The Effects of Growth Sequence on the Electronic Properties of Al-Ge-Ni Ohmic Contacts on (001) GaAs

1992 ◽  
Vol 281 ◽  
Author(s):  
W. V. Lampert ◽  
T. W. Haas ◽  
E. S. Lambers ◽  
Paul H. Holloway

ABSTRACTThe growth sequence of Al, Ge, and Ni metals was shown to dramatically affect the amount of heat treatment time required to convert the electrical properties from Schottky to ohmic behavior. Differences in the heat treatment times required to convert from rectifying to ohmic contact were dependent on the doping concentration of the contact layer and on the heat treatment temperature. Interdiffusion of component elements and phase formation have been studied to determine the origin of these effects. Auger depth profiles and X-ray diffraction have been used to determine the interdiffusion and phase formation resulting from various types of thermal processing. Elemental profiles and identification of phases of Ni-Ga, Ni-As, and Ni-Ga-Ge will be used to explain the origin of ohmic behavior.

1993 ◽  
Vol 300 ◽  
Author(s):  
W. V. Lampert ◽  
T. W. Haas ◽  
Paul H. Holloway

ABSTRACTThe growth sequence of Al, Ge, and Ni metals has been shown to dramatically affect the amount of heat treatment time required to convert the ohmic contact metallization from Schottky to ohmic behavior. Interpretation of interdiffusion and phase formation of the Al-Ge, Al-Ni, or Ni-Ge thin film couples were measured. Auger depth profiles and thin film X-ray diffraction were used to determine interdiffusion and phase formation resulting from various types of thermal processing. The effects of interdiffusion and formation of phases such as Ni-Ga, Ni-As, Ni-Ga-Ge, and Ni-As-Ge from the two element metallizations on GaAs will be used to explain the origin of ohmic behavior for the ternary Al-Ge-Ni contacts to GaAs.


1992 ◽  
Vol 260 ◽  
Author(s):  
W. V. Lampert ◽  
T. W. Haas ◽  
Paul H. Holloway

ABSTRACTElectrical characterization has demonstrated dramatic differences in the amount of heat treatment time required to convert the ohmic contact metallizations from Schottky to ohmic behavior, depending on the layering sequence of the Al, Ge, and Ni metals. Additional time differences were found to be dependent on the doping concentration of the contact layer of the GaAs and on the heat treatment temperature. For samples with Ge at the metal-semiconductor interface, the time required to convert from Schottky to ohmic behavior varies inversely with the doping concentration of the contact layer and directly with heat treatment temperature. Samples with Ni at the metal-semiconductor interface converted from Schottky to ohmic behavior much faster and had a much smaller dependence on the doping concentration and the heat treatment temperature. Models to explain these observations in terms of interdiffusion of the components and phases formed will be proposed.


2019 ◽  
Vol 798 ◽  
pp. 229-234 ◽  
Author(s):  
Puripat Kantha ◽  
Naris Barnthip ◽  
Kamonpan Pengpat ◽  
Tawee Tunkasiri ◽  
Nuttapon Pisitpipathsin

In this work, the thermal treatment temperature effect on phase formation and bioactivity of glass-ceramics based on the SiO2-Na2O-CaO-P2O5 system has been studied. The chemical composition of the system is 45 wt.% SiO2, 24.5 wt.% Na2O, 24.5 wt.% CaO and 6 wt.% P2O5 (45S5). The rice husk ash is used as the natural raw materials instead of commercial SiO2. All of the investigated compositions were prepared by melting the glass mixtures at 1350°C for 3 h. The resulting glass samples were heated at different thermal treatment temperatures ranging from 750 to 1050°C with fixed dwell-time for 4 h for crystallization. Phase identification of the 45S5 glass ceramics was carried out by X-Ray diffraction (XRD). Moreover, the physical properties such as density, porosity and mechanical properties were systematically investigated. It was found that, the increasing of heat treatment temperature led to the increasing of the Na2Ca2Si3O9 phase and obtaining better bioactive behavior after incubation of glass-ceramics in simulated body fluid (SBF) for 7 days. The maximum hardness value of 4.02 GPa was achieved after heating at 1050°C for 4 h. However, the density value has slightly changed with various heat treatment temperatures.


