Surface Chemistry Research Articles

Diethylene glycol reduced the water activity of aqueous electrolyte via regulating interphase chemistry for highly durable Zinc-ion batteries

The uncontrollable dendrite growth and parasitic side reactions of Zn lead to poor cycling stability, hindering the practical application of aqueous zinc-ion batteries. Here, we develop a new hybrid electrolyte with zinc trifluoromethanesulfonate dissolved in water and co-solvent diethylene glycol (DEG). DEG can not only alter the Zn2+ solvation structure with the co-participation of DEG and anion to reduce active water molecules, but also interrupt the hydrogen-bond network of the original water. DEG is more easily absorbed on Zn surface than H2O to regulate electric double layer. Based on these unique effects, DEG can regulate interface chemistry, forming a robust solid electrolyte interphase and adjusting Zn2+ stripping/plating behaviors, which suppress side reactions and dendrite growth. Their synergetic effect results in the great improved cycling stability of Zn anode with 5000 h in symmetric cell at 1 mA cm−2 and 1 mAh cm−2. The work shed light on the design of high-performance aqueous electrolyte to advance zinc-ion batteries.

Hydrogen peroxide electrosynthesis using commercial carbon blacks as catalysts: the influence of surface properties and adsorption performance

AbstractBACKGROUNDSurface properties and adsorption performance of carbon materials play a crucial role in the electrochemical two‐electron oxygen reduction to produce H2O2. However, there is still a lack of in‐depth research on commercial carbon blacks in this area. Herein, four typical commercial carbon blacks (Acetylene black (AB), Ketjen black EC 600JD, Vulcan XC 72 and Black Pearls 2000) were used as cathode catalysts to generate H2O2. Surface chemistry and pore structure of electrodes of the four carbon blacks were systematically characterized, and their effects on H2O2 adsorption, electrochemical generation and degradation were investigated.RESULTSAmong the four carbon blacks, AB has the highest content of C–O–C/COOH and CO, which are active groups catalyzing the two‐electron oxygen reduction reaction to generate H2O2. AB has the lowest level of defects and highest degree of graphitization, and AB‐modified graphite felt electrode (AB‐Ele) has the largest average pore diameter, smallest specific surface area and smaller charge transfer resistance. H2O2 production using AB‐Ele is the largest and reaches 567.7 mg L−1 at 180 min under a current density of 5 mA cm−2, and only decreases by 17.6% after 10 repeated uses.CONCLUSIONOverall, rich oxygen‐containing functional groups such as C–O–C, COOH and CO, high degree of graphitization, suitable surface area and porosity as well as weak H2O2 adsorption performance are beneficial for the two‐electron oxygen reduction reaction to generate H2O2. AB‐modified graphite felt electrode exhibits good catalytic activity and reusability in H2O2 electrosynthesis, demonstrating promising application prospects. © 2024 Society of Chemical Industry (SCI).

Improvement of UV resistance and mechanism in polypropylene wax on wood surface through maleic anhydride and β-nucleating agent modification

In China, beeswax is commonly used to protect hardwood surfaces through hot waxing, and is widely utilized in wood furniture and buildings. However, beeswax, with its low melting point and high cost, is prone to being destroyed and falling off, and has a short-term protective effect on wood under ultraviolet (UV) light. Polypropylene wax (PPW), with its low cost and high melting point, holds potential for application in wood protection. The introduction of maleic anhydride enhanced the combination of PPW and wood, resulting in excellent surface properties. Additionally, the β-nucleating agent (WBG-II) induced PPW to form β crystal structure, further enhancing the UV barrier property of the wax coating. After UV irradiation, the surface properties of the hot-waxed wood using the modified polypropylene wax exhibited minimal changes, including color, adhesion, hydrophobicity, and surface roughness. The chemical structure, crystalline structure, and surface morphology were analyzed by FTIR, XRD, and SEM to reveal the photodegradation mechanism of the surface wax coating. The results demonstrated that the co-modification of polypropylene wax by maleic anhydride and WBG-II has a positive effect on the long-term protection of wood substrate, providing a reference for wood protection, particularly for dark and precious wood, and helping to reduce deforestation.

