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Electrical and optical characterization of SiONC dielectric thin film deposited by polymer-source chemical vapor deposition
The electro-optical properties of SiONC dielectric thin films deposited by polymer-source chemical vapor deposition using an organosilane precursor has been investigated as a function of oxygen concentration in the films. SiONC thin films were characterized using capacitance-voltage ( C - V ), condu...
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Published in: | Journal of applied physics 2007-04, Vol.101 (8), p.084107-084107-5 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The electro-optical properties of SiONC dielectric thin films deposited by polymer-source chemical vapor deposition using an organosilane precursor has been investigated as a function of oxygen concentration in the films. SiONC thin films were characterized using capacitance-voltage (
C
-
V
), conductance-voltage (
G
-
V
), ellipsometry, and ultraviolet visible (UV-Vis) photospectroscopy. These measurements showed that the electro-optical properties of the films are greatly influenced by the atomic concentration of oxygen. The high frequency
C
-
V
measurement revealed a nearly ideal metal-oxide-semiconductor (MOS) structure behavior at high atomic concentration of oxygen (35 at.%). A relative dielectric constant as high as 6 is obtained at 10 kHz for samples with about 5 at.% of oxygen, which corresponds to high-
k
dielectric material. The interface trap density extracted from
G
-
V
measurement using Hill-Coleman method is as low as
3.2
×
10
10
(
cm
−
2
eV
−
1
)
, making these films a viable high-
k
dielectric alternative to
SiO
2
and SiON in MOS devices. The refractive index measured by ellipsometry at a wavelength of 632.8 nm shows a linear variation with atomic concentration of oxygen from 1.58 to 1.69. The optical energy band gap extracted from UV-Vis absorption spectra was found to vary between 4.40 and 5.25 eV. |
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ISSN: | 0021-8979 1089-7550 |
DOI: | 10.1063/1.2717607 |