Chemical Surface Modification Research Articles

Two-dimensional MXene-based nano-prodrug for synergistic chemo-photothermal therapy on cancer treatment

In cancer treatment, although prodrugs have been developed to overcome obstacles such as undesirable pharmacokinetic performance and serious off-target toxicity of most chemotherapeutics, the combination of prodrugs with nanotechnology could be used to overcome the shortcomings of conventional prodrug strategies and facilitate more efficient drug delivery and accumulation of anticancer prodrugs at specific sites/tissues. Phototherapy is a method that uses near-infrared (NIR) light to achieve local and non-invasive tumor therapy. The combination of chemotherapy and phototherapy has shown many therapeutic advantages, including synergistic therapeutic effects and the reduction of toxic and side effects of drugs through dose reduction. In this work, a hydrazone linkage was reported to conjugate Ti3C2Tx MXene nanosheets with doxorubicin hydrochloride (DOX) and methoxy poly(ethylene glycol) benzaldehyde (mPEG-CHO) through a chemical surface modification to form a two-dimensional (2D) nano-prodrug Ti3C2Tx-DOX/PEG (TDP) for synergistic chemo-photothermal therapy. First, hydrazide functionalized Ti3C2Tx was obtained. Then, the carbonyl group of DOX and the aldehyde group of mPEG-CHO can form a pH-responsive hydrazone bond with hydrazide-functionalized Ti3C2Tx. The high surface area of Ti3C2Tx could overcome the reduced drug loading caused by conjugation. Aqueous stability and biocompatibility were enhanced by the introduction of PEG, making the material capable of prolonged circulation in the body's bloodstream. By achieving excellent antitumor results with this nano-prodrug, we have added another brick to the edifice of Ti3C2Tx MXene as an anticancer drug carrier, and given new vitality to the study of anticancer prodrugs combined with nanotechnology.

Current Status of root Biomodification Agents in Periodontal Regeneration

Periodontitis can be defined as a multifactorial inflammatory disease of bacterial origin causing destruction of periodontal tissues. Achieving effective regeneration in periodontal therapy still remains a foremost goal. Chemical modification of tooth surface has been the most persistent effort to achieve periodontal regeneration. There are controversies regarding effectiveness of root biomodification due to a mixture of results from clinical and histological studies. This review provides an acumen about root biomodification in clinical conditions as well as a summary on the novel biomodification agents.

Surface Depassivation via B-O Dative Bonds Affects the Friction Performance of B-Doped Carbon Coatings.

Boron doping of diamond-like carbon coatings has multiple effects on their tribological properties. While boron typically reduces wear in cutting applications, some B-doped coatings show poor tribological performance compared with undoped films. This is the case of the tribological tests presented in this work in which an alumina ball is placed in frictional contact with different undoped and B-doped amorphous carbon coatings in humid air. With B-doped coatings, a higher friction coefficient at a steady state with respect to their undoped counterparts was observed. Estimates of the average contact shear stress based on experimental friction coefficients, surface topographies, and Persson's contact theory suggest that the increased friction is compatible with the formation of a sparse network of interfacial ether bonds leading to a mild cold-welding friction regime, as documented in the literature. Tight binding and density functional theory simulations were performed to investigate the chemical effect of B-doping on the interfacial properties of the carbon coatings. The results reveal that OH groups that normally passivate carbon surfaces in humid environments can be activated by boron and form B-O dative bonds across the tribological interfaces, leading to a mild cold-welding friction regime. Simulations performed on different tribological pairs suggest that this mechanism could be valid for B-doped carbon surfaces in contact with a variety of materials. In general, this study highlights the impact that subtle modifications in surface and interface chemistry caused by the presence of impurities can have on macroscopic properties, such as friction and wear.

