Abstract
While plasmas are now routinely employed to synthesize or remove nano- to micron-sized particles, the charge state (polarity and magnitude) of the particles remains relatively unknown. In this study, charging of nanoparticles was systematically characterized in low-temperature, atmospheric-pressure, flow-through plasmas previously applied for synthesis. Premade, charge-neutral nanoparticles of MgSO4, NaCl, and sea salt were introduced into the plasma to decouple other effects such as the reactive vapor precursor, and MgSO4 was selected as the focus because of its stability (i.e., no evaporation) in the plasma environment. The charge fraction and distribution of the particles was examined at the reactor outlet for different particle diameters (10–250 nm) as a function of plasma power and two types of power source, alternating current (AC) and radio frequency (RF). We found that the overall charge fraction increased with increasing plasma power and diameter for the RF plasma. A similar increasing trend was observed for the AC plasma with increasing particle diameter in the range of 50–250 nm, but the charge fraction increased with decreasing particle diameter in the range of 10–50 nm. The charge distribution was revealed to be bipolar, with particles supporting multiple charges for both the RF and AC plasmas, but the RF plasma produced a higher fraction of multiple charges. Differences in the characteristic timescales for particle charging in the AC and RF plasmas are a possible explanation of the trends observed in the experiments.
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