Atomic Electron Research Articles

Enhanced Electrochemical Detection of Nonelectroactive Compounds Based on Surface Supramolecular Interactions on Chevron-like Graphene Nanoribbons Modified through Click Chemistry.

In this study, we have developed a nanostructured electrochemical sensor based on modified graphene nanoribbons tailored for the analysis of nonelectroactive compounds via a surface competitive assay. Stigmasterol, a nonelectroactive phytosterol, was selected as a representative case. Chevron-like graphene nanoribbons, chemically synthesized, were immobilized onto glassy carbon electrodes and covalently functionalized to allow the on-surface formation of a supramolecular complex. To this end, the nanoribbons were first modified through a diazotization process by electrochemical reduction of a 4-azidoaniline diazonium salt, leaving the electrode surface with azide groups exposed to solution. Next, the incorporation of a ferrocene group, as a redox probe, was carried out by a click chemistry reaction between ethynylferrocene and these azide groups. Finally, the recognition event leads to the formation of a supramolecular complex between ferrocene and a macrocyclic receptor on the electrode surface. To this end, the receptors cucurbit[7]uril, cucurbit[8]uril, and β-cyclodextrin were evaluated, with the better results obtained with β-cyclodextrin. Atomic force microscopy and scanning electron microscopy measurements were performed for the morphological characterization of the resulting electrochemical platform surface. The ability of β-cyclodextrin to form an inclusion complex with ferrocene or with stigmasterol allows to perform a competitive assay, which translates into the decrease and recovery of the ferrocene electrochemical signal. For stigmasterol determination, a linear concentration range between 200 and 750 μM and a detection limit of 60 μM were obtained, with relative errors and relative standard deviations less than 7.1 and 9.8%, respectively.

Application of sculptured Mn conical (Spiral+helical) thin films for monitoring N2-CO and N2-CO2 gas mixtures: Gas ionization and field emission sensors

This study deals with the design and fabrication of Mn sculptured conical (spiral + helical) thin films as electrodes for the detection of gas mixtures of different percentages (N2-CO and N2-CO2) in a gas ionization and field emission face to face sensor. The electrodes were produced using oblique angle deposition (OAD) technique. X-ray diffraction (XRD), atomic force microscopy (AFM) and field emission electron microscopy (FESEM) as well as energy dispersive x-ray spectroscopy (EDS) confirmed crystallography, morphology and elemental composition of materials of the designed samples. The sharp tip of the nano-helices were aimed to act as an electric field enhancer by applying voltage. The results indicated that Paschen's law is not applicable for inter-electrodes gaps less than 15 μm at pressures higher than 250 mbar where the field emission process becomes the dominant reaction. Enhanced selectivity and sensitivity were obtained for CO, CO2 and their mixtures with N2 gas at lower concentrations and shorter inter-electrodes gaps (<100 μm). The ionization energies of different ionization channel reactions of N2, CO and particularly CO2 in the gas mixtures were used to explain the behavior of Paschen's curves in different pressure ranges. Highest sensitivity of the sensor was obtained for inter-electrodes gaps of less than 100 μm. Comparison of the results with the published literature showed better performance of the present sensors relative to previously reported works.

Dual-energy CT Radiomics Combined with Quantitative Parameters for Differentiating Lung Adenocarcinoma From Squamous Cell Carcinoma: A Dual-center Study