Influence of Chemical Treatment on the Physical and Mechanical Properties of Bamboo Fibers as Potential Reinforcement for Polymer Composites

ABSTRACT The growing concern for environmentally friendly biomaterials has spurred interest in natural fibers as a viable alternative to synthetic fibers in various industrial applications. Chemical treatment of natural fibers is necessary in cases where it is desired to enhance their properties and make them more suitable for various industrial applications. These treatments can remove impurities, increase fiber roughness for better adhesion, and modify surface chemistry, ultimately improving characteristics like tensile strength, thermal stability, and compatibility with matrix materials in composites. In this study, chemical treatments, including Sodium Hydroxide, Ammonium Hydroxide, and Potassium Permanganate, were applied to the Bamboo fibers to modify the fiber structure. The tensile strength, morphological characteristics, and degree of crystallinity of the treated fibers were examined. Results revealed that 5% Sodium Hydroxide treatment for 2 hours significantly improved tensile strength and crystallinity compared to other treatments. Chemical composition analysis, XRD, and FTIR analyses confirmed the removal of impurities and amorphous substances. Density measurements indicated a reduction in volume due to the elimination of low molecular weight impurities, leading to increased fiber density. This research provides valuable insights for the development of sustainable biomaterials in the construction and automotive industries such as wall panels, dashboards and door panels.

Surface-Modified Wheat Straw for the Production of Cement-Free Geopolymer Composite: Effects of Wheat Variety and Pre-Treatment Method

The development of new composite materials with specific properties and reduced environmental pollution can be achieved by the incorporation of agricultural residues, whose morphology is strongly affected by their variety and growing conditions. Herein, the functional properties of a cement-free geopolymer composite reinforced with straw from two wheat varieties (Ada and Malibu) were investigated through different straw pre-treatment methods and their surface modification with silane coupling agents. The characterization of the wheat surface and the geopolymer composites involved SEM-EDS, TGA, FTIR, and gas physisorption analysis methods supplemented with mechanical strength and moisture ingress measurements. Mild (23 °C) and severe (100 °C) physical pre-treatment methods with chemical soaking in 7.3 M isopropanol solution were applied on wheat straw. Tetraethoxysilane (TEOS) with octadecylamine was employed for chemical surface modification. The set of geopolymer compositions was prepared with untreated, pre-treated, and modified straws. The results revealed the hot pre-treatment method caused a higher degradation of siliceous layers of straw, especially in the Ada variety. The modification with TEOS resulted in irregular silane coating formation regardless of the wheat variety and pre-treatment method. Despite good interfacial bonding of the modified straw with the geopolymer matrix, the mechanical strength of the composites was reduced, although the resistance to water ingress slightly increased. Comparing both varieties, Ada wheat showed better performance than Malibu.

Immune-defensive microspheres promote regeneration of the nucleus pulposus by targeted entrapment of the inflammatory cascade during intervertebral disc degeneration

Sustained and intense inflammation is the pathological basis for intervertebral disc degeneration (IVDD). Effective antagonism or reduction of local inflammatory factors may help regulate the IVDD microenvironment and reshape the extracellular matrix of the disc. This study reports an immunomodulatory hydrogel microsphere system combining cell membrane-coated mimic technology and surface chemical modification methods by grafting neutrophil membrane-coated polylactic-glycolic acid copolymer nanoparticles loaded with transforming growth factor-beta 1 (TGF-β1) (T-NNPs) onto the surface of methacrylic acid gelatin anhydride microspheres (GM) via amide bonds. The nanoparticle-microsphere complex (GM@T-NNPs) sustained the long-term release of T-NNPs with excellent cell-like functions, effectively bound to pro-inflammatory cytokines, and improved the release kinetics of TGF-β1, maintaining a 36 day-acting release. GM@T-NNPs significantly inhibited lipopolysaccharide-induced inflammation in nucleus pulposus cells in vitro, downregulated the expression of inflammatory factors and matrix metalloproteinase, and upregulated the expression of collagen-II and aggrecan. GM@T-NNPs effectively restored intervertebral disc height and significantly improved the structure and biomechanical function of the nucleus pulposus in a rat IVDD model. The integration of biomimetic technology and nano-drug delivery systems expands the application of biomimetic cell membrane-coated materials and provides a new treatment strategy for IVDD.

Plasma Treatment Modifies Element Distribution in Seed Coating and Affects Further Germination and Plant Growth through Interaction with Soil Microbiome.

