Internal Site Research Articles

Electrochemical Sacrificial Alchemy: Crafting Hollow Hydroxide Hierarchy for Practical Aqueous Energy Storage Solution

AbstractEffective utilization of internal active sites in high‐mass loading electrode materials is essential for advancing practical energy storage. Herein, a novel electrochemical sacrificial alchemy for the first time to directly transform the solid Co‐Ni‐Zn carbonate hydroxide (CH) into its hollow structure with a strategic hierarchical architecture is introduced. In contrast to the complex and often cumbersome procedures of traditional methods, the approach is built on the simple electrochemically induced in situ etching and remodeling process. The experimental and theoretical analyses highlight the significant role of electric field force‐induced Zn sacrificial etching and hydroxide redeposition in creating internal cavities and regenerating external active sites, leading to the final hollow hierarchical structure with primary 1D hollow nanorod arrays and secondary reconstructed 2D nanoflakes, effectively exposing abundant energy storage sites. Benefiting from the synergistic effect, the resulting Co‐Ni‐Zn CH exhibited exceptional electrochemical performance. As proof of concept, a modular pouch‐type hybrid supercapacitor (HSC) composed of Co‐Ni‐Zn CH cathode achieved an ultrahigh energy density of 46.9 Wh kg−1. This device can efficiently power consumer electronics with a faster charging speed compared to commercial shared power banks. This research unveils a facile electrochemical approach for structuring electrode materials in energy storage solutions.

Accelerating Lithium Deposition Kinetics Via Lithiophilic Ag‐Decorated Graphitic Carbon Nitride Spheres for Stable Lithium Metal Anode

This study presents a novel Li metal host material with a unique hollow nano‐spherical structure that incorporates Ag nano‐seeds into a graphitic carbon nitride (g‐C3N4) shell layer, referred to as g‐C3N4@Ag hollow spheres. The g‐C3N4@Ag spheres provide a managed internal site for Li metal encapsulation and promote stable Li plating. The g‐C3N4 spheres are uniformly coated using polydopamine, which has an adhesive nature, to enhance lithium plating/stripping stability. The strategic presence of Ag nano‐seeds eliminates the nucleation barrier, properly directing Li growth within the hollow spheres. This design facilitates highly reversible and consistent lithium deposition, offering a promising direction for the production of high‐performance lithium metal anodes. These well‐designed g‐C3N4@Ag hollow spheres ensure stable Li plating/stripping kinetics over more than 500 cycles with a high coulombic efficiency of over 97%. Furthermore, a full cell made using LiNi0.90Co0.07Mn0.03O2 and Li‐g‐C3N4@Ag host electrodes demonstrated highly competitive performance over 200 cycles, providing a guide for the implementation of this technology in advanced lithium metal batteries.

The ‘Normality’ of civilian internment in Germany during the First World War: camps as sealed or entangled spaces?

ABSTRACT This article examines internment camps in Germany during the First World War and their entanglements with society. In particular, it discusses whether the internment sites were closed or semi-permeable spaces that were interwoven with their nearby environment. Based on this, the question of what kind of integration existed and what form it took will be answered. Furthermore, the article investigates the consequences and aftermaths of these experiences in post-war Germany. The conclusion raises some further questions for future studies.

Human 8-oxoguanine glycosylase OGG1 binds nucleosome at the dsDNA ends and the super-helical locations