Rationale and ObjectivesTo evaluate the ability of dual-energy CT(DECT)-based quantitative parameters and radiomics features to differentiate solid lung adenocarcinoma (ADC) from squamous cell carcinoma (SCC). MethodsThis study included 213 patients diagnosed with ADC and SCC who underwent DECT scans at two centers from November 2022 to December 2023. Patients at center 1 were randomly divided into training(n=114) and internal test set (n=50) in a 7:3 ratio, with center 2 serving as the external test set (n=49). Radiologic and clinical data were combined to establish a clinical-radiologic model. Ten types of DECT energy images including conventional images, iodine density (ID), effective atomic number (Zeff), electron density, and virtual monoenergetic images (VMI) were reconstructed in both arterial phases (AP) and venous phases (VP). Quantitative parameters were measured at the uniform enhanced solid portion of the tumor and normalized to the aorta, used to develop a quantification model and calculate the quantitative score (quantscore). Radiologists manually delineated the tumor ROI at the largest level for extracting radiomics features in these 10 energy images. These features were used to establish ten uni-energy models from which the best-performing features were selected to construct the final radiomics model and calculate a radiomics score (radscore). Then, a combined model was developed using the akaike information criterion(AIC) and compared with the clinical-radiological model to test its diagnostic validity. ResultsThe independent predictors of the clinical-radiological model included age, gender, and central or peripheral location, and the AUCs for the training set, internal test set, and external test set were 0.808, 0.837, and 0.802. The quantification model incorporated 40keV CT values, Zeff, normalized Zeff, and the slope of the spectral attenuation curve (λHU) in the AP and normalized ID, Zeff, and λHU in the VP. Uni-energy models based on AP ID maps, AP Zeff maps, and VP VMI 65keV significantly outperformed AUC = 0.5, and 11 radiomics features were selected from these three models to construct the final radiomics model. The combined model, incorporating age, gender, quantscore, and radscore, significantly outperformed the clinical-radiological model in the training set (AUC = 0.952 vs 0.808, P < 0.001), and demonstrated higher performance in both the internal and external test sets, although these differences did not reach statistical significance (AUC = 0.870 vs 0.837, for the internal test set [P = 0.542], 0.888 vs 0.802 for the external test sets [P = 0.128]). The evaluation of the combined model demonstrated good discriminative ability and potential for generalization. ConclusionsThe combined model, integrating quantitative parameters and radiomics features from DECT multi-energy images with clinical-radiological characteristics, can be used as a non-invasive tool to differentiate ADC from SCC.

Caesalpinia crista seed is used as an eco-friendly inhibitor to prevent the corrosion of aluminium in hydrochloric acid solutions

This investigation delves into the inhibitory impact of Caesalpinia crista (Kanchaki) seed extract (CCE) on the corrosion of aluminium alloy (AA6061) at temperatures varying between 303 and 333K, employing Potentiodynamic Polarisation (PDP), Electrochemical Impedance Spectroscopy (EIS), and weight loss methodologies. Findings demonstrate that CCE extract effectively safeguards Al against corrosion, with efficacy increasing at higher concentrations. The observed inhibitory action exhibits a cathodic-type behavior across all concentrations and temperatures, aligning well with Langmuir isotherm. Notably, the highest level of inhibitory efficiency, reaching 96.87 ​%, is attained at a concentration of 2.0 ​g/L and a temperature of 303 ​K for 3 hours. Consistency is observed between the results obtained through EIS and PDP. A plausible mechanism for preventing corrosion in Al alloy is proposed. Surface analysis techniques, such as Atomic Force Microscopy (AFM) and Scanning Electron Microscopy/Energy Dispersive X-ray analysis (SEM/EDX), validate the adsorption of the inhibitor onto Al alloy surfaces. Morphological examinations corroborate electrochemical findings, confirming protection against uniform corrosion in HCl solutions. Additional analyses involve the computation of activation energy and thermodynamic parameters, with a thorough discussion of the results.

Role of the magnetic layer interface, roughness, and thickness in the temperature-dependent magnetic properties of Al2O3/Co/CoO thin films deposited by magnetron sputtering

Using the methods of atomic force and electron microscopy and the magneto-optical Kerr effect, the role of the interface, roughness, and thickness of the magnetic layer in the temperature-dependent magnetic properties of thin Al2O3–Co films with a naturally oxidized cobalt surface was studied. The layers were deposited by magnetron sputtering. The thickness of the cobalt layer varied from 2 to 100 nm. For the first time, the dependences of coercive forces and exchange displacements on the thickness of the cobalt film in the temperature range from 80 to 300 K were obtained and analyzed. The contribution to the coercive force and exchange displacement from the oxidized cobalt surface increases as the temperature decreases below 160 K. The magnitude of the contribution depends on the base material on which the cobalt film is deposited and is maximum for a cobalt film with a thickness of ∼20 nm in the Al2O3/Co structure. A weakly magnetic layer was found at the Al2O3/Co interface. The behavior of the exchange bias in this layer is similar to the behavior of a ferromagnetic Co core with a naturally oxidized CoO shell. The thickness of this layer depends on the speed and order of deposition of the layers. When the order of deposition of layers (Co/Al2O3) changes, the behavior of the exchange displacement of the interface becomes similar to that observed in the ferromagnet/antiferromagnet system. That is, when the deposition order changes, the value of the exchange shift changes sign when the cobalt layer thickness is below 10 nm.

Treatment of pulp and paper mill effluent through combined aerobic and anaerobic suspended fixed-bed bioreactor.

