Nanostructured Surfaces Research Articles

Transparent, Antibiofouling Window Obtained with Surface Nanostructuring.

Biofouling is one of the key factors which limits the long-term performance of seawater sensors. Common measures to hinder biofouling include toxic paints, mechanical cleaning and UV radiation. All of these measures have various limitations. A very attractive solution would be to prevent biofilm formation by changing the surface structure of the sensor. This idea has been implemented successfully in various settings, but little work has been done on structuring optically transparent materials, which are often needed in sensor applications. In order to achieve good antibiofouling properties and efficient optical transparency, the structuring must be on the nanoscale. Here, we investigate a transparent, antibiofouling surface obtained by patterning a semihexagonal nanohole structure on borosilicate glass. The nanoholes are approximately 50 nm in diameter and 200 nm deep, and the interparticle distance is 135 nm, allowing the structure to be optically transparent. The antibiofouling properties of the surface were tested by exposing the substrates to the microalgae Phaeodactylum tricornutum for four different time intervals. This species was chosen because it is common in the Norwegian coastal waters. The tests were compared with unstructured borosilicate glass substrates. The experiments show that the nanostructured surface exhibits excellent antibiofouling properties. We attribute this effect to the relative size between the structure and the biofouling microorganism. Specifically, the small dimensions of the nanoholes, compared to the biofouling microorganism, make it more difficult for the microalgae to attach. However, lubrication of the substrates with FC-70 perfluorocarbon resulted in contamination at a rate comparable to the reference substrate, possibly due to the chemical attractiveness of the alkane chains in FC-70 for the microalgae.

Rolling contact fatigue property of gradient rare earth addition M50 bearing steel with surface nano-grains and its inhibited martensite decay

A gradient nanostructured surface layer of ∼600 μm in thickness was prepared on M50 steel with rare earth additions by a surface mechanical rolling treatment. The initial microstructure was refined into nanosized grains (∼29 nm in diameter) in the top surface layer, causing a significant increase of surface hardness. Meanwhile, the grain size increases, and the microhardness decreases gradually to the matrix values with increasing depth. Rolling contact fatigue tests showed that the fatigue lives are significantly increased by the gradient nanostructured surface layer. Analysis of failure mechanism revealed that both softening in the near surface layer and hardening in the subsurface occur under rolling contact testing. And surface spalling is the predominant failure mode, of which the cracks initiate from primary carbides in the top surface layer owing to surface softening. In gradient nanostructured samples, the nano-grains inhibit carbon migration by impeding dislocation movement in the near surface layer, so that martensite decay is suppressed. Consequently, the crack initiation is inhibited, and the fatigue property is enhanced.

Design of an FPGA-Based Controller for Fast Scanning Probe Microscopy.

Atomic-scale imaging using scanning probe microscopy is a pivotal method for investigating the morphology and physico-chemical properties of nanostructured surfaces. Time resolution represents a significant limitation of this technique, as typical image acquisition times are on the order of several seconds or even a few minutes, while dynamic processes-such as surface restructuring or particle sintering, to be observed upon external stimuli such as changes in gas atmosphere or electrochemical potential-often occur within timescales shorter than a second. In this article, we present a fully redesigned field programmable gate array (FPGA)-based instrument that can be integrated into most commercially available standard scanning probe microscopes. This instrument not only significantly accelerates the acquisition of atomic-scale images by orders of magnitude but also enables the tracking of moving features such as adatoms, vacancies, or clusters across the surface ("atom tracking") due to the parallel execution of sophisticated control and acquisition algorithms and the fast exchange of data with an external processor. Each of these measurement modes requires a complex series of operations within the FPGA that are explained in detail.

Surface thermomigration of 2D voids

In a thermal gradient, surface nanostructures have been experimentally observed to move due to thermomigration. However, analytical models that describe the thermomigration force acting on surfaces are still controversial. In this work, we start from a thermodynamic approach based on the Massieu function, which is used to describe thermomigration of single adatoms, to develop an expression for the velocity of thermomigrating 2D holes. The model can be simplified in two limiting cases: (i) When the hole motion is limited by adspecies diffusion, the velocity is independent from the hole size (as in our experiments). (ii) If the hole motion is limited by the attachment or detachment of species to or from steps, then the velocity is proportional to the hole width. We have studied the thermomigration of 2D monatomic deep holes on Si(100) using low energy electron microscopy. From the velocity measurements taken at different temperatures, we find, using our model, that the sum of the migration energy and the adatom creation energy is 1.95 ± 0.16 eV. This value is consistent with those found by other authors, reinforcing the validity of our thermomigration model.

