Freeze-drying Method Research Articles

Preparation and Characterization of Demineralized Bone Extracellular Matrix/Chitosan Porous Microcarriers

Composite porous microcarriers based on demineralized bone extracellular matrix (DBECM) and chitosan (Cs) were prepared using a combined emulsion and freeze-drying method. The effects of digestion by pepsin on the DBECM properties were investigated. The morphologies and porous structure of the DBECM/Cs porous microcarriers were observed by using a scanning electron microscope (SEM). The cytocompatibility of the DBECM/Cs porous microcarriers were studied by using cell counting kit-8 (CCK-8) and calcein acetoxymethyl ester/propidium iodide (CAM/PI). DBECM was digested into small pieces with a loose porous sponge structure and the digested DBECM showed an amorphous state. The resultant DBECM/Cs porous microcarriers showed a spherical shape and an interconnective porous structure. The CCK-8 and CAM/PI analyses indicated that the DBECM/Cs porous microcarriers were non-cytotoxic and showed good biocompatibility, providing a more favorable growth environment for cells.

Microstructured CNTs/Cellulose Aerogel for a Highly Sensitive Pressure Sensor.

Flexible sensors have been applied in human health monitoring and biomedical research, but producing high-performance piezoresistive sensors at low cost is still challenging. To address these shortcomings, we proposed a microstructured carbon nanotube (CNT)/cellulose aerogel-based pressure sensor. The sensor consists of three parts, i.e., cellulose/poly(vinyl alcohol)/CNT aerogel-based sensing layer and top and bottom thermoplastic polyurethane elastomer (TPU)/silver nanowire (Ag NW) nanofiber electrode. The aerogel is fabricated using a simple freeze-drying method and an easy electrospinning method to obtain the nanofiber-based electrode. Two TPU/Ag NW nanofiber electrodes sandwiched the aerogel with a microstructure in the middle. Benefiting from the microcone and micropore structures on the nanofiber electrode, the assembled sensors show a high sensitivity of 66.4 kPa-1, a significant detection boundary of 50 kPa, and an excellent response speed of 10 ms. The high sensing performance enables the sensor to monitor physiological signals, Morse code interactions, and gesture recognition. With the help of machine learning, the success rate of gesture recognition is as high as 98.8%. The preparation of this pressure sensor based on an aerogel shows excellent health and environmental monitoring potential as an artificial skin.

Highly Porous Particles of Cellulose Derivatives for Advanced Applications.

A chemical modification of cellulose diacetate by phthalate and nitrate was performed to increase solubility in organic solvents and change the electrical properties. The role of substituents on the conductivity, permittivity, and polarizability of cellulose films is revealed. It has been shown that highly porous micro particles can be obtained from cellulose derivatives by a simple and technological freeze-drying method. The resulting micro sized aerogels have a predominantly spherical morphology and amorphous structure. Suspensions of porous particles of nitro- and phthalylated cellulose derivatives in silicone oil have an increased dielectric permittivity compared to cellulose diacetate particles. Produced particles are novel promising material with tunable electrical properties for advanced applications in composites, including for electrorheological fluids.

Material Analysis and Conservation Treatment of Wooden Artifacts Excavated at the Ssangbuk-ri 280-10 Site in Buyeo, Korea

Numerous Baekje historical sites are located in Ssangbuk-ri, Buyeo, where a diverse array of wooden artifacts, including lacquerware, was excavated in a waterlogged condition. Consequently, comprehensive analysis and conservation treatments were undertaken. The study encompassed four wooden artifacts and one lacquerware. Species identification was conducted for all five artifacts, and the coating residue on the surface of one lacquerware was discerned using FT-IR. The results revealed that the Y-shaped and Drill-shaped wooden artifacts were crafted from Hard pine, the Square container with a handle from Juglans spp., the Arrow-shaped wooden object from Pyrus spp., and the Lacquerware from Castanea spp.. Additionally, the surface coating of the lacquerware was confirmed to be lacquer. Conservation treatments involved PEG(Polyethylene glycol) impregnation and freeze-drying methods, ensuring the stable storage and display of these artifacts.