The human glycosylase OGG1 extrudes and excises the oxidized DNA base 8-oxoguanine (8-oxoG) to initiate base excision repair and plays important roles in many pathological conditions such as cancer, inflammation, and neurodegenerative diseases. Previous structural studies have used a truncated protein and short linear DNA, so it has been unclear how full-length OGG1 operates on longer DNA or on nucleosomes. Here we report cryo-EM structures of human OGG1 bound to a 35-bp long DNA containing an 8-oxoG within an unmethylated Cp-8-oxoG dinucleotide as well as to a nucleosome with an 8-oxoG at super-helical location (SHL)-5. The 8-oxoG in the linear DNA is flipped out by OGG1, consistent with previous crystallographic findings with a 15-bp DNA. OGG1 preferentially binds near dsDNA ends at the nucleosomal entry/exit sites. Such preference may underlie the enzyme’s function in DNA double-strand break repair. Unexpectedly, we find that OGG1 bends the nucleosomal entry DNA, flips an undamaged guanine, and binds to internal nucleosomal DNA sites such as SHL-5 and SHL+6. We suggest that the DNA base search mechanism by OGG1 may be chromatin context-dependent and that OGG1 may partner with chromatin remodelers to excise 8-oxoG at the nucleosomal internal sites.

Stochastic Sensing of Chloride Anions Using an α-Hemolysin Pore with a semiaza-Bambusuril Adapter.

Pores containing molecular adapters provide internal selective binding sites, thereby allowing the stochastic sensing of analytes. Herein, we demonstrate that semiaza-bambusuril (BU) acts as a non-covalent molecular adapter when lodged within the lumen of the wild-type α-hemolysin (WT-αHL) protein pore. Because the bambusurils are recognized as anion receptors, the anion binding site within the adapter-nanopore complex allows the detection of chloride anions, thus converting a non-selective pore into an anion sensor.

Tunable sulfur vacancies in amorphous-crystalline AC-Bi2S3-x@C derived from CAU-17 for efficient capture of radioiodine: Comparison of sulfur vacancies in amorphous and crystalline structures

Solid-phase adsorption has been recognized as an effective method for the control of volatile radioactive iodine in spent fuel reprocessing plant off-gases. However, it is still a challenge to develop efficient and stable iodine capture adsorbents. In this work, sulfur-vacancy-rich amorphous-crystalline AC-Bi2S3-x@C was prepared by solvothermal vulcanization using CAU-17 as a precursor. Based on the synergistic effect of the amorphous structure and sulfur vacancy defects, AC-Bi2S3-x@C exhibited fast adsorption equilibrium time (15 min), distinguished iodine adsorption capacity (1763.9 mg g−1), high percentage of chemical adsorption (93.4 %) as well as favorable thermal and irradiation stability. Adsorption experiments and theoretical calculations verified that the amorphous structure not only enhance the charge transfer between sulfur vacancy defects and iodine molecules, but also offers rapid diffusion channels for iodine molecules to the interior of the adsorbent and sufficient internal binding sites to promote iodine molecule adsorption in its interior. The used adsorbent showed high iodine retention (92.3 %) and excellent chemical durability (normalized iodine leaching rate of 4.63 × 10-5 g m−2 d-1) in glass solidification. In general, this work presented a new concept in the design and synthesis of efficient radioactive iodine capture materials.

The city the earthquake built: internal displacement, international aid and state–society relations in the “fragile city” of Canaan

This paper revisits the case of Canaan – a massive informal settlement that emerged in the wake of the devastating 2010 earthquake in Haiti – in order to examine the often-forgotten aftermath of international aid programming in an urban, fragile-state context. Originally categorized as an (informal) internal displacement site, Canaan continued to expand in the years following the quake, reaching an estimated population of 300,000 by 2016. Using a qualitative case study of Canaan conducted nearly 15 years after its creation, the paper makes two interrelated arguments: first, that the ways in which the United Nations’ “durable solutions” framework is frequently understood and applied may be unrealistic and even deleterious for state–society relations in some fragile urban contexts. Second, even calls to shift (urban) internal displacement programming to a more development footing is far from a panacea if these interventions are not designed to be more politically nuanced, context-sensitive and modest about what can be achieved in such complex environments.

