Prussian Blue Research Articles

Fe3C@Fe decorated carbonized wood Fiber catalyst for organic dyes degradation: Preparation, characterization and mechanism

The extensive use of organic dyes has led to significant water pollution. Using lignocellulosic waste as a precursor for catalysts preparation for sewage remediation presents an effective alternative with numerous advantages in sustainability, cost-effectiveness, and environmental compatibility. In this work, wood fiber waste collected from wood processing plants was decorated with Prussian blue (PB) and then annealed to produce carbonized wood fiber catalyst (Fe3C@Fe-CB). In the presence of peroxymonosulfate (PMS), the prepared catalyst could achieve over 98.69 % efficiency in degrading methylene blue (MB) solutions (20 mg/L) in 60 min across a pH range of 3 to 11. Electrochemical test and electron paramagnetic resonance (EPR) analysis respectively verified that electron transfer pathway and radical pathway were the key factors for the degradation of MB. Cyclic degradation tests demonstrated that the degradation efficiency remained above 93.67 % after five recycling experiments. Moreover, the used magnetic catalyst can be easily recycled by magnet. This study proposed a facile and sustainable carbonized wood fiber catalyst decorated by Fe3C@Fe-CB, which could realize efficient elimination of organic dyes. Moreover, we offered a novel choice for dyes-polluted water treatment and paving a new route for converting low-value lignocellulosic waste to high-value utilizations.

A simplified ratiometric fluorescent sensing strategy for enhanced detection of alkaline phosphatase employing Prussian blue nanozymes and commercially available chromogen

The traditional nanozymes-based ratiometric fluorescence sensing platforms usually necessitate the supplementary addition of fluorescent probes, therefore greatly restricting its convenient and broad application. In this study, a highly sensitive and selective ratiometric fluorescence platform for alkaline phosphatase (ALP) detection was established, only employing Prussian blue (PB) nanozymes and a commercially available chromogen of o-phenylenediamine (OPD). PB nanozymes with remarkable peroxidase-like (POD-like) activity can effectively catalyze OPD chromogen to yield 2,3-diaminophenazine (OPDox) with an intense yellow fluorescence at 573 nm emission peak. Target ALP can facilitate ascorbic acid 2-phosphate (AAP) dephosphorylation to generate phosphate and ascorbic acid (AA). Significantly, both these two resultant hydrolysis products could effectively decrease the OPDox generation via a dual-path based inhibition on the PB nanozymes POD-like activity. On the other hand, the generated dehydroascorbic acid (DHAA) from AA oxidation would exclusively react with OPD chromogen to yield 3-(dihydroxyethyl)furo[3,4-b]quinoxaline-1-one (DFQ) with a strong blue fluorescent signal at 434 nm, which further providing a significant enhancement on the sensing selectivity of ALP detection. As a result, an increased yellow fluorescence of OPDox and decreased blue fluorescence of DFQ could be clearly observed with different ALP addition. A robust linear relationship between the fluorescence ratio of F434/F573 and ALP activity ranging from 0.25 U/L to 6 U/L was obtained, with a low detection limit of 0.112 U/L. This proposed method demonstrates high sensitivity, excellent selectivity, cost-effectiveness, and operational simplicity, yet enabling an effective detection of ALP levels in human serum.

An Electro‐Driven Dynamic and Multicolored Radiative Thermal Regulation Material for All‐Year‐Round Building Energy Saving

AbstractRational dynamic thermal regulation of both solar and thermal regions is of significant importance for building energy saving. In this work, an electro‐driven dynamic radiative thermal regulation material (EDRTRM) capable of switching the thermal regulation capacity between the heating, white cooling, and multicolored cooling (blue, green, and yellow) modes is designed. These multi‐modes with high thermal regulation power and color variation are achieved through a synergistic material combination involving an electrochromism of Prussian blue (PB) and the electrodeposition of copper (Cu) with a polyformaldehyde (POM)‐based mid‐infrared (MIR) emitter. Optical characterization confirmed the superior spectral performance of materials, with a remarkable modulation capability of power density up to 659 W m−2, indicating an exceptional heating and cooling performance, which is evidenced by a temperature modulation difference of up to 11 °C. Notably, the EDRTRM under a multi‐colored cooling mode also achieves a temperature reduction of ≈ 4–6 °C. The EnergyPlus simulations demonstrate that the EDRTRM can save a huge amount of energy consumption of 16.56 MJ m−2 in cities with seasonal temperature variations such as Beijing. This dual‐functional design not only maximizes thermal regulation capabilities but also satisfies aesthetic requirements, showcasing its potential for widespread practical application.