This study investigates the impact of plasma-seed interaction on germination and early plant development, focusing on Arabidopsis thaliana and Brassica napus. The investigation delves into changes in chemical composition, water absorption, and surface morphology induced by plasma filaments generated in synthetic air. These analyses were conducted using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Although plasma treatment enhanced water absorption and modified surface chemistry, its impact on germination demonstrated species- and context-dependent variations. Notably, the accelerated germination and morphogenesis of seedlings in microbiome-enriched (MB+) soil could be achieved also in microbiome-deprived (MB-) soil by short-term plasma treatment of seeds. Remarkably, the positive effects of plasma treatment on early developmental events (germination, morphogenesis) and later events (formation of inflorescences) were more pronounced in the context of MB- soil but were accompanied by a slight decrease in disease resistance, which was not detected in MB+ soil. The results underscore the intricate dynamics of plasma-plant interactions and stress the significance of accounting for the soil microbiome while designing experiments with potential field application.

Enhancing the dynamic thermal stability of metal oxide oil-based nanofluids through synchronous chemical modification and physical coating

The stability of oil-based nanofluid, especially dynamic thermal stability, hinders its practical application in industries. To enhance the stability of oil-based nanofluids, an excess amount of hexadecyl trimethoxysilane was employed to synchronously achieve chemical surface modification and physical coating of metal oxide nanoparticles. This process can efficiently render the nanoparticle surface lipophilic while introducing steric hindrance. The dynamic thermal stability and long-term durability of the nanofluids were confirmed through extended resting and thermal cycling experiments. Additionally, various characterization methods were employed to examine certain properties of the modified nanoparticles. The results reveal that the modified nanoparticles exhibit lipophilic characteristics, effective dispersion, and robust thermal stability. The nanofluids prepared using these modified nanoparticles remained stable for 3 months during resting periods and withstood 21 days of thermal cycling at 130 °C. This positions them as promising heat transfer mediums for mid-temperature industries. Importantly, this stabilization technique exhibits potential applicability across a wide range of hydrophilic metal oxide oil nanofluids, as suggested by mechanistic analysis. The exploration of dynamic thermal stability mechanisms is of great practical significance in promoting the large-scale application of nanofluids in industry and provides insights that could potentially resolve the longstanding challenge of nanofluid stability.

Interfacial Chemistry and Catalysis of Inorganic Materials.

Heterogeneous catalysis is essential to most industrial chemical processes. To achieve a better sustainability of these processes we need highly efficient and highly selective catalysts that are based on earth-abundant materials rather than the more conventional noble metals. Here, we discuss the potential of inorganic materials as catalysts for chemical transformations focusing in particular on the promising transition metal phosphides and sulfides. We describe our recent and current efforts to understand the interfacial chemistry of these materials that governs catalysis, and to tune catalytic reactivity by controlled chemical modification of the material surfaces and by use of interfacial electric fields.

Critical role of the composition of the cell culture medium on cell attachment and viability on PLA biocomposite scaffolds under in vitro assay conditions

In tissue engineering applications 3D scaffolds undertake the function of the native extracellular matrix (ECM) for cell attachment, survival, proliferation, and differentiation. For successful long-term implementation scaffolds need to mimic the ECM in vitro and in vivo. Many studies have focused on protein adsorption as the most critical factor for cell attachment. To improve protein adsorption on polymeric scaffolds various physical and chemical surface modification techniques, such as changing surface porosity, surface energy, and introducing various functional surface chemical groups have been investigated. It is well studied and documented that complex interactions between the biomaterial surface and the cell culture components in in vitro assay conditions define the scaffold performance. In this study influence of in vitro assay components on HepG2 liver cell attachment and proliferation on 3D printed poly(lactic acid) (PLA) scaffolds coated with various polymeric electrospun webs were investigated. MTT assays were performed on the scaffolds by using 3 different cell culture media; (i) basal cell culture medium (DMEM), (ii) DMEM supplemented with 10% albumin, and (iii) DMEM supplemented with 10% fetal bovine serum (FBS). Results obtained have shown dramatic improvement in cell attachment and proliferation in DMEM supplemented with 10% FBS when compared with DMEM and DMEM containing 10% albumin. Our findings clearly demonstrate synergistic effects of all bioactive components present in the FBS medium in significantly improving the HepG2 cell attachment and proliferation on polymeric scaffolds under in vitro conditions, regardless of the substrate structure, composition, and surface properties.