Role of nanostructured surface layers in enhancing pure titanium diffusion bonding above their destabilization temperatures

The benefits of the nanostructured materials are believed to be probably absent if they are used at high temperatures. In this study, enhanced diffusion bonding of pure Ti was investigated by introducing a nanostructured surface layer through the surface mechanical attrition treatment (SMAT) technique. Complete recrystallization and remarkable grain growth have taken place in the original nanostructured surface layer due to the diffusion bonding conditions far beyond the nanostructured Ti destabilization temperatures. However, they still played a significant role in enhancing the Ti/Ti interfacial bonding. The consistency analysis of relative grain boundary energy, relaxation time, and microstrain reveals that although the original nanocrystalline has disappeared, the newly formed grain boundaries (GBs) during recrystallization probably inherit part of non-equilibrium state of the corresponding GBs in the as-SMATed surface layer, where the atomic diffusivity may increase greatly compared to the general relaxed GBs in their coarse-grained polycrystalline counterparts. The presence of these high-energy non-equilibrium GBs retains ultrafast atomic diffusion paths, leading to a diffusion bonding temperature of at least 100 °C lower than the traditional approach. The joint achieved at a low temperature of 750 °C exhibited a shear strength approximately 2 times higher than that prepared using raw substrates.

Pollen-based natural nanostructures to realize nanoplasmonic biochips for single-molecule detection

In this work, a paradigm change in the development of the plasmonic-based bio/chemical sensing approaches is presented. The proposed idea is to use natural nanostructures instead of those fabricated by electron-beam lithography (EBL) tools. This sensing approach produces several advantages, such as high performances without an optimization step and a simple, low-cost, and eco-friendly production process with respect to other methods, which are still time-consuming with low scalability. In particular, pollen's nanostructures covered by gold nanofilms are used to realize gold nanogratings (GNG), similar to those made via EBL, to excite hybrid plasmonic phenomena. Bulk and binding sensitivities are evaluated and compared to nanoplasmonic sensors, particularly those achieved via an EBL-based chip. As proof of principle, an estrogen receptor (ERα) is immobilized on the plasmonic nanostructured surfaces of both EBL-based and pollen-based chips and interrogated by the same custom 3D-printed holder through a transmission-based experimental setup, exploiting polymer optical fibers (POFs). The experimental results demonstrate that the proposed pollen-based nanoplasmonic biosensor shows performance very similar to an EBL-based nanoplasmonic biosensor, indicating the equivalence between the two nanoplasmonic biosensors. The biosensor exhibited a detection limit better than 1 aM for the estradiol, demonstrating the capabilities of the proposed sensing approach towards single-molecule detection.

Platelet interaction and performance of antibacterial bioinspired nanostructures passivated with human plasma

The ever-increasing ageing of the world population is demanding superior orthopedic devices. Issues such as implant infection, poor osseointegration, or chronic inflammation remain problematic to the lifespan and long-term efficacy of implants. Fabrication of materials with bioinspired nanostructures is one emerging antibacterial strategy to prevent implant infection, however their interactions with blood components, and whether they retain their bactericidal properties in an environment displaying a complex protein corona, remains largely unexplored. In the present study, titanium alloy, commercially pure and plasma-sprayed titania were hydrothermally etched, passivated with human native plasma to develop a protein corona, and then incubated with either Staphylococcus aureus, Pseudomonas aeruginosa or human platelets. Surface analysis was first used to characterize the topography, chemical composition or crystallinity of each material. Fluorescence staining and SEM were performed to evaluate the nanostructure bactericidal properties, as well as to study platelet attachment and morphology. Composition of platelet supernatant was studied using ELISA and flow cytometry. Overall, our study showed that the bioinspired nanostructured surfaces displayed both impressive antibacterial properties in a complex environment, and a superior blood biocompatibility profile in terms of platelet activation (particularly for titanium alloy). Additionally, the amount of pro-inflammatory cytokines released by platelets was found to be no different to that found in native plasma (background levels) and, in some cases, presented a more pro-healing profile with an increased secretion of factors such as TGF-β, PDGF-BB or BMP-2. The nanostructured surfaces performed equally, or better, than hydroxyapatite-coated titanium which is one of the current gold standards in orthopedics. Although further in vivo studies are required to validate these results, such bioinspired nanostructured surfaces certainly show promise to be safely applied to medical device surfaces used in orthopedics and other areas.

