The effect of particle morphology on unipolar diffusion charging of nanoparticle agglomerates in the transition regime

We investigated the effect of particle morphology on unipolar diffusion charging of nanoparticle agglomerates consisting of multiple primary spheres. In the unipolar diffusion charging of non-spherical agglomerates, geometric surface area and electrical capacitance of particles, which are related to particle morphology, are known as important parameters to determine mean charge per particle. From mobility analysis we found that the geometric surface area of chain-like agglomerates is only larger than that of spherical particles with the same mobility diameter for mobility size range below d_m=80 nm. We estimated the electrical capacitance of agglomerates with a newly developed model based on electrostatics and mobility theories. The results show that the electrical capacitance of chain-like agglomerates becomes significantly larger compared to that of spheres with the same mobility diameter as particles become larger. Our analysis results indicate that loose agglomerates have larger mean charge per particle compared to compact particles with the same mobility diameter because the electrical capacitance of agglomerates becomes larger as particle morphology becomes looser. Our experimental data show that mean charge per particle for silver agglomerates is larger than that for fully coalesced silver spheres with the same mobility diameter as agglomerates by about 24%. The experimental data is in good agreement with estimates of mean charge per particle for silver agglomerates.     

Nanoparticulate PdZn as a Novel Catalyst for ZnO Nanowire Growth

ZnO nanowires have been grown by chemical vapour deposition (CVD) using PdZn bimetallic nanoparticles to catalyse the process. Nanocatalyst particles with mean particle diameters of 2.6 ± 0.3 nm were shown to catalyse the growth process, displaying activities that compare well with those reported for sputtered systems. Since nanowire diameters are linked to catalyst morphology, the size-control we are able to exhibit during particle preparation represents an advantage over existing approaches in terms of controlling nanowire dimensions, which is necessary in order to utilize the nanowires for catalytic or electrical applications.     

Evaluating the Mobility of Nanorods in Electric Fields

The mobility of a nonspherical particle is a function of both particle shape and orientation. In turn, the higher magnitude of electric field causes nonspherical particles to align more along the field direction, increasing their mobility or decreasing their mobility diameter. In previous works, Li et al. developed a general theory for the orientation-averaged mobility and the dynamic shape factor applicable to any axially symmetric particles in an electric field, and applied it to the specific cases of nanowires and doublets of spheres. In this work, the theory for a nanowire is compared with experimental results of gold nanorods with known shape determined by TEM images. We compare the experimental measured mobility sizes with the theoretical predicted mobility in the continuum, free molecular, and the transition regime. The mobility size shift trends in the electric fields based on our model, expressed both in the free molecular regime and in the transition regime, are in good agreement with the experimental results. For rods of dimension: width d_r = 17 nm and length L_r = 270 nm, where one length scale is smaller than the mean free path and one larger, the results clearly show that the flow regime of a slender rod is mostly controlled by the diameter of the rod (i.e., the smallest dimension). In this case, the free molecule transport properties best represented our nanorod. Combining both theory and experiment we show how, by evaluating the mobility as a function of applied electric field, we can extract both rod length and diameter.

Copyright 2013 American Association for Aerosol Research     

The effect of nanowire length and diameter on the properties of transparent, conducting nanowire films

This article describes how the dimensions of nanowires affect the transmittance and sheet resistance of a random nanowire network. Silver nanowires with independently controlled lengths and diameters were synthesized with a gram-scale polyol synthesis by controlling the reaction temperature and time. Characterization of films composed of nanowires of different lengths but the same diameter enabled the quantification of the effect of length on the conductance and transmittance of silver nanowire films. Finite-difference time-domain calculations were used to determine the effect of nanowire diameter, overlap, and hole size on the transmittance of a nanowire network. For individual nanowires with diameters greater than 50 nm, increasing diameter increases the electrical conductance to optical extinction ratio, but the opposite is true for nanowires with diameters less than this size. Calculations and experimental data show that for a random network of nanowires, decreasing nanowire diameter increases the number density of nanowires at a given transmittance, leading to improved connectivity and conductivity at high transmittance (>90%). This information will facilitate the design of transparent, conducting nanowire films for flexible displays, organic light emitting diodes and thin-film solar cells.     

