg/g VS hydrolytic nanozyme bolstered the relative abundance of genes encoding acetyl-CoA carboxylase (accABCD) and involving in glycolysis (hxk and pfkA). These quantities were higher (8.31 − 34.14%) than that without nanozyme addition. The enhanced relative abundance of ackA, pta, cdhCDE, mvhAD, fpoABCDHIJKLMNO, vhoC, rnfABCDEG, mtrABCDEFGH, and hdrABC in the Ce-MOF-150 test indicated that the high proton conductivity of nanozyme facilitated acetoclastic methanogenesis and membrane-bound electron transport system, thereby enhancing methane production. These findings contribute to the expanding understanding of the application of artificial nanozymes as biocatalysts for solid waste resource recovery, providing a promising approach for methane production from sewage sludge.

Design strategies for MOFs-derived Ce10-xZrxOy catalysts with polyhedral coordination to enhance soot combustion

Various cerium-based metal–organic frameworks (Ce-MOFs and Ce10-xZrx-MOFs) and their derivatives (Ce10-xZrxOy complex oxide catalysts) with different structures and properties by modulating the organic ligands (i.e., trimesic acid (BTC), 1,2,4,5-benzenetetracarboxylic acid (PMA), and terephthalic acid (BDC)) and transition metal elements via the solvothermal method. The performance of these catalysts was tested in the diesel soot oxidation reaction. In contrast, morphology engineering and the introduction of heteroatom zirconium to modify CeO2 can significantly improve the catalytic activity and stability of the catalyst. Among them, the best Ce5Zr5Oy-BDC shows remarkable catalytic performance for soot oxidation, converting 90% of soot particles into CO2 at about 410 °C. A series of characterization results demonstrate that the engineering of morphology provides a highly active polycrystalline surface for the adhesion of reactants, and the electron transfer system caused by Zr doping weakens the Ce-O bond. With the help of their combined action, the exposed polycrystal surfaces greatly enhance the oxygen vacancy content and the ability to generate reactive oxygen species. The DFT investigations shows that the presence of Zr can weaken the Ce-O link, result in favorable defect structures, and the reactive oxygen species of formation were promoted. This study provides an idea for the design of non-precious metal catalysts with high activity and stability.

MOF-Derived CeO2 Nanorod as a Separator Coating Enabling Enhanced Performance for Lithium-Sulfur Batteries.

The deployment of Li-S batteries in the commercial sector faces obstacles due to their low electrical conductivity, slow redox reactions, quick fading of capacity, and reduced coulombic efficiency. These issues stem from the "shuttle effect" associated with lithium polysulfides (LiPSs). In this work, a haystack-like CeO2 derived from a cerium-based metal-organic framework (Ce-MOF) is obtained for the modification of a polypropylene separator. The carbon framework and CeO2 coexist in this haystack-like structure and contribute to a synergistic effect on the restriction of LiPSs shuttling. The carbon network enhances electron transfer in the conversion of LiPSs, improving the rate performance of the battery. Moreover, CeO2 enhances the redox kinetics of LiPSs, effectively reducing the "shuttle effect" in Li-S batteries. The Li-S battery with the optimized CeO2 modified separator shows an initial discharge capacity of 870.7 mAh/g at 2 C, maintaining excellent capacity over 500 cycles. This research offers insights into designing functional separators to mitigate the "shuttle effect" in Li-S batteries.

Unveiling CO2 Dynamics in Perfluorinated Cerium-Based Metal–Organic Frameworks with UiO-66 and MIL-140 Topologies by Solid State NMR

Unveiling CO₂ Dynamics in Perfluorinated Cerium-Based Metal–Organic Frameworks with UiO-66 and MIL-140 Topologies by Solid State NMR

Hydrogen sulfide chemiresistive sensor based on swift heavy ion irradiated cerium-based metal–organic framework/graphene oxide composite

