NP Size Research Articles

Temperature Effects on the Optical Properties of Bismuth Nanoparticles Prepared by PLAL for Antibacterial Activity

Bismuth nanoparticles (Bi NPs) constitute a promising technology for combating infectious illnesses and bacterial resistance to antibacterial treatments. Bi NPs were synthesized by Pulsed Laser Ablation in Liquid (PLAL) using a 532 nm second-harmonic generation Nd:YAG laser. Bi NPs samples were prepared in 10, 35, 50, 75, and 90 ˚C water for various laser energies and number of laser pulses. Ultraviolet-visible (UV-Vis) spectra measurements revealed a characteristic plasmonic absorption band indicative of metallic bismuth nanosized particles. Field emission scanning electron microscopy (FESEM) analysis showed that the water temperature during the ablation process affected the size and morphology of Bi NPs. The average Bi NP size at 60 ˚C was 28 nm, considerably smaller than the 55 nm average observed at 10 ˚C. The antimicrobial properties of Bi NPs against two opportunistic pathogens, E. coli and S. aureus, were assessed. For S. aureus, the inhibition zone of Bi NPs prepared at 60 ˚C was greater than that of samples prepared at 10 ˚C. Further, Bi NPs exhibited lower potency against E. coli than S. aureus in both samples.

Magnetic vortex γ-Fe2O3 nanospheres decorated with gold nanoparticles for dual hyperthermia treatment

In this work, multifunctional systems with potential applications for dual control of thermal heat delivery are developed. For this purpose, the nanosystems produced consist of vortex iron oxide nanospheres (VIONS) decorated with different amounts of gold nanoparticles (AuNPs). The VIONS were synthesized using the solvothermal reduction method, resulting in a 204 ± 24 nm diameter and meeting the requirements for biomedical applications. Magnetic measurements revealed that these systems are composed mainly of maghemite (γ-Fe2O3), exhibiting relatively low coercivity and moderate saturation magnetization, both of which serve as indicative attributes of an exceptional magnetic vortex state as validated by electron holography microscopy. The decoration with gold NPs was achieved through deposition-precipitation, involving the deposition of gold hydroxide on the surface of the previously amine-modified iron oxide NPs, followed by the concurrent reduction of Au3+. Furthermore, the gold NP size modulation was investigated by consecutively adding Au3+ to obtain gold NPs that interact with light differently depending on their size. The study provides crucial information that can aid the decoration of magnetic iron oxide nanospheres with AuNPs with tailored magnetic and optical properties; consequently, they may be promising candidates for magnetic and photothermal hyperthermia based on three-dimensional magnetic vortex structures.

Review of Antimicrobial Properties of Titanium Dioxide Nanoparticles

There is a growing interest in the utilization of metal oxide nanoparticles as antimicrobial agents. This review will focus on titanium dioxide nanoparticles (TiO2 NPs), which have been demonstrated to exhibit high antimicrobial activity against bacteria and fungi, chemical stability, low toxicity to eukaryotic cells, and therefore high biocompatibility. Despite the extensive research conducted in this field, there is currently no consensus on how to enhance the antimicrobial efficacy of TiO2 NPs. The aim of this review is to evaluate the influence of various factors, including particle size, shape, composition, and synthesis parameters, as well as microbial type, on the antibacterial activity of TiO2 NPs against bacteria and fungi. Furthermore, the review offers a comprehensive overview of the methodologies employed in the synthesis and characterization of TiO2 NPs. The antimicrobial activity of TiO2 exhibits a weak dependence on the microorganism species. A tendency towards increased antibacterial activity is observed with decreasing TiO2 NP size. The dependence on the shape and composition is more pronounced. The most pronounced antimicrobial potential is exhibited by amorphous NPs and NPs doped with inorganic compounds. This review may be of interest to specialists in biology, medicine, chemistry, and other related fields.

