Academic literature on the topic 'Atomic layer epitaxy ZnS'

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Journal articles on the topic "Atomic layer epitaxy ZnS"

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Hyvärinen, Jaakko, Martti Sonninen, and Runar Törnqvist. "Mass spectrometry study of ZnS atomic layer epitaxy process." Journal of Crystal Growth 86, no. 1-4 (January 1988): 695–99. http://dx.doi.org/10.1016/0022-0248(90)90797-o.

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Wu, Yi-hong, Takashi Toyoda, Yoichi Kawakami, Shizuo Fujita, and Shigeo Fujita. "Atomic Layer Epitaxy of ZnS on GaAs Substrates by Metalorganic Molecular Beam Epitaxy." Japanese Journal of Applied Physics 29, Part 2, No. 5 (May 20, 1990): L727—L730. http://dx.doi.org/10.1143/jjap.29.l727.

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Oikkonen, M., T. Tuomi, and M. Luomajärvi. "Density of ZnS thin films grown by atomic layer epitaxy." Journal of Applied Physics 63, no. 4 (February 15, 1988): 1070–74. http://dx.doi.org/10.1063/1.340009.

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Tadokoro, Toyoyasu, Shin-ichi Ohta, Takashi Ishiguro, Yukio Ichinose, Satoshi Kobayashi, and Naoki Yamamoto. "Atomic layer epitaxy growth of ZnS on (100)GaAs using molecular beam epitaxy system." Journal of Crystal Growth 148, no. 3 (March 1995): 223–31. http://dx.doi.org/10.1016/0022-0248(94)00149-g.

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Ihanus, Jarkko, Mikko Ritala, Markku Leskelä, Thomas Prohaska, Roland Resch, Gernot Friedbacher, and Manfred Grasserbauer. "AFM studies on ZnS thin films grown by atomic layer epitaxy." Applied Surface Science 120, no. 1-2 (November 1997): 43–50. http://dx.doi.org/10.1016/s0169-4332(97)00226-2.

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Kim, Y. G., Y. S. Nam, K. S. Baek, and S. K. Chang. "Structural properties of ZnS/GaAs epilayers grown by atomic-layer epitaxy." Current Applied Physics 9, no. 6 (November 2009): 1304–6. http://dx.doi.org/10.1016/j.cap.2008.10.010.

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Koukitu, Akinori, Takayuki Miyazawa, Hitoshi Ikeda, and Hisashi Seki. "Atmospheric pressure atomic layer epitaxy of ZnS using Zn and H2S." Journal of Crystal Growth 123, no. 1-2 (September 1992): 95–100. http://dx.doi.org/10.1016/0022-0248(92)90013-9.

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Hsu, Chin-Tsar, M. Yokoyama, and Y. K. Su. "Growth of znse/zns strained-layer superlattice on si substrates by atomic layer epitaxy." Materials Chemistry and Physics 51, no. 2 (November 1997): 102–6. http://dx.doi.org/10.1016/s0254-0584(97)80276-3.

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Chen, Nyen-Ts, Meiso Yokoyama, and Herng-Yih Ueng. "Atomic layer epitaxy growth of ZnS Se1− epitaxial layers lattice-matched to Si substrates." Journal of Crystal Growth 216, no. 1-4 (June 2000): 152–58. http://dx.doi.org/10.1016/s0022-0248(00)00433-4.

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Innocenti, M., G. Pezzatini, F. Forni, and M. L. Foresti. "CdS and ZnS Deposition on Ag(111) by Electrochemical Atomic Layer Epitaxy." Journal of The Electrochemical Society 148, no. 5 (2001): C357. http://dx.doi.org/10.1149/1.1360208.

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Dissertations / Theses on the topic "Atomic layer epitaxy ZnS"

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Fernandes, Valéria Cristina. "Estudo dos processos de eletrodeposição de filmes finos de Se, ZnSe e PbS." Universidade Federal de São Carlos, 2008. https://repositorio.ufscar.br/handle/ufscar/6099.