Herein, we report ultrahigh sensitive and selective hydrogen sulfide (H2S) chemiresistive sensor using SHI irradiated cerium-based metal–organic framework (MOF)/graphene oxide composite (Ce-BTC/GO). The solvothermal synthesized Ce-BTC/GO coated on an indium tin oxide (ITO) electrode, irradiated by the 100 MeV Au+ ion at the fluence rate 5 × 1010 ions/s, 5 × 1011 ions/s and 5 × 1012 ions/s has been tested for chemiresistive sensing of H2S. As irradiated, Ce-BTC/GO was multi-parametrically tested for XRD, FE-SEM, FTIR spectroscopy, Raman spectroscopy and I-V characteristics for its structural, morphological, spectroscopic and electrical characteristics. The result reveals that the irradiation treatment greatly affects the electric characteristics of the GO, achieving dramatic conductivity modulation in the presence of H2S gas, it also creates the surface sites for the H2S absorption and hence shows excellent real-time sensing performance below the maximum residue limit established by OSHA (Occupational Safety and Health Administration). SHI irradiated Ce-BTC/GO sensor also shows excellent response/recovery time, ultrahigh reproducibility, good repeatability and stability at room temperature. The sensor allows the detection of H2S with a sensitivity of 54.70% in a concentration range of 10–100 ppm with a limit of detection 10 ppm.

Dual-mode photoelectrochemical radar based on CdS quantum dot and Ce-MOF for detection of low-abundance disease-associated proteins

Herein, we developed a convenient and versatile dual-mode electrochemiluminescence (ECL) and photoelectrochemistry (PEC) sensing radar for the detection of Prostate-specific antigen (PSA), which has important implications for detection of low-abundance disease-associated proteins. Cerium-based metal-organic framework (Ce-MOFs) were firstly modified on the electrode, showing well ECL and PEC property. In particular, a unique multifunctional Au@CdS quantum dots (QDs) probe loaded numerous QDs and antibody was fabricated, not only displaying strong ECL and PEC signals, but also having specific recognition to PSA. After the signal probe was linked to the electrode by immune reaction, much amplified signals of ECL and PEC were generated for double-mode detection of PSA. Therefore, this work proposed a multifunctional Au@CdS QDs signal probe with excellent ECL and PEC performance, and developed an ultrasensitive photoelectric biosensing platform for dual-mode detection, which provides an effective method for health monitoring of cancer patients.

Enhanced electrochemical performance of cerium-based metal organic frameworks derived from pyridine-2,4,6-tricarboxylic acid for energy storage devices

Modern era demands development of hybrid supercapacitor amalgamating characteristics of battery and supercapacitor is a single unit. Various contender electrode materials have been used so far, however, metal organic frameworks, having rich porosity and distinctive electrochemical properties can be integrated in energy storage devices to improve electrochemical performance. Herein, we have synthesized Ce-PTA-MOF from pyridine-2,4,6-tricarboxylic acid which was structurally as well as electrochemically characterized. Effects of different concentrations of KOH electrolyte on electrochemical properties of Ce-PTA-MOF electrode has been investigated using three electrodes assembly and practical applications of hybrid supercapacitor device has also been explored by fabricating it with activated carbon. The stability and capacitive-diffusive contributions of the hybrid supercapacitor has been analyzed by theoretical approach. The specific capacity, maximum energy density and power density were calculated as 115 C/g, 26.75 Wh/kg and 5760 W/kg respectively which showed efficiency of 99.2 % even after 5000 GCD cycles. High energy density and power density with extraordinary stability make Ce-PTA-MOF electrode a promising candidate for futuristic hybrid supercapacitor devices.

Ultrasound Trigger Ce-Based MOF Nanoenzyme For Efficient Thrombolytic Therapy.

The inflammatory damage caused by thrombus formation and dissolution can increase the risk of thrombotic complications on top of cell death and organ dysfunction caused by thrombus itself. Therefore, a rapid and precise thrombolytic therapy strategy is in urgent need to effectively dissolve thrombus and resist oxidation simultaneously. In this study, Ce-UiO-66, a cerium-based metal-organic framework (Ce-MOF) with reactive oxygen species (ROS) scavenging properties, encapsulated by low-immunogenic mesenchymal stem cell membrane with inflammation-targeting properties, is used to construct a targeted nanomedicine Ce-UiO-CM. Ce-UiO-CM is applied in combination with external ultrasound stimulation for thrombolytic therapy in rat femoral artery. Ce-UiO-66 has abundant Ce (III)/Ce (IV) coupling sites that react with hydrogen peroxide (H2O2) to produce oxygen, exhibiting catalase (CAT) activity. The multi-cavity structure of Ce-UiO-66 can generate electron holes, and its pore channels can act as micro-reactors to further enhance its ROS scavenging capacity. Additionally, the porous structure of Ce-UiO-66 and the oxygen produced by its reaction with H2O2 may enhance the cavitation effects of ultrasound, thereby improving thrombolysis efficacy.