Evaluation of antibacterial activity on nanoline-array surfaces with different spacing

Extensive research has been conducted on anti-biofouling or antibacterial surfaces, with nanostructured surfaces that mimic cicada and dragonfly wings emerging as promising candidates for mechano-bactericidal applications. These biomimetic nanostructured surfaces are capable of exerting a bactericidal effect by directly damaging the membranes of bacteria attached to nanostructures. Although research on bactericidal effect using various nanostructures have been conducted, no specific studies have yet reported on the antibacterial efficiency of the surface having nanoline array, especially regarding the spacing between nanolines. This study details the fabrication of nanoline array via ultraviolet (UV) molding with polyurethane acrylate (PUA), noted for its UV sensitivity and rapid curing, enabling the fabrication of precise and scalable nanoscale structures. Investigation into the nanoline array’s antibacterial effects against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) reveals that nanoline spacing critically influences bacterial adherence and viability, with specific spacings enhancing antibacterial properties. Scanning electron microscopy (SEM) and confocal microscopy analyses show that surface topography significantly affects bacterial behavior, with specific spacings leading to varied bacterial responses, including membrane damage and altered attachment patterns. The study highlights the potential of nanoline array in fabricating surfaces with tailored antibacterial properties, emphasizing the importance of nanoscale design in influencing bacterial interaction and viability. We also confirm the relative mechanical rigidity of the nanoline array, which exhibits antibacterial effects, through both experimental observations and numerical analysis. This indicates our proposed nanoline-array surface could have potential future applications in mechanical anti-bacterial functions that require such structural robustness.

Surface Nanostructuring of Copper Using Fluoride and Chloride

AbstractCopper is an active electrocatalyst for various energy conversion reactions, but its performance depends on the structure of the active surface sites. In this work, we propose a simple strategy to tailor both the roughness and the active site's geometry of copper. To modify the surface of copper, we oxidize and reduce a copper polycrystalline electrode in 0.1 M solutions containing both sodium fluoride and sodium chloride with different chloride/fluoride molar ratios: (0.1‐x) M NaF+x M NaCl. To address the anion effect on the changes in surface geometry, we recorded the voltammetric fingerprints of the modified electrodes using lead underpotential deposition (UPD). The voltammetric analysis suggested that while chloride induces (n10) sites, fluoride promotes an increase in the active surface area and the growth of low‐coordinated sites with (110) or (111) geometry. Solutions containing both fluoride and chloride anions induced (n10) motifs covered by nanometric clusters, as observed by scanning electron microscopy, forming a highly defect‐rich surface. Our work provides a direct link between electrochemical response and ex‐situ structural characterization, and compares, in detail, the effect of chloride and fluoride on the surface nanostructuring of copper.

A combined multilevel computational and experimental approach for interfacial screening and mechanical reinforcement of basalt fiber/polyamide 66 composites

Silane coupling agents (SCAs) can improve fiber-resin interface issues, yet selecting an appropriate SCA experimentally is resource-intensive. Herein, a multi-level screening method combining simulation and experiments is proposed to identify SCA-enhancing bonding between SCAs and polyamide 66 (PA66) and the basalt fiber (BF) −PA66 interface. SCAs with organic groups composed of N and O exhibited superior interaction with PA66 due to the more pronounced negative and positive electrostatic potential (ESP) distributions. In SCAs-grafted BF-PA66 models, SCAs not only altered BF surface nanostructure but also changed the arrangement of PA66 main chains from parallel to interpenetrating BF surface atoms. Besides, (3-ureapropyl)trimethoxysilane (SCA6) significantly improved BF-PA66 bonding, which was experimentally validated by enhanced interlaminar shear and mechanical properties. O atoms on SCA6 and PA66 are more electronically bound and have the smallest ESP extremum, providing strong polar interaction sites. Additionally, both simulations and experiments demonstrated a transformation from adhesive to cohesive failure.