Synthesis of tellurium nanotubes by galvanic displacement

Tellurium nanotubes with controlled diameter and wall thickness were synthesized by galvanic displacement of cobalt nanowires and their temperature dependent field effect transistor and magnetoresistance properties were systematically investigated. The nanotube diameter was slightly larger than the sacrificial cobalt nanowire diameter with a wall thickness of range from 15 to 30 nm depending on the diameter of cobalt nanowires. Te nanotubes show p-type semiconducting property with the field effect carrier mobility of approx. 0.01 cm²/V s which is relatively lower than other 1D nanostructure. Low mobility might be attributed to porous morphology with small grain size (<10 nm). Temperature dependent mobility also exhibiting a Conwell-Weisskopf relationship to temperatures below 250 K, indicating that the dominant scattering sites are ionized impurity centers. Unique MR behavior was observed from nanotube with a maximum magnetoresistance ratio of 37% at 260 K.     

Bipolar diffusion charging characteristics of single-wall carbon nanotube aerosol particles

Bipolar diffusion charging characteristics of airborne single-wall carbon nanotube (SWCNT) agglomerates were investigated in the mobility diameter range of 100–1000 nm. Neutral fractions of three types of SWCNT aerosols following bipolar charge equilibrium in a radioactive source were experimentally measured to infer their electrical charging characteristics. Significant deviation from Boltzmann and Fuchs stationary charge equilibrium was observed, with neutral fractions of SWCNT particles lower by 30–53% compared to that of spherical particles of the same mobility. Particles with mobility diameter larger than 400 nm showed high electrical charging efficiencies compared to that of mobility-equivalent spherical particles. Higher charging efficiencies of SWCNT particles were attributed to their higher electrical capacitance resulting from complex nonspherical morphologies. Numerical calculations using idealized fiber geometries confirmed the qualitative trend in the experimental data. The electrical capacitance of nanotubes particles deduced from experimentally measured neutral fractions were also found to be higher by a factor ranging from 1.6 to 4.6 compared to that of mobility-equivalent spherical particles, indicating high charge carrying capacity. The charging-equivalent diameters of nanotube particles were computed and were found to be higher than their mobility diameter by a factor of 2.85–4.34.     

Multiple charging of ultrafine particles in a corona charger

The charge distribution on ultrafine aerosol particles in the size range below 35 nm has been measured using a corona-based unipolar charger, in which ion generation and aerosol charging take place simultaneously in the region around a sharp-point discharge electrode. The mean number of charges per particle predicted by Fuchs’ diffusion charging theory is in relatively good agreement with the experimental results, and this implies that diffusion charging is the predominant mechanism in spite that the electric field in the charging region is very high. Since a steady state is unattainable in unipolar charging, the charge distribution depends on the geometry and operating conditions of each particular charger. When the present device operates under the conditions (nt-product) which yield the maximum charging efficiency, double charge appears on particles with diameter as small as 15 nm. At larger values of nt, 32 nm particles can acquire up to five charges. The critical particle diameter above which multiple charging occurs is about four times smaller than for bipolar radioactive chargers. In order to use corona charging in aerosol particle size measurement by electrical methods, the required mobility data inversion is thus straightforward for particle diameter below about 15 nm, but becomes quite complex for larger sizes.     

