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We investigated the possibility of using a layer of quantum dots (QDs) deposited on the microparticle surface for the measurement of the charge the microparticle acquires when immersed into a plasma. To that end, we performed the calculations of the Stark shift of the photoluminescence spectrum of QDs caused by the fluctuating local electric field. In our calculations, we assumed the plasma-delivered surplus electrons to be distributed on the surface of a microparticle. According to our calculations, the Stark shift will acquire measurable values when the lifetime of the quasi-stationary configuration of the surplus electrons will be determined by their diffusion along the surface. Experiments with flat QD-covered floating plasma-facing surfaces suggest that measurable Stark shift of the photoluminescence spectrum can be achieved. Based on our model, modern microscopic plasma-surface interaction theories and analysis of the experiments, we suggest the possible design of the charge microsensor, which will allow to measure the charge accumulated on its surface by means of visible-light optics.

The dynamics of carbonaceous nanoparticle (NP) evolution in its cyclic growth process in a capacitively coupled RF plasma is studied using multiple diagnostic methods. We designed a simple method using biased substrates for spatiotemporal collection of growing NPs at different positions inside the particle cloud and at different time steps during the growth cycle. In addition, self-bias voltage and laser light scattering are in situ measured to monitor the nanoparticle growth. Subsequently, the collected nanoparticles are characterized by scanning electron microscopy (SEM). Correlations between the self-bias voltage and SEM results are presented. We show that different threshold potentials are needed to overcome the confinement of the NPs for collection. This is explained with the spatial and temporal variation of the plasma potential, the NP size, and the ion drag inside the particle cloud. Moreover, the arrangement of the locally collected NPs on the substrate is found to depend on the bias voltage applied to it. Finally, we demonstrate the possibility to control the self-organization and deposition patterns of the nanoparticles by changing the substrate orientation.