Preparation of an imidazolium-based poly(ionic liquid) functionalized magnetic three-dimensional graphene oxide for magnetic solid phase extraction of pyrethroids from tea samples

In this work, an imidazolium-based poly(ionic liquid) (poly(1-dodecyl-3-vinyl-imidazolium bromide) functionalized magnetic three-dimensional graphene oxide (Fe3O4@3D-GO@poly(ImC12+Br−)) was synthesized via a vacuum freezing-drying method and used as a magnetic solid phase extraction (MSPE) adsorbent for the efficient extraction of pyrethroid pesticides from tea samples. The prepared Fe3O4@3D-GO@poly(ImC12+Br−) was confirmed by scanning electron microscopy (SEM), Fourier transform infrared spectrometry (FT-IR), vibrating sample magnetometer (VSM) and X-ray photoelectron spectrogram (XPS). Due to its large specific surface area and the ability to offer multiple intermolecular interactions, including π-π stacking, hydrophobic and hydrogen bond interactions, the prepared Fe3O4@3D-GO@poly(ImC12+Br−) showed high extraction efficiency for pyrethroids. The experimental parameters were optimized by a combination of single-factor method and Box-Behnken design to improve the extraction efficiency. Under the optimum conditions, coupled with high performance liquid chromatography (HPLC), a sensitive analytical method was developed for the determination of pyrethroids, and the proposed method showed wide linear ranges (1.00–100 μg L−1) with correlation coefficients (R) ranging from 0.9980 to 0.9994, low limits of detection (0.100 μg L−1) and good repeatability with intra-day relative standard deviations (RSDs) in the range of 2.90–5.53 % and inter-day RSDs in the range of 1.83–7.76 %. Moreover, the developed method was successfully applied to the determination of pyrethroids in tea samples and satisfactory recoveries ranging from 82.37 % to 114.34 % were obtained. The results showed that the developed Fe3O4@3D-GO@poly(ImC12+Br−) was an ideal, effective and selective material for the extraction and enrichment of pyrethroids from tea samples.

Superhydrophobic Cellulose Nanofiber Aerogels for Efficient Hemostasis with Minimal Blood Loss.

Reducing unnecessary blood loss in hemostasis is a major challenge for traditional hemostatic materials due to uncontrolled blood absorption. Tuning the hydrophilic and hydrophobic properties of hemostatic materials provides a road to reduce blood loss. Here, we developed a superhydrophobic aerogel that enabled remarkably reduced blood loss. The aerogel was fabricated with polydopamine-coated and fluoroalkyl chain-modified bacterial cellulose via a directional freeze-drying method. Primarily, the hydrophobic feature prevented blood from uncontrolled absorption by the material and overflowing laterally. Additionally, the aerogel had a dense network of channels that allowed it to absorb water from blood due to the capillary effect, and fluoroalkyl chains trapped the blood cells entering the channels to form a compact barrier via hydrophobic interaction at the bottom of the aerogel, causing quick fibrin generation and blood coagulation. The animal experiments reveal that the aerogel reduced the hemostatic time by 68% and blood loss by 87 wt % compared with QuikClot combat gauze. The study demonstrates the superiority of superhydrophobic aerogels for hemostasis and provides new insights into the development of hemostatic materials.

Blood Coagulation Activities and Influence on DNA Condition of Alginate-Calcium Composites Prepared by Freeze-Drying Technique.

The aim of this research was to synthesize and characterize alginate-calcium composites using a freeze-drying method, with a focus on their potential applications in biomedicine. This study specifically explored the biochemical properties of these composites, emphasizing their role in blood coagulation and their capacity to interact with DNA. Additionally, the research aimed to assess how the cross-linking process influences the structural and chemical characteristics of the composites. Detailed analyses, including microscopic examination, surface area assessment, and atomic absorption spectrometry, yielded significant results. The objective of this study was to examine the impact of calcium chloride concentration on the calcium content in alginate composites. Specifically, the study assessed how varying concentrations of the cross-linking solution (ranging from 0.5% to 2%) influence the calcium ion saturation within the composites. This investigation is essential for understanding the physicochemical properties of the materials, including calcium content, porosity, and specific surface area. The results are intended to identify the optimal cross-linking conditions that maximize calcium enrichment efficiency while preserving the material's structural integrity. The study found that higher calcium chloride concentrations in alginate cross-linking improve the formation of a porous structure, enhanced by two-stage freeze-drying. Increased calcium levels led to a larger surface area and pore volume, and significantly higher calcium content. Furthermore, assays of activated partial thromboplastin time (aPTT) showed a reduction in clotting time for alginate composites containing calcium ions, indicating their potential as hemostatic agents. The aPTT test showed shorter clotting times with higher calcium ion concentrations, without enhanced activation of the extrinsic clotting pathway. The developed alginate material with calcium effectively supports hemostasis and reduces the risk of infection. The study also explored the capacity of these composites to interact with and modify the structure of plasmid DNA, underscoring their potential for future biomedical applications.

