Neon Atomic Spectrum Measurement Based on the Frank-Hertz Experiment

Author(s):  
Jinghua Sun ◽  
Xiao Zhang ◽  
Guangkuo Guo
2021 ◽  
Vol 103 (3) ◽  
Author(s):  
M. Andriamirado ◽  
A. B. Balantekin ◽  
H. R. Band ◽  
C. D. Bass ◽  
D. E. Bergeron ◽  
...  

Electronics ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 65
Author(s):  
Quan Zhao ◽  
Ling Tong ◽  
Bo Gao

The classical two-channel push-pull chirp transform spectrometer (CTS) has been widely applied in satellite-borne remote sensing systems for earth observation and deep space exploration. In this paper, we present two simplified structures with single M(l)-C(s) CTS arrangements for the spectral analysis of stationary signals. A simplified CTS system with a single M(l)-C(s) arrangement and a time delay line was firstly developed. Another simplified structure of CTS with a M(l)-C(s) arrangement and a frequency conversion channel was also developed for spectral analysis of stationary signals. Simulation and experiment results demonstrate that the two simplified arrangements can both realize spectrum measurement for the stationary signals and obtain the same frequency resolution, amplitude accuracy and system sensitivity as that of the classical two-channel push–pull CTS system. Compared to the classical CTS structure, the two simplified arrangements require fewer devices, save power consumption and have reduced mass. The matching problem between the two channels can be avoided in the two simplified arrangements. The simplified CTS arrangements may have potential application in the spectrum measurement of stationary signals in the field of aviation and spaceflight.


2021 ◽  
Vol 1739 ◽  
pp. 012035
Author(s):  
Shuifa Shen ◽  
Feipeng Wang ◽  
Yupeng Yan ◽  
Jiejie Shen ◽  
Yan Li ◽  
...  

2015 ◽  
Vol 23 (22) ◽  
pp. 29245 ◽  
Author(s):  
Qian Zhou ◽  
Jie Qin ◽  
Weilin Xie ◽  
Zhangweiyi Liu ◽  
Yitian Tong ◽  
...  

1990 ◽  
Vol 201 ◽  
Author(s):  
Honglie Shen ◽  
Genqing Yang ◽  
Zuyao Zhou ◽  
Guanqun Xia ◽  
Shichang Zou

AbstractDual implantations of Si+ and P+ into InP:Fe were performed both at 200°C and room temperature. Si+ ions were implanted by 150keV with doses ranging from 5×1013 /cm2 to 1×1015 /cm2, while P+ ions were implanted by 110keV. 160keV and 180keV with doses ranging from 1×l013 /cm2 to 1×1015 /cm2. Hall measurements and photoluminescence spectra were used to characterize the silicon nitride encapsulated annealed samples. It was found that enhanced activation can be obtained by Si+ and P+ dual implantations. The optimal condition for dual implantations is that the atomic distribution of implanted P overlaps that of implanted si with the same implant dose. For a dose of 5×l014 /cm2, the highest activation for dual implants is 70% while the activation for single implant is 40% after annealing at 750°C for 15 minutes. PL spectrum measurement was carried out at temperatures from 11K to 100K. A broad band at about 1.26eV was found in Si+ implanted samples, of which the intensity increased with increasing of the Si dose and decreased with increasing of the co-implant P+ dose. The temperature dependence of the broad band showed that it is a complex (Vp-Sip) related band. All these results indicate that silicon is an amphoteric species in InP.


Three lines in the atomic spectrum of tin, λ 3262 Å, λ 3283 Å and λ 6454Å have been studied in emission under high resolution with the use of light sources containing enriched isotopic samples. Results are reported for isotope shifts in these lines for the abundant stable isotopes ( A ≽ 116). Pressure-scanned Fabry–Perot etalons provided the necessary resolution; the spectrograms for λ 6454 Å were recorded and analysed by digital techniques, and for this line hyperfine structure constants required in the interpretation of the data were also evaluated. The results for the three lines are not in good agreement with earlier work, but are shown to be self-consistent by means of a King plot. Their interpretation in terms of the nuclear charge distribution is considered in the following paper.


Author(s):  
Robert T Devine ◽  
Leonard L Romero ◽  
Devin W Gray ◽  
David T Seagraves ◽  
Richard H Olsher ◽  
...  

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