Cupric Doping Hollow Prussian Blue Nanoplatform for Enhanced Cholesterol Depletion: a Promising Strategy for Breast Cancer Therapy and Metastasis Inhibition.

The dysregulated cholesterol metabolism in breast cancer cells drives malignancy, invasion, and metastasis, emphasizing the significance of reducing abnormal cholesterol accumulation for effective cancer treatment and metastasis inhibition. Despite its promise, cholesterol oxidase (ChOx) encounters challenge due to limited catalytic efficiency and susceptibility to harsh conditions. To overcome these hurdles, biocompatible nanoplatforms (Cu-HPB/C) tailored for efficient cholesterol depletion are introduced. Cu2+-doped hollow Prussian blue (Cu-HPB) acts as a carrier, shelter, and enhancer for ChOx, bolstering tumor-targeting ability, stability, and enzymatic activity. Tumor-responsive released Cu2+ notably augments ChOx activity, facilitating cholesterol depletion and disrupting lipid rafts, thereby impeding cell invasion and migration. Additionally, H2O2 generated from the oxidase reaction enhances Cu-HPB's chemo dynamic therapeutic efficacy. Transcriptomic analysis validates Cu-HPB/C's impact on cholesterol homeostasis and reveals cell death mechanisms including oxidative stress, ferroptosis, cuproptosis, and apoptosis. Demonstrating therapeutic efficacy in both 4T1 tumor subcutaneous and metastasis mouse models, the study presents a direct and effective strategy for tumor therapy and metastasis inhibition through enhanced cholesterol depletion.

Insights on Prussian Blue Analogue Cathode Material Engineered with Polypyrrole Surface Protection Layer for Aqueous Rechargeable Zinc Metal Battery.

One of the key intricacies against using Prussian blue analogues (PBAs)in aqueous batteries is their gradual dissolution in aqueous electrolytes, resulting in inadequate cycling stability. Besides, the rate capability of PBAs is limited due to their poor electrical conductivity. To overcome these challenges, it is essential to tune the physical and chemical properties of PBAs at the nano regime without affecting the inherent charge storage properties, especially at high-voltage operating conditions. Through this work, a strategy is demonstrated to enhance the electrochemical performance of vanadium-based PBA (V-PBA) by surface engineering using a conducting polymer nano-skin (V-PBA/PPy) for aqueous zinc metal batteries. The polypyrrole (PPy) nano-skin over the V-PBA nanoparticles acts as an electron percolation path to ameliorate the poor electronic conductivity of the otherwise pristine V-PBA. Interestingly, the V-PBA with an optimized polypyrrole coating (V-PBA/PPy-2) exhibits an enhanced specific capacity (173 mAh g-1 at 0.10 A g-1) than the pristine V-PBA counterpart (80 mAh g-1) and 85% capacity retention up to 500 cycles. The DFT calculation confirms the synergistic interaction between PPy and V-PBA and the presence of PPy favors the adsorption of Zn.

Impact of Sodium on the Water Dynamics in Prussian Blue Analogues

Impact of Sodium on the Water Dynamics in Prussian Blue Analogues

Peroxynitrite-Free Nitric Oxide-Embedded Nanoparticles Maintain Nitric Oxide Homeostasis for Effective Revascularization of Myocardial Infarcts.

Revascularization is crucial for treating myocardial infarction (MI). Nitric oxide (NO), at an appropriate concentration, is recognized as an ideal and potent pro-angiogenic factor. However, the application of NO in the treatment of MI is limited. Improper NO supplementation is harmful to revascularization because NO is converted into harmful peroxynitrite (ONOO-) in MI tissues with high reactive oxygen species (ROS) levels. We overcome these obstacles by embedding biliverdin and NO into Prussian blue (PB) nanolattices to obtain an ONOO--free NO-embedded nanomedicine (OFEN). Unlike previous NO donors, OFEN provides NO stably and spontaneously for a longer time (>7 days), which makes it possible to maintain a stable concentration of NO, suitable for angiogenesis, through dose optimization. More importantly, based on the synergy between PB and biliverdin, OFEN converts ROS into beneficial O2 and inhibits the production of ONOO- from the source. OFEN specifically targets MI tissues and achieves sustained and stable NO delivery at the MI site. OFEN effectively promotes revascularization in the MI tissue, significantly reduces myocardial death and fibrosis, and ultimately promotes the complete recovery of cardiac function. Our strategy provides a promising approach for the treatment of myocardial and other ischemic diseases.