Vanillin-crosslinked gelatin-polyvinyl alcohol aerogels: Improved physicochemical properties and antimicrobial activity

Crosslinking is a promising way to fabricate high-performance aerogels. In this study, vanillin (Van) crosslinked gelatin–polyvinyl alcohol (Gel−PVA) aerogels were prepared by vacuum freeze-drying method. The effects of different addition levels of Van on FTIR spectra, microstructures and physicochemical properties including water stability, mechanical properties, thermal stability and thermal insulation properties of aerogels were characterized, and antimicrobial activity of aerogels were validated. The results showed that Van exerted its crosslinking function through Schiff base bonding with Gel and hydrogen bonding with Gel and PVA. Although Van addition caused a slight decline in the thermal insulation performance and the obvious increase in pore diameter of aerogels, moderate Van crosslinking contributed to water stability, mechanical properties and thermal stability of aerogels. Besides, Van crosslinked Gel−PVA aerogel could effectively inhibit the growth of E. coli and B. cinerea. This suggests that the aerogel has promising applications in antimicrobial food packaging.

Binary and Ternary Inclusion Complexes of Niflumic Acid: Synthesis, Characterization, and Dissolution Profile.

Although niflumic acid (NA) is one of the most used non-steroidal anti-inflammatory drugs, it suffers from poor solubility, low bioavailability, and significant adverse effects. To address these limitations, the complexation of NA with cyclodextrins (CDs) is a promising strategy. However, complexing CDs with low molecular weight drugs like NA can lead to low CE. This study explores the development of inclusion complexes of NA with 2-hydroxypropyl-β-cyclodextrin (2HP-β-CD), including the effect of converting NA to its sodium salt (NAs) and adding hydroxypropyl methylcellulose (HPMC) on complex formation. Inclusion complexes were prepared using co-evaporation solvent and freeze-drying methods, and their CE and Ks were determined through a phase solubility study. The complexes were characterized using physicochemical analyses, including FT-IR, DSC, SEM, XRD, DLS, UV-Vis, 1H-NMR, and 1H-ROESY. The dissolution profiles of the complexes were also evaluated. The analyses confirmed complex formation for all systems, demonstrating drug-cyclodextrin interactions, amorphous drug states, morphological changes, and improved solubility and dissolution profiles. The NAs-2HP-β-CD-HPMC complex exhibited the highest CE and Ks values, a 1:1 host-guest molar ratio, and the best dissolution profile. The results indicate that the NAs-2HP-β-CD-HPMC complex has potential for delivering NA, which might enhance its therapeutic effectiveness and minimize side effects.

Carbon-intercalated halloysite-based aerogel efficiently encapsulating phase change materials with excellent photothermal conversion and energy storage

Latent heat storage systems based on organic phase change materials (PCMs) are considered to be an efficient solar energy utilization strategy, but leakage vulnerability and insensitivity to sunlight of PCMs limit their further application in energy storage. In this work, a new hierarchical porous aerogel was constructed with the carbon intercalated halloysite nanotubes (CHNTs) as the assembly units for PCMs encapsulation to improve the load weight, stability and sunlight absorption. The CHNTs were first successfully synthesized through intercalation and carbonization, with the aim of increasing their specific surface area and sunlight absorption.Subsequently, the CHNTs/polyvinyl alcohol (PVA) aerogels with 3D honeycomb structure were prepared by self-assembly using a freeze-drying method, which can significantly promote the encapsulation ratio of lauric acid (LA) in the pores of both aerogels and CHNTs. The CHNTs can not only improve compressive strength of the aerogels and shape stability of the composite PCMs, but also enhance light absorption ability of the composites compared to pristine HNTs. As a support material, CHNTs aerogel (CHNP) loaded more than 92 wt% PCM (LA@CHNP) and exhibited an extremely high latent heat capacity (170.9 J/g). The LA@CHNP had good structural and thermal stability in 300 cycles without visible leakage. Besides, solar energy absorption increased from 43 % to 98 %, and the solar-to-thermal energy conversion efficiency increased to 95.88 %, which could be attributed to 3D porousness and carbon nanolayers of the CHNTs. We have successfully synthesized an eco-friendly and facile composite LA@CHNP, which will contribute to the design of advanced composites with excellent solar energy storage properties, and provide a new direction for the application of carbonized materials.