Chemical modification of nanotubular Ti surfaces with calcium phosphate and strontium ranelate for biomedical applications

Titanium (Ti) and its alloys are widely used as dental implants due to their notable properties, including corrosion resistance, biocompatibility, and mechanical stability. The anodization process can create a unique nanotubular (NT) structure on the surface of Ti, which offers significant potential for improving the performance of this biomaterial. This study deals with the chemical modification of an NT Ti surface by the incorporation of calcium phosphate (CaP) and strontium ranelate (SrR). A comprehensive set of analytical techniques was used to study these surface modifications on Ti, including atomic force microscopy, water contact angle measurements, scanning electron microscopy, thermal diffusivity, X-ray diffraction, and X-ray photoelectron spectroscopy. Examination of the surface morphology after immersion revealed the presence of deposits, occasionally with partial blocking of the TiO2 nanotubes. Both surface morphology and chemical analysis demonstrated the successful incorporation of CaP and SrR. In addition, in vitro evaluations demonstrated the exceptional promise of the prepared samples for biomedical applications, exhibiting high cell viability, non-toxicity, and osteogenic properties. These results underscore the potential of these modified surfaces to significantly advance the field of dental implantology.

Antifouling strategies for electrochemical sensing in complex biological media.

Surface fouling poses a significant challenge that restricts the analytical performance of electrochemical sensors in both in vitro and in vivo applications. Biofouling resistance is paramount to guarantee the reliable operation of electrochemical sensors in complex biofluids (e.g., blood, serum, and urine). Seeking efficient strategies for surface fouling and establishing highly sensitive sensing platforms for applications in complex media have received increasing attention in the past. In this review, we provide a comprehensive overview of recent research efforts focused on antifouling electrochemical sensors. Initially, we present a detailed illustration of the concept about biofouling along with an exploration of four key antifouling mechanisms. Subsequently, we delve into the commonly employed antifouling strategies in the fabrication of electrochemical sensors. These encompass physical surface topography (micro/nanostructure coatings and filtration membranes) and chemical surface modifications (PEG and its derivatives, zwitterionic polymers, peptides, proteins, and various other antifouling materials). The progress in antifouling electrochemical sensors is proposed concerning the antifouling mechanisms as well as sensing capability assessments (e.g., sensitivity, stability, and practical application ability). Finally, we summarize the evolving trends in the field and highlight some key remaining limitations.

Surface Modification of Polystyrene with Boronic Acid for Immunoaffinity-Based Cell Enrichment.

Obtaining an enriched and phenotypically pure cell population from heterogeneous cell mixtures is important for diagnostics and biosensing. Existing techniques such as fluorescent-activated cell sorting (FACS) and magnetic-activated cell sorting (MACS) require preincubation with antibodies (Ab) and specialized equipment. Cell immunopanning removes the need for preincubation and can be done with no specialized equipment. The majority of the available antibody-mediated analyte capture techniques require a modification to the Abs for binding. In this work, no antibody modification is used because we take advantage of the carbohydrate chain in the Fc region of Ab. We use boronic acid as a cross-linker to bind the Ab to a modified surface. The process allows for functional orientation and cleavable binding of the Ab. In this study, we created an immunoaffinity matrix on polystyrene (PS), an inexpensive and ubiquitous plastic. We observed a 37% increase in Ab binding compared with that of a passive adsorption approach. The method also displayed a more consistent antibody binding with 17 times less variation in Ab loading among replicates than did the passive adsorption approach. Surface topography analysis revealed that a dextran coating reduced nonspecific antibody binding. Elemental analysis (XPS) was used to characterize the surface at different stages and showed that APBA molecules can bind upside-down on the surface. While upside-down antibodies likely remain functional, their elution behavior might differ from those bound in the desired way. Cell capture experiments show that the new surface has 43% better selectivity and 2.4-fold higher capture efficiency compared to a control surface of passively adsorbed Abs. This specific surface chemistry modification will allow the targeted capture of cells or analytes with the option of chemical detachment for further research and characterization.

Synthesis of Photoluminescent 2D Self-Assembled Silver Thiolate Nanoclusters for Sensors and Biomolecule Support.