Organic coating strategy with oxidized oxygen anion capture to suppress lattice oxygen evolution of Ni-rich cathode materials at high voltage

Ni-rich layered oxide has attracted widespread attention due to its high capacity of over 200 mAh·g−1 at 4.5 V. However, how to solve its lattice oxygen evolution problem during high-voltage cycling remains the major challenge nowadays. It is still important to design stable and efficient Ni-rich layered oxides. Herein, an organic coating strategy was proposed for this challenge. Specifically, (C3H3N)n (PAN) was employed as a proof-of-concept organic coating with better electro-negativity on LiNi0.8Co0.1Mn0.1O2 to inhibit the lattice oxygen evolution. The CN functional groups in the PAN coating can adsorb Oα− (α < 2) and provide it with electrons for its reduction to stable O2−, thus inhibiting the continuous outward migration. As expected, in a voltage range of 2.7–4.5 V, the modified Ni-rich electrode displayed a high-capacity retention of 86.3 % after 200 cycles at 1C, 75.1 % after 350 cycles at 5C, and 83.1 % after 100 cycles at 1C and 55 °C. Furthermore, it also exhibited a high discharge specific capacity of 235.3 mAh·g−1 with a capacity retention of 75.5 % after 200 cycles under a cut-off voltage of 4.7 V. This innovative organic coating strategy presents new insights into suppressing the lattice oxygen evolution under high-voltage cycling by manipulating the surface chemistry of Ni-rich materials.

AFM-IR investigation of thin PECVD SiO x films on a polypropylene substrate in the surface-sensitive mode.

Thin silicon oxide films deposited on a polypropylene substrate by plasma-enhanced chemical vapor deposition were investigated using atomic force microscopy-based infrared (AFM-IR) nanospectroscopy in contact and surface-sensitive mode. The focus of this work is the comparison of the different measurement methods (i.e., contact mode and surface-sensitive mode) with respect to the chemical surface sensitivity. The use of the surface-sensitive mode in AFM-IR shows an enormous improvement for the analysis of thin films on the IR-active substrate. As a result, in this mode, the signal of the substrate material could be significantly reduced. Even layers that are so thin that they could hardly be measured in the contact mode can be analyzed with the surface-sensitive mode.

Simulation of Hydrogen Adsorption in Hierarchical Silicalite: Role of Electrostatics and Surface Chemistry.

Adsorption in nanoporous materials is one strategy that can be used to store hydrogen at conditions of temperature and pressure that are economically viable. Adsorption capacity of nanoporous materials depends on surface area which can be enhanced by incorporating a hierarchical pore structure. We report grand canonical Monte Carlo (GCMC) simulation results on the adsorption of hydrogen in hierarchical models of silicalite that incorporate 4 nm wide mesopores in addition to the 0.5 nm wide micropores at 298 K, using different force fields to model hydrogen. Our results suggest that incorporating mesopores in silicalite can enhance adsorption by at least 20% if electrostatic interactions are not included and up to 100% otherwise. Incorporating electrostatic interactions results in higher adsorption by close to 100% at lower pressures for hierarchical silicalite whereas for unmodified silicalite, it is less significant at all pressures. Hydroxylating the mesopore surface in hierarchical silicalite results in an enhancement in adsorption at pressures below 1 atm and suppression by up to 20% at higher pressures. Temperature dependence at selected pressures exhibits expected decrease in adsorption amounts at higher temperatures. These findings can be useful in the engineering, selection, and optimization of nanoporous materials for hydrogen storage.

Recyclable Homogeneous Catalysis Enabled by Dynamic Coordination on Rhodium(II) Axial Sites of Metal-Organic Polyhedra.

The activity of catalytic nanoparticles is strongly dependent on their surface chemistry, which controls colloidal stability and substrate diffusion toward catalytic sites. In this work, we studied how the outer surface chemistry of nanostructured Rh(II)-based metal-organic cages or polyhedra (Rh-MOPs) impacts their performance in homogeneous catalysis. Specifically, through post-synthetic coordination of aliphatic imidazole ligands onto the exohedral Rh(II) axial sites of Rh-MOPs, we solubilized a cuboctahedral Rh-MOP in dichloromethane, thereby enabling its use as a homogeneous catalyst. We demonstrated that the presence of the coordinating ligand on the surface of the Rh-MOP does not hinder its catalytic activity in styrene aziridination and cyclopropanation reactions, thanks to the dynamic Rh-imidazole coordination bond. Finally, we used similar ligand exchange post-synthetic reactions to develop a ligand-mediated approach for precipitating the Rh-MOP catalyst, facilitating the recovery and reuse of Rh-MOPs as homogeneous catalysts.