Impact of Ultrasound Pre-Treatment on the Drying Kinetics and Quality of Chicken Breast-A Comparative Study of Convective and Freeze-Drying Methods.

Fresh meat has a limited shelf life and is prone to spoilage. Drying serves as a common method for food preservation. Non-thermal techniques such as ultrasound treatment (US) can positively affect the drying processes and alter the final product. The study aimed to evaluate the impact of US pre-treatment on the hot air (HA) and freeze-drying (FD) of chicken breast meat and the quality of the dried products. US pre-treatment had a varied impact depending on the drying method used. The contact US method extended the HA drying time (about 50%) but improved water removal during FD (about 30%) compared to the untreated samples. Both methods resulted in low water content (<8.3%) and low water activity (<0.44). While rehydration properties (RR) and hygroscopicity (H) were not significantly affected by US pre-treatment in HA drying (about 1.35% and about 1.1, respectively), FD noticed differences due to shrinkage and porosity variations (RR: 2.4-3.2%, H: 1.19-1.25). The HA-dried samples exhibited notably greater tissue shrinkage and a darker surface color than the FD meat. Ultrasonic processing holds substantial potential in creating dried meat products with tailored characteristics. Hence, meticulous consideration of processing methods and parameters is of utmost importance.

Ultralight and rigid PBO nanofiber aerogel with superior electromagnetic wave absorption properties

Polymer-based aerogels are emerging as promising candidates for lightweight and high performance electromagnetic (EM) wave absorption materials. In this study, an ultralight and rigid poly(p-phenylene benzobisoxazole) nanofiber (PNF) based composite aerogel with excellent EM wave absorption performance was fabricated with cobalt-nickel alloy (CoNi) nanoparticles and carbon nanotubes (CNTs) as magnetic and conductive fillers, respectively. A CNT/PNF composite aerogel was first prepared through a sol-gel and freeze-drying method, and then CoNi nanoparticles were introduced therein through hydrothermal reaction and thermal annealing to obtain the CoNi/CNT/PNF aerogel. CNTs and PNFs were interwoven and constructed a three-dimensional conductive/magnetic cage-like skeleton structure decorating with magnetic CoNi nanoparticles. The cage-like skeleton structure allowed the dissipation of EM waves through multiple mechanisms encompassing conduction loss, magnetic loss, multiple reflection, scattering, and absorption. When its thickness was 4 mm, the CoNi/CNT/PNF aerogel showed a minimal reflection loss of −44.7 dB (at 6.88 GHz), and its broad effective absorption bandwidth covered the entire X-band and Ku-band and most of the C-band (12.32 GHz, from 5.68 GHz to 18 GHz). In addition, the rigid aerogel exhibited an ultralow density (0.107 g/cm3), excellent thermal insulation, and flame retardancy, demonstrating its potential application as a high-performance EM wave absorption material in the fields of aerospace and national defense.

Zn-substituted Co3O4 crystal anchored on porous carbon nanofibers for high performance supercapacitors

Metal-organic frameworks (MOFs) are a promising class of electrode materials for supercapacitors. In this work, MOF-derived transition metal oxide/carbon nanofiber composites (ZnCoO/C) are synthesized through a freeze-drying method followed by a carbonization process. The crystal structure of the ZnCoO/C product is regulated by changing the ratio of Co to Zn, which in turn influences its electrode properties. The electrochemical tests reveal that the ZnCoO/C-2 electrode demonstrates an impressive specific capacitance of 356.3 F g-1 at 1 A g-1 and maintains a capacitance retention exceeding 77 % after 10,000 cycles, which exhibits a good cycling stability. It is found that appropriate Zn substitution can diminish the crystallinity of the material, augment the active sites, and enhance the specific capacitance of the electrode material. Considering the heteroatom substitution tends to introduce vacancy defects in the crystals, this work theoretically explores the effect of oxygen vacancies on the electrode materials. As the oxygen vacancy concentration increases, the band gap and the adsorption energy of the models decrease; conversely, the formation energy of the models shows an increasing tendency. This indicates that an increase in oxygen vacancies can enhance the electrical conductivity of electrode materials and facilitate their kinetic process but destroy the stability of crystal. This research explores the interplay between the microstructure and the electrochemical performance of electrode materials, providing a foundational reference for the design of structurally optimized high-performance electrodes and further elucidating the energy storage mechanisms in supercapacitors.