Enhanced decontamination of surface radioactive contamination using a hydrogel coating composited with Prussian blue

Enhanced decontamination of surface radioactive contamination using a hydrogel coating composited with Prussian blue

Copper peroxide-decorated Prussian blue for effective bacterial elimination via photothermal-enhanced and H2O2-releasing chemodynamic therapy

Bacterial infection is a major impediment towards wound healing and threaten human health worldwide. Traditional antibiotic therapy poses a high risk of inducing bacterial resistance, thus nanomaterial-based synergistic bactericidal strategy as effective alternatives have received tremendous attention. Herein, a NIR/pH-dual responsive nanoplatform was fabricated for synergistic photothermal and chemodynamic therapy (PTT/CDT). Prussian blue (PB) were employed as supporting material, while copper peroxide (CP) were growth in situ on PB surface, resulting in a core-shell structured nanoplatform (designated as PC). PB core served as photothermal/Fenton catalyst dual agents, and CP shell could co-release Cu2+ and H2O2 under acidic bacterial infection environment, realizing synergistic PTT and H2O2-releasing CDT. Under NIR irradiation, PC exhibited photothermal-enhanced Fenton-like reaction feature and the hyperthermia facilitated Cu2+ release, leading to the rapid conversion of H2O2 into toxic •OH to effectively kill Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus), eradicating S. aureus biofilm. Moreover, the released Cu2+ could improve the bactericidal effect of CDT via the depletion of GSH and significantly promote cell migration. Furthermore, in vivo experiments demonstrated PC with good biocompatibility exhibited robust bactericidal effect and promoted wound healing. Overall, this versatile nanoplatform offered an efficacious and safe antibiotic-free strategy for bacterial infection treatments.

Defect-Engineered Coordination Compound Nanoparticles Based on Prussian Blue Analogues for Surface-Enhanced Raman Spectroscopy.

Surface-enhanced Raman spectroscopy (SERS) is a powerful tool for label-free chemical analysis. The emergence of nonmetallic materials as SERS substrates, offering chemical signal enhancements, presents an exciting direction for achieving reproducible and biocompatible SERS, a challenge with traditional metallic substrates. Despite the potential, the realm of nonmetallic SERS substrates, particularly nanoparticles, remains largely untapped. Here, we present defect-engineered coordination compounds (DECCs) based on Prussian blue analogues (PBAs) as a class of nonmetallic nanoparticle-based SERS substrates. We demonstrate the utility and flexibility of the DECC template by incorporating various metal (M) elements into PBAs to synthesize nanoparticles that deliver substantial chemical mechanism (CM)-based enhancements to the Raman signal with a ∼ 108-fold increase. The introduction of the M-PBA-based DECC nanoparticles as a class of SERS substrates represents a pioneering stride, enabling the straightforward and systematic exploration of a library of compounds for SERS-based analysis of a wide range of target molecules, especially biomolecules.

Valence switching of bismuth in ferricyanide as cathode materials for sodium-ion batteries

Sodium-ion batteries (SIBs) are considered potential alternatives to lithium-ion batteries, and the key to their widespread use lies in finding efficient and cost-effective cathode materials. Ferricyanides have emerged as promising candidates for SIBs cathodes due to their low cost and open channel structure allowing for favorable ion and electron transport. However, traditional ferricyanides such as Prussian blue (PB) and its analogs (PBAs) have a limited two-electron transfer capacity, which hampers their practical application. Bi-based ferricyanide materials with multiple valence states, low toxicity and abundant resources are attractive for electrochemical reactions and enable multiple electron transfers to develop high-capacity cathode materials. In this study, we synthesized a rod-like BiHCF·4H2O sample using a simple coprecipitation method. After dehydration, the rod-like BiHCF compounds with a robust framework and reduced lattice water defects demonstrated good electrochemical performance in SIBs. The rod-like BiHCF electrode exhibited a specific capacity of 221 mAh g−1 at 20 mA g−1 based on a three-electron transfer of Bi3+/Bi0. A full SIBs composed of a BiHCF cathode and Bi anode demonstrated acceptable performance, indicating potential for practical applications. This work provides valuable insights into the development of redox-active site substitution strategies for high performance positive electrode materials in SIBs.