The influence of the particle size and size synergistic effect of nano-copper on the tribological properties of lubricants

Friction and wear reduction are urgently sought to promote energy savings and performance of precision manufacturing equipment. The molecular dynamics (MD) simulation unveils the detailed lubrication mechanisms of the particle size effect of single Cu NPs and the size synergy effect of multiple Cu NPs. By setting various particle sizes and quantities, the tribological properties of the lubrication system under multiple complex conditions are compared. The stress, strain, wear volume, friction force, normal force, and temperature at the fluid-solid boundary are quantitatively calculated. The results indicate that the average values of friction force are maximally reduced approximately 83.65 %, the wear rate is maximally decreased 22.5 %, the max stress is maximally reduced 22.46 % and the peak temp is maximally reduced 8 % after the addition of Cu NPs. The tribological properties improves as particle size increases, but there is an optimal Cu NP size that yields the best tribological properties. In addition, the tribological properties of the multiple particles are superior to those of the single particle. The results indicate that small and uniform Cu NPs show superior tribological properties over dispersed sizes, small Cu NPs can contribute to improve the overall tribological properties of the system primarily comprises large Cu NPs.

A study using physical sphere-in-contact models to investigate the structure of close-packed nanoparticles supported on flat hexagonal, square and trigonal lattices

The tailored design of nanoparticles becomes more important with the advancement of heterogeneous catalysis and materials science. The formation of nanoparticles in catalysts with a specific geometry of the active site becomes necessary to improve activity and selectivity in catalysis. Here we have used physical sphere-in-contact models of various nanoparticles with hexagonal, square and trigonal geometries on flat close-packed surfaces to understand how the distribution of (100) and (111) sites changes as a function of nanoparticle (NP) size in a simplified model of nanoparticle supported metals. The results from this approach clearly show that in 2-layer NPs that have a hexagonal base have 2–3 times more (100) sites than the square and trigonal base NPs as a function of the number of atoms in the NP. In 3D isotropic NPs, this phenomenon is even more pronounced than the 2-layer NPs. We derive equations that estimate the number of (100), (111), the number of atoms and the aspect ratio as a function of n. These equations are important in tailoring the properties of NPs supported on close-packed metal surfaces, which may find applications in materials science, nanotechnology and catalysis.

Cu nanoparticles immobilized in mesopores generated in zeolite for high-performing CO2 hydrogenation to methanol

Copper nanoparticles (Cu NPs) are commonly used as catalyst active components in CO2 hydrogenation reactions. However, they often lose their catalytic activity due to sintering in most reaction environments. This study explores a solution for Cu-supported catalysts used for methanol production from CO2 hydrogenation by fixing Cu NPs in the mesopores generated in zeolite. Mesopores were generated in NaY zeolite by partially dealuminating its framework. High-resolution (scanning) transmission electron microscopy (HR(S)TEM) and CO adsorption measurements confirm that the synthesized mesoporous zeolite-supported Cu NPs are highly dispersed and fixed within the mesopores. In comparison with conventional microporous zeolite-supported Cu NPs (2 wt%), Cu NPs (2 wt%, average size of 2.2 nm) in mesoporous zeolite increased methanol production from ∼26 mmolgCu−1h−1 to approximately 56 mmolgCu−1h−1 at 250 °C. By further modifying the mesoporous zeolite with Zr (2 wt%), Cu NPs increased in size, and the methanol production rate increased approximately 2.2 folds to 125 mmolgCu−1h−1 under similar conditions due to zeolite electronic modification and the newly formed Zr-zeolite/Cu interface. However, the addition of Zr significantly increased the Cu NP size and moved part of them out of the mesopores, lowering their stability. In situ DRIFTS experiments reveal CO2 hydrogenation proceeds through the formate route via a direct formation of dominantly carbonate (*CO3), which hydrogenates to formate (*HCOO) and traces of methoxy (*H3CO), and subsequently methanol (CH3OH). This study reports the design of active and stable catalysts for CO2 hydrogenation to methanol by engineering Cu NPs in zeolite pores.