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This work describes studies on the underpotential deposition (UPD) of selenium, zinc, as well for Zn/Se systems deposited on polycrystalline Pt electrodes in acid solutions. The effects of Zn presence in the Se dissolution process were also investigated in the UPD and bulk potential range, 0.6 and 0.03 V respectively. The measurements were carried out using cyclic voltammetry and electrochemical quartz crystal microbalance (EQCM). Furthermore Lead sulfide (PbS) multilayers were grown on a single crystal Ag(111) substrate by Electrochemical Atomic Layer Epitaxy (ECALE) method. For Zn UPD in sulfuric acid, two different processes were observed, which are attributed to the dissolution of submonolayer of Znads and H-atoms adsorbed on the electrode surface. For Se UPD was observed that hydrogen desorption were completely inhibited indicating that Se film recovered the Pt surface. The deposition of UPD Se in perchloric acid solution showed the transference of 4 electrons with 1.4 and 1.12 active sites of Pt occupied by 1 Se ad-atom in the UPD and bulk potential range, respectively. In the evaluation of the Se monolayers dissolution process formed at 0.03 V during 2000 s a process not mentioned in the literature it was observed which was evaluated by the technique MECQ. The experimental results obtained by this technique allowed to end that the dissolution process occurred by two stages, and the first involved the participation of 6e-. The dissolution mechanism with 6e- happens with the participation of water in the dissolution process of Se, leading to the formation of an oxygenated selenium compound which in next step undergo slow oxidation and is dissolved as soluble Se(VI) species. Then the total dissolution process of Se occurs in a six-electron transfer reaction. For Se deposition in the Zn presence the dissolution charges associated with Se UPD increase, indicating that the presence of Zn favors the deposition of UPD Se. In the case of PbS multilayers on Ag (111) the voltammetric analysis of the first PbUPD and SUPD peaks indicates a mechanism of two-dimensional growth, which is consistent with epitaxial growth. Electrochemical stripping measurements indicate that the amount of Pb and S deposited in a given number of cycles is a function of the number of cycles employed, again suggesting a layer-by-layer growth. This result indicates that the amount of Pb and S in these films corresponds to the stoichiometric 1:1 ratio, indicating the formation of a compound.
Este trabalho descreve os estudos da deposicao em regime de subtensao (DRS) de Se, Zn, assim como para sistemas Zn/Se depositados sobre eletrodos policristalinos de Pt em solucoes acidas. Os efeitos da presenca de Zn no processo de dissolucao de Se tambem foram investigados em uma regiao de potenciais de DRS e deposicao massiva 0,6 V e 0,03 V, respectivamente. As medidas foram realizadas usando voltametria ciclica e microbalanca eletroquimica de cristal de quartzo (MECQ). Alem disso, multicamadas de sulfeto de chumbo (PbS) foram crescidas sobre substrato de Ag(111) utilizando o metodo de deposicao eletroquimica de camadas atomicas epitaxiais (ECALE). Para a DRS de Zn em meio de acido sulfurico dois processos distintos foram observados os quais foram atribuidos a submonocamadas de Znads e atomos de H adsorvidos sobre a superficie do eletrodo. Para a DRS do Se observou-se a inibicao completa da dessorcao de hidrogenio o que indicou recobrimento total da superficie de Pt por ad-atomo de Se. A deposicao de Se em meio de acido perclorico mostrou a transferencia de 4 eletrons com 1,4 e 1,12 sitios da Pt ocupados por cada ad-atomo de Se, em potenciais de deposicao em DRS e sobretensao, respectivamente. Na avaliacao do processo de dissolucao das monocamadas de Se formadas a 0,03 V e por um tempo de deposicao de 2000 s um processo nao mencionado na literatura foi observado o qual foi avaliado pela tecnica MECQ. Os resultados experimentais obtidos por esta tecnica permitiram concluir que o processo de dissolucao do Se ocorria por duas etapas, sendo que a primeira envolvia a participacao de uma 6 eletrons e a segunda de 4 eletrons. O mecanismo de dissolucao com 6 eletrons ocorre com a participacao de agua no processo de dissolucao do Se, levando a formacao de compostos de Se oxigenados, os quais em uma etapa posterior sofrem uma oxidacao lenta e se dissolvem como especies soluveis de Se(VI). Entao o processo total de dissolucao de Se ocorre em uma reacao de transferencia de 6 eletrons. Ja para a deposicao de Se na presenca de Zn pode-se concluir, devido ao aumento da carga de dissolucao da DRS de Se, que a presenca de Zn favorece o processo de deposicao do Se. No caso das multicamadas de PbS o estudo voltametrico das primeiras camadas de Pb DRS e S DRS indicam um mecanismo de crescimento bidimensional, que e consistente com o crescimento epitaxial. As cargas medidas no processo de dissolucao das camadas indicaram que a quantidade de Pb e S depositados para um dado numero de ciclos e uma funcao do numero de ciclos realizados, sugerindo novamente um crescimento camada por camada Este resultado sugere que a quantidade de Pb e S nos filmes possuem uma relacao estequiometrica de 1:1, indicando a formacao de um composto.
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Yeo, Philip Sinclair. "Role of gallium precursors in atomic layer epitaxy of GaAs." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape11/PQDD_0019/MQ51515.pdf.