Study of a Nanoparticle Charger Containing Multiple Discharging Wires in a Tube

Abstract

A unipolar charger containing multiple discharging wires in a tube (inner diameter: 50 mm) was developed and tested in order to increase the aerosol flow rate and the charging efficiency of nanoparticles. Four gold wires of 25 µm in diameter and 15 mm in length were used as the discharging electrodes to generate positive ions (N_i) from 2.72 × 10⁸ ions/cc to 3.87 × 10⁹ ions/cc in concentration at the discharging voltage of + 4.0 ～ + 10 KV. Monodisperse NaCl particles of 10 ～ 50 nm in diameter were used to test the charging efficiency and the particle loss of charged particles with different aerosol flow rates, corona voltages and sheath flow rates. The sheath air near the tube wall was found to increase the extrinsic charging efficiency, and the highest efficiency was obtained at + 6.0 KV discharging voltage, 10 L/min aerosol flow rate and 9 L/min sheath flow rate. The extrinsic charging efficiency increased from 10.6% to 74.2% when the particle diameter was increased from 10 to 50 nm. The TDMA (tandem differential mobility analyzer) method was used to determine the charge distribution and the mean charge per particle and it was found that the Fuchs charging theory corrected for the extrinsic charging efficiency matched with the experimental data very well.     

Wavelength-Resolved UV Photoelectric Charging Dynamics of Nanoparticles: Comparison of Spheres and Aggregates

The objective of this work is to understand the charging dynamics of metal nanoparticles under wavelength-selected UV irradiation, with a particular focus on the effect of particle structure on the quantum yield. We employed an ion mobility analysis technique to measure the size-resolved single charging efficiency of structure-controlled silver nanoparticles (spheres vs. aggregates) in the mobility diameter (D _m) range of 10 ～ 100 nm. We found that the measured particle charging efficiency follows D ² _m dependence for both spherical and aggregate particles. Based on the measured charging efficiency and calculated particle photon absorption cross section, we are also able to determine the mobility size dependence of photoelectric quantum yield for both spheres and aggregates. The quantum yield of spheres is a constant for larger particles (50 nm or larger) but significantly enhanced as particle size decreases. The quantum yield of aggregates is shown to be particle structure dependent and does not behave as a simple summation of individual primary particles. The aggregate particles have higher quantum yield compared with spheres of the same mobility size but is offset by the lower photon absorption cross section, and thus overall charging efficiency of aggregates is lower than spheres of the same mobility size.

© 2013 American Association for Aerosol Research     

Ag nanowires and its application as electrode materials in electrochemical capacitor

Silver nanowires were synthesized on a large scale by using anodic aluminum oxide (AAO) film as templates and serving ethylene glycol as reductant. Their morphological and structural characterizations were characterized with field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and selected area electron diffraction (SAED). The electrochemical properties of silver nanowires as electrode materials for electrochemical capacitors were investigated by cyclic voltammetry (CV) and galvanostatic charge/discharge technique in 6 M KOH aqueous electrolyte. The Ag₂O/Ag coaxial nanowires were formed by the incomplete electrochemical oxidation during the charge step. The maximum specific capacitance of 987 F g^?1 was obtained at a charge–discharge current density of 5 mA cm^?2.     

Experimental investigation and numerical modeling of the orientation angle of silver nanowires passing through polyester filters

In the present study, we measured the penetration of silver nanowires with the mobility diameter in the range from 200 to 400 nm through two different types of polyester filters: the screen filter with the solidity of 0.505 and fibrous filter with the solidity of 0.278. The orientation angles of silver nanowires passing through the single layer and multi-layers of polyester filter were experimentally estimated on the basis of the single fiber efficiency theory. In the case of the screen filter, the orientation angle obtained by fitting the experimental data for single layer was found to be close to 40?, indicating a random orientation of nanowires near the filter. However, the fibrous filter has the orientation angle much larger than 40?. The orientation angle can be affected by inhomogeneity of the filter. In particular, in the case of the fibrous filter, the solidity and fiber diameter may affect the orientation angle. For multi-layers of both screen and fibrous filters, it is difficult to determine the typical orientation angle and the fibrous filter tends to have a larger orientation angle than the screen filter. In addition, we carried out numerical simulations on the penetration of silver nanowires through the five layers of screen filter and the single layer of both screen and fibrous filters. Numerical prediction was carried out by using the three-dimensional numerical model determined by solidity and thickness of fibrous filter. Numerical predictions are highly congruent with experimental results and theoretical prediction.