Proton-driven bilateral interfacial chemistry and electrolyte structure reconstruction enable highly reversible zinc metal anodes

Uncontrolled dendrite growth, severe parasitic reactions on the Zn metal anode (ZMA), and the dissolution of cathode active materials have significantly limited the development of aqueous zinc ion batteries. Herein, 3-(Cyclohexylamino)-1-propanesulfonic acid (CAPS) featured with zwitterion as a multifunctional additive is introduced into the 2 M ZnSO4 aqueous electrolyte to simultaneously regulate the interfacial chemistry of the Zn anode and the cathode, as well as the solvated structure of Zn2+, thereby improving the interfacial and structural stability of both electrodes. Thereinto, the preferentially adsorbed CAPS zwitterion onto the ZMA surface favors for constructing a cationic protective layer originated from the electrostatic shielding effect of the cationic group (>NH2+), inhibiting the growth of dendrites. Meanwhile, the CAPS zwitterion can self-regulate the bilateral interfacial pH by forming the conjugate acid-base pair, suppressing hydrogen evolution reaction and Zn anode surface corrosion. Additionally, the CAPS zwitterion alters the solvated structure of Zn2+, weakening H2O molecule activity and reducing the dissolution of vanadium element from cathode. Consequently, the Zn||Zn symmetric cells harvest excellent cycling stability (1 mA cm−2, 1 mAh cm−2, 2300 h), and the Zn||Cu asymmetric cells display a high average Coulombic Efficiency of 99.7 % after 1600 cycles in the ZnSO4+CAPS electrolyte.

Additive-Free Anode with High Stability: Nb2CTx MXene Prepared by HCl-LiF Hydrothermal Etching for Lithium-Ion Batteries.

MXenes, represented by Ti3C2Tx, have been widely studied in the electrochemical energy storage fields, including lithium-ion batteries, for their unique two-dimensional structure, tunable surface chemistry, and excellent electrical conductivity. Recently, Nb2CTx, as a new type of MXene, has attracted more and more attention due to its high theoretical specific capacity of 542 mAh g-1. However, the preparation of few-layer Nb2CTx nanosheets with high-quality remains a challenge, which limits their research and application. In this work, high-quality few-layer Nb2CTx nanosheets with a large lateral size and a high conductivity of up to 500 S cm-1 were prepared by a simple HCl-LiF hydrothermal etching method, which is 2 orders of magnitude higher than that of previously reported Nb2CTx. Furthermore, from its aqueous ink, the viscosity-tunable organic few-layer Nb2CTx ink was prepared by HCl-induced flocculation and N-methyl-2-pyrrolidone treatment. When using the organic few-layer Nb2CTx ink as an additive-free anode of lithium-ion batteries, it showed excellent cycling performance with a reversible specific capacity of 524.0 mAh g-1 after 500 cycles at 0.5 A g-1 and 444.0 mAh g-1 after 5000 cycles at 1 A g-1. For rate performance, a specific capacity of 159.8 mAh g-1 was obtained at a high current density of 5 A g-1, and an excellent capacity retention rate of about 95.65% was achieved when the current density returned to 0.5 A g-1. This work presents a simple and scalable process for the preparation of high-quality Nb2CTx and its aqueous/organic ink, which demonstrates important application potential as electrodes for electrochemical energy storage devices.

Supportive suggestions for successful Surface Science Spectra SIMS submissions

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Gradient heating activated ammonium persulfate oxidation for efficient preparation of high-quality chitin nanofibers

APS is a cheap and eco-friendly oxidant which enables one-step extraction of nanochitin (NCh) from fishery wastes. However, it is challenging to improve the preparation efficiency and NCh quality simultaneously, owing to the uneven or uncontrollable oxidation. Herein, we propose a simple and controllable way to isolate chitin nanofibers (ChNFs) from squid pen by gradient heating activated (GHA)- ammonium persulfate (APS) oxidation. Compared to the isothermal activated (ITA)-APS oxidation, our strategy reduced the mass ratio of squid pen to APS from 1:45 to 1:6 and reaction time from 15 h to 8 h. Meanwhile, the as-prepared ChNFs exhibited high yield (91.5 %), light transmittance (98 % at 500 nm), crystallinity index (96.9 %), and carboxyl content (1.53 mmol/g). GHA-APS oxidation involved multiple continuous heating and isothermal stages. The former stimulates a moderate activation of APS and enhances the oxidation rate, while the latter provides a duration for surface chemistry. This non-isothermal heating facilitates the continuous decomposition of APS at a relatively high and consistent rate, thereby enhances its oxidation efficiency. Furthermore, green assessments indicate this method is simple, time-saving, eco-friendly and cost-effective. Overall, this work introduces a novel perspective for the industrial extraction of high-efficiency and high-quality nanomaterials.