Sia-m7G: Predicting m7G Sites through the Siamese Neural Network with an Attention Mechanism

Background: The chemical modification of RNA plays a crucial role in many biological processes. N7-methylguanosine (m7G), being one of the most important epigenetic modifications, plays an important role in gene expression, processing metabolism, and protein synthesis. Detecting the exact location of m7G sites in the transcriptome is key to understanding their relevant mechanism in gene expression. On the basis of experimentally validated data, several machine learning or deep learning tools have been designed to identify internal m7G sites and have shown advantages over traditional experimental methods in terms of speed, cost-effectiveness and robustness. Aims: In this study, we aim to develop a computational model to help predict the exact location of m7G sites in humans. Objective: Simple and advanced encoding methods and deep learning networks are designed to achieve excellent m7G prediction efficiently. Methods: Three types of feature extractions and six classification algorithms were tested to identify m7G sites. Our final model, named Sia-m7G, adopts one-hot encoding and a delicate Siamese neural network with an attention mechanism. In addition, multiple 10-fold cross-validation tests were conducted to evaluate our predictor. Results: Sia-m7G achieved the highest sensitivity, specificity and accuracy on 10-fold crossvalidation tests compared with the other six m7G predictors. Nucleotide preference and model visualization analyses were conducted to strengthen the interpretability of Sia-m7G and provide a further understanding of m7G site fragments in genomic sequences. Conclusion: Sia-m7G has significant advantages over other classifiers and predictors, which proves the superiority of the Siamese neural network algorithm in identifying m7G sites.

Modification on different recycled fine aggregates by biological CaCO3: Physical properties and packing state

MICP was a modification method often used to modify recycled fine aggregates (RFAs) in recent years. The paper studied the mechanism of modifying two RFAs with different particle grading by MICP. The results showed a corresponding alteration in the proportion of internal mineralization sites and external mineralization sites within RFAs with the variation in particle size, thereby impacting the amount and proportion of internal and external CaCO3. The internal and external CaCO3 improved the properties and packing state (closer to the MAA model) of the RFAs, respectively. The use of <1.18 mm RFAs could take into account both improvement efficiency.

Zinc-cluster-based MOF with super selective separation adsorption catalyzes direct chemical conversion of CO2 from quasi-polluted air

The CO2 in the atmosphere has a serious impact on the human living environment. Direct utilization of the discharged CO2 to produce useful chemicals is challenging due to the practical presence of mixed compositions and low concentrations for CO2. Metal-organic frameworks (MOFs) with high internal surface areas, porosity and open metal site potentially possess superior adsorption separation capacity for CO2 gas, and on this basis, it can be used as a catalyst to achieve efficient chemical conversion of CO2. We demonstrate the synthesis and characterization of MOF ([Zn4O(ntba)2]n, MOF 1, H3ntba=4,4',4''-nitrilotribenzoic acid) with excellent selective adsorption properties from quasi- polluted air (O2, N2, CO2, CH4) and as heterogeneous catalysts for direct efficient CO2 chemical conversion. Detailed structural analysis reveals show that zinc ions behave multiple open metal sites and two coordination modes in the polyhedral zinc clusters building unit forming a 3D porous network by polyhedral zinc clusters building unit. Thanks to its structural features, at the 273 K and 100kPa, due to the ideal specific surface area and porosity, MOF 1 have ideal adsorption-separation performance for CO2, its values of adsorption and separation ratio are 75.7 cm3g−1, 373(CO2/N2), 79(CO2/O2), 13(CO2/CH4), respectively. The cycloaddition catalytic reaction investigations show that MOF 1 can be employed as a highly efficient catalyst for converting CO2 with a yield of 78 %. The result of this experiment offers the potential to directly utilize low-concentration and mixed CO2 while avoiding the economic and environmental costs of obtaining purified CO2 feeds tocks.