Understanding the growth kinetics of polydopamine nanoparticles as a function of the temperature and the type of alcohol used as solvent media in their polymerization

Currently, one of the bottlenecks in the large-scale production of particles used for biomedical purposes is reproducibility achieving sizes less than 100 nm. For this reason, the main purpose of this work was to elucidate how the size of polydopamine nanoparticles (PDA NPs), which are widely used in cancer nanomedicine, was affected by several synthesis parameters to facilitate their production scaling-up. Specifically, PDA NPs growth kinetics were investigated as a function of the polymerization temperature (15–50 °C) and the type of alcohol (ethanol, 2-propanol, or a mixture of both) used to produce them, finding that an increase in temperature and the amount of 2-propanol in the solvent media allowed smaller NPs to be obtained. Based on the results achieved, a mathematical model capable of predicting PDA NP diameter as a function of the temperature and reaction time, the NH4OH concentration, and the type of alcohol used to synthesize them was proposed. Also, PDA solubility in the different media was studied to explain NP size behavior depending on the type of alcohol employed, which conditioned the formation of PDA oligomers. Finally, additional assays were conducted to confirm that an increase in the synthesis temperature did not affect some of the most important properties of PDA NPs from a biomedical point of view: their Fe3+-loading capacity and their inherent antitumor activity. Therefore, the results obtained in this research could be useful to scale-up the obtaining of 100 nm PDA NPs in a reproducible manner hereafter without significantly altering their outstanding physical-chemical properties.

Metal-organic framework-derived carbon-supported high-entropy alloy nanoparticles applied in ammonia borane hydrolytic dehydrogenation

While high-entropy alloy nanoparticle (HEA NP) catalysts from a sacrificial high-entropy-MOF (HE-MOF) have been attractive, their conventional characterizations may be misleading. Here, we report HEA NPs on HE-MOF-derived carbon (HE-MDC) via direct pyrolysis of MnFeCoNiCu HE-MOF in Ar and H2 at different temperatures and durations with a fast-ramping rate. With the profound investigations of the metal NPs on HE-MDCs by synchrotron radiation X-ray diffraction and absorption, we revealed that the Ar-treated HE-MDCs had either Cu-dominant solid solution or phase-segregated metal NPs, whereas H2 pyrolysis yielded well-dispersed HEA NPs on HE-MDCs. For ammonia borane hydrolysis, although the metal NP size in H2-treated HE-MDC was not the smallest, it showed the fastest dehydrogenation rate (TOF=5.76 molH₂∙min−1∙molcat-1), 2 ∼ 4 times faster than the Ar-treated HE-MDCs. It emphasized the crucial role of elemental uniformity in the HEA NPs over the traditionally reported catalyst size.

Assessment of enhancing curcumin’s solubility versus uptake on its anti-cancer efficacy

Curcumin (CUR) exhibits anti-inflammatory and anti-cancer activities. However, its poor solubility and bioavailability limit its therapeutic applications. Several CUR nano-formulations have been developed to enhance its solubility and uptake, thereby improving its anti-cancer activity. Despite this, studies comparing the effect of enhanced CUR solubility versus cellular uptake on its anti-cancer efficacy are lacking. Therefore, CUR nanofibers (CUR NF) were synthesized by electrospinning using a water-soluble polymer to enhance CUR solubility. While CUR nanoparticles (CUR NP) were synthesized by nanoprecipitation method using a water-insoluble polymer to enhance CUR cellular uptake. Both nano-formulations aim to improve CUR cellular concentration and anti-cancer activity against various cancer cells. CUR NF and CUR NP were successfully synthesized at drug load (DL%) of 10 %, 20 %, and 40 % w/w. Both nano-formulations were characterized, and CUR dissolution, release, cytotoxicity, IC50, and cellular uptake were assessed. A gradual increase in NF diameter and NP size was observed as the drug load% increased compared to the placebo. NF showed a rapid CUR release and increased solubility by 16–38 fold. In contrast, NP sustained CUR release and resulted in only a 2-fold increase in solubility. Both formulations significantly reduced cell viability and IC50 compared to free CUR. However, CUR NP demonstrated higher cell toxicity (70–80 %) than CUR NF (60 %) and reduced IC50 up to 4 μM compared to 11 μM for NF. Enhancing CUR solubility or uptake can significantly increase its cellular concentration and anti-cancer activity. However, enhancing CUR cellular uptake by NP demonstrated superior anti-cancer effect compared to enhancing its solubility by NF.