Silver thiolate nanoclusters (Ag NCs) show distinctive optical properties resulting from their hybrid nature, metallic and molecular, exhibiting size-, structure-, and surface-dependent photoluminescence, thus enabling the exploitation of Ag NCs for potential applications in nanobiotechnology, catalysis, and biomedicine. However, tailoring Ag NCs for specific applications requires achieving long-term stability and may involve modifying surface chemistry, fine-tuning ligand composition, or adding functional groups. In this study, we report the synthesis of novel Ag NCs using 2-ethanephenylthiolate (SR) as a ligand, highlight critical points addressing stability, and characterize their optical and structural properties. A preliminary electrical characterization revealed high anisotropy, well suited for potential use in electronics/sensing applications. We also present the synthesis and characterization of Ag NCs using 10-carboxylic 2-ol thiolate (SR'COOH) having a terminal carboxylic group for conjugation with amine-containing molecules. We present a preliminary assessment of its bioconjugation capability using bovine serum albumin as a model protein indicating its prospective application as a biomolecule support.

Comparable Toxicity of Surface-Modified TiO2 Nanoparticles: An In Vivo Experimental Study on Reproductive Toxicity in Rats.

Nanoparticles (NPs), a distinct class of particles ranging in size from 1 to 100 nm, are one of the most promising technologies of the 21st century, and titanium dioxide NPs (TiO2 NPs) are among the most widely produced and used NPs globally. The increased application of TiO2 NPs raises concerns regarding their global safety and risks of exposure. Many animal studies have reported the accumulation of TiO2 NPs in female reproductive organs; however, evidence of the resultant toxicity remains ambiguous. Since the surface area and chemical modifications of NPs can significantly change their cytotoxicity, we aimed to compare the toxic effects of pristine TiO2 powder with surface-modified TiO2 powders with salicylic acid (TiO2/SA) and 5-aminosalicylic acid (TiO2/5-ASA) on the ovaries, oviducts, and uterus on the 14th day following acute oral treatment. The results, based on alterations in food and water intake, body mass, organ-to-body mass ratio, hormonal status, histological features of tissues of interest, and antioxidant parameters, suggest that the modification with 5-ASA can mitigate some of the observed toxic effects of TiO2 powder and encourage future investigations to create NPs that can potentially reduce the harmful effects of TiO2 NPs while preserving their positive impacts.

Surface modification strategies of 304 austenitic stainless steel plate with different micromorphology and composition for improved mechanical interlocking and chemical bonding in metal–epoxy joints

304 austenitic stainless-steel (SS) strip-based carbon fiber metal laminates (CFMLs) have raised significant concerns, in terms of their mechanical performance. On top of that, the hybrid laminates’ interlamination performance is vital in regulating their failure patterns. Along these lines, in this work, SS strips with regulatable micromorphology and composition were obtained by using physical and chemical surface modification strategies, including polishing, acid etching, anodization, and thermal treatment. The shear strength of the treated-SS/epoxy single lap joints (two treated-SS strips bonded by the epoxy resin via hot curing process) was systematically explored, and the origins of the enhancement mechanism were attributed to the resulting surface microstructure, as well as the possible chemical reactions between the treated surface and the curing agent. The etching-anodizing-thermally treated-SS (EAT-SS)/epoxy joint exhibited the maximum shear strength (16.04 MPa) and work of fracture (5.85 kJ·m−2) due to the substantial cohesive failure pattern of the epoxy. The encouraging enhancement was mainly attributed to the synergistic effect of the micro-annular pit and the nanoporous array structure of the EAT-SS surface. These effects induced a significant mechanical interlock and a plausible chemical reaction at the interface, which led to improved bonding strength between the epoxy and treated-SS surface. Overall, in this work, it was demonstrated that the combination of the anodization and thermal treatment can effectively improve the interlamination bonding properties between the SS strip and the epoxy resin due to the combination effect of mechanical interlocking and chemical bonding.

Broadband-Tunable Vanadium Dioxide (VO2)-Based Linear Optical Cavity Sensor.

Sensors fabricated by using a silicon-on-insulator (SOI) platform provide promising solutions to issues such as size, power consumption, wavelength-specific nature of end reflectors and difficulty to detect ternary mixture. To address these limitations, we proposed and investigated a broadband-thermally tunable vanadium dioxide (VO2)-based linear optical cavity sensor model using a finite element method. The proposed structure consists of a silicon wire waveguide on a silicon-on-insulator (SOI) platform terminated with phase-change vanadium oxide (VO2) on each side to provide light confinement. A smooth transmission modulation range of 0.8 (VO2 in the insulator state) and 0.03 (VO2 in the conductive phase state) in the 125 to 230 THz spectral region was obtained due to the of Fabry-Pérot (FP) effect. For the 3.84 μm cavity length, the presented sensor resulted in a sensitivity of 20.2 THz/RIU or 179.56 nm/RIU, which is approximately two orders of magnitude higher than its counterparts in the literature. The sensitivity of the 2D model showed direct relation with the length of the optical cavity. Moreover, the change in the resonating mode line width Δν of approximately 6.94 THz/RIU or 59.96 nm/RIU was also observed when the sensor was subjected to the change of the imaginary part k of complex refractive index (RI). This property of the sensor equips it for the sensing of aternary mixture without using any chemical surface modification. The proposed sensor haspotential applications in the areas of chemical industries, environmental monitoring and biomedical sensing.