© 2017 American Association for Aerosol Research     

Structural Property Effect of Nanoparticle Agglomerates on Particle Penetration through Fibrous Filter

Most filtration studies have been conducted with spherical particles; however, many aerosol particles are agglomerates of small primary spheres. Filtration efficiency tests were conducted with silver NP agglomerates, with the agglomerate structure controlled by altering the temperature of a sintering furnace. The mobility diameter and mass of the silver NP agglomerates were measured using a differential mobility analyzer together with an aerosol particle mass analyzer. From these measurements, it was found that the fractal-like dimension, D _fm, varied from 2.07 to 2.95 as the sintering temperatures was increased from ambient to 600°C. The agglomerates were essentially fully coalesced at 600°C allowing direct comparison of the filtration behavior of the agglomerate to that of a sphere with the same mobility diameter. Other agglomerate properties measured include the primary diameter, the agglomerate length and aspect ratio, and the dynamic shape factor.

Agglomerate filtration modeling with no adjustable parameters has been investigated in terms of diffusion, impaction, and interception. The model results agree qualitatively with the experimental results in the particle size range of 50 to 300 nm. The results indicated that the larger interception length of agglomerates is responsible for the smaller penetration through a fibrous filter in comparison to spherical particles with the same mobility diameters.     

Measuring aerosol active surface area by direct ultraviolet photoionization and charge capture in continuous flow

Abstract

Direct ultraviolet photoionization electrically charges particles using a mechanism distinct from diffusion charging. The purpose of this study is to evaluate aerosol photoemission theory as a function of aerosol particle size, concentration, material, and morphology. Particles are classified using an aerodynamic aerosol classifier (AAC) and subsequently measured with a scanning mobility particle sizer (SMPS) and photoionization measurement system in parallel. This configuration allows direct comparison of photo-emission from high concentrations of initially neutral, monodisperse aerosols with different morphologies or materials. Under all examined conditions, the overall photoelectric yields of particles of self-similar material (silver and unconditioned soot) and morphology (sintered spheres and agglomerates) are each linearly proportional to the second moment of the mobility-equivalent diameter distribution, even in the transition regime (mobility diameter 30–200?nm), with agglomerate silver particles resulting in 5× higher photoelectric yield than unconditioned soot from a propane flame. It is shown for the first time that the photoelectric yield is significantly higher (2.6×) for fractal-like agglomerate silver particles than sintered, close-packed spherical particles of the same material and mobility-equivalent diameter, which is inferred to be due to the larger material surface area exposed externally to the particle surroundings. It is demonstrated that photoelectric measurements of aerosols reflect the photoelectrically active surface area which depends on the particle morphology and therefore the state of sintering.

Copyright © 2019 American Association for Aerosol Research     

Large-scale synthesis of SiC/PyC core-shell structure nanowires via chemical liquid-vapor deposition

In carbon/carbon (C/C) composites, SiC/PyC core-shell structure nanowires were successfully fabricated via chemical liquid-vapor deposition (CLVD). The influences of heat-treatment temperature on the microstructure and composition of SiC nanowires were studied, and meanwhile the growth mechanism of SiC nanowires was discussed. Additionally, the microstructure and morphology of SiC/PyC core-shell structure nanowires were also investigated. The results displayed that the low heat-treatment temperature could not meet the requirements of SiC nanowires growth, but the too high temperature made the nanowires appear agglomerate easily. Only when the heat-treatment temperature was 1800 °C, SiC nanowires possessed a uniform distribution. The diameter of SiC nanowire was about 300 nm, and there was a SiO₂ layer with the thickness of about 1 nm existing on the surface of SiC nanowire. The growth behavior of SiC nanowire was governed by vapor-solid (V–S) mechanism. After the PyC deposition, SiC/PyC core-shell structure nanowires were constructed, and the nanowires were about 450 nm in diameter. These nanowires displayed a core-shell structure with three layers, which were SiC nanowire core, SiO₂ interlayer and PyC shell, respectively. Meanwhile, SiC/PyC core-shell structure nanowires connected the matrices with each other, and the core-shell structure nanowires generated a stable network.     