Design and fabrication of MnCo2O4@MnCo2S4 Core@Shell nanostructured arrays decorated over the rGO sheets for high-performance asymmetric supercapacitor

In order to create reliable and effective energy storage systems, it is crucial to choose electrode materials that exhibit high stability and energy density. In this work, MnCo2S4@MnCo2O4 core@shell nanoneedle-like nanostructures (MCS@MCO/rGO) are synthesised over a rGO sheet using an innovative and easy hydrothermal technique. Electrolyte transport and sulphur incorporation during charge-discharge reactions are both made easier by the core@shell nanostructured arrays' large active surface area. With an appropriate pore size distribution centred at 13.4 nm and a high surface area of 125.4 m2g-1, the ternary electrodes composed of MCS@MCO and rGO have a rich mesoporous structure. A specific capacitance of 1346 Fg-1 at 1 Ag-1 demonstrates the exceptional performance of the MCS@MCO/rGO ternary electrode. The MCS@MCO/rGO ternary electrodes show a remarkable cyclic stability of 88.9 % capacity retention over 10,000 cycles, according to the cycling stability studies. With an impressive power density of 1010 Wkg-1 and remarkable cycling stability (95.5 % retention of the original capacitance after 10,000 cycles), the manufactured MCS@MCO/rGO//AC ACS displays an impressive energy density of 57.5 Whkg-1. The mesoporous structure is excellent for increasing the characteristics of supercapacitor electrodes, as these astounding results can demonstrate.

How substrate surface area and surface curvature determine kinetics and titanate formation during non-hydrothermal alkali treatment of titanium microspheres

Titanium surface nanostructuring using alkali treatment gains significant attention in a wide range of fields, such as biomaterials, (photo)catalysis, (metal/ion) sorption, CO2 capture, electrochromism and sodium-ion batteries. Even though the physicochemical properties and application potentials of the surface nanostructures are fairly well understood, there is still debate about their exact formation mechanism, limiting knowledge based structural control through altered synthesis conditions. Moreover, this knowledge is largely focused on hydrothermal synthesis conditions, whereas non-hydrothermal conditions might provide benefits towards industrial application. Also the impact of substrate properties, rather than chemical reaction conditions, on the nanostructure formation is only limitedly reported in literature. This work reveals new fundamental knowledge of non-hydrothermal alkali treatment of titanium, using microspheres by implementing, for the first time, in-situ hydrogen measurement during alkali treatment in combination with the ex-situ determination of the sodium and oxygen content in the recovered alkali treated samples, providing critical information on the role of dissolution apart from the precipitation process. The effect of surface area and surface curvature on the dissolution and precipitation process, and the resulting impact on the physicochemical properties of the obtained titanate layer is studied. This shows the much larger impact on dissolution in contrast to precipitation, knowledge that is lacking in literature, but important when implementing alkali surface nanostructuring on complex (e.g. 3D printed) substrates, and considering the prospective shift from lab-scale to industry. The Ti dissolution step was found to be mainly controlled by the total surface area, while the rate determining step was found to be the titanate precipitation, not influenced by either surface area or particle size.The changes in oxygen content in the samples after transformation of titanate into TiO2 provided a novel method for its quantification. The microspheres were analysed chemically (Raman), structurally (XRD) and morphologically (SEM, MIP), screening the effect of surface area, particle size and reaction time on the growth behaviour of the titanate layer. The porous layer structurally corresponds to Na2Ti2O4(OH)2 for all evaluated conditions, with pores in the range of 10–600 nm. Increasing surface area and particle size results in local and non-uniform titanate growth, while titanate nanowire and strut formation between the microspheres were enhanced by reduced microsphere size and prolonged reaction times.

Stable Magnetite@La-Fe Oxide Core-Shell Nanostructures Prepared via Lattice Lock for Reusable Extraction of Phosphate Anions.

Stable magnetic core-shell nanostructures are developed by lattice locking lanthanide-iron (La-Fe) oxide shells with magnetite cores to prevent the release of La from the surfaces of the magnetite nanostructures. The resulting core-shell nanostructures demonstrate excellent outstanding regeneration performance and high adsorption capacity for phosphate (115 mg P·g-1). These nanostructures release minimal La from the magnetite core surfaces after adsorbent regeneration, with a La loss of only 20% compared to the control sample, Mag@La(OH)3. La3+ ions were released at concentrations ranging from 1 to 2.3 μg·L-1 at pH levels of 4 to 8, which is within the metal content range found in natural aquatic environments. These results demonstrate the high stability of the nanostructures after regeneration. Furthermore, the adsorbent exhibits high extraction capacity across a wide pH range of 4 to 10 and performs well even in the presence of interfering anions at phosphate-to-anion molar ratios of 1:5, 1:25, and 1:100. Microscopic and spectroscopic analyses reveal that the primary extraction mechanism of phosphate in the La-containing shells is surface precipitation. This approach not only improves the use of magnetic core-shell nanostructures as adsorbents but also demonstrates the creation of a broad range of stable magnetic functional materials for diverse applications.