Synergistic Electrocatalyst-Cathode Architecture for Stable Long-Term Cycling Lithium-Sulfur Batteries

Lithium-sulfur (Li-S) batteries are a promising candidate for next-generation energy storage owing to the high theoretical capacity of sulfur (1,675 mAh g−1). However, the intrinsically low electrical conductivity of sulfur and complex multistep electrolyte-mediated redox reactions involving soluble lithium polysulfide intermediates engender critical challenges toward practical realization. Specifically, migration and diffusion of higher-order lithium polysulfides provokes continuous loss of active sulfur species, yielding premature capacity fade. Electrochemical kinetics also remain sluggish due to the insulating nature of sulfur cathodes, which require engineering designs to accelerate charge transfer.Rational morphological and compositional cathode tuning represents a compelling strategy for addressing fundamental Li-S limitations. Herein, we develop an extended cathode architecture composed of a porous carbon nanotube network decorated with homogenously dispersed nanocatalysts. Electron microscopy and spectroscopy analysis verify platinum group metals are well-incorporated both within internal channels and external surface sites of conductive carbon nanotubes. The composite framework affords multifaceted functionality arising from synergistic chemical and structural attributes of components. Nanocatalyst sites demonstrate a pronounced chemical affinity toward soluble polysulfide intermediates, effectively localizing them within cathode, minimizing diffusional losses toward the anode. This anchoring phenomenon is complemented by the inherent microporosity of the high-surface-area nanotube network, further obstructing polysulfide migration through a confinement effects. Concurrently, noble metal nanoparticles facilitate the redox conversion of trapped higher-order polysulfides into solid Li2S alleviating the precipitation of electrically insulating discharge products. The excellent electrical conductivity of CNTs ensures efficient charge transport to all incorporated sulfur active materials, further maximizing reversible utilization.As a result of complementary polysulfide confinement and electrocatalytic conversion functionalities, Li-S coin cells exhibit enhanced reversible capacities exceeding 900 mAh g−1 for over 500 cycles at 0.558 A g−1. Notably, over 500 cycles, minimal capacity decay of 0.018% per cycle and 92% retention of the initial capacity are obtained at moderate sulfur loadings highlighting the exceptional cycling stability enabled by engineered cathodes. Outstanding rate performance is also demonstrated with the delivery of 854 mAh g−1 capacity at a very high current density of 1.675 A g−1. Our rationally designed cathode architecture provides critical mechanistic insight toward addressing fundamental bottlenecks to progress Li-S technologies.

Structural insights into the cooperative nucleosome recognition and chromatin opening by FOXA1 and GATA4

Mouse FOXA1 and GATA4 are prototypes of pioneer factors, initiating liver cell development by binding to the N1 nucleosome in the enhancer of the ALB1 gene. Using cryoelectron microscopy (cryo-EM), we determined the structures of the free N1 nucleosome and its complexes with FOXA1 and GATA4, both individually and in combination. We found that the DNA-binding domains of FOXA1 and GATA4 mainly recognize the linker DNA and an internal site in the nucleosome, respectively, whereas their intrinsically disordered regions interact with the acidic patch on histone H2A-H2B. FOXA1 efficiently enhances GATA4 binding by repositioning the N1 nucleosome. Invivo DNA editing and bioinformatics analyses suggest that the co-binding mode of FOXA1 and GATA4 plays important roles in regulating genes involved in liver cell functions. Our results reveal the mechanism whereby FOXA1 and GATA4 cooperatively bind to the nucleosome through nucleosome repositioning, opening chromatin by bending linker DNA and obstructing nucleosome packing.

Stochastic Sensing of Chloride Anions Using an α‐Hemolysin Pore with a semiaza‐Bambusuril Adapter

AbstractPores containing molecular adapters provide internal selective binding sites, thereby allowing the stochastic sensing of analytes. Herein, we demonstrate that semiaza‐bambusuril (BU) acts as a non‐covalent molecular adapter when lodged within the lumen of the wild‐type α‐hemolysin (WT‐αHL) protein pore. Because the bambusurils are recognized as anion receptors, the anion binding site within the adapter‐nanopore complex allows the detection of chloride anions, thus converting a non‐selective pore into an anion sensor.

