Positive and negative ions produced by radioactive sources and corona discharges in gases find a number of applications, including charging aerosol particles prior to their measurement by electrical and/or electrical mobility techniques. The degree to which these ions can charge aerosol particles depends on their mobility and mass; properties that are strongly affected by the composition of the carrier gas and the impurities that it contains. We show that when the purity of the carrier gas is increased, the mobility of both positive and negative ions increases by more than 50%, whereas the respective masses reduce by more than 50%. In most cases, the dominant positive species is N ₄ ⁺, whereas NO ₂ ^- and NO ₃ ^- prevail for the negative polarity. Differences in ion mobility and mass resulting from the two ionization methods (i.e., radioactive source and corona discharges) remain limited. When volatile methyl siloxanes (VMS) are introduced deliberately to the gas, the mobility of the cations decreases by 39% and their mass increases by 385%, while the dominant mobility and mass peaks of the negative ions remains almost unaffected. Interestingly, introduction of VMS also leads to consistent and reproducible positive ion properties across all variations of the experiments, which can be especially relevant for charging aerosol particles in a reproducible manner. Taken together, the new measurements we report in this paper corroborate prior knowledge that the composition and purity of the carrier gas strongly influence the properties of positive and negative ions generated in aerosol neutralizers, and provide new evidence regarding their evolution in the presence of impurities.

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Spark ablation is a highly effective and versatile method for producing nanoparticles from bulk conductive electrode materials. For a number of applications, however, the production throughput of the process needs to be increased with respect to the current state of the art. Here we show that this can be achieved by decreasing the diameter of the employed bulk-material electrodes from ca. 12 to 0.15 mm, corroborating previous observations, and demonstrate that the throughput is associated with the ablation efficiency (i.e., the energy spent to produce nanoparticles per total input energy) that respectively increases by a factor of 10. It is also shown that the commonly used theory for predicting the mass of nanoparticles produced by spark ablation cannot capture this effect, and thus we extend it to account for heat losses that affect the process when electrode diameter reduces below ca. 2 mm. Through this exercise we also show that reduced heat losses associated with thinner electrodes provide an effective recipe to increase the ablation efficiency, also referred as the nanoparticle production yield. The new extended theory for estimating spark ablation nanoparticle mass production throughput is also accompanied by an empirical equation predicting its dependence on electrode diameter.

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Experimental evidence shows that hydroxylated metal ions are often produced during cluster synthesis by atmospheric pressure spark ablation. In this work, we predict the ground state equilibrium structures of AgOkHm± clusters (k and m = 1–4), which are readily produced when spark ablating Ag, using the coupled cluster with singles and doubles (CCSD) method. The stabilization energy of these clusters is calculated with respect to the dissociation channel having the lowest energy, by accounting perturbative triples corrections to the CCSD method. The interatomic interactions in each of the systems have been investigated using the frontier molecular orbital (FMO), natural bond orbital (NBO) and quantum theory of atoms in molecules (QTAIM) methods. Many of the ground states of these ionic clusters are found to be stable, corroborating experimental observations. We find that clusters having singlet spin states are more stable in terms of dissociation than the clusters that have doublet or triplet spin states. Our calculations also indicate a strong affinity of the ionic and neutral Ag atom towards water and hydroxyl radicals or ions. Many 3-center, 4-electron (3c/4e) hyperbonds giving rise to more than one resonance structure are identified primarily for the anionic clusters. The QTAIM analysis shows that the O–H and O–Ag bonds in the clusters of both polarities are respectively covalent and ionic. The FMO analysis indicates that the anionic clusters are more reactive than the cationic ones. Using the cluster structures predicted by the CCSD method, we calculate the collision cross sections of the AgOkHm± family, with k and m ranging from 1 to 4, by the trajectory method. In turn, we predict the electrical mobilities of these clusters when suspended in helium at atmospheric pressure and compare them with experimental measurements.@en

Silver oxide cluster cations (AgnOm+) can readily be produced by a number of methods including atmospheric-pressure spark ablation of pure silver electrodes when trace amounts of oxygen are present in the carrier gas. Here we determine the equilibrium geometries of AgnOm+ clusters (n = 1-4; m = 1-5) using accurate coupled cluster with singles and doubles (CCSD) method, while the stabilization energies are calculated with additional perturbative triples correction (CCSD(T)). Although a number of stable states have been identified, our results show that the AgnOm+ clusters with m = 1 are more stable than those with m ≥ 2 due to the absence of the terminally attached O2 molecule, corroborating recent observations by mass spectrometry. Using the computed structures, we calculate the electrical mobilities of the AgnOm+ clusters and label the values on a respective experimentally determined spectrum in an attempt to better interpret the occurrence of the peaks and troughs in the measurements.

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The potential of using atmospheric-pressure spark ablation for production of atomic clusters has been shown in the recent past. In this study we used this method to produce atomic clusters in Argon and investigated their chemical composition with an atmospheric pressure interface time-of-flight mass spectrometer (APi-TOF-MS). Both anionic and cationic silver and gold clusters were generated and characterised. The carrier gas was used directly from the gas cylinder without the application of any additional gas purification. As a result, the carrier gas stream contained trace impurities of N₂, O₂, and H₂O, as well as radicals such as O, OH, and H and their ionized forms resulting from the plasma created by the sparks. The experimental results show that different reactivities towards oxygen and water traces can be observed depending on the number of metal atoms in the clusters, their polarity, as well as their compositions; e.g., Au_n⁻ shows less reactive behaviour towards oxygen and hydrogen compared to Ag_n⁻. The results also show that certain cluster types can be generated at large enough quantities by atmospheric-pressure spark ablation, which considering the low installation and operating cost of the technique can pave the way towards its exploitation for numerous technological applications.

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