scholarly journals Polyatomic Ion-Induced Electron Emission (IIEE) in Electrospray Thrusters

Aerospace ◽  
2020 ◽  
Vol 7 (11) ◽  
pp. 153
Author(s):  
Jared M. Magnusson ◽  
Adam L. Collins ◽  
Richard E. Wirz

To better characterize the lifetime and performance of electrospray thrusters, electron emission due to electrode impingement by the propellant cation 1-ethyl-3-methylimidazolium (EMI+) has been evaluated with semi-empirical modeling techniques. Results demonstrate that electron emission due to grid impingement by EMI+ cations becomes significant once EMI+ attains a threshold velocity of ∼9×105 cm s−1. The mean secondary electron yield, γ¯, exhibits strong linearity with respect to EMI+ velocity for typical electrospray operating regimes, and we present a simple linear fit equation corresponding to thruster potentials greater than 1 kV. The model chosen for our analysis was shown to be the most appropriate for molecular ion bombardments and is a useful tool in estimating IIEE yields in electrospray devices for molecular ion masses less than ∼1000 u and velocities greater than ∼106 cm s−1. Droplet-induced electron emission (DIEE) in electrospray thrusters was considered by treating a droplet as a macro-ion, with low charge-to-mass ratio, impacting a solid surface. This approach appears to oversimplify back-spray phenomena, meaning a more complex analysis is required. While semi-empirical models of IIEE, and the decades of solid state theory they are based upon, represent an invaluable advance in understanding secondary electron emission in electrospray devices, further progress would be gained by investigating the complex surfaces the electrodes acquire over their lifetimes and considering other possible emission processes.

2021 ◽  
Vol 11 (11) ◽  
pp. 4801
Author(s):  
Xiangping Zhu ◽  
Junjiang Guo ◽  
Xiangxin Li ◽  
Rundong Zhou ◽  
Dan Wang ◽  
...  

MgO is a kind of high secondary electron yield (SEY) material with important applications in electron multipliers. MgO coatings can be used as the electron emission layer for multiplier dynode to improve the electron gain significantly. However, the SEY investigation on ultrathin MgO coatings is not complete and needed to be supplemented urgently. In this work, a series of MgO coatings with increasing thickness were prepared by atomic layer deposition. SEY properties and energy spectra were characterized, and the effect of coating thickness on SEY was systematically analyzed. Experimental results show that SEY of MgO/Si samples rises as the coating thickness increases. Merely, SEY almost does not change with the coating thickness when the thickness exceeds 30 nm. Then, a SEY semi-empirical theory was employed to interpret the SEY regularities of MgO coatings by regarding the coating samples as ideal double-layer structures. Theoretical calculation quantitatively explained the SEY variation observed during the experiments, and further quantified the SEY contribution level of top coating and bottom substrate for the 1 nm and 20 nm MgO coatings. The work is of great significance for comprehending the SEY of ultrathin MgO coatings and expanding the applications of nanoscale coatings with high SEY.


Author(s):  
R. D. Heidenreich

This program has been organized by the EMSA to commensurate the 50th anniversary of the experimental verification of the wave nature of the electron. Davisson and Germer in the U.S. and Thomson and Reid in Britian accomplished this at about the same time. Their findings were published in Nature in 1927 by mutual agreement since their independent efforts had led to the same conclusion at about the same time. In 1937 Davisson and Thomson shared the Nobel Prize in physics for demonstrating the wave nature of the electron deduced in 1924 by Louis de Broglie.The Davisson experiments (1921-1927) were concerned with the angular distribution of secondary electron emission from nickel surfaces produced by 150 volt primary electrons. The motivation was the effect of secondary emission on the characteristics of vacuum tubes but significant deviations from the results expected for a corpuscular electron led to a diffraction interpretation suggested by Elasser in 1925.


Author(s):  
T. Koshikawa ◽  
Y. Fujii ◽  
E. Sugata ◽  
F. Kanematsu

The Cu-Be alloys are widely used as the electron multiplier dynodes after the adequate activation process. But the structures and compositions of the elements on the activated surfaces were not studied clearly. The Cu-Be alloys are heated in the oxygen atmosphere in the usual activation techniques. The activation conditions, e.g. temperature and O2 pressure, affect strongly the secondary electron yield and life time of dynodes.In the present paper, the activated Cu-Be dynode surfaces at each condition are investigated with Scanning Auger Microanalyzer (SAM) (primary beam diameter: 3μmϕ) and SEM. The commercial Cu-Be(2%) alloys were polished with Cr2O3 powder, rinsed in the distilled water and set in the vacuum furnance.Two typical activation condition, i.e. activation temperature 730°C and 810°C in 5x10-3 Torr O2 pressure were chosen since the formation mechanism of the BeO film on the Cu-Be alloys was guessed to be very different at each temperature from the results of the secondary electron emission measurements.


Author(s):  
E. F. Lindsey ◽  
C. W. Price ◽  
E. L. Pierce ◽  
E. J. Hsieh

Columnar structures produced by DC magnetron sputtering can be altered by using RF biased sputtering or by exposing the film to nitrogen pulses during sputtering, and these techniques are being evaluated to refine the grain structure in sputtered beryllium films deposited on fused silica substrates. Beryllium is brittle, and fractures in sputtered beryllium films tend to be intergranular; therefore, a convenient technique to analyze grain structure in these films is to fracture the coated specimens and examine them in an SEM. However, fine structure in sputtered deposits is difficult to image in an SEM, and both the low density and the low secondary electron emission coefficient of beryllium seriously compound this problem. Secondary electron emission can be improved by coating beryllium with Au or Au-Pd, and coating also was required to overcome severe charging of the fused silica substrate even at low voltage. The coating structure can obliterate much of the fine structure in beryllium films, but reasonable results were obtained by using the high-resolution capability of an Hitachi S-800 SEM and either ion-beam coating with Au-Pd or carbon coating by thermal evaporation.


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