This study explored using ultrafiltration (UF) membranes to treat pulp and paper mill wastewater, implementing a novel Taguchi experimental design to optimize operating conditions for pollutant removal and minimal membrane fouling. Researchers examined four factors: pH, temperature, transmembrane pressure, and volume reduction factor (VRF), each at three levels. Optimal conditions (pH10, 25°C, 6bar, VRF 3) led to a 35% reduction in flux due to fouling and high pollutant rejections: total hardness (83%), sulfate (97%), spectral absorption coefficient (SAC254) (95%), and chemical oxygen demand (COD) (89%). Conductivity had a lower rejection rate of 50%. Advanced imaging techniques like atomic force microscopy (AFM) and scanning electron microscopy (SEM) revealed reduced membrane fouling under these conditions. The Taguchi method effectively identified optimal conditions, significantly improving wastewater treatment efficiency and promoting environmental sustainability in the pulp and paper industry. PRACTITIONER POINTS: This study optimized UF membrane conditions for pulp and paper mill wastewater, reducing fouling and enhancing pollutant removal, offering practical strategies for industrial treatment. AFM and SEM provided key insights into membrane fouling and mitigation, promoting real-time diagnosis and optimization for enhanced treatment efficiency. Prioritizing anaerobic fixed-bed systems in wastewater treatment is beneficial for achieving high COD removal efficiency. Optimizing hydraulic retention time (HRT) in these systems can further improve their overall effectiveness and sustainability.

Evaluation of AGeX3 structured perovskite solar cells based on density functional theory

Abstract Density functional theory (DFT), as a theory to explore the electron microscopic structure of materials, guides and promotes the rapid development of the perovskite field. In the context of the global energy revolution, “green”, “safe”, and “sustainable” have become the keywords in the field of perovskite research. Because of its abundant reserves on the earth, less harm to the environment and human health, strong stability, and other advantages, germanium has been widely concerned in the field of perovskite solar cells (PSCs). In this study, the differential charge densities, the total densities of states (TDOS), the partial densities of states (PDOS), and the thermodynamic properties of four AGeX3 germanium-based perovskite materials are calculated by using Materials Studio (MS). It is found that Ge atomic orbital electrons play a crucial role in the absorption of photon energy and the generation of photocurrent. The PSCs of the AGeX3 structure will perform better. This study contributes to the realization of efficient germanium-based PSCs in experiments, provides a broad prospect for researchers in this field, and plays a vital role in the future research of germanium-based perovskite.

Elucidating the effect of cyclic plasticity on strengthening mechanisms and fatigue property of 5xxx Al alloys

The strength of non-heat-treatable 5xxx Al alloys is derived from solid solution strengthening and strain hardening, the absence of a precipitation strengthening response results in their lower strength. In this study, significant improvements in strength can be achieved by subjecting three different Mg concentrations 5xxx Al alloys to cyclic plasticity. A quantitative analysis of the respective contributions to the yield strength has been conducted by combining transmission electron microscopy and atom probe tomography. Additionally, the fatigue performance and fatigue mechanism of the cyclic strengthened 5xxx Al alloys have been thoroughly studied due to its transformation from non-heat-treatable to precipitation strengthening. We demonstrate that the high-cycle fatigue (HCF) strength of the cyclically strengthened state only experiences a minor improvement compared to the as-received state, which is significantly disproportionate to the enhancement in tensile strength. This disparity is primarily attributed to the changes in microstructure and fatigue mechanisms, resulting in a reduction in fatigue ratio. This study provides important insights for expanding research on cyclic plasticity methods in fatigue performance, and can aid in the development of improved processes for optimal fatigue resistance.

Cleaning of laser-induced periodic surface structures on copper by gentle wet chemical processing