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Arès, Richard. "Growth mechanisms of atomic layer epitaxy studied in situ by reflectance difference spectroscopy." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq24289.pdf.

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Watanabe, Joy Kimi. "Silicon preparation techniques for nucleation and growth studies of zinc sulfide deposited by atomic layer epitaxy." Diss., The University of Arizona, 1992. http://hdl.handle.net/10150/185938.

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Zinc sulfide with a direct bandgap of 3.6 eV is a potential candidate as blue-light emitting diodes and lasers. Initial growth of ZnS on Si(100) substrates by atomic layer epitaxy (ALE), a deposition technique in which film growth ideally proceeds in a 2-dimensional, layer-by-layer manner, has been investigated. The interaction between the first layer of atoms of the film and the substrate surface initiates film growth and affects the resulting structure. Work has focused on the effects of surface composition, (particularly on the role of sulfur) on the initial growth of ZnS on Si(100), and thus the chemical composition must be well controlled and characterized. Three methods have been used to process Si(100) substrates. The first was a wet chemical clean with either HF or H₂O passivation followed by a low temperature (700-800°C) anneal in UHV. The second processing method was ion sputter cleaning with a post-sputter anneal at 800-900°C. The third technique irradiated substrates held in UHV with a beam from a KrF excimer laser. Initial layers of ZnS (from Zn and H₂S) were then deposited onto processed substrates. Samples were characterized by in-situ angle resolved x-ray photoelectron spectroscopy (ARXPS) to determine the chemical composition of the surface and also the coverage and thickness of contamination and film layers. The main impurities on the surface were oxygen and carbon. The first two processing techniques had difficulty in either eliminating those impurities or caused additional contamination. Elimination of the impurities was achieved using excimer laser irradiation with a pre-dose of reactive gas. The substrate surface could also be chemically modified in a controlled manner using excimer laser irradiation. Deposition studies of initial sulfur and zinc layers onto the processed substrates determined the temperature during ALE growth should be held at 250-310°C. Uniform coverage of both sulfur and zinc was difficult to obtain, but experiments indicated sulfur adhesion improved with the presence of oxygen, and zinc adhesion improved when oxide or sulfide layers were present on the surface.
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Törndahl, Tobias. "Atomic Layer Deposition of Copper, Copper(I) Oxide and Copper(I) Nitride on Oxide Substrates." Doctoral thesis, Uppsala University, Department of Materials Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4651.

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Thin films play an important role in science and technology today. By combining different materials, properties for specific applications can be optimised. In this thesis growth of copper, copper(I) oxide and copper(I) nitride on two different substrates, amorphous SiO2 and single crystalline α-Al2O3 by the so called Atomic Layer Deposition (ALD) techniques has been studied. This technique allows precise control of the growth process at monolayer level on solid substrates. Other characteristic features of ALD are that it produces films with excellent step coverage and good uniformity even as extremely thin films on complicated shaped substrates.

Alternative deposition schemes were developed for the materials of interest. It was demonstrated that use of intermediate water pulses affected the deposition pathways considerably. By adding water, the films are thought to grow via formation of an oxide over-layer instead of through a direct reaction between the precursors as in the case without water.