Controlling In Planta Gold Nanoparticle Synthesis and Size for Catalysis.

Gold nanoparticles (Au-NPs) are used as catalysts for a diverse range of industrial applications. Currently, Au-NPs are synthesized chemically, but studies have shown that plants fed Au deposit, this element naturally as NPs within their tissues. The resulting plant material can be used to make biomass-derived catalysts. In vitro studies have shown that the addition of specific, short (∼10 amino acid) peptide/s to solutions can be used to control the NP size and shape, factors that can be used to optimize catalysts for different processes. Introducing these peptides into the model plant species, Arabidopsis thaliana (Arabidopsis), allows us to regulate the diameter of nanoparticles within the plant itself, consequently influencing the catalytic performance in the resulting pyrolyzed biomass. Furthermore, we show that overexpressing the copper and gold COPPER TRANSPORTER 2 (COPT2) in Arabidopsis increases the uptake of these metals. Adding value to the Au-rich biomass offers the potential to make plant-based remediation and stabilization of mine wastes financially feasible. Thus, this study represents a significant step toward engineering plants for the sustainable recovery of finite and valuable elements from our environment.

In Vitro Toxicological Insights from the Biomedical Applications of Iron Carbide Nanoparticles in Tumor Theranostics: A Systematic Review and Meta-Analysis.

(1) Background: Despite the encouraging indications regarding the suitability (biocompatibility) of iron carbide nanoparticles (ICNPs) in various biomedical applications, the published evidence of their biosafety is dispersed and relatively sparse. The present review synthesizes the existing nanotoxicological data from in vitro studies relevant to the diagnosis and treatment of cancer. (2) Methods: A systematic review was performed in electronic databases (PubMed, Scopus, and Wiley Online Library) on December 2023, searching for toxicity assessments of ICNPs of different sizes, coatings, and surface modifications investigated in immortalized human and murine cell lines. The risk of bias in the studies was assessed using the ToxRTool for in vitro studies. (3) Results: Among the selected studies (n = 22), cell viability emerged as the most frequently assessed cellular-level toxicity endpoint. The results of the meta-analysis showed that cell models treated with ICNPs had a reduced cell viability (SMD = -2.531; 95% CI: -2.959 to -2.109) compared to untreated samples. A subgroup analysis was performed due to the high magnitude of heterogeneity (I2 = 77.1%), revealing that ICNP concentration and conjugated ligands are the factors that largely influence toxicity (p < 0.001). (4) Conclusions: A dose-dependent cytotoxicity of ICNP exposure was observed, regardless of the health status of the cell, tested organism, and NP size. Inconsistent reporting of ICNP physicochemical properties was noted, which hinders comparability among the studies. A comprehensive exploration of the available in vivo studies is required in future research to assess the safety of ICNPs' use in bioimaging and cancer treatment.

Size-dependent plasmonic activity of AuNPs for the rational design of catalysts for organic reactions

The rational design of plasmonic catalysts encompasses the manipulation of nanoparticle (NP) size: the smaller the AuNPs size is, the higher catalytic activity occurs.