Removal of malachite green in wastewater and its mechanism by three-dimensional graphene oxide-based aerogels

Malachite green (MG) is a significant water pollutant due to its widespread use and harmful properties, making its effective removal crucial. Graphene oxide (GO) has emerged as a promising material for dye adsorption. Doping GO into cellulose aerogels enhances mechanical properties and prevents GO dissolution. Many reports claim the advantages of GO in adsorption, but challenges remain in understanding and optimizing the adsorption of MG in three-dimensional cellulosic GO (CLGO) aerogels. In this study, three-dimensional CLGO aerogels were prepared using the freeze-drying method. They achieved an MG maximum adsorption capacity of 33.98 mg g−1, and the adsorbent still had 97.04 % adsorption capacity at the seventh adsorption–desorption cycle. The photothermal properties of the CLGO aerogels were also studied, contributing to the development of the zero-liquid discharge (ZLD) post-processing concept. Molecular force field simulations indicated that π-π interaction is the primary force between MG and CLGO aerogels in the absorption process. We believe our research will guide the future optimization of MG specialized absorbent.

Comparison of oven drying and freeze drying methods for the production of fast melt films containing quetiapine fumarate

Background Quetiapine fumarate (QTP) is commonly prescribed for schizophrenic patient, typically available in tablet or oral suspension form, presenting challenges such as administration difficulties, fear of choking and distaste for its bitter taste. Fast melt films (FMF) offer an alternative dosage form with a simple development process, ease of administration and rapid drug absorption and action onset. Objective This study aims to prepare FMF with different formulations using solvent casting methods and to compare the effects of different drying methods, including oven drying and freeze drying, on the properties of the films. Methods Various formulations were created by manipulating polymer types (starch, hydroxypropyl methylcellulose (HPMC) and guar gum) at different concentrations, along with fixed concentrations of QTP and other excipients. Characterization tests including surface morphology, weight, thickness, pH, tensile strength, elongation length, Young’s modulus, folding endurance and disintegration time were conducted. The optimal FMF formulation was identified and further evaluated for moisture and drug content, dissolution behavior, accelerated stability, X-ray diffraction (XRD), and palatability. Results FMF containing 10 mg guar gum/film developed using oven drying emerged as the optimum choice, exhibiting desirable film appearance, ultra-thin thickness (0.453 ± 0.002 mm), appropriate pH for oral intake (pH 5.0), optimal moisture content of 11.810%, rapid disintegration (52.67 ± 1.53 s), high flexibility (folding endurance > 300 times) and lower Young’s modulus (1.308 ± 0.214). Conclusion Oven drying method has been proven to be favorable for developing FMF containing QTP, meeting all testing criteria and providing an alternative option for QTP prescription.

Construction of dielectric and magnetic coupling cobalt salt/chitosan derived Co/C hybrid aerogels for high-performance infrared/radar compatible applications

In virtue of mutually exclusive stealth mechanisms, effectively protecting from infrared detection and attenuating microwaves through composition and structure design remains a formidable challenge. To achieve high-efficiency infrared/radar compatible stealth, in this work, 0D magnetic Co nanoparticles were successfully in situ grown onto the renewable biomass chitosan-based 3D porous carbon skeletons via facile liquid reaction, freeze-drying, and calcination method. Herein, the as-prepared Co/C hybrid aerogels exhibit dielectric and magnetic coupling network, and the relevant infrared/radar compatible stealth property can be regulated by adjusting the addition amount of Co salt. The minimum thermal conductivity value reached 0.095 W m−1 K−1 at 60 °C, and the lowest infrared emissivity of 0.717 in the 8–14 μm band was also achieved. Furthermore, the minimum reflection loss (RLmin) value of −44.70 dB at a relatively thin thickness of 1.35 mm and the maximum effective absorption bandwidth (EAB) of 5.45 GHz at only 1.5 mm appeared in the optimal Co/C hybrid aerogel with the most appropriate Co content. Compared with perfect conductive layer (PEC), the simulated radar cross section (RCS) signals of Co/C composites covered PEC have been significantly reduced by 18.44 dB m2 at the scanning angle of 80°. This study inspires the exploration of the elaborate design strategy and facile construction method for environment-friendly infrared/radar compatible hybrid aerogels in the future.