MRS Advances ◽  
2018 ◽  
Vol 3 (11) ◽  
pp. 563-567 ◽  
Author(s):  
Quentin Altemose ◽  
Katrina Raichle ◽  
Brittani Schnable ◽  
Casey Schwarz ◽  
Myungkoo Kang ◽  
...  

ABSTRACTTransparent optical ZnO–Bi2O3–B2O3 (ZBB) glass-ceramics were created by the melt quenching technique. In this work, a melt of the glass containing stoichiometric ratios of Zn/Bi/B and As was studied. Differential scanning calorimeter (DSC) measurements was used to measure the thermal behavior. VIS/NIR transmission measurements were used to determine the transmission window. X-ray diffraction (XRD) was used to determine crystal phase. In this study, we explore new techniques and report a detailed study of in-situ XRD of the ZBB composition in order to correlate nucleation temperature, heat treatment temperature, and heat treatment duration with induced crystal phase.


2007 ◽  
Vol 124-126 ◽  
pp. 1031-1034
Author(s):  
Bong Soo Jin ◽  
Bok Ki Min ◽  
Chil Hoon Doh

To find out suitable Si surface treatment and heat treatment conditions, acid treatment of Si wafer was done for lithium polysilicate electrolyte coating on Si wafer. In case of HCl treatment, the wet angle of a sample is 30o, which is the smallest wet angle of other acid in this experiment. Acid treatment time is 10 min, which is no more change of wet angle. Lithium polysilicate electrolyte was synthesized by hydrolysis and condensation of lithium silicate solution using perchloric acid. Thermal analysis of lithium polysilicate electrolyte shows the weight loss of ~23 % between 400 and 500 , which is due to the decomposition of LiClO4. The XRD patterns of the obtained lithium polysilicate electrolyte also show the decrement of LiClO4 peak at 400 . The optimum heat treatment temperature is below 400 , which is the suitable answer for lithium polysilicate electrolyte.


2020 ◽  
pp. 0734242X2095740
Author(s):  
Haijun Bi ◽  
Huabing Zhu ◽  
Lei Zu ◽  
Yong Gao ◽  
Song Gao ◽  
...  

Spent lithium iron phosphate (LFP) batteries contain abundant strategic lithium resources and are thus considered attractive secondary lithium sources. However, these batteries may contaminate the environment because they contain hazardous materials. In this work, a novel process involving low-temperature heat treatment is used as an alternative pretreatment method for recycling spent LFP batteries. When the temperature reaches 300°C, the dissociation effect of the anode material gradually improves with heat treatment time. At the heat treatment time of 120 minutes, an electrode material can be dissociated. The extension of heat treatment time has a minimal effect on quality loss. The physicochemical changes in thermally treated solid cathode and anode materials are examined through scanning electron microscopy with energy-dispersive X-ray spectroscopy. The heat treatment results in the complete separation of the materials from aluminium foil without contamination. The change in heat treatment temperature has a small effect on the quality of LFP material shedding. When the heat treatment temperature reaches 300°C and the time reaches 120 minutes, heat treatment time increases, and the yield of each particle size is stable and basically unchanged. The method can be scaled up and may reduce environmental pollution due to waste LFP batteries.


2019 ◽  
Vol 285 ◽  
pp. 146-152
Author(s):  
Nai Yong Li ◽  
Han Xiao ◽  
Chi Xiong ◽  
De Hong Lu ◽  
Rong Feng Zhou

The semi-solid extruded ZCuSn10P1 copper alloy were annealed at different temperatures and time. The influences of heat treatment temperature and holding time on the microstructure of semi-solid ZCuSn10P1 copper alloy were investigated. The results show that with the increase of heat treatment temperature, the morphology of the semi-solid microstructure was improved, the sharp angle around the primary phase α-Cu and the liquid droplets were reduced. With the increase of heat treatment time, the solid-liquid segregation of the semi-solid structure was improved. The average grain size of the solid phase increased with the increasing of the holding time. After heat treatment, the solid solubility of the primary phase α-Cu increased, and the Sn and P elements in the liquid phase continued to diffuse to the primary phase α-Cu. The microstructure of semi-solid copper alloy was the most uniform after heat treatment at 350°C for 120 min.