Perfect Is Perfect: Nickel Prussian Blue Analogue as A High-Efficiency Electrocatalyst for Hydrogen Peroxide Production.

Prussian blue analogues (PBA) are a large family of functional materials with diverse applications such as in electrochemical fields. However, their use in the emerging two-electron oxygen reduction reaction for clean production of hydrogen peroxide (H2O2) is lagging. Herein, a general solvent exchange induced reconstruction strategy is demonstrated, through which an abnormal NiNi-PBA superstructure is synthesized as a high-performance electrocatalyst for H2O2 generation. The resultant NiNi-PBA superstructure has a stoichiometric composition with saturated lattice water, and a leaf-like morphology composed of interconnected small-size nanosheets with identical orientation and predominate {210} side surface exposure. Our studies show that the Ni-N centers on {210} facets are the active sites, and the saturated lattice H2O favors a six-coordinated environment that results in high selectivity. The "perfect" structure including stoichiometric composition and ideal facet exposure leads to a high selectivity of ~100 % and H2O2 yield of 5.7 mol g-1 h-1, superior to the reported MOF-based electrocatalysts and most other electrocatalysts.

Perfect Is Perfect: Nickel Prussian Blue Analogue as A High‐Efficiency Electrocatalyst for Hydrogen Peroxide Production

AbstractPrussian blue analogues (PBA) are a large family of functional materials with diverse applications such as in electrochemical fields. However, their use in the emerging two‐electron oxygen reduction reaction for clean production of hydrogen peroxide (H2O2) is lagging. Herein, a general solvent exchange induced reconstruction strategy is demonstrated, through which an abnormal NiNi‐PBA superstructure is synthesized as a high‐performance electrocatalyst for H2O2 generation. The resultant NiNi‐PBA superstructure has a stoichiometric composition with saturated lattice water, and a leaf‐like morphology composed of interconnected small‐size nanosheets with identical orientation and predominate {210} side surface exposure. Our studies show that the Ni−N centers on {210} facets are the active sites, and the saturated lattice H2O favors a six‐coordinated environment that results in high selectivity. The “perfect” structure including stoichiometric composition and ideal facet exposure leads to a high selectivity of ~100 % and H2O2 yield of 5.7 mol g−1 h−1, superior to the reported MOF‐based electrocatalysts and most other electrocatalysts.

Prussian Blue-Carbonized wood photothermal composites for efficient solar evaporation and seawater desalination

Freshwater scarcity, exacerbated by environmental pollution, poses a significant global challenge. This study addresses these challenges by developing a Prussian blue/carbonized wood (PB/CW) photothermal composite for solar desalination. The PB/CW composite exhibits enhanced solar absorption and photothermal conversion. The integration of Prussian blue (PB) on the honeycomb structure of wood facilitates efficient water transport and minimizes heat loss, underscoring the composite’s potential in practical solar desalination applications. Under natural sunlight, the PB/CW system achieves an evaporation rate of 4.39 kg m-2 h-1, demonstrating its high efficiency in converting solar energy into water evaporation. This work offers a novel and effective approach to designing low-cost, high-efficiency solar evaporators, advancing the field of sustainable desalination technology.

A Bacterial Capturing, Neural Network-Like Carbon Nanotubes/Prussian Blue/Puerarin Nanocomposite for Microwave Treatment of Staphylococcus Aureus-Infected Osteomyelitis.

Staphylococcus aureus (S. aureus)-infected osteomyelitis is a deep tissue infection that cannot be effectively treated with antibiotics. Microwave (MW) thermal therapy (MTT) and MW dynamic therapy (MDT) based on MW-responsive materials are promising for the therapy of bacteria-infected osteomyelitis occurring in deep tissues that cannot be effectively treated with antibiotics. In this work, the MW-responsive system of carbon nanotubes (CNTs)/Prussian blue (PB)/puerarin (Pue) with stable network-like structures is constructed. The PB is grown in situ on the CNTs, and its introduction not only reduces the aggregation of the network-like structures of the CNTs, but the large specific surface area and mesoporous structure can also provide many active sites for the adsorption of oxygen and polar molecules. Pue is a natural anti-inflammatory material that reduces inflammation at the infection site. The composite of the CNTs and PB avoids the skin effect and thus can improve dielectric and reflection losses. The MW thermal response of CNTs/PB/Pue is mainly due to the occurrence of reflection loss, dielectric loss, multiple reflections and scattering, interface polarization, and dipole polarization. In addition, under MW irradiation, the CNTs/PB/Pue can produce reactive oxygen species (ROS), such as singlet oxygen (1O2), hydroxyl radical (·OH).