Nanotechnology and Its Application in Dentistry: A Systematic Review of Recent Advances and Innovations.

Background: This study looks at the clinical applications of nanotechnology in dentistry, with an emphasis on implantology, preventive care, orthodontics, restorative dentistry, and endodontics. Methods: Following PRISMA criteria and registered in PROSPERO (ID: CRD 564245), a PubMed, Scopus, and Web of Science search was conducted for studies from January 2014 to April 2024. The criteria were English-language research on nanotechnology in dental coatings, with a focus on clinical trials and observational studies. The electronic database search yielded 8881 publications. Following the screening process, 17 records were selected for qualitative analysis. Results: Nanotechnology has revolutionized dentistry. In orthodontics, nanoparticles improve antibacterial characteristics, durability, and biocompatibility, lowering bacterial colonization and plaque. In preventative care, Casein Phosphopeptide-Amorphous Calcium Phosphate (CPP-ACP) combined with stannous fluoride (SnF2) and nano-sized sodium trimetaphosphate (TMPnano) substantially remineralizes enamel. Nanostructured surfaces in dental implants, particularly those containing calcium, improve osseointegration and stability. Nanoparticles in restorative dentistry improve composite and adhesive strength, aesthetics, and longevity. Conclusions: Nanotechnology improves dental materials and equipment, resulting in better treatment outcomes and increased patient comfort. Its integration provides more effective treatments, which improves dental care and patient outcomes. More research is needed to overcome present problems and expand nanotechnology's medicinal applications.

Interfacial dynamics mediate surface binding events on supramolecular nanostructures

The dynamic behavior of biological materials is central to their functionality, suggesting that interfacial dynamics could also mediate the activity of chemical events at the surfaces of synthetic materials. Here, we investigate the influence of surface flexibility and hydration on heavy metal remediation by nanostructures self-assembled from small molecules that are decorated with surface-bound chelators in water. We find that incorporating short oligo(ethylene glycol) spacers between the surface and interior domain of self-assembled nanostructures can drastically increase the conformational mobility of surface-bound lead-chelating moieties and promote interaction with surrounding water. In turn, we find the binding affinities of chelators tethered to the most flexible surfaces are more than ten times greater than the least flexible surfaces. Accordingly, nanostructures composed of amphiphiles that give rise to the most dynamic surfaces are capable of remediating thousands of liters of 50 ppb Pb2+-contaminated water with single grams of material. These findings establish interfacial dynamics as a critical design parameter for functional self-assembled nanostructures.

Bioinspired Nanostructures by Soft‐Template Electropolymerization from Di‐Substituted Triphenylamine

AbstractWe report a bioinspired approach to tune surface nanostructures by soft‐template electropolymerization in micellar conditions. Monomers highly favoring π‐stacking interactions are particularly interesting for favoring the polymer deposition in one direction. Here, original triphenylamine‐based monomers di‐substituted by thiophene and carbazole are investigated. Conjugated building blocks monomers are tested to favor deposition vs polymerization, even if the monomers are not perfectly planar. The carbazole derivatives have a much higher electrodeposition capacity than the thiophene derivatives, which is unexpected if thiophene and carbazole are taken alone. Moreover, in all electrodeposited films, monomer seems to be present as shown by cyclic voltammetry experiments, confirming previous works. The amount of monomer vs oligomers is highly dependent on the investigated monomer. For the resulting surface structures, hollow spheres and nanoribbons are particularly formed with some investigated monomers by cyclic voltammetry while nanotubes are observed at constant potential. The formation of nanotubes indicates a polymer growth more favored in one direction. These surfaces are less hydrophobic (water contact angle up to 111.5°) compared to films with spherical nanoparticles but these results can be explained only by the presence of air inside the surface roughness.