Honeycomb-like macroporous crosslinked chitosan assisted EDTA-intercalated Ca-Mg-Al layered hydrotalcite composite foams for efficient U(VI) biosorption

The biosorption is considered to be highly efficient for the separation of radionuclide from radioactive wastewater. Herein, the crosslinked chitosan assisted EDTA intercalated Ca-Mg-Al layered double hydroxides composite foam (CS-EDTA-LDH) was synthesized by combining EDTA intercalation and freeze-drying methods. The macroporous and ultralight properties of CS-EDTA-LDH facilitates its rapid adsorption and facile recovery, and the inorganic/organic incorporation can avoid pore collapse and provide numerous adsorption sites, while the EDTA intercalation can enhance the complex capture of U(VI). The CS-EDTA-LDH presents various functional groups (carboxyl, hydroxyl and amino groups) for U(VI) adsorption, and the adsorption capacity for U(VI) reached 272.3 mg/g at pH 5.0 and 298 K. The adsorption kinetics of U(VI) conformed to PSO equation, whereas the isotherms conformed to the Freundlich model, indicating heterogeneous adsorption with diffusion process as a rate-controlling step. The thermodynamic parameters indicate that U(VI) adsorption by CS-EDTA-LDH is endothermic and spontaneous in nature. The adsorption mechanism is related to the synergic complexation by multi-functional groups, ion exchange, and possible isomeric substitution. Overall, CS-EDTA-LDH could be a promising biosorbent for the cleanup of radioactive pollution due to its high performance for U(VI) adsorption and facile recovery.

A Strategic Synthesis of Orange Waste-Derived Porous Carbon via a Freeze-Drying Method: Morphological Characterization and Cytocompatibility Evaluation.

Porous carbon materials from food waste have gained growing interest worldwide for multiple applications due to their natural abundance and the sustainability of the raw materials and the cost-effective synthetic processing. Herein, orange waste-derived porous carbon (OWPC) was developed through a freeze-drying method to prevent the demolition of the original biomass structure and then was pyrolyzed to create a large number of micro, meso and macro pores. The novelty of this work lies in the fact of using the macro-channels of the orange waste in order to create a macroporous network via the freeze-drying method which remains after the pyrolysis steps and creates space for the development of different types of porous in the micro and meso scale in a controlled way. The results showed the successful preparation of a porous carbon material with a high specific surface area of 644 m2 g-1 without any physical or chemical activation. The material's cytocompatibility was also investigated against a fibroblast cell line (NIH/3T3 cells). OWPC triggered a mild intracellular reactive oxygen species production without initiating apoptosis or severely affecting cell proliferation and survival. The combination of their physicochemical characteristics and high cytocompatibility renders them promising materials for further use in biomedical and pharmaceutical applications.

Physicochemical Properties, Antioxidant Capacity and Sensory Acceptability of Instant Rosehip Teas Prepared by Spray-Drying and Freeze-Drying Methods

Physicochemical Properties, Antioxidant Capacity and Sensory Acceptability of Instant Rosehip Teas Prepared by Spray-Drying and Freeze-Drying Methods

Regulating the closed pore structure of biomass-derived hard carbons towards enhanced sodium storage

Hard carbon (HC) stands out as a promising anode material for sodium storage due to its unique structure. However, the pore structure regulation of HC still poses a significant challenge. Herein, we propose a combined method of hydrothermal pretreatment, freeze-drying, and high-temperature carbonization to regulate the pore structure of HC. During the hydrothermal processes, the assembly of graphene oxide (GO) with starch facilitates the formation of open pores, which are subsequently transformed into closed pores during high-temperature carbonization. Impressively, a hard carbon with a reversible capacity of 434 mA h g −1 at 30 mA g −1 has been prepared through the structure regulation. Compared to the sample without structural regulation, it demonstrates a remarkable increase of 184.21 mA h g−1, with an enhancement rate of 73.80 %. Simultaneously, the skeletal structure of GO serves as a conductive network and framework support, enabling favorable rate performance and excellent cycling stability. Furthermore, the sodium storage mechanism is deduced as “adsorption -- intercalation -- pore filling”. Overall, this study can offer valuable insights into pore structure regulation for anode materials and shed light on sodium storage mechanisms.