Artificial nociceptor based on interface engineered ferroelectric volatile memristor

Recent advancements in neuromorphic computing driven by memristors, which emulate biological synapses and neurons, have spurred the development of innovative information technologies. To extend memristor applications to artificial nervous systems, electronic receptors are crucial for converting external stimuli into signals for the internal nervous system. Key requirements for integrating neuron devices into neuromorphic computing include achieving threshold behavior, minimizing power consumption, and ensuring compatibility with complementary metal-oxide semiconductor (CMOS) technology. Hafnium-based ferroelectric memristors are known for their robust ferroelectric properties at nanoscales and compatibility with CMOS technology. However, their non-volatile resistive switching has historically limited their suitability for neuron sensory applications requiring threshold switching. This study demonstrates threshold switching behavior in a TiN/Hf0.67Zr0.33O2(HZO)/TiOx/TiN heterostructure by incorporating a nanoscale TiOx interfacial layer as an oxygen reservoir. This layer facilitates the formation of oxygen vacancies within the ferroelectric HZO layer, serving as internal charge trap sites. As a result, hafnium-based ferroelectric memristors exhibit volatile switching characteristics, enabling them to function as nociceptive devices through internal charge trapping and detrapping mechanisms. These volatile memristors are suitable for artificial nociceptor systems requiring responses such as threshold detection, relaxation, allodynia, and hyperalgesia to external stimuli. This capability opens avenues for developing advanced humanoid robots capable of rapid adaptation and response in challenging environments such as outer space or hazardous conditions, leveraging real-time sensory processing for effective operation and survival.

Factors influencing circuit lifetime in paediatric continuous kidney replacement therapies – results from the EurAKId registry

BackgroundContinuous kidney replacement therapy (CKRT) has recently become the preferred kidney replacement modality for children with acute kidney injury (AKI). We hypothesise that CKRT technical parameters and treatment settings in addition to the clinical characteristics of patients may influence the circuit lifetime in children.MethodsThe study involved children included in the EurAKId registry (NCT 02960867), who underwent CKRT treatment. We analysed patient characteristics and CKRT parameters. The primary end point was mean circuit lifetime (MCL). Secondary end points were number of elective circuit changes and occurrence of dialysis-related complications.ResultsThe analysis was composed of 247 children who underwent 37,562 h of CKRT (median 78, IQR 37–165 h per patient). A total of 1357 circuits were utilised (3, IQR 2–6 per patient). MCL was longer in regional citrate anticoagulation (RCA), compared to heparin (HA) and no anticoagulation (NA) (42, IQR 32-58 h; 24, IQR 14-34 h; 18, IQR 12-24 h, respectively, p < 0.001). RCA was associated with longer MCL regardless of the patient’s age or dialyser surface. In multivariate analysis, MCL correlated with dialyser surface area (beta = 0.14, p = 0.016), left internal jugular vein vascular access site (beta = -0.37, p = 0.027), and the use of HA (beta = -0.14, p = 0.038) or NA (beta = -0.37, p < 0.001) vs. RCA. RCA was associated with the highest ratio of elective circuit changes and the lowest incidence of complications.ConclusionAnticoagulation modality, dialyser surface, and vascular access site influence MCL. RCA should be considered when choosing first-line anticoagulation for CKRT in children. Further efforts should focus on developing guidelines and clinical practice recommendations for paediatric CKRT.Graphical abstractA higher resolution version of the Graphical abstract is available as Supplementary information

