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Effect of the anodization conditions on the growth and volume expansion of porous alumina films in malonic acid electrolyte

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F15%3APU117146" target="_blank" >RIV/00216305:26620/15:PU117146 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.surfcoat.2015.04.030" target="_blank" >http://dx.doi.org/10.1016/j.surfcoat.2015.04.030</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.surfcoat.2015.04.030" target="_blank" >10.1016/j.surfcoat.2015.04.030</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effect of the anodization conditions on the growth and volume expansion of porous alumina films in malonic acid electrolyte

  • Original language description

    Galvanostatic formation of nanoporous anodic films on aluminumwas performed in 0.6 M malonic acid electrolyte over a wide current density range in order to define the relationship between the anodizing behavior, oxide growth, dissolution and volume expansion of the oxide. The volume expansion and aluminum dissolution increase with raising the current density, the latter indicating an increasing potential difference across the electrolyte/barrier-layer interface. The same potential difference promotes dissociation of the acid molecules and incorporation of electrolyte-derived species into the film. The increase of volume expansion occurs in three phases, resulting fromthe two dissociation steps of malonic acid and from the change in the oxide growth mechanism at higher current densities. Infrared spectroscopy showed an enhanced presence of OH in films formed at higher current densities, indicating that lower coordination of aluminumaswell as anion incorporation contributes to volume expansion of the oxide. The current appeared to be 100% ionic in the interval of 5–100 mA cm-2, while being about 10% electronic beyond this range. At higher current densities a selflocalizing mechanism concentrates the ionic current to a smaller, spot-like area that moves continuously along the sample consuming steadily the whole metal thickness under the spot and thus forming a porous anodic film of highly self-ordered morphology, without physical imperfections. The volume expansion factor of the oxide becomes independent of the anodization current density under these conditions

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/GA14-29531S" target="_blank" >GA14-29531S: Formation and properties of novel self-organized mixed-oxide 3-D nanostructured films for use in advanced microdevices (AnoNanoFilm)</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Surface and Coatings Technology

  • ISSN

    0257-8972

  • e-ISSN

  • Volume of the periodical

    275

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    8

  • Pages from-to

    18-25

  • UT code for WoS article

    000357753900004

  • EID of the result in the Scopus database

    2-s2.0-84930863806