TY - JOUR
T1 - Chemical vapor deposition precursor chemistry. 5. The photolytic laser deposition of aluminum thin films by chemical vapor deposition
AU - Glass, John A.
AU - Hwang, Seong Don
AU - Datta, Saswatti
AU - Robertson, Brian
AU - Spencer, James T.
N1 - Funding Information:
Acknowledgements-Wew ish to thank Prof. Peter A. Dowbenfo rh ist echnicaals sistancaen dv aluabled iscussions duringt hec ourseo f thisw ork.W e also wish to thankP rof. TheresaB . Freedmanfo r here nthusiastiacs sistancwe ith the MNDO quantumc hemicacl alculationsF. inally, we wish to thank the National ScienceF oundation( Grant Nos MSS-89-0979C3H E-9521572a nd OSR-92-21655I)n, ternational BusinessM achines, the General Electric Company and the Wright-PattersonL aboratory( Award No. F33615-90-C-5291)f or supporto f this work.
PY - 1996/5
Y1 - 1996/5
N2 - Thin films of very high purity aluminum were formed from the laser photolysis of trimethylamine alane (TMAA) using both ultraviolet (pulsed nitrogen) and visible (argon ion) laser irradiation on a variety of substrates including gold, Si(111), GaAs(110) and Teflon (PTFE). At thicknesses of up to 1 μm, nearly linear growth rates of 377 Ås-1 and 112Ås-1 were observed. The formation of volatile species formed during the deposition of aluminum from TMAA was investigated by quadrupole mass spectrometry (QMS) of the reactant gas stream. The highest intensity post-deposition mass fragments were observed at m/z 58, 43 and42amucorresponding to [NC3H8]+, [NC2H5]+ and [NC2H4]+, respectively. These species arise from the dissociation and subsequent fragmentation of the trimethylamine ligand from the starting TMAA complex. Semi-empirical quantum chemical calculations (MNDO) for TMAA provided further support that photolysis of this precursor should result in principally ligand dissociation processes since the LUMO orbital is primarily an aluminum-nitrogen antibonding interaction. The deposited materials were also characterized by X-ray emission spectroscopy (XES), scanning electron microscopy (SEM), and Laser Microprobe Mass Analysis (LAMMA) techniques.
AB - Thin films of very high purity aluminum were formed from the laser photolysis of trimethylamine alane (TMAA) using both ultraviolet (pulsed nitrogen) and visible (argon ion) laser irradiation on a variety of substrates including gold, Si(111), GaAs(110) and Teflon (PTFE). At thicknesses of up to 1 μm, nearly linear growth rates of 377 Ås-1 and 112Ås-1 were observed. The formation of volatile species formed during the deposition of aluminum from TMAA was investigated by quadrupole mass spectrometry (QMS) of the reactant gas stream. The highest intensity post-deposition mass fragments were observed at m/z 58, 43 and42amucorresponding to [NC3H8]+, [NC2H5]+ and [NC2H4]+, respectively. These species arise from the dissociation and subsequent fragmentation of the trimethylamine ligand from the starting TMAA complex. Semi-empirical quantum chemical calculations (MNDO) for TMAA provided further support that photolysis of this precursor should result in principally ligand dissociation processes since the LUMO orbital is primarily an aluminum-nitrogen antibonding interaction. The deposited materials were also characterized by X-ray emission spectroscopy (XES), scanning electron microscopy (SEM), and Laser Microprobe Mass Analysis (LAMMA) techniques.
KW - A. electronic materials
KW - A. organometallic compounds
KW - A. thin films
KW - B. vapor deposition
KW - D. microstructure
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U2 - 10.1016/0022-3697(96)80011-4
DO - 10.1016/0022-3697(96)80011-4
M3 - Article
AN - SCOPUS:0030145355
SN - 0022-3697
VL - 57
SP - 563
EP - 570
JO - Journal of Physics and Chemistry of Solids
JF - Journal of Physics and Chemistry of Solids
IS - 5
ER -