Robust and washable silk fiber-based electrochemical biosensor for high-performance sensing of hydrogen peroxide

Wearable electronics, especially fiber-based biosensors, show promise in large-scale production and reusability compared with conventional wafer-based electronics. However, it is challenging to use wearable electronics, with less intensity and non-wash ability, to produce fiber-based biosensors for textiles. Here, a robust and washable Prussian blue (PB)-functionalized silk fiber (PB-SF) flexible electrode is reported. Modified cyanotype is successfully employed to immobilize PB nanoparticles (∼18.32 nm) onto silk fibers for hydrogen peroxide (H2O2) detection. The intrinsic mechanical properties of silk fibers are well maintained with slight increases in stress (∼10 %) and strain (∼16 %). Furthermore, the PB-SF electrode displays good electrochemical H2O2 sensing performance with a sensitivity of 716.54 μA/mM·cm2, a linear range of 0.01–0.6 mM and a low detection limit of 10 μM (S/N = 3). Notably, the hybrid PB-SF electrode adapts to mechanical deformations with a series of angles and the electrical signals are not compromised obviously even after 100 home laundry washing cycles. PB modified silk fibers is simple, easy-operating and cost-effective electrode that is suitable for large-scale production as it can be integrated into e-textiles through typical textile processing methods.

Teratoid hepatoblastoma with small cell undifferentiated histology in polysplenia patient: a case report

Abstract Introduction/Objective Hepatoblastoma (HB) with teratoid is a uncommon variant of mixed epithelial and mesenchymal components. Conversely, HB with small cell undifferentiated (SCUD) is extremely rare, with only nine documented cases showing retained INI-1 expression in the literature. The prognosis of SCUD remains debatable. In this report, we describe the first case of combined teratoid HB with a SCUD component that preserved INI-1 expression with a favorable outcome. Methods/Case Report A 2-year-old girl with polysplenia syndrome presented with a right liver mass detected during ultrasound screening. The alpha fetoprotein levels were significantly elevated to 148,000. MRI revealed a 7.2 cm lesion, staged as Pre-Treatment Extent 2 (PRETEXT) in the right anterior liver. She underwent cholecystectomy and right hepatectomy. Resection specimen revealed a mixed neoplasm comprising epithelial components (fetal and embryonal) and mesenchymal components. Additionally, notable findings include small cell component and teratoid features, characterized by melanin pigment and neuroectodermal elements. All the neoplastic cells showed reactivity with CD34, reticulin, SALL4, beta-catenin, GPC-3, arginase-1, chromogranin, and glutamine synthetase. Notably, the teratoid area only displayed positivity for CD56 and NSE, while vimentin highlighted capillaries, vessels and focally staining small cells. Furthermore, CK19 highlighted the small cell components and the bile ducts in the background liver. Importantly, INI-1 staining was retained in all tumor cells, including the small cell component. Synaptophysin and Prussian blue were negative in all lesional cells. After a 2-year follow-up, no recurrence was observed. Results (if a Case Study enter NA) NA Conclusion This case underscores the diagnostic challenge posed by small cell undifferentiated (SCUD) hepatoblastoma. Moreover, it contributes to the understanding of this rare variant of hepatoblastoma and suggests a potential favorable prognosis associated with retained INI-1 staining in the SCUD component.

Organic Dye Molecule Intercalated Prussian Blue for Simultaneously Enhancing Coloration Efficiency and Energy Storage Capacity in Electrochromic Battery.

The dual-functional device combining electrochromic properties and energy storage has gained numerous attentions in the field of energy-saving smart electronics. However, achieving simultaneous optimization of coloration efficiency and energy storage capacity of materials poses a significant challenge. This study presents a novel approach by incorporating methyl orange into Prussian blue channels (PB-MO films) to adjust the internal electronic structure of Prussian blue. This modification allows the active layer to simultaneously improve the electrochromic and energy storage performance. The introduction of methyl orange not only alters the ratio of Fe3+/Fe2+ within the framework through the coordination reaction of Fe3+ with methyl orange, but also improves the reaction kinetics after intercalating organic dye molecules, including charge transfer resistance, diffusion capability of ions and capacitive contribution. The PB-MO films demonstrate remarkable properties: high optical contrast (81.4% at 670nm), excellent coloration efficiency (265 cm2C-1), and significant specific capacity (84 mAh m-2 at 0.05 A m-2), outperforming pure PB films. The PB-MO films are ideally suited for applications in displays and intelligent energy storage fields, boasting both high coloration efficiency and substantial energy storage capacity, thus advancing promote the development of dual-functional electrochromic devices.

