@article{
 title = {Anodic stability of electrodeposited ruthenium: galvanostatic, thermogravimetric and X-ray photoelectron spectroscopy studies},
 type = {article},
 year = {1995},
 identifiers = {[object Object]},
 pages = {3045-3049},
 volume = {30},
 publisher = {CHAPMAN HALL LTD},
 city = {2-6 BOUNDARY ROW, LONDON, ENGLAND SE1 8HN},
 id = {38a6546f-cd11-3239-8ca4-6931771b0276},
 created = {2016-11-30T14:26:31.000Z},
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 profile_id = {12182ba0-f80b-33ff-8da5-1813b38b682d},
 group_id = {49ce86ba-a52a-36eb-a7fb-9e42f732edd5},
 last_modified = {2017-03-14T17:25:32.499Z},
 read = {false},
 starred = {false},
 authored = {false},
 confirmed = {true},
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 citation_key = {ISI:A1995RG75600005},
 source_type = {article},
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 abstract = {The anodic stability of an electrodeposited ruthenium electrode was measured by anodic galvanostatic polarization in 0.5 mol dm(-3) H2SO4 solution. The role of water and adsorbed hydroxyl groups in electrode stability was determined by means of thermogravimetric analysis. A continuous weight loss due to water removal and condensation of hydroxyl groups was detected between 120 and 430 degrees C. The loss of a hydrous component of the oxide layer was in direct correlation with the increase of the anodic stability. Between 430 and 480 degrees C a weight gain was detected on the thermogravimetric curve. It was attributed to the formation of the ruthenium oxide layer in a higher oxidative state. This finding was confirmed by X-ray photoelectron spectroscopy measurements.},
 bibtype = {article},
 author = {Marijan, D and Čukman, Dunja and Vuković, Marijan and Milun, Milorad},
 journal = {Journal of Materials Science},
 number = {12}
}

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