scholarly journals Roozeboom's Type II of Solid Solution

Nature ◽  
1944 ◽  
Vol 153 (3887) ◽  
pp. 530-530
Author(s):  
A. N. CAMPBELL
Keyword(s):  
Author(s):  
А.А. Семакова ◽  
В.В. Романов ◽  
Н.Л. Баженов ◽  
К.Д. Мынбаев ◽  
К.Д. Моисеев

The results of a study of the electroluminescence of the asymmetric InAs/InAs1−ySby/InAsSbP LED heterostructures with a molar fraction of InSb in the ternary solid solution in the active region y=0.15 and y=0.16 in the temperature range 4.2−300 K are presented. Based on the experimental data, the formation of a staggered type II heterojunction at the InAs1−ySby/InAsSbP heterointerface was determined. The dominant contribution of the interface radiative transitions at the type II heterointerface in the temperature range 4.2−180 K was shown, which makes it possible to minimize the temperature dependence of the operating wavelength of the LEDs.


2017 ◽  
Vol 308 ◽  
pp. 173-180 ◽  
Author(s):  
Julia Wind ◽  
Paula Kayser ◽  
Zhaoming Zhang ◽  
Ivana Radosavljevic Evans ◽  
Chris D. Ling
Keyword(s):  

1997 ◽  
Vol 31 (8) ◽  
pp. 763-767 ◽  
Author(s):  
T. I. Voronina ◽  
T. S. Lagunova ◽  
M. P. Mikhailova ◽  
K. D. Moiseev ◽  
M. A. Sipovskaya ◽  
...  

2008 ◽  
Vol 310 (23) ◽  
pp. 4846-4849 ◽  
Author(s):  
K.D. Moiseev ◽  
V.V. Romanov ◽  
T.I. Voronina ◽  
T.S. Lagunova ◽  
M.P. Mikhailova ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1340
Author(s):  
Angelina V. Zhurenok ◽  
Dina V. Markovskaya ◽  
Evgeny Y. Gerasimov ◽  
Alexander S. Vokhmintsev ◽  
Ilya A. Weinstein ◽  
...  

Two types of photocatalysts, 1%Pt/Cd1−xZnxS/g-C3N4 (x = 0.2–0.3) and Cd1−xZnxS/1%Pt/g-C3N4 (x = 0.2–0.3), were synthesized by varying the deposition order of platinum, and a solid solution of cadmium and zinc sulfides onto the surface of g-C3N4. The characterization of photocatalysts showed that, for 1%Pt/Cd1−xZnxS/g-C3N4, small platinum particles were deposited onto a solid solution of cadmium and zinc sulfides; in the case of Cd1−xZnxS/1%Pt/g-C3N4, enlarged platinum clusters were located on the surface of graphitic carbon nitride. Based on the structure of the photocatalysts, we assumed that, in the first case, type II heterojunctions and, in the latter case, S-scheme heterojunctions were realized. The activity of the synthesized samples was tested in hydrogen evolution from triethanolamine (TEOA) basic solution under visible light (λ = 450 nm). A remarkable increase in hydrogen evolution rate compared to single-phase platinized 1%Pt/Cd1−xZnxS photocatalysts was observed only in the case of ternary photocatalysts with platinum located on the g-C3N4 surface, Cd1−xZnxS/1%Pt/g-C3N4. Thus, we proved using kinetic experiments and characterization techniques that, for composite photocatalysts based on Cd1−xZnxS and g-C3N4, the formation of the S-scheme mechanism is more favorable than that for type II heterojunction. The highest activity, 2.5 mmol H2 g−1 h−1, with an apparent quantum efficiency equal to 6.0% at a wavelength of 450 nm was achieved by sample 20% Cd0.8Zn0.2S/1% Pt/g-C3N4.


2018 ◽  
Vol 60 (3) ◽  
pp. 585
Author(s):  
В.В. Романов ◽  
Э.В. Иванов ◽  
К.Д. Моисеев

AbstractSingle heterostructures of type II n ^+-InA s/n ^0-InAs_0.59Sb_0.16P_0.25, based on an intentionally undoped epitaxial layer with an electronic type of conductivity are obtained by metalorganic vapor phase epitaxy (MOVPE). In the heterostructure, a transition layer of modulated composition is formed near the heterointerface in the bulk of the quaternary solid solution. The existence of a radiative recombination channel due to the presence of localized hole states in quantum wells formed in the transition layer near the heterointerface is shown. It is demonstrated that the maximum of the intensity of the electroluminescence spectrum of the heterostructure under study is rearranged when a forward external bias is applied. The results of this study can be used in the development of tunable light-emitting diodes operating in the midinfrared range of 2–4 μm.