Synergistic enhancement of CO2/N2 separation performance via Ce-MOF-infused chitosan mixed matrix membrane.

Reticular chemistry, exemplified by metal-organic frameworks (MOFs), has proven invaluable in creating porous materials with finely tuned structures to address critical global energy and environmental challenges. In this context, the need for efficient carbon dioxide (CO2) capture and utilization has taken center stage. One promising approach involves the integration of MOFs into polymer matrix to develop mixed matrix membranes (MMMs). In this work, cerium-based MOFs (Ce-MOF) were selected due to their robust CO2 capture capabilities, while chitosan (CS) was chosen as the polymer matrix due to its reasonably good selectivity and balanced CO2 permeance for the development of MMMs for CO2/N2 (20/80 vol%) separation. A comprehensive suite of analytical techniques, including FTIR, XRD, FESEM, XPS, TGA, EDX, FETEM, and BET, was applied for precise characterization of both the MOF and MMMs. Various operational parameters, such as Ce-MOF content and temperature, were systematically explored to investigate the CO2 capture efficiency of the synthesized MMMs. The results revealed that the optimized Ce-MOF-embedded CS MMMs consistently outperformed the bare CS membranes.

Enhanced carbohydrate-based plastic performance by incorporating cerium-based metal-organic framework for food packaging application

The development of biodegradable active packaging films with hydrophobic characteristics is vital for extending the shelf life of food and reducing the reliance on petroleum-based plastics. In this study, novel hydrophobic cerium-based metal-organic framework (Ce-MOF) nanoparticles were successfully synthesized. The Ce-MOF nanoparticles were then incorporated into the cassava starch matrix at varying concentrations (0.5 %, 1.5 %, 3 %, and 4 % w/w of total solid) to fabricate cassava-based active packaging films via the solution casting technique. The influence of Ce-MOF on the morphology, thermal attributes, and physicochemical properties of the cassava film was subsequently determined through further analyses. Biomedical analysis including antioxidant activity and the cellular morphology evaluation in the presence of the films was also conducted. The results demonstrated that the consistent dispersion of Ce-MOF nanofillers within the cassava matrix led to a significant enhancement in the film's crystallinity, thermal stability, antioxidant activity, biocompatibility, and hydrophobicity. The introduction of Ce-MOF also contributed to the film's reduced water solubility. Considering these outcomes, the developed cassava/Ce-MOF films undoubtedly have significant potential for active food packaging applications.

Comparative Investigation of Phosphate Adsorption Efficiencies of MOF-76 (Ce) and Metal Oxides Derived from MOF-76 (Ce).

Phosphate pollution is a very challenging problem for the water environment. Phosphate mixed with water in various ways causes eutrophication. To sustain life in aquatic systems, phosphate ions must be cleaned. Therefore, it is very important to remove phosphate in wastewater. Here, an adsorption method has been tried for the removal of phosphate. MOF-76 (Ce), a cerium-based metal-organic framework, was synthesized by a hydrothermal method. Since metal oxides are known to be successful in phosphate adsorption, CeO2 nanoparticles were also obtained by pyrolysis of this MOF structure. The phosphate adsorption efficiencies of both adsorbents were compared. The characterization methods (SEM, FTIR, XRD, and TGA) were applied to adsorbents. The kinetic, isotherm, and thermodynamics studies were applied to experimental results. At 298 K, the adsorption capacity of MOF-76 (Ce) is higher than that of CeO2, according to Langmuir isotherm qm values. The qm values are 72.97 and 55.71 mg/g, respectively. Both adsorbents follow the pseudo second-order kinetic model. It has been found that MOF-76 (Ce) has a pH-selective property in phosphate adsorption. No change was observed in the phosphate adsorption capacity of CeO2 with pH. In terms of thermodynamics, the endothermic reaction is valid for both adsorbents.