Unveiling polycrystalline silicon channel dissolution mechanism in wet etching process of 3D NAND fabrication

3D NAND is one of the most promising storage devices due to its high storage density and low energy consumption. Selective wet etching of Si3N4 by hot-concentrated phosphoric acid (PA) solution is a key process for 3D NAND fabrication. However, the channel material, polycrystalline silicon (poly-Si), is unexpectedly dissolved due to its inevitable exposure to the PA etching solution, which causes device failure and thus limits the stacking density of 3D NAND. Herein, to avoid the detrimental dissolution of poly-Si, we unveil the mechanism of poly-Si dissolution in PA solution from kinetic and thermodynamic perspectives. We find that the etch process shows a two-stage reaction, in which H2O plays a key role in lowering the activation barrier for poly-Si etching. Further thermodynamic analysis demonstrates that poly-Si prefers to be oxidized by H2O to suboxide rather than to SiO2. Combined with surface chemistry characterization, we propose the dissolution mechanism as a two-stage process involving the dissolution of suboxide interface and bulk poly-Si, where the nucleophilic substitution of Si–H with Si–OH on bulk poly-Si surface determines the overall etch rate. This study advances the 3D NAND development by establishing a theoretical foundation for identifying and implementing efficacious strategies to impede detrimental dissolution.

Nanoplastic Size and Surface Chemistry Dictate Decoration by Human Saliva Proteins.

Environmental pollution with plastic polymers has become a global problem, leaving no continent and habitat unaffected. Plastic waste is broken down into smaller parts by environmental factors, which generate micro- and nanoplastic particles (MNPPs), ultimately ending up in the human food chain. Before entering the human body, MNPPs make their first contact with saliva in the human mouth. However, it is unknown what proteins attach to plastic particles and whether such protein corona formation is affected by the particle's biophysical properties. To this end, we employed polystyrene MNPPs of two different sizes and three different charges and incubated them individually with saliva donated by healthy human volunteers. Particle zeta potential and size analyses were performed using dynamic light scattering complemented by nanoliquid chromatography high-resolution mass spectrometry (nLC/HRMS) to qualitatively and quantitatively reveal the protein soft and hard corona for each particle type. Notably, protein profiles and relative quantities were dictated by plastic particle size and charge, which in turn affected their hydrodynamic size, polydispersity, and zeta potential. Strikingly, we provide evidence of the latter to be dynamic processes depending on exposure times. Smaller particles seemed to be more reactive with the surrounding proteins, and cultures of the particles with five different cell lines (HeLa, HEK293, A549, HepG2, and HaCaT) indicated protein corona effects on cellular metabolic activity and genotoxicity. In summary, our data suggest nanoplastic size and surface chemistry dictate the decoration by human saliva proteins, with important implications for MNPP uptake in humans.

Strategies for the quantification and characterization of nanoplastics in AOPs research

There is a growing interest in developing new targeted degradation technologies for the removal of micro- and nanoplastics (NPs) in water, corresponding to increased public concerns regarding their potential negative impacts on urban water systems, and consequently on human life quality. Recently, Advanced Oxidation Processes (AOPs) have been proposed as promising treatment alternatives for effective degradation of NPs in water. However, the selection of appropriate analytical methods for monitoring these oxidation tests remains a challenge. Herein, the feasibility of different characterization strategies for monitoring the evolution of NPs in water upon oxidation tests was systematically studied using polystyrene (PS) NPs of different particle sizes (D0 = 140, 252, 460, and 909 nm) as model plastic pollutants. To quantify NPs in water, Total Organic Carbon (TOC), Chemical Oxygen Demand (COD) and turbidity measurements were assessed. Moreover, turbidity was correlated to the particle size and PS NPs concentration by developing a response surface. Among the analytical techniques employed to characterize the solid particles, transmission electronic microscopy (TEM) was used to evaluate morphology and particle size. Alternatively, the viability of Dynamic Light Scattering (DLS), Nanoparticle Tracking Analysis (NTA) and Atomic Force Microscopy (AFM) to determine particle size is discussed. Chemical surface modifications were explored by Fourier-Transform Infrared Spectroscopy (FTIR). As a proof of concept, the degradation of PS NPs in water upon photo-Fenton oxidation was investigated at ambient conditions and fully characterized using the mentioned techniques.