Nanocomposites Based on Thermoplastic Acrylic Resin with the Addition of Chemically Modified Multi-Walled Carbon Nanotubes.

The main goal of this work was an improvement in the mechanical and electrical properties of acrylic resin-based nanocomposites filled with chemically modified carbon nanotubes. For this purpose, the surface functionalization of multi-walled carbon nanotubes (MWCNTs) was carried out by means of aryl groups grafting via the diazotization reaction with selected aniline derivatives, and then nanocomposites based on ELIUM® resin were fabricated. FT-IR analysis confirmed the effectiveness of the carried-out chemical surface modification of MWCNTs as new bands on FT-IR spectra appeared in the measurements. TEM observations showed that carbon nanotube fragmentation did not occur during the modifications. According to the results from Raman spectroscopy, the least defective carbon nanotube structure was obtained for aniline modification. Transmission light microscopy analysis showed that the neat MWCNTs agglomerate strongly, while the proposed modifications improved their dispersion significantly. Viscosity tests confirmed, that as the nanofiller concentration increases, the viscosity of the mixture increases. The mixture with the highest dispersion of nanoparticles exhibited the most viscous behaviour. Finally, an enhancement in impact resistance and electrical conductivity was obtained for nanocomposites containing modified MWCNTs.

Well-established carbon nanomaterials: modification, characterization and dispersion in different solvents

Three different types of carbon nanomaterials, SWCNTs, MWCNTs and GNPs were prepared, modified, characterized, and their dispersibility behavior in three different solvents was evaluated. The carbon nanotubes were synthesized by using the well-known chemical vapor deposition method and the graphene nanoplatelets by wet physicochemical treatment techniques. Their characterization was accomplished by using various advanced techniques, such as powder X-ray diffraction and Raman spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and N2 adsorption at 77 K. Furthermore, the carbon nanostructures were modified via plasma treatment and wet chemical surface modification in order to enhance their dispersion characteristics, for achieving more homogenous suspensions and therefore to be remained dispersed over a reasonable period of time without any sedimentation. The effect of treatment parameters and the use of different solvents were thoroughly studied mainly by optical methods, but also by using the DIN/EN classified ISO method of oil absorption and UV–Vis spectroscopy. The enhanced dispersion rate is observed in both CNTs and GNPs materials following their surface treatment, especially when using the solvent n-methyl-2-pyrrolidone. The aforementioned studied nanomaterials are perfect candidate fillers for preparing polymeric mixed matrix membranes.Graphical abstract

Defect passivation in methylammonium/bromine free inverted perovskite solar cells using charge-modulated molecular bonding

Molecular passivation is a prominent approach for improving the performance and operation stability of halide perovskite solar cells (HPSCs). Herein, we reveal discernible effects of diammonium molecules with either an aryl or alkyl core onto Methylammonium-free perovskites. Piperazine dihydriodide (PZDI), characterized by an alkyl core-electron cloud-rich-NH terminal, proves effective in mitigating surface and bulk defects and modifying surface chemistry or interfacial energy band, ultimately leading to improved carrier extraction. Benefiting from superior PZDI passivation, the device achieves an impressive efficiency of 23.17% (area ~1 cm2) (low open circuit voltage deficit ~0.327 V) along with superior operational stability. We achieve a certified efficiency of ~21.47% (area ~1.024 cm2) for inverted HPSC. PZDI strengthens adhesion to the perovskite via -NH2I and Mulliken charge distribution. Device analysis corroborates that stronger bonding interaction attenuates the defect densities and suppresses ion migration. This work underscores the crucial role of bifunctional molecules with stronger surface adsorption in defect mitigation, setting the stage for the design of charge-regulated molecular passivation to enhance the performance and stability of HPSC.