For growth of copper(I) nitride from Cu(hfac)2 and ammonia no film growth occurred without adding water to the growth process. The Cu3N films could be transformed into conducting copper films by post annealing. In copper growth from CuCl and H2 the water affected film growth on the alumina substrates considerably more than on the fused silica substrates. The existence of surface -OH and/or -NHx groups was often found to play an important role, according to both theoretical calculations and experimental results.

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Lindahl, Erik. "Thin Film Synthesis of Nickel Containing Compounds." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-111484.

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CHOLLET, FREDERIC. "Epitaxie à basse température de couches silicium et Si(1-x)Gex : étude par microscopie à force atomique." Université Joseph Fourier (Grenoble), 1997. http://www.theses.fr/1997GRE10183.

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Les couches epitaxiees a basse temperature (<650c) offrent des perspectives interessantes en vue de la fabrication de dispositifs microelectroniques sophistiques, integrant des structures fragiles comme des profils de dopants tres minces ou des films heteroepitaxies metastables. Ces couches doivent etre structuralement parfaites afin d'atteindre les caracteristiques electriques attendues. Ce travail est motive par l'etude de la morphologie de surface de couches epitaxiales de si et si#1#-#xge#x deposees sur si(100) par cvd a basse temperature (550-800c). La caracterisation physique a principalement ete effectuee par microscopie a force atomique (afm). La preparation de surface des substrats avant epitaxie est une etape critique. C'est pourquoi la surface du si(100) a ete etudiee apres nettoyage par voie humide et apres recuit sous hydrogene vis a vis de la nano-rugosite, des terminaisons atomiques et des contaminants adsorbes. Les premiers instants de l'homoepitaxie de si ont ete etudies en detail. Deux modes de croissance (l'un lisse l'autre rugueux) dependant a la fois des parametres de substrat et de depot sont observes. Le mode lisse se caracterise par une croissance en terraces, alors que le mode rugueux correspond a une croissance par facettage. La morphologie de surface resultante a ete reliee a la couverture dynamique en hydrogene du front de croissance. D'autres mecanismes de croissance entrent en jeu dans les films si#1#-#xge#x en raison des contraintes existantes. Des films de si#1#-#xge#x contraints en compression et en tension ont ete etudies. Les films en compression presentent une croissance stranski-krastanov sans defaut permettant une relaxation partielle de la contrainte au travers d'ondulations de surface. Pour les films en tension, la topographie finale depend fortement de la diffusion de surface des ad-atomes.
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Ahmed, Mustafa M. Abdalla. "Alternating-Current Thin-Film Electroluminescent Device Characterization." Doctoral thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2008. http://www.nusl.cz/ntk/nusl-233432.

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Jádrem této disertační práce bylo studovat optické a elektrické charakteristiky tenkovrstvých elektroluminiscenčních součástek řízených střídavým proudem (ACTFEL) a zejména vliv procesu stárnutí luminiforů na jejich optické a elektrické vlastnosti. Cílem této studie měl být příspěvek ke zvýšení celkové účinnosti luminoforů, vyjádřené pomocí jasu, účinnosti a stability. Vzhledem k tomu, že současnou dominantní technologií plochých obrazovek je LCD, musí se další alternativní technologie plošných displejů porovnávat s LCD. Výhodou ACTFEL displejů proti LCD je lepší rozlišení, větší teplotní rozsah činnosti, větší čtecí úhel, či možnost čtení při mnohem vyšší intenzitě pozadí. Na druhou stranu je jejich nevýhodou vyšší energetická náročnost, problém s odpovídající barevností tří základních barev a podstatně vyšší napětí nutné pro činnost displeje. K dosažení tohoto cíle jsme provedli optická, elektrická a optoelektrická měření ACTFEL struktur a ZnS:Mn luminoforů. Navíc jsme studovali vliv dotování vrstvy pomocí KCl na chování mikrostruktury a na elektroluminiscenční vlastnosti (zejména na jas a světelnou účinnost) ZnS:Mn luminoforů. Provedli jsme i některá, ne zcela obvyklá, měření ACTFEL součástek. Vypočítali jsme i rozptylový poměr nabitých barevných center a simulovali transportní charakteristiky v ACTFEL součástkách. Studovali jsme vliv stárnutí dvou typů ZnS:Mn luminoforů (s vrstvou napařenou či získanou pomocí epitaxe atomových vrstev) monitorováním závislostí svítivost-napětí (L-V), velikost vnitřního náboje - elektrické pole luminoforu (Q-Fp) a kapacitance-napětí (C-V) ve zvolených časových intervalech v průběhu stárnutí. Provedli jsme krátkodobá i dlouhodobá měření a pokusili jsme se i o vizualizaci struktury luminoforu se subvlnovým rozlišením pomocí optického rastrovacího mikroskopu pracujícího v blízkém poli (SNOM). Na praktickém případu zeleného Zn2GeO4:Mn (2% Mn) ACTFEL displeje, pracujícího při 50 Hz, jsme také studovali stabilitu svítivosti pomocí měření závislosti svítivosti na napětí (L-V) a světelné účinnosti na napětí (eta-V). Přitom byl zhodnocen význam těchto charakteristik. Nezanedbatelnou a neoddělitelnou součástí této práce je i její pedagogický aspekt. Předložený text by mohl být využit i jako učebnice pro studenty na mé univerzitě v Lybii.
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Lee, Nien-chung, and 李年中. "The Study of ZnS Thin Films by Atomic Layer Epitaxy." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/97810032775445755086.