Laser-induced periodic surface structures (LIPSS) attract considerable attention due to the manifold applications enabled by these self-organised structures ranging from optical colouring to bio-mimicking or wetting effects. The mechanism of LIPSS-formation at metal surfaces includes laser-ablation processes that results in phase transitions, explosive material removal and partial redeposition of the ablation products in the form of nanoscopic debris or even sub-micrometre-sized spherical particles in case of melt ejection. For some applications, these particulates, debris, and microscopic features on top of the periodic surface structures are disadvantageous. We studied wet-chemical cleaning approaches to remove redeposited material from LIPSS to enhance their applicability. LIPSS on copper with a lateral periodicity of ∼ 365 nm, that were fabricated by ultrashort pulse laser exposure(λ: 515 nm, tp: 260 fs), were cleaned with different liquids ranging from solvents to microemulsions. The surface morphologies were characterised by scanning electron microscopy (SEM), atomic force microscopy (AFM) and transmission electron microscopy(TEM) to study the surface topography, the size and density of surface particulates as well as other surface contaminations before and after wet cleaning. The LIPSS surface composition was analysed by X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and Energy-dispersive x-ray spectroscopy (EDX) at the FIB-cross sections. The different cleaning approaches are classified with respect to their capability to remove particles and contaminations as well as to their influence on the morphology and shape of LIPSS pattern, whereby substantial differences are found. At least two wet-chemical solutions enable the removal of nanoparticles with only minor modification of the LIPSS topography. The main effect of wet cleaning is the detachment of particulates including sub-micrometre-sized spheres due to a gentle and selective etching of the interface region between the LIPSS and the redeposited material that comprise of modified copper and copper oxides.

On novel Ni-rich phase formed during aging of an additively manufactured ultra-high strength CoFeNi alloy

The precipitation mechanism of strengthening phase of a body-centered-cubic (BCC) structured CoFeNi multi-principal element alloy produced by additive manufacturing was studied by transmission electron microscopy (TEM) and atom probe tomography (APT). The hardness of CoFeNi alloy achieved the peak value of 554.79 ± 9.86 HV after aging for 160 h at 400 °C. The CoFeNi alloy exhibited an ultrahigh compressive yield strength and ultimate compressive strength up to 1.8 GPa and 2.3 GPa respectively, whilst maintains a strain of 18.9 %. The microstructure of the alloy exhibited nanoscale lamellar Ni-rich phase with high stability homogeneously distributed in BCC matrix after aging at 400 °C. The novel Ni-rich phase containing about 50 at. % Ni with a hexagonal structure is the mainly precipitation strengthening phase, and has coherent orientation relationship with the BCC matrix in the<101>bcc∥<112¯0>Niand 111bcc∥{0001}Ni. Based on the experimental results, the precipitation mechanisms of the Ni-rich phase were discussed in detail. The current work provides a possible new direction to design high-strength alloy by introducing the novel Ni-rich phase.

A semiempirical model for low energy electron–atom transport cross sections: The case of noble gases

A semiempirical approach to describe low energy electron–atom transport cross sections of easy implementation and reproduction is presented. The heart of the model is an energy independent two-parameter potential that was adjusted to reproduce the accurate total cross sections for He, Ne, Ar and Kr, measured with a threshold photoelectron source technique from meV up to 20 eV. Once the potential was conceived, the model was validated by comparing the values obtained for the calculated scattering lengths and phase shifts with the respective quantities previously reported in the literature. We close the article by presenting the momentum transfer and viscosity cross sections. Good agreement is found when compared to the similar data obtained from swarm experiments, from phase shifts according to differential cross section measurements and to the cross sections reported by sophisticated ab initio relativistic many-body calculations. Tables for the phase shifts and cross sections are provided for direct use and applications.

One-pot radiolytically synthesized reduced graphene oxide-gold nanoparticles composites and exploration in energy storage

Graphene and its composites are of primary importance, particularly in the field of energy storage. Numerous bottom-up and top-down methods have been proposed in the literature to produce these materials with enhanced physicochemical properties. Recently, an innovative and green methodology was developed based on ionizing radiation, allowing the quantitative synthesis of graphene oxide-based materials. With the aim to extend this strategy for the preparation of hybrid nanomaterials, the objective of this work was the one-pot synthesis of nanocomposites composed of reduced graphene oxide – gold nanoparticles (rGO-AuNPs) via gamma ray-induced radiolytic reduction. UV–Vis Absorption Spectroscopy, Fourier Transform Infrared Spectroscopy, Raman Spectroscopy and X-ray Photoemission Spectroscopy were utilized to comprehensively evaluate the reduction degree of graphene oxide and the formation of gold nanoparticles. Atomic Force Microscopy and Scanning Electron Microscopy were employed to obtain the morphological and topographical information on synthesized nanocomposites. Thermal properties were investigated by Thermogravimetric Analysis and electrical properties were investigated using Cyclic Voltammetry and Potentiostatic Charge and Discharge method. The results demonstrated the successful reduction of graphene oxide and gold ions through the drastic transformation of oxygen-containing functional groups and the formation of gold nanoparticles. Electrical characterization results highlighted the excellent electrical properties of radiosynthesized rGO-AuNPs composites and their great potential for supercapacitance application.

