The creation of a spatially extended stable DC complex plasma crystal is a big experimental challenge and a topical area of research in the field of dusty plasmas. In this paper we describe a newly built and commissioned dusty plasma experimental (DPEx-II) device at the Institute for Plasma Research. The device can support the formation of large sized Coulomb crystals in a DC glow discharge plasma. The plasma in this L-shaped table-top glass chamber is produced between a circular anode and a long tray shaped cathode. It is characterized with the help of various electrostatic probes over a range of discharge conditions. The dust particles are introduced by a dust dispenser to form a strongly coupled Coulomb crystal in the cathode sheath region. The unique asymmetric electrode configuration minimizes the heating of dust particles and facilitates the formation of crystalline structures with a maximum achievable dimension of 40 cm × 15 cm using this device. A larger crystal has numerous advantages over smaller ones, such as higher structural homogeneity, fewer defects, lower statistical errors due to finite size effects etc. A host of diagnostics tools are provided to characterize the Coulomb crystal. Results of a few initial experiments aimed at demonstrating the technical capabilities of the device and its potential for future dusty plasma research, are reported.
In this work, concept of virtual cathode and its existence in dusty plasma has been studied by theoretical and numerical analysis. Using basic equations of charge dust, ions, and electrons, the non‐monotonic behaviour of the potential in presence of charged dust has been calculated and plotted as a function of dust density. It has been found that there is a change in potential between cathode and sheath potential and subsequently changes the threshold wall temperature as compared to that of without dust conditions. The threshold wall temperature has been increased due to the ability of micro‐particles acquiring electron charge and hence, reducing potential at the wall. Further, for different values of α (depends on dust density); threshold temperature remained the same for observed virtual cathode. Hence, behaviour of potential has been plotted as a function of α with increasing wall temperatures for two dust charge values (1 and 1,000). Considering no dust charge, it has been observed that, at lower dust density, double layer like structure is formed near the emissive wall. But this double layer structure gets diminishes with increasing dust density. Hence, below a threshold dust density, virtual cathode near to the emissive wall is not possible. While for Zd = 1,000, the formation of virtual cathode appeared even at very small dust density. However, irrespective of variation of potential difference near the wall and existence of virtual cathode at different emission regime the threshold wall temperature remains same. Effect of dust potential dependency on threshold wall temperature has also been discussed in this study.
We report the measurement of photoexcitation cross-sections of three firststep uranium transitions (0 → 16900.38 cm −1 , 0 → 17361.89 cm −1 and 620 → 17361.89 cm −1 ) using saturation method. These measurements were performed on a resonance ionization mass spectrometry (RIMS) set-up consisting of Nd:YAG-pumped dye lasers, a reflectron time-of-flight mass spectrometer and high-temperature atomic vapour source. The uranium vapours were excited and photoionized by two-colour, three-photon photoionization scheme using Nd:YAG-pumped dye laser system. The resultant photoion signal was monitored as a function of dye laser fluence used for first step excitation to measure the excitation cross-section values. A new approach was adopted to overcome the large uncertainties associated with such measurements. With this approach the crosssection of transitions whose value is already reported in the literature was measured as a bench mark. By normalizing the measured value to the reported value, a scaling factor was derived. This scaling factor was used to scale up the cross-section values of other transitions measured by this method.
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