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碩士
國立成功大學
電機工程研究所
83
Atomic Layer Epitaxy is a stepwise deposition process by su- pplying the sources materials alternatively.This deposition te- chnique provides monolayer control of the deposited film thick- ness and uniform growth over a large area. ZnS layers were grown epitaxially onto (100)GaAs,(100)Si, (222)ITO substrates under low pressure in a horizontal vaper phase epitaxial reactor using DMZn for the group II source and H2S gas for the group VI source.In this study, We varied the growth condition, including change of the substrate temperature, the mole fraction of DMZn,the mole fraction of H2S,the purge H2 duration, the pressure of reaction chamber ...etc.In order to privide high quality ZnS epitaxial films. In ZnS grown on GaAs,the present process provides the mono- layer growth over a wide range of growth condition in a self- limiting manner.High crystalline quality of the epitaxially grown layers can be obtained by XRD,SEM,EPMA and PL,in spite of very large lattice mismatch (4.4 %) between ZnS and GaAs. In ZnS grown on Si and ITO glasses,The ZnS films have high crystalline quality and the epitaxial layers had a mirror-like surface.But the growth rate was still at 0.7 monolayer over a wise range of growth condition.It may be possible because the adsorption of the reactions on the substrates is weak; and much higher flows or flow times may be needed for monolayer
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Chen, Ying-Zhang, and 陳盈璋. "The electrical and optical properties of ZnS/ZnSe strained-layer superlattice by Atomic Layer Epitaxy." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/01947596128001604228.

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碩士
國立成功大學
電機工程學系
87
In this dissertation, we will discuss the effects and roles of ZnS/ZnSe strained-layer superlattices (SLSs) for introducing it into the Electroluminescent devices. The SLSs layer is grown on n-type silicon by Atomic Layer Epitaxy (ALE) which modified in a low pressure, horizontal-type, MOCVD system using dimethylzinc, hydrogen sulphide and hydrogen selenide as the reactants. The formation of SLSs structure is evident from the altering behavior of each fluctuation profile by SIMS. The electrical property of SLSs schottky diode is investigated by current-voltage measurement. It is found that at least 16 periods of ZnS/ZnSe (1600 A) will represent as low cut-in voltage as 0.52V. ZnS:Tm phosphor layer is deposited on SLSs/Si and discuss the role of SLSs as a buffer layer. Under photoluminescence spectra performed at room temperature, an unnecessary peak around 4000A is suppressed while compare it with one which have a ZnSe buffer layer with comparable thickness. All this point out the appropriateness of SLSs as an electron-transmission layer and buffer layer in Electroluminescent devices.
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Books on the topic "Atomic layer epitaxy ZnS"

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Suntola, T., and M. Simpson, eds. Atomic Layer Epitaxy. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0.

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Kääriäinen, Tommi. Atomic layer deposition: Principles, characteristics, and nanotechnology applications. 2nd ed. Beverly, MA: Scrivener Publishing, 2013.