Optical Properties of Germanium Nanoparticles Prepared by Laser Ablation

The synthesis of germanium nanoparticles (Ge NPs) through pulsed laser ablation in deionized water is investigated for Nanophotonics and optoelectronic applications. This study delves into the influence of laser pulse energy on Ge NP properties, specifically highlighting size control and optical characteristics. Our findings reveal a significant reduction in Ge NP size, from an initial 30 nm to 20 nm, as the laser pulse energy increases. Notably, we observed size-dependent blue luminescence from the synthesized Ge NPs. This controlled synthesis holds promise for optoelectronics and sensing applications. The study provides valuable insights into precise Ge NP synthesis and underscores their intriguing optical properties, paving the way for advanced Nanophotonic devices.

Cost-effective synthesis of copper sulfide nanoparticles and flexible films for photocatalytic and antibiotic applications

Herein, we investigate the effects of temperature and thiourea addition rate on the synthesis of copper sulfide nanoparticles (CuS NPs) via a chemical co-precipitation method, exploring their impact on the size and morphology of CuS NPs. Our systematic approach resulted in the successful synthesis of CuS NPs with significantly smaller nanoflower sizes than previously reported in the literature, providing insights into the nucleation and growth mechanisms under various synthesis conditions. Furthermore, the photocatalytic activity of the synthesized CuS NPs with three types of distinctive morphologies, namely, nanoflowers with 50 nm diameter (F-50), nanoflowers with 200 nm diameter, and nanogravels with 50 nm diameter, is comparatively analyzed. Notably, the F-50 exhibits a superior photocatalytic performance compared to the other samples, demonstrating the considerable influence of the NP size and morphology on their functional properties. Furthermore, the antibacterial property of the small CuS nanoflowers is examined using an antibacterial film fabricated by coating the NPs on a polyethylene terephthalate substrate, which is widely used as a protective or packaging film in various industries because of its transparency and flexibility. The antibacterial film can be used to kill both gram-positive and -negative bacteria effectively. This research contributes significantly to the understanding and optimization of CuS NP synthesis and application, emphasizing the potential of small-sized nanoflower CuS NPs in photocatalysis and antibacterial applications.

Gallium nanoparticles as antireflection structures on III-V solar cells

The integration of nanostructures on top of solar cells has been previously demonstrated as an effective method to increase the collection efficiency by coupling to sunlight. In this work, this approach is implemented by using core-shell gallium nanoparticles (Ga-NPs) as functional light scatterers on III-V solar cells, investigating how the Ga-NPs affect their photovoltaic performance. The effect is studied in GaAs and in GaAsSbN superlattice-based solar cells with different bandgaps for a wide range of Ga-NPs sizes. After NP size optimization, average improvements in the short-circuit current around 18 % are obtained in both types of solar cells with these nanostructures. The underlying physical mechanism is studied by performing optical measurements and simulations. It is found that the Ga-NPs can be treated as an antireflection coating due to both their geometry and the refractive index in the cases when their localized surface plasmon resonances do not spectrally overlap with the solar cell absorption range. Lastly, a facile method to attenuate the plasmonic effect of the Ga-NPs it is also shown as a proof of concept. In this method, an annealing treatment at low temperature is performed causing an improvement of the photovoltaic performance. This work demonstrates that Ga-NPs can successfully enhance the efficiency of III-V solar cells in a very controllable manner and paves the way for the design of new functional nanostructures.

