scholarly journals Non-Contact Determination of Free Carrier Concentration in n-GaInAsSb

2003 ◽  
Vol 799 ◽  
Author(s):  
James E. Maslar ◽  
Wilbur S. Hurst ◽  
Christine A. Wang ◽  
Daniel A. Shiau

ABSTRACTGaSb-based semiconductors are of interest for mid-infrared optoelectronic and high-speed electronic devices. Accurate determination of electrical properties is essential for optimizing the performance of these devices. However, electrical characterization of these semiconductors is not straightforward since semi-insulating (SI) GaSb substrates for Hall measurements are not available. In this work, the capability of Raman spectroscopy for determination of the majority carrier concentration in n-GaInAsSb epilayers was investigated. Raman spectroscopy offers the advantage of being non-contact and spatially resolved. Furthermore, the type of substrate used for the epilayer does not affect the measurement. However, for antimonide-based materials, traditionally employed Raman laser sources and detectors are not optimized for the analysis wavelength range dictated by the narrow band gap of these materials. Therefore, a near-infrared Raman spectroscopic system, optimized for antimonide-based materials, was developed.Ga0.85In0.15As0.13Sb0.87 epilayers were grown by organometallic vapor phase epitaxy with doping levels in the range 2 to 80 × 1017 cm-3, as measured by secondary ion mass spectrometry. For a particular nominal doping level, epilayers were grown both lattice matched to n-GaSb substrates and lattice-mismatched to SI GaAs substrates under nominally identical conditions. Single magnetic field Hall measurements were performed on the epilayers grown on SI GaAs substrates, while Raman spectroscopy was used to measure the carrier concentration of epilayers grown on GaSb and the corresponding SI GaAs substrates. Contrary to Hall measurements, Raman spectra indicated that the GaInAsSb epilayers grown on GaSb substrates have higher free carrier concentrations than the corresponding epilayers grown on SI GaAs substrates under nominally identical conditions. This is contrary to the assumption that for nominally identical growth conditions, the resulting carrier concentration is independent of substrate, and possible mechanisms will be discussed.

1997 ◽  
Vol 134 (1-2) ◽  
pp. 272 ◽  
Author(s):  
P. Weinmann ◽  
G. Menard ◽  
B. Lacroix ◽  
L. Delaigue ◽  
M. Jouan ◽  
...  

2008 ◽  
Vol 34 (1) ◽  
pp. 37-39 ◽  
Author(s):  
O. S. Komkov ◽  
A. N. Pikhtin ◽  
Yu. V. Zhilyaev ◽  
L. M. Fedorov

1998 ◽  
Vol 6 (A) ◽  
pp. A35-A44 ◽  
Author(s):  
R.A. Taylor

A new fiber optic sensor was developed to measure the mass of optically thin cotton samples by integrating light transmission and reflectance signals. High speed measurements of cotton strength requires an accurate determination of the specimen mass without use of laborious cut-and-weigh methods. A previous high speed sensor measured changes in visible light transmission which required secondary measurements of fiber fineness to adjust the data for light scattering. Fiber orientation also affected scattering which required a precise control on specimen preparation. The new sensor measures fiber specimen transflectance using near infrared light. Because cellulose (the basic compound in cotton) exhibits strong absorption bands, its concentration can be accurately measured using near infrared absorbance. In this report we show that an integratinq sensor gave the best measurement of cotton fiber mass. Additionally, we demonstrated its accuracy over a wide range of fiber orientations using a novel fiber specimen tension experiment.


PLoS ONE ◽  
2012 ◽  
Vol 7 (2) ◽  
pp. e32406 ◽  
Author(s):  
Narahara Chari Dingari ◽  
Gary L. Horowitz ◽  
Jeon Woong Kang ◽  
Ramachandra R. Dasari ◽  
Ishan Barman

1998 ◽  
Author(s):  
Stephen Rudin ◽  
Afshin Divani ◽  
Ajay K. Wakhloo ◽  
Baruch B. Lieber ◽  
William Granger ◽  
...  

2019 ◽  
Vol 89 (23-24) ◽  
pp. 4875-4883 ◽  
Author(s):  
Jing Huang ◽  
Chongwen Yu

The rapid and accurate determination of flax fiber composition is necessary for its application, but until now it has mainly been tested by the wet chemical method, which is time-consuming and not environmentally friendly. In this paper, near-infrared (NIR) spectroscopy was studied to determinate the main composition of flax, in which 43 flax samples were tested according to the traditional Chinese wet chemical component test standard. Five sets of spectra were generated to show the characteristic of each sample; in total 215 spectra sets were collected using a Fourier transform near-infrared spectrometer. The methods of partial least squares (PLS) and principal component regression (PCR) were used to establish the relationships between the data from the chemical and NIR methods. PLS proved to be a better quantitative method than PCR, based on the value of the coefficient of multiple determination for calibration ( Rc2) and prediction ( Rp2), the ratio of performance to standard deviate (RPD) and the root mean square error of prediction (RMSEP). With the best pretreatment method, the spectral range of 10,000–4000 cm–1yielded a better predictive result than the full range, with Rc2of 0.968, Rp2of 0.955, RMSEP of 1.060%, RPD of 4.641 for cellulose and Rc2of 0.958, Rp2of 0.906, RMSEP of 0.678%, RPD of 3.305 for hemicellulose, while the spectral range 6900–5600 cm–1yielded a better predictive result with Rc2of 0.936, Rp2of 0.769, RMSEP of 0.455%, and RPD of 2.366 for lignin. The study shows that NIR models can provide a simple and fast way to analyze flax fiber composition, which is also beneficial to evaluate its quality.


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