Hydroxyl group modification improves the selectivity of metal single atom on poly(heptazine imide) for electrocatalytic acetylene semi-hydrogenation

Electrocatalytic semi-hydrogenation of acetylene to ethylene has recently attracted attention as a process for removing acetylene from ethylene-rich gas streams due to its mild conditions and energy-saving advantages. However, developing catalysts with low cost and high selectivity for acetylene semi-hydrogenation remains a huge challenge. Here, we investigated the effect of hydroxyl group modification on the acetylene semi-hydrogenation selectivity of poly(heptazine imide) (PHI) supported metal single atom catalyst under alkaline conditions by density functional theory calculations. The results show that hydroxyl group as ligand not only increases the steric resistance of acetylene adsorption, but also acts as electron-withdrawing group to delocalize the electrons of metal atoms, weaken the interaction with acetylene and subsequent intermediates, and make the adsorption moderate, which is beneficial to the desorption of ethylene and avoid over-hydrogenation. The Ni-OH/PHI and Fe-2OH/PHI are capable of achieving the selective hydrogenation of acetylene to ethylene and have good thermodynamic stability, which can be used as ideal catalysts for the electrocatalytic semi-hydrogenation of acetylene to selectively generate ethylene. This study provides theoretical guidance for the rational design of electrocatalysts for the selective semi-hydrogenation of acetylene.

Novel Superhard Boron Nitrides, B2N3 and B3N3: Crystal Chemistry and First-Principles Studies.

Tetragonal and hexagonal hybrid sp3/sp2 carbon allotropes C5 were proposed based on crystal chemistry and subsequently used as template structures to identify new binary phases of the B-N system, specifically tetragonal and hexagonal boron nitrides, B2N3 and B3N3. The ground structures and energy-dependent quantities of the new phases were computed within the framework of quantum density functional theory (DFT). All four new boron nitrides were found to be cohesive and mechanically (elastic constants) stable. Vickers hardness (HV), evaluated by various models, qualified all new phases as superhard (HV > 40 GPa). Dynamically, all new boron nitrides were found to be stable from positive phonon frequencies. The electronic band structures revealed mainly conductive behavior due to the presence of π electrons of sp2-like hybrid atoms.

Effect of Calcination Temperature on Green Powder From Ensis sp. Shell Waste

Ensis sp. is a primary source of protein from the Nyumbun Tradition in Jambi Province, and it is becoming solid waste after tradition. This study explored the effect of calcination temperature on green powder derived from Ensis sp. shell waste. Before characterization, the powder was treated at room temperature, 800 °C, and 900 °C. After that, the powder material was studied using Atomic Absorption Spectroscopy (AAS) and Scanning Electron Microscope (SEM) instruments. The material was shifted using a 200 mesh sieve. Temperature of 800 and 900 °C showed similar Ca content of 443 and 447,6 mg/g, respectively. The morphology of the two samples was different due to the other temperature conditions used. Higher temperatures induce decomposition, leading to a decrease in particle size. The product of this process could be used as a promising heterogeneous catalyst, so it reduced the existence of shell waste.

Cinnamaldehyde- and nonanal-incorporated polyvinyl alcohol/colloidal silicon dioxide films with synergistic antifungal activities

Biodegradable materials may help solve the problem of environmental pollution caused by conventional synthetic food packaging. Here, various amounts of colloidal silicon dioxide [CSD, 5, 10, and 15 wt% based on polyvinyl alcohol (PVA)] and 1 % SCAN, a 1:1 (v:v) combination of cinnamaldehyde and nonanal, were added to fabricate PVA-based films. Microstructure analyses using atomic force and scanning electron microscopes revealed that the films had uniform CSD dispersion, and the surface roughness rose along with the CSD concentration. The addition of SCAN prevented UV light transmission. In addition, the introduction of CSD enhanced the water-resistance abilities and tensile strengths of the composite films. The PVA/SCAN films exerted remarkable antifungal activities against Aspergillus flavus owing to a synergistic effect between cinnamaldehyde and nonanal. Furthermore, the PVA/SCAN/CSD film, contrasted with the PVA film containing SCAN alone, attenuated the SCAN loss during storage and also continually released SCAN from the film. In peanut preservation, the PVA/SCAN/CSD composite film was superior to the single-element films in antifungal activity, showing decreases of 76.66 % and 85.33 % in the production of conidia and aflatoxin B1, respectively. In conclusion, the PVA/SCAN/CSD composite film with high UV barrier, water-resistance ability, excellent mechanical properties and antifungal activity possesses a promising application potential in food packaging.