Insights into the writing process of the mask-free nanoprinting fluid force microscopy technology

Platelets are activated immediately when contacting with non-physiological surfaces. Minimization of surface-induced platelet activation is important not only for platelet storage but also for other blood-contacting devices and implants. Chemical surface modification tunes the response of cells to contacting surfaces, but it requires a long process involving many regulatory challenges to transfer into a marketable product. Biophysical modification overcomes these limitations by modifying only the surface topography of already approved materials. The available large and random structures on platelet storage bags do not cause a significant impact on platelets because of their smallest size (only 1–3 μm) compared to other cells. We have recently demonstrated the feasibility of the mask-free nanoprint fluid force microscope (FluidFM) technology for writing dot-grid and hexanol structures. Here, we demonstrated that the technique allows the fabrication of nanostructures of varying features including grid, circle, triangle, and Pacman-like structures. Characteristics of nanostructures including height, width, and cross-line were analyzed and compared using atomic force microscopy imaging. Based on the results, we identified several technical issues, such as the printing direction and shape of structures that directly altered nanofeatures during printing. Importantly, both geometry and interspace governed the degree of platelet adhesion, especially, the structures with triangular shapes and small interspaces prevent platelet adhesion better than others. We confirmed that FluidFM is a powerful technique to precisely fabricate a variety of desired nanostructures for the development of platelet/blood-contacting devices if technical issues during printing are well controlled.

Highly reversible zinc metal anode enabled by strong Brønsted acid and hydrophobic interfacial chemistry

Uncontrollable zinc (Zn) plating and hydrogen evolution greatly undermine Zn anode reversibility. Previous electrolyte designs focus on suppressing H2O reactivity, however, the accumulation of alkaline byproducts during battery calendar aging and cycling still deteriorates the battery performance. Here, we present a direct strategy to tackle such problems using a strong Brønsted acid, bis(trifluoromethanesulfonyl)imide (HTFSI), as the electrolyte additive. This approach reformulates battery interfacial chemistry on both electrodes, suppresses continuous corrosion reactions and promotes uniform Zn deposition. The enrichment of hydrophobic TFSI– anions at the Zn|electrolyte interface creates an H2O-deficient micro-environment, thus inhibiting Zn corrosion reactions and inducing a ZnS-rich interphase. This highly acidic electrolyte demonstrates high Zn plating/stripping Coulombic efficiency up to 99.7% at 1 mA cm–2 ( > 99.8% under higher current density and areal capacity). Additionally, Zn | |ZnV6O9 full cells exhibit a high capacity retention of 76.8% after 2000 cycles.

Enhancing 3D poly[ɛ]caprolactone scaffold properties through alkaline hydrolysis for improved chondrocyte culture: Morphological, physicochemical, and biocompatibility evaluations

This study investigates the impact of alkaline hydrolysis on the morphology, physicochemical properties, and mechanical strength of poly[ε]caprolactone (PCL) scaffolds fabricated using a melt-based electrohydrodynamic process. We systematically analyzed how a brief, 5-min alkaline hydrolysis treatment influenced scaffold characteristics compared to longer durations (15 and 30 min). Results demonstrated that the short-duration treatment significantly increased fiber diameter and reduced pore size while modifying the scaffold's surface chemistry. Importantly, the 5-min treatment optimized the water contact angle to 55–65°, enhancing hydrophilicity which facilitated superior cell attachment and proliferation of the C28/I2 immortalized human chondrocyte cell line. Mechanical testing revealed that while alkaline hydrolysis decreased the scaffold's Young's modulus, a 5-min treatment maintained sufficient mechanical integrity for potential tissue engineering applications, in contrast to the more substantial degradation observed with longer treatments.Biocompatibility evaluations showed that the scaffolds, particularly those treated for 5 min, supported cell viability and proliferation without inducing cytotoxic effects. The molecular analysis indicated a favorable upregulation of chondrogenic genes such as SOX9 and COL2A1, and a downregulation of COL1A1, suggesting potential benefits for cartilage tissue engineering. These findings highlight that precise control over the duration of alkaline hydrolysis can significantly enhance PCL scaffold properties, suggesting a scalable and cost-effective method for scaffold optimization in regenerative medicine applications. The results pave the way for further in vivo studies to validate these promising in vitro findings and explore the clinical applicability of the optimized scaffolds.