2020 ◽  
Vol 117 (1) ◽  
pp. 107 ◽  
Author(s):  
Xiangyu Wu ◽  
Liang-pin Wu ◽  
Jian-bo Xie ◽  
Ping Shen ◽  
Jian-xun Fu

Te is an alloy element which is capable of improving the morphology of sulfide in free-cutting steel. In this paper, the effect of modification and mechanism of action of Te on sulfide was studied by addition of various Te masses to the Y1Cr13 free-cutting stainless steel. The results revealed that the typical sulfide in Y1Cr13 was MnS, and when Te content exceeded 170 ppm, it was transformed into a solid solution and precipitated as MnTe in Te–Mn–S solution. The solid solution of Te in MnS coarsened MnS and improved its hardness. The precipitated MnTe enveloped MnS and absorbed the rolling stress in high temperature. Both forms of Te improved the morphology of MnS, promoted the transition from type II to type I and III as the Te content increased. The effect of the modification was good, and it was mainly ascribed to the precipitation of MnTe.


2008 ◽  
Vol 42 (12) ◽  
pp. 1403-1407
Author(s):  
V. V. Romanov ◽  
K. D. Moiseev ◽  
T. I. Voronina ◽  
T. S. Lagunova ◽  
Yu. P. Yakovlev

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 593 ◽  
Author(s):  
Jiangang Jiao ◽  
Feng Han ◽  
Liandang Zhao ◽  
Jun Duan ◽  
Mengxi Wang

The Jinchuan Ni-Cu-PGE deposit is the single largest magmatic Ni-sulfide deposit in the world, with three different hypotheses on its ore-forming processes (e.g., in-situ sulfide segregation of sulfide-bearing magma, deep segregation with multiple injections of magma, and hydrothermal superimposition) mainly based on study of whole-rock geochemistry and isotopes (e.g., S-Sr-Nd-Hf). In this study, we mainly concentrated on magnetite textural and geochemical characteristics from different sulfide ores to clarify the genetic types and geochemical difference of the Jinchuan magnetite, and to explore a new credible ore-forming process by magnetite formation process when combined with detailed deposit geology. Three types of magnetite from massive and disseminated sulfide ores were observed by different textural analysis, and they were shown to have different genetic types (mainly in geochemistry) and trace elemental features. Type I magnetite is subhedral to anhedral from massive Ni- (or Fe-) and Cu-rich sulfide ores, with apparent magmatic origin, whereas Type II (dendritic or laminar crystals) and III magnetite (granular crystals as disseminated structures) from disseminated Cu-rich sulfide ores may have precipitated from late stage of melts evolved from a primitive Fe-rich and sulfide-bearing system with magmatic origin, but their geochemistry being typical of hydrothermal magnetite, videlicet, depletions of Ti (< 20 ppm), Al (< 51 ppm), Zr (0.01–0.57 ppm), Hf (0.03–0.06 ppm), Nb (0.01–0.14 ppm), and Ta (0.01–0.21 ppm). Such different types of magnetite can be clearly distinguished from concentrations and ratios of their trace elements, such as Ti, V, Co, Ni, Zn, Zr, Sn, Ga, and Ni/Cr. Those different types of Jinchuan magnetite crystallized from (evolved) sulfide-bearing systems and their geochemistries in trace elements are controlled mainly by evolution of ore-related systems and geochemical parameters (e.g., T and fO2), with the former playing a predominant role. Combining the previous literature with this study, we propose that the Jinchuan deposit formed by multiple pluses of sulfide-bearing magma during fractional crystallization, with the emplacing of more fractionated and sulfide-bearing magma during sulfide segregation playing a predominant role. During this multiple emplacement and evolving of sulfide-bearing systems, Type I magmatic magnetite crystallized from primitive and evolved Fe-rich MSS (monosulfide solid solution), while Type II and III magnetite crystallized from evolved Fe-rich MSS to Cu-rich ISS (intermediate solid solution) during sulfide fractionation, with those Type II and III magnetite having much higher Cu contents compared with that of Type I magnetite.


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