Little-Cost Potentiometric and Spectrophotometric Procedures for Cephalothin Assessment in Pure and Biological Fluids.

Low-cost potentiometric and spectrophotometric procedures for cephalothin (CPI) determination in pure and biological fluids were investigated. The potentiometric technique is created through titration of CPI with an aqueous medium of 0.1 M NaOH at an ionic strength of μ = 0.3 M sodium chloride and room temperature by a combined glass pH electrode. Using the standard addition method, we found that the detection and quantitative limits were 0.042 mg/mL, with the standard deviation SD = 0.011, correlation coefficient R = 0.9880 (n = 5), and linear concentration ranges from 0.042 to 0.82 mg/mL. This technique was utilized to assess CPI in pure solutions, urine, and serum with suitable results. No interference was exposed in the presence of public components of the samples under study. Recovery of CPI for pure and biological fluids is in the range of 98.2-101%. Also, the spectrophotometric method has been performed through the formation of the Prussian Blue (PB) complex. The reaction between the acidic hydrolysis product of CPI (T = 60 °C) and the mixture of Fe3+ with hexacyanoferrate (III) ions (HCF(III)) was detected for the spectrophotometric determination of the drug. The maximum absorbance of the formed complex was measured at λ = 283 nm with 2.0 × 103 L mol-1 cm-1 molar absorptivity. Reaction states have been advanced to acquire the PB complex of great sensitivity and longer stability. In optimal states, the absorbent of the PB compound was attained to grow linearly with the increase in the concentration of CPI, which agrees with the correlation coefficient values. The detection and quantitative limits were 0.000036 and 0.0012 mg/mL, respectively, with the standard deviation, SD = 0.0005, correlation coefficient, R = 0.9955 (n = 5), and the linearity range of the calibration plot 0.0005-0.02 mg/mL CPI. The planned technique was positively utilized for the detection of CPI in both urine and serum models. The results fit well with the data found from the potentiometric method.

Optimization of sodium-ion battery cathode performance by nickel-based Prussian blue epitaxial growth with iron-based Prussian blue core-shell structure

To address the structural defects and poor electrical conductivity of conventional Prussian blue analogues (PBAs) samples, in this study, nickel hexacyanoferrate (NiHCF) and nickel hexacyanoferrate epitaxially grown with iron hexacyanoferrate (Ni@FeHCF-X) series of samples were successfully synthesized by co-precipitation combined with epitaxial growth technique, and their structural and electrochemical properties were systematically characterized. X-ray powder diffractometer (XRD) results show that all the samples maintain a cubic crystal system structure, and the diffraction peaks of the (220) and (400) crystal planes are shifted to a lower angle with the epitaxial growth of ferric hexacyanoferrate (FeHCF). The successful embedding of Fe was confirmed by inductively coupled plasma (ICP) measurement data. Scanning electron microscope (SEM) images show that the samples are in a cubic morphology, and the surfaces gradually become rounded from sharp to rounded with the increase of the Fe content. High-resolution transmission electron microscope (HRTEM) and energy-dispersive spectrometer (EDS) analyses confirm the successful construction of the core-shell structure and the homogeneous distribution of the elements. Electrochemical testing showed that the Ni@FeHCF-X samples exhibited higher specific capacities and superior rate performance compared to NiHCF, particularly the Ni@FeHCF-4 sample, which delivered a high specific capacity of 73.4 mAh·g⁻¹ at a current density of 100 mA·g⁻¹, significantly outperforming the 38.2 mAh·g⁻¹ achieved by NiHCF. Additionally, the capacity retention rate of Ni@FeHCF-4 reached 42.16 %. Electrochemical impedance spectroscopy (EIS) further confirmed the reduced charge transfer resistance and enhanced reversibility of the electrochemical reactions in the Ni@FeHCF-X samples. These results demonstrate that Ni@FeHCF-4 significantly enhances the electrochemical performance of the samples in aqueous sodium-ion battery, providing new insights into the design of cathode materials for sodium-ion batteries.