2012 ◽  
Vol 184-185 ◽  
pp. 1175-1180
Author(s):  
Guo Liang Li ◽  
Xiao Hua Jie ◽  
Bi Xue Yang

Amorphous Cr–C alloy coating was prepared by electrodepositing. The microhardness of the coating was tested after annealing from 100°C to 800°C and the crystallization evolution was studied by the analysis of X-ray diffraction (XRD) and differential scanning caborimetry (DSC). The results showed that the crystallization evolution of the coating began at 300°C and finished around 450°C, and intermetallic compound Cr7C3and Cr23C6appeared when heat treatment temperature reached around 600°C. The microhardness, corrosion resistance as well as the adhesion of the coating all increased first with the temperature and then dropped until it attained the proper values. The microhardness reached the maximum of 1610HV0.025at 600°C. While the corrosion resistance and the adhesion force attained the peak value at about 400°C.


Author(s):  
Shouyu Zhang ◽  
Junfu Lu ◽  
Jianmin Zhang ◽  
Qing Liu ◽  
Guangxi Yue

The effect of heat treatment on the reactivity and crystallinity of char prepared from the vitrinite of two coals (YX, JJ) was investigated by using XRD and TGA in this paper. The results from TGA show that the reactivity of the chars from YXV and JJV decreases with the increase of heat treatment temperature. The reactivity of YXV char decreases quickly and significantly as heat treatment time increases. However, after heat treatment time of 60 min, it decreases slowly. The effect of heat treatment time on the reactivity of JJV char is small. The results from XRD show that the crystallinity of coal-char is determined by the intensity of heat treatment. When heat treatment time is more than 60 minutes, the turbostratic crystallite of YXV char prepared under 900°C changes remarkably and becomes more orderly. The aromatic layer stacking heights (Lc) of YXV Char when heat treated above 900°C increased with the increase of heat treatment time. The effect of heat treat time on Lc of JJV char is small, but under heat treatment temperature of 1200°C, the crystalline of JJV char grows distinctly. There is a good parallel relationship between the crystalline growth and deactivation of the chars. It can be concluded that the growth of the crystalline is the main reason for the deactivation of coal-char.


2017 ◽  
Vol 46 (5) ◽  
pp. 356-361 ◽  
Author(s):  
Liliya Frolova ◽  
Alexander Pivovarov ◽  
Tatyana Butyrina

Purpose The purpose of this work is to study the patterns of pigment colour formation and to develop metal compositions for obtaining spinels using the precipitation and heat treatment methods. Design/methodology/approach Precursor materials were prepared using co-precipitation method. Phase composition of pigments were determined by X-ray diffraction. Colour of pigments was determined spectrophotometry. Modelling of colour formation was performed using simplex method. Planning in the future to carry out full synthesis of pigments of blue, red and yellow colours. Findings The paper deals with the results of theoretical and experimental research on the synthesis pigments of blue, red and yellow colours based on Fe-Co-Al-O spinel. The influence of the chromophore cation content and the heat treatment temperature on optical and colour characteristics of pigments were studied. Originality/value The resulting composition-property diagrams make it possible to evaluate the effect of chromophore cations and heat treatment on the colour formation for Fe2O3-Al2O3-CoO system. Crystal-phase composition of the pigments is installed and its relationship with the optical colour characteristics. That makes it possible carry out targeted synthesis of pigments blue, red and yellow colours in further. The phase composition of pigments and its relationship with optical and colour properties has been established thus enabling the directed synthesis of blue, red and yellow pigments.


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