Controlled synthesis of ultra-long AlN nanowires in different densities and in situ investigation of the physical properties of an individual AlN nanowire

The controlled synthesis of different growth densities of ultra-long AlN nanowires has been successfully realized by nitridation of Al powders for the first time. These AlN nanowires have an average diameter of about 100 nm and their mean length is over 50 μm. All the synthesized ultra-long nanowires are pure single crystalline h-AlN structures with a growth orientation of [0001]. We preferred the self-catalyzing vapor-liquid-solid (VLS) mechanism to illustrate their growth process. Although the sample with the middle growth density (3.2×10(7) per cm2) of AlN nanowire performs the best field emission (FE) properties, the emission uniformity is not good enough for field emission display applications, which may be attributed to their low intrinsic conductivity. Moreover, the electrical transport and FE properties of an individual ultra-long AlN nanowire are further investigated in situ to find the decisive factor responsible for their FE behaviors. An individual AlN nanowire is observed to have a mean 1 nA field of 440 V μm(-1) and 1 μA field of 480 V μm(-1) as well as an average electrical conductivity of about 2.7×10(-4)Ω(-1) cm(-1), which is lower than that of some cathode materials with excellent FE properties. Therefore we come to the conclusion that the electrical conductivity of the AlN nanowire must be improved to a higher level by some effective ways in order to realize their practical FE device applications.     

The Nano-Particle Mass Classifier (Nano-PMC): Development,Characterization, and Application for Determining the Mass,Apparent Density,and Shape of Particles with Masses Down to the Zeptogram Range

Existing aerosol particle mass classifiers (PMCs) can classify particles having masses down to ca. half an attogram (i.e., 10^?18 g), which corresponds to a diameter of ca. 10 nm for spherical particles with standard density (1 g/cm³). Here, we describe an improved design of such a classifier, namely, the nano-PMC, which can classify particles with masses down to 20 zeptograms (10^?21 g). The response of the classifier was characterized with spherical polystyrene-latex and ammonium sulfate particles, produced by atomization and mobility classification. Measured responses were compared with predictions by a numerical trajectory-based model that considers particle diffusivity. Measurements and predictions of the mean mass of the particles penetrating the classifier agreed within experimental uncertainty (<6%). Differences in the spectrum width could be attributed to recirculation flows occurring in the classification channel.

To demonstrate the capabilities of a nano-PMC, we used it in a tandem configuration with a differential mobility analyzer to determine (1) the size-dependent shape factor of cubic sodium chloride particles having diameters from 15 to 120 nm, and (2) the apparent density and mass–mobility coefficient of coalesced and aggregated silver particles generated by spark ablation. Measurements of the shape factor of the cubic sodium chloride particles show good agreement with previous observations. Coalesced silver particles exhibited an apparent density that was lower compared with that of bulk silver, suggesting a slightly non-spherical particle shape. The mass–mobility scaling exponent of aggregated silver particles determined by the measurements was 2.3 ± 0.1.

