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Control of a Metal-Electrode Work Function by Solid-State Diffusion of Nitrogen

Published online by Cambridge University Press:  01 February 2011

R.J.P. Lander
Affiliation:
Philips Research Leuven, Kapeldreef 75, 3001 Leuven, Belgium
J.C. Hooker
Affiliation:
Philips Research Leuven, Kapeldreef 75, 3001 Leuven, Belgium
J.P. van Zijl
Affiliation:
Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands
F. Roozeboom
Affiliation:
Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands
M.P.M. Maas
Affiliation:
Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands
Y. Tamminga
Affiliation:
Philips CFT, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands
R.A.M. Wolter
Affiliation:
Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands
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Abstract

The work function of a metal gate electrode has been adjusted with the introduction of nitrogen by solid-source diffusion from an over-stoichiometric TiN1+x layer. RBS measurements have shown that measurable concentrations of nitrogen can be diffused into a 10nm Ta layer at moderate anneal temperatures (>500°C), and that this concentration increases with temperature in the range 500-1000°C. Capacitance-voltage measurements have been carried out on 10nm tantalum layers on Al2O3. These measurements have indicated that the work function of tantalum changes by -0.08eV due to the presence of the over-stoichiometric TiN1+x covering layer during anneal (800°C/30”). Similar C-V measurements have been carried out on 10nm molybdenum layers on SiO2 and on Al2O3 dielectrics. These have shown that the work function of molybdenum is substantially different for metal stacks with the TiN1+x covering layer after a similar anneal. The work function changes by -0.52eV for molybdenum on SiO2 and by -1.1eV for molybdenum on Al2O3. The results suggest great potential for molybdenum as a candidate for a single-metal dual-work function approach to integrating metal gates into future CMOS technologies.

Type
Research Article
Copyright
Copyright © Materials Research Society 2002

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