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Sherman, Arthur. Atomic layer deposition for nanotechnology: An enabling process for nanotechnology fabrication. Ivoryton, Conn: Ivoryton Press, 2008.

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International Symposium on Atomic Layer Epitaxy and Related Surface Processes (3rd 1994 Sendai, Japan). ALE-3: Proceedings of the third International Symposium on Atomic Layer Epitaxy and Related Surface Processes, Sendai, Japan, 25-27 May 1994. Amsterdam: North-Holland, 1994.

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Suntola, T. Atomic Layer Epitaxy. Springer, 2011.

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Atomic Layer Epitaxy. Springer, 1989.

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T, Suntola, and Simpson M, eds. Atomic layer epitaxy. Glasgow: Blackie, 1990.

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Atomic Layer Epitaxy of Copper. Uppsala Universitet, 1999.

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Atomic layer growth and processing: Symposium held April 29 - May 1, Anaheim, California, U.S.A. Pittsburgh: Materials Research Society, 1991.

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Book chapters on the topic "Atomic layer epitaxy ZnS"

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Cornelissen, Hugo J., D. A. Cammack, and R. J. Dalby. "Atomic Layer Epitaxy of ZnSe/ZnSxSe1-X Superlattices." In Growth and Optical Properties of Wide-Gap II–VI Low-Dimensional Semiconductors, 257–61. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5661-5_25.

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Leskelä, M., and L. Niinistö. "Chemical aspects of the ALE process." In Atomic Layer Epitaxy, 1–39. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0_1.

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Pakkanen, T. "Theoretical aspects of ALE growth mechanisms." In Atomic Layer Epitaxy, 40–62. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0_2.

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Mason, N. J. "Comparison of ALE with other techniques." In Atomic Layer Epitaxy, 63–109. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0_3.

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Tischler, M. A., and S. M. Bedair. "Atomic layer epitaxy of III-V compounds." In Atomic Layer Epitaxy, 110–54. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0_4.

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Yao, T. "Atomic layer epitaxy of II-VI compounds." In Atomic Layer Epitaxy, 155–80. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0389-0_5.

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Aliano, Antonio, Giancarlo Cicero, Hossein Nili, Nicolas G. Green, Pablo García-Sánchez, Antonio Ramos, Andreas Lenshof, et al. "Atomic Layer Epitaxy (ALE)." In Encyclopedia of Nanotechnology, 171. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100045.

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Varazo, Kris, Travis L. Wade, Billy H. Flowers, Marcus D. Lay, Uwe Happek, and John L. Stickney. "Morphology in Electrochemical Atomic Layer Epitaxy." In Thin Films: Preparation, Characterization, Applications, 83–93. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0775-8_6.

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Pessa, Markus. "Atomic Layer Epitaxy of Compound Semiconductors." In Thin Film Growth Techniques for Low-Dimensional Structures, 221–23. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-9145-6_12.

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Sanders, Brian W. "Atomic layer epitaxy of phosphor thin films." In Solid State Luminescence, 293–312. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1522-3_9.

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Conference papers on the topic "Atomic layer epitaxy ZnS"

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Tanaka, Yuji, Yusuke Masuda, Hiroshi Kumagai, Tsutomu Shinagawa, and Ataru Kobayasi. "Atomic layer epitaxy of TiO 2 /ZnO multilayers for water-window attosecond optics." In SPIE LASE: Lasers and Applications in Science and Engineering, edited by Michel Meunier, Andrew S. Holmes, Hiroyuki Niino, and Bo Gu. SPIE, 2009. http://dx.doi.org/10.1117/12.808169.

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Murata, Masaki, Yuji Tanaka, Yasutaka Sanjo, Hiroshi Kumagai, Tsutomu Shinagawa, and Masaya Chigane. "Atomic layer epitaxy of TiO 2 /ZnO multilayer optics using ZnO buffer layer for water-window x-ray." In SPIE MOEMS-MEMS, edited by Winston V. Schoenfeld, Jian Jim Wang, Marko Loncar, and Thomas J. Suleski. SPIE, 2011. http://dx.doi.org/10.1117/12.874377.

