The effect of interfacial reactions on the electrical properties of a polycrystalline (poly) gate stack were evaluated in terms of annealing conditions and the results were compared with those of a conventional poly- system. In the poly- gate stack, silicate formation was the dominant reaction at the poly- interface after annealing at 900 °C, resulting in the significant decrease in leakage current. From x-ray photoelectron spectroscopy analysis, the binding states of Hf silicates were clearly observed at a binding energy of about 16.1 eV in Hf spectra and 102.7 eV in Si spectra. However, in the poly- gate stack, the accumulation capacitance became undeterminable and the leakage current increased suddenly after annealing at 900 °C due to silicide formation at the poly- interface. The differences in reactions between a poly- interface and a poly- interface are attributed to the accumulation of Ge.
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8 September 2003
Research Article|
September 08 2003
Evaluation of the electrical properties and interfacial reactions for the polycrystalline gate stack
Sung Kwan Kang;
Sung Kwan Kang
Department of Ceramic Engineering, Yonsei University, Seoul 120-749, Korea
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Suheun Nam;
Suheun Nam
Department of Ceramic Engineering, Yonsei University, Seoul 120-749, Korea
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Byung Gi Min;
Byung Gi Min
Department of Ceramic Engineering, Yonsei University, Seoul 120-749, Korea
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Seok Woo Nam;
Seok Woo Nam
Department of Ceramic Engineering, Yonsei University, Seoul 120-749, Korea
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Dae-Hong Ko;
Dae-Hong Ko
Department of Ceramic Engineering, Yonsei University, Seoul 120-749, Korea
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Mann-Ho Cho
Mann-Ho Cho
Surface Analysis Group, Korea Research Institute of Standards and Science, Daejeon, 305-600, Korea
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Appl. Phys. Lett. 83, 2004–2006 (2003)
Article history
Received:
February 27 2003
Accepted:
July 21 2003
Citation
Sung Kwan Kang, Suheun Nam, Byung Gi Min, Seok Woo Nam, Dae-Hong Ko, Mann-Ho Cho; Evaluation of the electrical properties and interfacial reactions for the polycrystalline gate stack. Appl. Phys. Lett. 8 September 2003; 83 (10): 2004–2006. https://doi.org/10.1063/1.1608487
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