Deep learning models for assisted decision-making in performance optimization of thin film nanocomposite membranes

The performance of thin film nanocomposite nanofiltration membranes (TFNNMs) is frequently constrained by the trade-off between the permeability and rejection/selectivity of the membrane. In this study, to provide assisted decision-making in performance optimization of TFNNMs, we utilized a dataset comprising four categories of impact parameters, including membrane manufacturing conditions, membrane performance, nanoparticle material performance, and organic solvent nanofiltration conditions, and trained a dual output neural network (D-ANN) to simulate the relative permeability (RP) and relative rejection/selectivity (RR) of TFNNMs. The D-ANN model outperformed conventional machine learning models and single-output neural networks in predicting both RP and RR, indicating its potential in uncovering correlations between output variables. The Shapley additive explanation method was employed to elucidate the contribution and marginal effects of each influencing parameter on RP and RR, among them, NP size, NP loading, water contact angle, and chloride concentration were influential parameters that are important for both RP and RR. Based on the D-ANN model, we extrapolated two sets of unknown data and achieved good predictive performance (RP-error <15%, RS-error <7% for most sample points). Furthermore, we observed that the predicted performance of the data points rarely exceeded the actual performance, indicating a low probability of overestimation. Based on these premises, the influential parameters can be optimized using the D-ANN model, which ultimately led to exceptional performance for a total of 22 datasets in four pairs of organic solvent and solute purifications guided by the D-ANN model. This study demonstrates that the D-ANN model can provide decisions for the performance optimization of TFNNMs while highlighting the enhancement of nanofiltration performance by thin film nanocomposites, significantly facilitating the design of high-performance TFNNMs.

Tuning LSPR of Thermal Spike-Induced Shape-Engineered Au Nanoparticles Embedded in Si3N4 Thin-Film Matrix for SERS Applications.

While gold nanoparticles (Au NPs) are widely used as surface-enhanced Raman spectroscopy (SERS) substrates, their agglomeration and dynamic movement under laser irradiation result in the major drawback in SERS applications, viz., the repeatability of SERS signals. We tune the optical and structural properties of size- and shape-modified Au NPs embedded in a thin silicon nitride (Si3N4) matrix by intense electronic excitation with swift heavy ion (SHI) irradiation with the aim of overcoming this classical SERS disadvantage. We demonstrate the shape evolution of a single layer of Au NPs inserted between amorphous Si3N4 thin films under fluences of 120 MeV Au9+ ions ranging between 1 × 1011 and 1 × 1013 ions cm-2. This shape modification results in the gradual blue shift of the localized surface plasmon resonance (LSPR) dip until 1 × 1012 ions/cm2 and then a sudden diminishment at 1 × 1013 ions/cm2. Finite domain time difference (FDTD) simulations further justify our experimental optical spectra. The dynamical NP aggregation and dissolution, in addition to NP elongation and deformation at different fluences, are noted from 2D grazing incidence small-angle X-ray scattering (GISAXS) profiles, as well as cross-sectional transmission electron microscopy (X-TEM). The systematic shape evolution of metal NPs embedded in the insulating matrix is shown to be due to thermal spike-induced localized melting and a localized pressure hike upon SHI irradiation. Utilizing this specific control over the characteristics of Au NPs, viz., shape, size, interparticle gap, and corresponding optical response via SHI irradiation, we demonstrate their applications as very stable SERS substrates, where the separation between NPs and analyte does not alter under laser illumination. Thus, these irradiated SERS active substrates with controlled NP size and gap provide the optimal conditions for creating localized electromagnetic hotspots that amplify the SERS signals, which do not alter with time or laser exposure. We found that the film irradiated with 1 × 1011 exhibits the highest SERS intensity due to its optimal NP size distribution and shape. Thus, not only our study provides a SERS substrate for stable and repeatable signals but also the understanding depicted here opens new research avenues in designing SERS substrates, photovoltaics, optoelectronic devices, etc. with ion beam irradiation.

Targeted Anticancer Drug Delivery Using Chitosan, Carbon Quantum Dots, and Aptamers to Deliver Ganoderic Acid and 5-Fluorouracil.