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FUJITA, Shigeo, Yi-hong WU, Yasunori MIYAZAKI, Takashi TOYODA, Yoichi KAWAKAMI, and Shizuo FUJITA. "Sulfur-Passivation Pretreatment of GaAs Surface for Layer-by-Layer Growth and Atomic Layer Epitaxy of ZnSe by MOMBE." In 1990 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1990. http://dx.doi.org/10.7567/ssdm.1990.s-d-6.

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Takeda, T., T. Yao, T. Kurosu, and M. Iida. "Atomic-Layer Epitaxy of ZnSe and ZnTe Single Crystalline Films and its Application to the Fabrication of ZnSe /ZnTe Superlattices." In 1985 Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1985. http://dx.doi.org/10.7567/ssdm.1985.b-3-1.

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Hernández-Calderón, I., and J. C. Salcedo-Reyes. "Photoluminescence study of the substitution of Cd by Zn during the growth by atomic layer epitaxy of alternate CdSe and ZnSe monolayers." In 7TH INTERNATIONAL CONFERENCE ON LOW DIMENSIONAL STRUCTURES AND DEVICES: (LDSD 2011). AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4878294.

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Murata, Masaki, Yuji Tanaka, Hiroshi Kumagai, Tsutomu Shinagawa, and Ataru Kobayashi. "Atomic layer epitaxy of ZnO and TiO 2 thin films on c-plane sapphire substrate for novel oxide soft x-ray mirrors." In OPTO, edited by Ferechteh H. Teherani, David C. Look, Cole W. Litton, and David J. Rogers. SPIE, 2010. http://dx.doi.org/10.1117/12.840834.

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Usui, Akira, and Haruo Sunakawa. "Chloride Atomic Layer Epitaxy of InGaP." In 1988 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1988. http://dx.doi.org/10.7567/ssdm.1988.d-8-2.

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Bedair, S. M. "Recent progress in atomic layer epitaxy." In Critical Review Collection. SPIE, 1993. http://dx.doi.org/10.1117/12.141398.

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Dip, Anthony, Peter C. Colter, G. M. Eldallal, and Salah M. Bedair. "Atomic-layer epitaxy of device-quality Al0.3Ga0.7As." In Semiconductors '92, edited by Roger J. Malik, Chris J. Palmstrom, Salah M. Bedair, Harold G. Craighead, and Randall L. Kubena. SPIE, 1992. http://dx.doi.org/10.1117/12.137644.

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Hashemi, Majid, J. Ramdani, Brian McDermott, Kimberly G. Reid, John R. Hauser, and Salah M. Bedair. "Planar-doped structures by atomic layer epitaxy." In High-Speed Electronics and Device Scaling, edited by Lester F. Eastman. SPIE, 1990. http://dx.doi.org/10.1117/12.20918.

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Reports on the topic "Atomic layer epitaxy ZnS"

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Gat, R., T. I. Hukka, and M. P. D'Evelyn. Progress Toward Atomic Layer Epitaxy of Diamond Using Radical Chemistry. Fort Belvoir, VA: Defense Technical Information Center, May 1993. http://dx.doi.org/10.21236/ada265409.

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Hukka, T. I., R. E. Rawles, and M. P. D'Evelyn. Novel Method for Chemical Vapor Deposition and Atomic Layer Epitaxy Using Radical Chemistry. Fort Belvoir, VA: Defense Technical Information Center, June 1992. http://dx.doi.org/10.21236/ada252873.

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Eres, G. Kinetic modeling of the atomic layer epitaxy window in group IV semiconductor growth. Office of Scientific and Technical Information (OSTI), February 1995. http://dx.doi.org/10.2172/10113197.

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Davis, Robert F., and Salah Bedair. Atomic Layer Epitaxy Group IV Materials: Surface Processes, Thin Films, Devices and Their Characterization. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada238506.

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Davis, Robert F., Salah Bedair, Jill Little, Robert Macintosh, and Joe Sumakeris. Atomic Layer Epitaxy of Silicon, Silicon/Germanium and Silicon Carbide via Extraction/Exchange Processes. Fort Belvoir, VA: Defense Technical Information Center, January 1991. http://dx.doi.org/10.21236/ada231348.

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Trilayer Josephson junctions produced by atomic layer-by-layer FORCE (Flexible Oxide Reaction Controlled Epitaxy). Final report. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/399704.

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