Gas-phase hydrogenation processes of cationic carbon clusters

ABSTRACT In this work, the gas-phase ion–atom collision reaction between large cationic carbon clusters and H-atoms is investigated. The carbon cluster cations (C$_{48-2*n}$$^+$, n = [0$-$8]) are produced from the photo-fragmentation processes of large PAH (dicoronylene, DC, C$_{48}$H$_{20}$) cations. The hydrogenated carbon cluster cations are efficiently formed (e.g. C$_{44/46}$H$_{9}$$^+$), and no even–odd hydrogenated mass patterns are observed. The hydrogenation behaviour and hydrogenation rate for these carbon cluster cations are the same. With theoretical calculations, the formation and bending processes of carbon cluster cations, the structure of these newly formed hydrogenated carbon cluster cations, and the bonding energies for the hydrogenation pathways are investigated. During the formation process of carbon clusters, the zigzagged edges gradually increase, and the planar configuration tends towards a bent and folded molecular configuration, i.e. from graphene to fullerene structures. The bending process with higher exothermic energies provides a reasonable explanation for the formation of the ‘magic numbers’ (e.g. C-atoms = 44) carbon clusters and their greater stability. The exothermic energy for each hydrogenation reaction pathway is relatively high; consequently, the forms and the hydrogenated states of carbon clusters are complex. The hydrogenation ability of edge carbon sites is higher than that of internal carbon sites; after bending and folding, the hydrogenation ability of these originally internal carbon sites becomes higher due to structural caged. As a result, under the co-evolution interstellar chemistry network, the (hydrogenation) states and forms of carbon compounds are complicated and diverse in the ISM.

Spatiotemporally Controlled Release of Etamsylate from Bioinspired Peptide-Functionalized Nanoparticles Arrests Bleeding Rapidly and Improves Clot Stability in a Rabbit Internal Hemorrhage Model.

Achieving rapid clotting and clot stability are important unmet goals of clinical management of noncompressible hemorrhage. This study reports the development of a spatiotemporally controlled release system of an antihemorrhagic drug, etamsylate, in the management of internal hemorrhage. Gly-Arg-Gly-Asp-Ser (GRGDS) peptide-functionalized chitosan nanoparticles, with high affinity to bind with the GPIIa/IIIb receptor of activated platelets, were loaded with the drug etamsylate (etamsylate-loaded GRGDS peptide-functionalized chitosan nanoparticles; EGCSNP). Peptide conjugation was confirmed by LCMS, and the delivery system was characterized by DLS, SEM, XRD, and FTIR. In vitro study exhibited 90% drug release till 48 h fitting into the Weibull model. Plasma recalcification time and prothrombin time tests of GRGDS-functionalized nanoparticles proved that clot formation was 1.5 times faster than nonfunctionalized chitosan nanoparticles. The whole blood clotting time was increased by 2.5 times over clot formed under nonfunctionalized chitosan nanoparticles. Furthermore, the application of rheometric analysis revealed a 1.2 times stiffer clot over chitosan nanoparticles. In an in vivo liver laceration rabbit model, EGCSNP spatially localized at the internal injury site within 5 min of intravenous administration, and no rebleeding was recorded up to 3 h. The animals survived for 3 weeks after the injury, indicating the strong potential of the system for the management of noncompressible hemorrhage.

Hierarchical metal–organic framework nanoarchitectures for catalysis

Metal–organic frameworks (MOFs) have garnered significant attention in the field of catalysis due to their unique advantages such as diverse coordination geometry, variable metal nodes, and organic linkers, facilitating precise structural and compositional control for achieving programmable catalytic functionalities. Although their inherent microporous structure could provide excellent shape selectivity during catalysis, it typically impedes the mass transfer process, thereby reducing the use of internal active sites and overall catalytic efficiency. Additionally, employing single MOFs as catalysts presents challenges in achieving complex catalytic reactions that require multifunctional active sites. In recent years, considerable research efforts have focused on designing and constructing hierarchical nanostructured MOFs to alleviate substrate diffusion limitations by introducing secondary nanopores, shortening diffusion distances via the construction of low-dimensional nanoarchitectures, and constructing multifunctional catalysts by integrating distinct MOFs with suitable functions. This review provides a comprehensive overview of the design, synthesis methods, and formation mechanisms of MOF-based hierarchical nanostructures in recent years. Subsequently, it further highlights their applications in thermal catalysis, electrocatalysis, and photocatalysis, along with the relationship between their hierarchical nanostructures and catalytic performances. Finally, it provides an outlook on the challenges and potential development directions of hierarchically structured MOF nanocatalysts.