Breast cancer is a malignancy that affects mostly females and is among the most lethal types of cancer. The ligand-functionalized nanoparticles used in the nano-drug delivery system offer enormous potential for cancer treatments. This work devised a promising approach to increase drug loading efficacy and produce sustained release of 5-fluorouracil (5-FU) and Ganoderic acid (GA) as model drugs for breast cancer. Chitosan, aptamer, and carbon quantum dot (CS/Apt/COQ) hydrogels were initially synthesized as a pH-sensitive and biocompatible delivery system. Then, CS/Apt/COQ NPs loaded with 5-FU-GA were made using the W/O/W emulsification method. FT-IR, XRD, DLS, zeta potentiometer, and SEM were used to analyze NP's chemical structure, particle size, and shape. Cell viability was measured using MTT assays in vitro using the MCF-7 cell lines. Real-time PCR measured cell apoptotic gene expression. XRD and FT-IR investigations validated nanocarrier production and revealed their crystalline structure and molecular interactions. DLS showed that nanocarriers include NPs with an average size of 250.6 nm and PDI of 0.057. SEM showed their spherical form, and zeta potential studies showed an average surface charge of +37.8 mV. pH 5.4 had a highly effective and prolonged drug release profile, releasing virtually all 5-FU and GA in 48 h. Entrapment efficiency percentages for 5-FU and GA were 84.7±5.2 and 80.2 %±2.3, respectively. The 5-FU-GA-CS-CQD-Apt group induced the highest cell death, with just 57.9 % of the MCF-7 cells surviving following treatment. 5-FU and GA in CS-CQD-Apt enhanced apoptotic induction by flow cytometry. 5-FU-GA-CS-CQD-Apt also elevated Caspase 9 and downregulated Bcl2. Accordingly, the produced NPs may serve as pH-sensitive nano vehicles for the controlled release of 5-FU and GA in treating breast cancer.

Controllable Preparation and Size-Dependent SERS Performance of 35–410 nm Quasi-spherical Au NPs

Uniform Au NPs with definite but different sizes will serve as a perfect model for studying the influence of NP size on surface-enhanced Raman scattering (SERS) performance. In this study, using tri-hydroxymethyl aminomethane (Tris-base) as a stabilizer and FeCl2 as a reducing agent, Au NPs with the size of 110–410 nm were prepared by a one-step method by simply changing the amount of FeCl2. In the preparation of small particle size Au NPs, sodium citrate was introduced as an auxiliary stabilizer, and 35–85 nm Au NPs were prepared in one step. In addition, the synthetic Au NPs of different sizes were loaded onto the glass substrate and 4-MOTP was used as the probe molecule to monitor their SERS properties. The results showed that the SERS activity results showed a “volcanic shape” with the change of nanoparticle size at a fixed excitation wavelength. The 160 nm Au NPs have the best SERS performance when the excitation wavelength is 633 nm.

Capacitively coupled nonthermal plasma synthesis of aluminum nanocrystals for enhanced yield and size control

Uniform-size, non-native oxide-passivated metallic aluminum nanoparticles (Al NPs) have desirable properties for fuel applications, battery components, plasmonics, and hydrogen catalysis. Nonthermal plasma-assisted synthesis of Al NPs was previously achieved with an inductively coupled plasma (ICP) reactor, but the low production rate and limited tunability of particle size were key barriers to the applications of this material. This work focuses on the application of capacitively coupled plasma (CCP) to achieve improved control over Al NP size and a ten-fold increase in yield. In contrast with many other materials, where NP size is controlled via the gas residence time in the reactor, the Al NP size appeared to depend on the power input to the CCP system. The results indicate that the CCP reactor assembly, with a hydrogen-rich argon/hydrogen plasma, was able to produce Al NPs with diameters that were tunable between 8 and 21 nm at a rate up ∼ 100 mg h−1. X-ray diffraction indicates that a hydrogen-rich environment results in crystalline metal Al particles. The improved synthesis control of the CCP system compared to the ICP system is interpreted in terms of the CCP’s lower plasma density, as determined by double Langmuir probe measurements, leading to reduced NP heating in the CCP that is more amenable to NP nucleation and growth.