Copyright 2015 American Association for Aerosol Research     

Silver Nanowire Penetration Through Screen Filter

Understanding the filtration characteristics of fibrous particles is important since those particles have caused health and environmental concerns. Due to the straight morphology of metal nanowires, unlike carbon nanotube (CNT) particles nanowires can be considered as appropriate test material to evaluate existing filtration theory for cylindrical particles. We measured the penetration of silver nanowires in the size range of d_m = 200 to 400 nm through screen mesh filter. By using Li et al. (2012)'s theory, we determined the orientation status of silver nanowires inside differential mobility analyzer (DMA) and calculated the dynamic shape factor of nanowires. Theoretical penetration was obtained by using single fiber theory with modified interception parameter including orientation angle between a filter wire and a particle. The orientation angle obtained by fitting experimental data into single fiber theory for the 1 layer of screen mesh filter is found to be close to 40° indicating random orientation of nanowires near filter. However, in the experiments with multi-layers of screen mesh, any tendency related to the orientation angle was not found. We performed numerical simulations for the filtration processes such as impaction, diffusion, interception, and interception of diffusing particles by introducing modified slip correction factor. Overall, when interception of diffusing particles is considered in addition to diffusion and interception, numerically simulation results and theoretical prediction agree better with experimental data regarding the penetration of silver nanowires through the 1 layer of screen mesh filter.

Copyright 2014 American Association for Aerosol Research     

Particle Emission Characteristics of a Gas Turbine with a Double Annular Combustor

The total climate, air quality, and health impact of aircraft black carbon (BC) emissions depend on quantity (mass and number concentration) as well as morphology (fractal dimension and surface area) of emitted BC aggregates. This study examines multiple BC emission metrics from a gas turbine with a double annular combustor, CFM56-5B4-2P. As a part of the SAMPLE III.2 campaign, concurrent measurements of particle mobility, particle mass, particle number concentration, and mass concentration, as well as collection of transmission electron microscopy (TEM) samples, allowed for characterization of the BC emissions. Mass- and number-based emission indices were strongly influenced by thrust setting during pilot combustion and ranged from <1 to 208 mg/kg-fuel and 3 ×× 10¹² to 3 ×× 10¹⁶ particles/kg-fuel, respectively. Mobility measurements indicated that mean diameters ranged from 7 to 44 nm with a strong dependence on thrust during pilot-only combustion. Using aggregation and sintering theory with empirical effective density relationships, a power-law relationship between primary particle diameter and mobility diameter is presented. Mean primary particle diameter ranged from 6 to 19 nm; however, laser-induced incandescence (LII) and mass-mobility-calculated primary particle diameters demonstrated opposite trends with thrust setting. Similarly, mass-mobility-calculated aggregate mass specific surface area and LII-measured surface area were not in agreement, indicating both methods need further development and validation before use as quantitative indicators of primary particle diameter and mass-specific surface area.

Copyright 2015 American Association for Aerosol Research     

Ozone-free post-DBD aerosol bipolar diffusion charger: Evaluation as neutralizer for SMPS size distribution measurements

A postplasma neutralizer for submicron particles size measurements by mobility analysis has been evaluated. Bipolar ion currents have been measured downstream a dielectric barrier discharge (DBD) to estimate the ion fluxes at the inlet of charging volume and the n_i·τ product that define the theoretical maximal concentration that can be neutralized. Charge distributions were measured versus DBD voltage, aerosol diameter and concentration for monodisperse aerosols. It is confirmed that the charge distribution of particles depends on the ratio of initial positive and negative ion currents controlled by the DBD voltage leading to a tuneable mean charge of aerosol in this post-DBD bipolar charger. As expected from Gunn's law, the mean charge and the variance are proportional to particle diameter above 50 nm and independent of the aerosol concentration. The size distributions measured with ⁸⁵Kr and post-DBD neutralizer present the same modal diameters and a maximal overestimation of the total concentration of 10%, for aerosol from 15 to 730 nm with concentrations up to 6 × 10¹² m^?3. This post-DBD bipolar charger can be used for submicron aerosol neutralization and thus for scanning mobility particle sizer size distribution measurements in air as well as in nitrogen to suppress ozone downstream DBD.

Copyright © 2017 American Association for Aerosol Research