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Iron Thin Films from Fe(CO)[sub 5] and FeCp[sub 2]∕H[sub 2]O under Atmospheric Pressure
Author(s) -
François Senocq,
F.D. Duminica,
F. Maury,
Thomas Delsol,
Constantin Vahlas
Publication year - 2006
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/1.2352050
Subject(s) - chemical vapor deposition , metalorganic vapour phase epitaxy , thin film , analytical chemistry (journal) , atmospheric pressure , metal , chemistry , partial pressure , hydrogen , iron pentacarbonyl , electron microprobe , deposition (geology) , atmospheric temperature range , materials science , layer (electronics) , mineralogy , inorganic chemistry , metallurgy , nanotechnology , oxygen , epitaxy , environmental chemistry , paleontology , oceanography , organic chemistry , physics , sediment , geology , meteorology , biology
Iron layers were first obtained from iron pentacarbonyl in metallorganic chemical vapor deposition MOCVD process under\udatmospheric pressure, in the temperature range 473–773 K, in a vertical cold wall reactor. Films of good purity were obtained with or without hydrogen as co-reactant, no chemical additives being used. The experiments showed that the velocity of the gas stream and, to a lower extent, the precursor molar fraction are the key parameters to be controlled, in order to monitor film growth rate and purity. In a second step, Fe thin layers were obtained by atmospheric pressure MOCVD starting from the reactive gas mixture FeCp2 and H2O in the temperature range 973–1073 K. A thermochemical simulation of the Fe-C-H-O system allowed optimum processing conditions to be approached. X-ray diffraction and microprobe analysis showed that the highest iron content in the layer was obtained for H2O/FeCp2 ratios between 4 and 6. Film growth occurs in two steps: the initial formation of a black, powdered, and porous layer that becomes densified as a result of the grain growth on increasing the deposition time in order to form compact gray metal films. This two-step mechanism was confirmed by kinetic and in situ IR pyrometric observations

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