Trimethylaluminum-based Atomic Layer Deposition of MO 2 (M=Zr, Hf): Gate Dielectrics on In 0.53 Ga 0.47 As(001) Substrates

As post-Si era for digital device is incipient, In0.53Ga0.47As is good candidate among n-type active channels with high electron mobility but - unlike Si - it lacks a well-established technology for dielectric gating which may bear aggressive device scaling. Here we propose a viable route for the at...

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Veröffentlicht in:ECS transactions 2013-03, Vol.50 (13), p.11-19
Hauptverfasser: Molle, Alessandro, Cianci, Elena, Lamperti, Alessio, Wiemer, Claudia, Baldovino, Silvia, Lamagna, Luca, Spiga, Sabina, Fanciulli, Marco, Brammertz, Guy, Merckling, Clement, Caymax, Matty
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Sprache:eng
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Zusammenfassung:As post-Si era for digital device is incipient, In0.53Ga0.47As is good candidate among n-type active channels with high electron mobility but - unlike Si - it lacks a well-established technology for dielectric gating which may bear aggressive device scaling. Here we propose a viable route for the atomic layer deposition (ALD) of high-κ dielectrics taking advantage from the well-known self-cleaning effect of the trimethylaluminum (TMA) precursor on the III-V compound surfaces. In this respect, the incorporation of Al2O3 cycles both as pre-conditioning surface treatment and inside the ALD growth of a MO2 host matrix (M=Zr, Hf) is here investigated. Al:MO2/In0.53Ga0.47As heterojunctions have been scrutinized by in situ spectroscopic ellipsometry and ex situ chemical depth-profiling analysis which validate a good physical quality of the oxide and elucidate the effect of the pre-conditioning cycles at the interface level. The resulting MOS capacitors have been characterized by means of multifrequency capacitance-voltage measurements and conductance analysis therein yielding a permittivity of 19{plus minus}1 both for Al:HfO2 and Al:ZrO2 and similar electrical quality of the interfaces. On the other hand, Al:HfO2 appears to be electrically more robust against leakage and endowed with a lower frequency dispersion in accumulation.
ISSN:1938-5862
1938-6737
DOI:10.1149/05013.0011ecst