Bioinspired poly-dopamine/nano-hydroxyapatite: an upgrading biocompatible coat for 3D-printed polylactic acid scaffold for bone regeneration.

Poly-lactic acid (PLA) has been proposed in dentistry for several regenerative procedures owing to its biocompatibility and biodegradability. However, the presence of methyl groups renders PLA hydrophobic, making the surface less ideal for cell attachment, and it does not promote tissue regeneration. Upgrading PLA with inductive biomaterial is a crucial step to increase the bioactivity of the PLA and allow cellular adhesion. Our purpose is to evaluate biocompatibility, bioactivity, cellular adhesion, and mechanical properties of 3D-printed PLA scaffold coated with poly-dopamine (PDA) and nano-hydroxyapatite (n-HA) versus PLA and PLA/n-HA scaffolds. The fused deposition modelling technique was used to print PLA, PLA with embedded n-HA particles, and PLA scaffold coated with PDA/n-HA by immersion. After matrices characterization for their chemical composition and surface properties, testing the compressive strength was pursued using a universal testing machine. The bioactivity of scaffolds was evaluated by monitoring the formation of calcium phosphate compounds after simulated body fluid immersion. The PLA/PDA/n-HA scaffold showed the highest compressive strength which was 29.11 ± 7.58 MPa with enhancing calcium phosphate crystals deposition with a specific calcium polyphosphate phase formed exclusively on PLA/PDA/n-HA. With cell viability assay, the PDA/n-HA-coated matrix was biocompatible with increase in the IC50, reaching ⁓176.8 at 72 without cytotoxic effect on the mesenchymal stem cells, promoting their adhesion and proliferation evaluated by confocal microscopy. The study explored the biocompatibility, bioactivity, and the cell adhesion ability of PDA/n-HA coat on a 3D-printed PLA scaffold that qualifies its use as a promising regenerative material.

Insights into the Formation Mechanism of Reactive Oxygen Species in the Interface Reaction of SO2 on Hematite.

The interplay between sulfur and iron holds significant importance in their atmospheric cycle, yet a complete understanding of their coupling mechanism remains elusive. This investigation delves comprehensively into the evolution of reactive oxygen species (ROS) during the interfacial reactions involving sulfur dioxide (SO2) and iron oxides under varying relative humidity conditions. Notably, the direct activation of water by iron oxide was observed to generate a surface hydroxyl radical (•OH). In comparison, the aging of SO2 was found to markedly augment the production of •OH radicals on the surface of α-Fe2O3 under humid conditions. This augmentation was ascribed to the generation of superoxide radicals (•O2-) stemming from the activation of O2 through the Fe(II)/Fe(III) cycle and its combination with the H+ ion to produce hydrogen peroxide (H2O2) on the acidic surface. Moreover, the identification of moderate relative humidity as a pivotal factor in sustaining the surface acidity of iron oxide during SO2 aging underscores its crucial role in the coupling of iron dissolution, ROS production, and SO2 oxidation. Consequently, the interfacial reactions between SO2 and iron oxides under humid conditions are elucidated as atmospheric processes that enhance oxidation capacity rather than deplete ROS. These revelations offer novel insights into the mechanisms underlying •OH radical generation and oxidative potential within atmospheric interfacial chemistry.

Identification and Functional Characterization of a Surfactant-like Protein Region in Flagellin FliC for Stabilizing Selenium Nanoparticles and Enhancing Bioavailability.

Biogenic selenium nanoparticles (SeNPs) are the most favorable Se form for nutritional supplementation due to their high stability, low toxicity, and high activity. However, the interaction between the surface-binding proteins and their stable biogenic SeNPs, as well as their impact on the stability and bioavailability of SeNPs, remains to be understood. In vitro stabilization experiments revealed an amino acid segment (F(235-386)) in Rahnella aquatilis' flagellin FliC, with surfactant-like properties, stabilizing SeNPs under harsh conditions. FliC and F(235-386) were employed as stabilizers to synthesize SeNPs (FliC@SeNPs and F(235-386)@SeNPs), and surface chemistry analysis revealed coordination reactions between the proteins and Se atoms on the surface of SeNPs. Both FliC and F(235-386) enhanced SeNPs uptake in wheat seedlings but reduced it in bacteria and yeast. This study highlights FliC's core function in stabilizing SeNPs and enhancing their bioavailability, paving the way for agricultural and nutritional applications.