Effective adsorption of methyl orange dye from water samples over copper(II) Schiff-base complex-immobilized cerium-based metal-organic framework

Herein, a copper(II) Schiff-base complex derived from the condensation of salicylaldehyde (Sal) with amino groups of a cerium-based metal-organic framework of type, UiO-66-NH2(Ce), denoted here Cu(II)/Sal@UiO-66(Ce), has been prepared and characterized by EDX, SEM, FT-IR, BET and XRD, as well as thermal gravimetric analysis (TGA) techniques. The nominal nanostructure including dual-metal sites (Ce and Cu) was considered as a novel adsorbent for removing methyl orange (MO, as an organic contaminant) dye from aqueous media. Accordingly, various key experimental factors such as the pH, mass of adsorbent, contact time, and eluent type were tested and optimized. Based on experimental outcomes, the adsorption of MO for Cu(II)/Sal@UiO-66(Ce) reaches a maximum of 98.8 % efficiency at a pH of 6 and a maximum extraction capacity of 454.5 mg/g. Also, the limit of detection (LOD) and relative standard deviation (RSD%) were 0.63 μg/L and 2.4 %, respectively, under the optimum condition. Reusability, short adsorption time, and low-cost cerium-based MOF are the other advantages of the corresponding adsorbent. In addition, the porous adsorbent was applicable for the MO adsorption from environmental water samples.

Tuning the Cerium-Based Metal-Organic Framework Formation by Template Effect and Precursor Selection.

The novel metal-organic framework [(CH3)2NH2]2[Ce2(bdc)4(DMF)2]·2H2O (Ce-MOF, H2bdc-terephthalic acid, DMF-N,N-dimethylformamide) was synthesized by a simple solvothermal method. Ce-MOF has 3D connectivity of bcu type with a dinuclear fragment connected with eight neighbors, while three types of guest species are residing in its pores: water, DMF, and dimethylammonium cations. Dimethylamine was demonstrated to have a decisive templating effect on the formation of Ce-MOF, as its deliberate addition to the solvothermal reaction allows the reproducible synthesis of the new framework. Otherwise, the previously reported MOF Ce5(bdc)7.5(DMF)4 (Ce5) or its composite with nano-CeO2 (CeO2@Ce5) was obtained. Various Ce carboxylate precursors and synthetic conditions were explored to evidence the major stability of Ce-MOF and Ce5 within the Ce carboxylate-H2bdc-DMF system. The choice of precursor impacts the surface area of Ce-MOF and thus its reactivity in an oxidative atmosphere. The in situ PXRD and TG-DTA-MS study of Ce-MOF in a nonoxidative atmosphere demonstrates that it eliminates H2O and DMF along with (CH3)2NH guest species in two distinct stages at 70 and 250 °C, respectively, yielding [Ce2(bdc)3(H2bdc)]. The H2bdc molecule is removed at 350 °C with the formation of novel modification of Ce2(bdc)3, which is stable at least up to 450 °C. According to the total X-ray scattering study with pair distribution function analysis, the most pronounced local structure transformation occurs upon departure of DMF and (CH3)2NH guest species, which is in line with the in situ PXRD experiment. In an oxidative atmosphere, Ce-MOF undergoes combustion to CeO2 at a temperature as low as 390 °C. MOF-derived CeO2 from Ce-MOF, Ce5, and CeO2@Ce5 exhibits catalytic activity in the CO oxidation reaction.

Engineering Ultra‐Small Cerium‐Based Metal–Organic Frameworks Nanozymes for Efficient Antioxidative Treatment of Dry Eye Disease

AbstractDry eye disease (DED) is a widespread ophthalmic illness that inflicts massive economic and medical burdens on society. Although oxidative stress is closely associated with the onset of DED, barely any quantities of antioxidants are clinically available owing to low efficiency, toxicity, and poor bioavailability. Cerium‐based nanozymes possess promising enzyme‐mimetic activities in scavenging reactive oxygen species (ROS). Moreover, the ultra‐small metal–organic frameworks (MOFs) have the potential for more efficient drug delivery, ROS elimination, and therapeutic efficacy. However, the development of ultra‐small cerium‐based MOFs (Ce‐MOFs) is limited to a small minority due to challenges in the synthetic process and stability. By simply adjusting raw ingredients concentrations, three types of Ce‐MOFs with distinct particle sizes are synthesized: Ce‐MOF 1 (213 nm), Ce‐MOF 2 (36 nm), and Ce‐MOF 3 (2 nm). In comparison, the obtained ultra‐small Ce‐MOF 3 exhibited superior ROS scavenging and antioxidant capacity, decreased cytotoxicity, and excellent ocular penetration. Therapeutically, Ce‐MOF 3 is demonstrated to be highly efficient in alleviating DED by suppressing oxidative stress and inflammation, boosting corneal epithelial repair, and facilitating tear secretion recovery. The novel ultra‐small Ce‐MOF 3 may serve as a promising alternative treatment for DED and other ROS‐related disorders when combined with ocular biocompatibility.