Thermoplasmonic Effect Enables Indirect ON-OFF Control over the Z-E Isomerization of Azobenzene-Based Photoswitch.

Proper formulation of systems containing plasmonic and photochromic units, such as gold nanoparticles and azobenzene derivatives, yields materials and interfaces with synergic functionalities. Moreover, gold nanoparticles are known to accelerate the Z-E isomerization of azobenzene molecules in the dark. However, very little is known about the light-driven, plasmon-assisted Z-E isomerization of azobenzene compounds. Additionally, most of the azobenzene-gold hybrids are prepared with nanoparticles of small, isotropic shapes and azobenzene ligands covalently linked to the surface of nanostructures. Herein, a formulation of an innovative system combining azobenzene derivative, gold nanorods, and cellulose nanofibers is proposed. The system's structural integrity relies on electrostatic interactions among components instead of covalent linkage. Cellulose, a robust scaffold, maintains the material's functionality in water and enables monitoring of the material's plasmonic-photochromic properties upon irradiation and at elevated temperatures without gold nanorods aggregation. Experimental evidence supported by statistical analysis suggests that the optical properties of plasmonic nanometal enable indirect control over the Z-E isomerization of the photochromic component with near-infrared irradiation by triggering the thermoplasmonic effect. The proposed hybrid material's dual plasmonic-photochromic functionality, versatility, and ease of processing render a convenient starting point for further advanced azobenzene-related research and 3D printing of macroscopic light-responsive structures.

Functionalization of nanostructured surfaces: From the impact on morphological control during synthesis to the effect on colloidal dispersion

Functionalization of nanostructured surfaces: From the impact on morphological control during synthesis to the effect on colloidal dispersion

Impact of helium nanobubbles on tungsten fuzz nanostructure conductivity

Explosive electron emission splashes occurring in plasma interactions with nanostructured surfaces can be induced by Joule energy release under reduced conductivity. Distribution of helium nanobubbles inside tungsten at an elevated energy of implanted helium ions has been studied via numerical molecular dynamic modeling, and its impact on the nanostructure conductivity has been estimated. Average concentration and size of nanobubbles were calculated to be about n = 1020 cm−3 and r = 3 Å, respectively, at the helium fluence of about 2 × 1015 cm−2. The distribution of nanobubbles becomes more flat and extends deeper into the bulk material with increasing impact energy. At energies below about 300 eV, most nanobubbles form within a depth of 10 nm, corresponding to the characteristic size of the nanowires. At higher energies, a significant portion of the nanobubbles forms deeper in the material. An approach for estimating the electron scattering frequency in tungsten by helium nanobubbles has been proposed, taking into account the volume porosity of the W-fuzz nanostructure and scaling the helium content to the experimentally measured one. The resulting value for the tungsten fuzz nanostructure was 2.27 × 1016 s−1 and the resistivity was 1.92 mΩ cm that is 364 times larger than the normal tungsten resistivity, the conductivity of 521 S/cm was 0.275% from the normal tungsten one. The corresponding estimation of thermal conductivity via Wiedemann–Franz law gave 3.8 mW cm−1 K−1, which agrees well with recent measurements.

Plasmon-Promoted Interatomic Hot Carriers Regulation Enhanced Electrocatalytic Nitrogen Reduction Reaction.

Utilizing hot carriers for efficient plasmon-mediated chemical reactions (PMCRs) to convert solar energy into secondary energy is one of the most feasible solutions to the global environmental and energy crisis. Finding a plasmonic heterogeneous nanostructure with a more efficient and reasonable hot carrier transport path without affecting the intrinsic plasmonic properties is still a major challenge that urgently needs to be solved in this field. Herein, the mechanism by which plasmon-promoted interatomic hot electron redistribution on the surface of Au3Cu alloy nanoparticles promotes the electrocatalytic nitrogen reduction reaction (ENRR) is successfully clarified. The localized surface plasmon resonance (LSPR) effect can boost the transfer of plasmon hot electrons from Au atoms to Cu atoms, trigger the interatomic electron regulation of Au3Cu alloy nanoparticles, enhance the desorption of ammonia molecules, and increase the ammonia yield by approximately 93.9 %. This work provides an important reference for rationally designing and utilizing the LSPR effect to efficiently regulate the distribution and mechanism of plasmon hot carriers on the surface of heterogeneous alloy nanostructures.