Ionic Liquids Boost Anthraquinone Hydrogenation over Pd‐based Bimetallic Pincer Catalysts

AbstractA series of bimetallic‐ionic liquid (IL) pincer catalysts Pd−M@IL were synthesized using low Pd‐loading amount (0.3 %) and adopting six kinds of ion liquids with the cation containing the imidazole ring, and then evaluated the catalytic activities toward 2‐ethylanthraquinone hydrogenation reaction with the purpose to produce H2O2. Under the reaction conditions of 60 °C, 0.30 MPa and 15 min reaction time, over the catalysts Pd−La@[BMIm]Ac/alu and Pd−La@[VBIM]Br/alu achieved high hydrogenation efficiency(9.4 g/L and 8.5 g/L) but also high selectivity toward the active anthraquinone (98.9 % and 99.6 %). Through characterizations of STEM, TPD, in‐situ XPS, etc., it illustrates that the pincer catalysts Pd−La@[BMIm]Ac/alu and Pd−La@[VBIM]Br/alu have much better dispersity than the bimetallic Pd−La/alu, these two ionic liquids of [BMIm]Ac and [VBIM]Br provide different local environment around Pd−La sites, which in turn modulate the catalytic activity of the pincer‐catalysts toward anthraquinone hydrogenation. DFT calculations disclose the unique electron transfer between ILs ([BMIm]Ac and [VBIM]Br) and Pd−La clusters and subsequent changes of energy barriers for anthraquinone hydrogenation. The work illuminates a facile strategy to design novel hydrogenation catalysts through combining the pincer microenvironment partially encapsulated by the cation and the anion of ionic liquids with the internal bimetallic sites.

Enhancement of hydrogen bonds between proteins and polyphenols through magnetic field treatment: Structure, interfacial properties, and emulsifying properties

In food systems, proteins and polyphenols typically coexist in a non-covalent manner. However, the inherent rigid structure of proteins may hinder the binding sites of polyphenols, thereby limiting the strength of their interaction. In the study, magnetic field (MF) treatment was used to enhance non-covalent interactions between coconut globulin (CG) and tannic acid (TA) to improve protein flexibility, enhancing their functional properties without causing oxidation of polyphenols. Based on protein structure results, the interaction between CG and TA caused protein structure to unfold, exposing hydrophobic groups. Treatment with a MF, particularly at 3 mT, further promoted protein unfolding, as evidenced by a decrease in α-helix structure and an increase in coil random. These structural transformations led to the exposure of the internal binding site bound to TA and strengthening the CG-TA interaction (polyphenol binding degree increased from 62.3 to 68.2%). The characterization of molecular forces indicated that MF treatment strengthened hydrogen bonding-dominated non-covalent interactions between CG and TA, leading to improved molecular flexibility of the protein. Specifically, at a MF treatment at 3 mT, CG-TA colloidal particles with small size and high surface hydrophobicity exhibited optimal interfacial activity and wettability (as evidenced by a three-phase contact angle of 89.0°). Consequently, CG-TA-stabilized high internal phase Pickering emulsions (HIPPEs) with uniform droplets and dense gel networks at 3 mT. Furthermore, the utilization of HIPPEs in 3D printing resulted in consistent geometric shapes, uniform surface textures, and distinct printed layers, demonstrating superior printing stability. As a result, MF treatment at 3 mT was identified as the most favorable. This research provides novel insights into how proteins and polyphenols interact, thereby enabling natural proteins to be utilized in a variety of food applications.