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Please use this identifier to cite or link to this item: https://libeldoc.bsuir.by/handle/123456789/45043
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dc.contributor.authorInberg, A.-
dc.contributor.authorBogush, V. A.-
dc.contributor.authorCroitoru, N.-
dc.contributor.authorShacham-Diamand, Y.-
dc.date.accessioned2021-09-07T08:59:56Z-
dc.date.available2021-09-07T08:59:56Z-
dc.date.issued2007-
dc.identifier.citationElectrochemical Study of the Mechanism of Ag(W) Electroless Deposition / Inberg A. [et al.] // Journal of The Electrochemical Society. – 2007. – Vol. 154, № 1. – Р. D1–D4. – DOI: 10.1149/1.2372696.ru_RU
dc.identifier.urihttps://libeldoc.bsuir.by/handle/123456789/45043-
dc.description.abstractWe present an electrochemical study of the mechanism of silver-tungsten, Ag W , thin film electroless deposition from the solutions that are used for micro-systems-metallization applications. Ag W electroless films were deposited on palladium-activated surface of thin silicon dioxide layers on silicon substrates from ammonia-acetic or benzoate silver complex basedsolutions at room temperature using hydrazine hydrate as a reducing agent. These solution compositions have been investigated.The adsorption mechanism of tungsten incorporation into Ag coating on the positively charged silver surface was proposed and its co-deposition with silver due to interfacial catalytic interaction between tungsten and silver ions in form of Ag2 W 2O7 was shown.The kinetics of the Ag W electroless deposition process was analyzed by mixed potential theory. It was shown that the anodiccharge-transfer reaction for ammonia-acetic solution and the diffusion of reduced silver ions to substrate for benzoate complexhave controlled this process.ru_RU
dc.language.isoenru_RU
dc.publisherElectrochemical Societyru_RU
dc.subjectпубликации ученыхru_RU
dc.subjectelectrochemical depositionru_RU
dc.subjectchemical recoveryru_RU
dc.subjectelectrochemicaru_RU
dc.titleElectrochemical Study of the Mechanism of Ag(W) Electroless Depositionru_RU
dc.typeСтатьяru_RU
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