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Maskaeva  L. N.  Yurk  V. M.  Markov  V. F.  Voronin  V. I. 《Physics of the Solid State》2020,62(10):1949-1959
Physics of the Solid State - Comparative experimental data, using dynamic light scattering methods, scanning electron and atomic force microscopy, on the composition, crystal structure,...  相似文献   
2.
The boundary conditions of the formation of PbSe and concomitant impurity phases, Pb(OH)2 and PbCN2, were determined by calculation of the ionic equilibria in the Pb2+–Na3C5Н6О7–CH4N2Se system. Complex kinetic studies of the PbSe deposition from an ammonia–citrate mixture containing ascorbic acid as antioxidant for selenourea were performed. PbSe films 250 to 425 nm thick were synthesized by the hydrochemical method based on the results obtained. The absence of impurities in the deposited samples was confirmed by X-ray diffraction analysis.  相似文献   
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Spectrophotometric method was used to study the kinetics of the process in which aqueous solutions of selenurea of various compositions are oxidized. Significant differences between the stabilities of selenurea solutions were revealed in relation to the selenurea concentration and also to the acidity, or alkalinity of a medium. It was shown that the stability of selenurea solutions is affected by additives of various antioxidants: sodium sulfite Na2SO3, ascorbic acid C6H8O6, hydroxylamine chloride NH2OH·HCl, hydrazine hydrate N2H4·H2O, and tin chloride SnCl2·2H2O. It was found that using a 1 : 1 mixture of antioxidants Na2SO3 and C6H8O6 substantially raises their antioxidant activity and stabilizes the aqueous solutions of selenurea during up to five days. A hydro-chemical precipitation in the acetate—ethylenediamine reaction system in the presence of the antioxidants under study was used to obtain lead selenide films of stoichiometric composition with thicknesses of 230?670 nm. With the Na2SO3 + C6H8O6, Na2SO3, C6H8O6, and SnCl2 antioxidants used to stabilize selenurea solutions, a tendency is observed toward a decrease in the lattice constants of PbSe films from 6.1531 ± 0.0003 to 6.1367 ± 0.0002 Å, an increase in the share of nanosize particles, and rise in the PbSe energy gap width from 0.78 to 1.0 e V.

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