Revealing the regularities of electron correlation energies associated with valence electrons in atoms in the first three rows of the periodic table

Although correlation energy in an atom can be decomposed into different components such as inter- and intra-orbital pair-correlation energies (PCE), it is generally believed that the PCEs in different atoms cannot be the same. In this work, we find that when the correlation energy is defined as the difference between the exact ground-state energy and the unrestricted Hartree–Fock energy, the PCEs associated with the valence electrons of the atoms in the same row of the periodic table have the same values. For two specific orbitals, the inter-orbital correlation energy is the same between two electrons of parallel or anti-parallel spins.

Analysis of Defect Structures during the Early-Stages of PVT Growth of 4H-SiC Crystals

To better understand the effects of various growth parameters during the early-stages of PVT growth of 4H-SiC on resulting defect structures, multiple short duration growths have been carried out under varying conditions of seed quality, nucleation rate, thermal gradients, and N incorporation. Besides the replication of TSDs/TMDs and TEDs as well as the deflection of TSDs/TMDs into Frank dislocations, synchrotron monochromatic beam x-ray topography (SMBXT) studies also reveal the formation of stacking faults bounded by Frank dislocations. Using ray tracing simulations to characterize the Frank dislocations, three types of stacking faults are revealed: Type 1 stacking fault resulting from 2D nucleation of 6H polytype on terraces; Type 2 stacking fault resulting from macrostep overgrowth of the surface growth spiral steps of TSDs/TMDs which separate into c/2 or c/4 increments; Type 3 stacking fault resulting from vicinal step overgrowth of surface growth spiral steps of TSDs/TMDs which separate into c/4 and 3c/4 increments. Analysis of atomic resolution scanning transmission electron microscopy (STEM) images reveals the mechanism of the Type 3 fault.

Constructing Ni/CeO2 synergistic catalysts into LiAlH4 and AlH3 composite for enhanced hydrogen released properties

The high hydrogen release temperature and thermodynamic stability of the coordination hydride LiAlH4 render it unsuitable for direct application. This work intends to improve the hydrogen release properties via compositing LiAlH4 and AlH3 with similar initial hydrogen release temperatures and introduce efficient additive Ni/CeO2 composite. The thermal stability of the composite system LiAlH4-AlH3 is enormously reduced compared to that of LiAlH4. In addition, the preferential release of hydrogen from LiAlH4 in the composite system provides additional heat for the subsequent release of hydrogen from AlH3, accelerating the hydrogen release process. As a result, LiAlH4-AlH3-Ni/CeO2 composite performs enhanced hydrogen release performance with a hydrogen release capacity of 8.27 wt% hydrogen within 300 ℃ and a dehydrogenation onset temperature as low as 72.9 ℃. The enthalpy change of the first step hydrogen release reaction decreases from −11.99 kJ mol−1 (LiAlH4) to −2.02 kJ mol−1 (LiAlH4-AlH3). Theoretical calculations indicate that both atomic dehybridisation and electron redistribution expedite the breaking of the Al-H bond and the consequent release of hydrogen.

Influence of Deposition Parameters on the Plasmonic Properties of Gold Nanoantennas Fabricated by Focused Ion Beam Lithography.

The behavior of plasmonic antennas is influenced by a variety of factors, including their size, shape, and material. Even minor changes in the deposition parameters during the thin film preparation process may have a significant impact on the dielectric function of the film, and thus on the plasmonic properties of the resulting antenna. In this work, we deposited gold thin films with thicknesses of 20, 30, and 40 nm at various deposition rates using an ion-beam-assisted deposition. We evaluate their morphology and crystallography by atomic force microscopy, X-ray diffraction, and transmission electron microscopy. Next, we examined the ease of fabricating plasmonic antennas using focused-ion-beam lithography. Finally, we evaluate their plasmonic properties by electron energy loss spectroscopy measurements of individual antennas. Our results show that the optimal gold thin film for plasmonic antenna fabrication of a thickness of 20 and 30 nm should be deposited at the deposition rate of around 0.1 nm/s. The thicker 40 nm film should be deposited at a higher deposition rate like 0.3 nm/s.