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  • American Vacuum Society  (4)
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  • American Vacuum Society  (4)
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  • 1
    Online Resource
    Online Resource
    American Vacuum Society ; 1995
    In:  Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena Vol. 13, No. 4 ( 1995-07-01), p. 1434-1441
    In: Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena, American Vacuum Society, Vol. 13, No. 4 ( 1995-07-01), p. 1434-1441
    Abstract: The surface topography of doped polysilicon films was investigated by atomic force microscopy for a wide range of doping and process conditions. These low-pressure chemical vapor deposition silicon films were approximately 350 nm thick. The amorphous films were in situ phosphorus doped during deposition at 550 °C, while the crystalline films were deposited at 625 °C and subsequently diffusion doped using either PH3 or POCl3 gases. Measured resistivities ranged from 700 to 10 000 μΩ cm corresponding to secondary ion mass spectrometry phosphorus concentrations that ranged from 8.45 to 0.95×1020 cm−3. In situ doped films exhibited the smoothest surface topography with a peak-to-valley surface roughness of 11 nm. The surface roughness values were 50 nm for PH3 doped poly films, and as high as 135 nm for the POCl3 doped films. Atomic force microscopy grain size analysis showed uniform distributions for the in situ and PH3 doped films with grain sizes of 130 and 200 nm, respectively. POCl3 doped poly-Si showed bimodal grain size distributions, with the secondary grains measuring 500 nm in size and the normal grains averaging 225 nm. These secondary grains increased the surface roughness and their occurrence correlates with chlorine concentration. The number of secondary grains and their size increases with higher phosphorus content. Following the polyoxide growth, the surface roughness increased 3× to 5× with POCl3 doping, but the surface topography increased only slightly for PH3 and in situ doped poly-Si. After removing the polyoxide, the surface roughness decreased for the diffusion doped films. In situ doped films retained their smooth surface following the oxidation and removal of the oxide.
    Type of Medium: Online Resource
    ISSN: 1071-1023 , 1520-8567
    RVK:
    Language: English
    Publisher: American Vacuum Society
    Publication Date: 1995
    detail.hit.zdb_id: 3117331-7
    detail.hit.zdb_id: 3117333-0
    detail.hit.zdb_id: 1475429-0
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    American Vacuum Society ; 1993
    In:  Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena Vol. 11, No. 4 ( 1993-07-01), p. 1287-1296
    In: Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena, American Vacuum Society, Vol. 11, No. 4 ( 1993-07-01), p. 1287-1296
    Abstract: Titanium nitride films deposited by low-pressure chemical vapor deposition (LPCVD) on Si(100) using TiCl4 and NH3 as reactants, were investigated as a function of deposition temperature between 400 and 700 °C. LPCVD TiN depositions were carried out in a rapid thermal chemical vapor deposition system with a total deposition pressure of 155 mTorr. Stoichiometric TiN films were formed regardless of the deposition temperature and composition was uniform across the entire film. Depending on deposition temperature, varying amounts of chlorine (Cl) and oxygen (O) impurities are found in the TiN films. Films deposited at lower temperatures (400 and 550 °C) contained more than 5 at. % Cl, while the films produced at 700 °C contained as little as 1 at. % Cl. For the films deposited at 650 and 700 °C, the bulk of the TiN films is oxygen-free. LPCVD TiN deposition rates of 400 Å/min with no appreciable incubation time were routinely achieved. The LPCVD TiN deposition process is surface reaction controlled with an activation energy of 35 kJ/mol. Excellent TiN film conformality was observed. Electrical resistivity of the TiN films was found to decrease with increasing deposition temperature. Resistivity in the range of 85 μΩ cm was observed. Polycrystalline ∂-TiN phase with a preferred orientation of (200) was observed at all deposition temperatures. These TiN films have columnar grain structure. The TiN/Si interface is smooth, and no voids are observed at the silicon substrate interface, a prerequisite for good adhesion. An increase in the average grain size and lattice parameter was observed with increasing deposition temperature. While increasing the deposition temperature increases the TiN film growth rate, it also produces larger TiN grains and rougher surface morphology. The reliability of the TiN films as a diffusion barrier between aluminum and silicon was evaluated by diode leakage current measurements, which remained low after being thermally stressed up to 550 °C.
    Type of Medium: Online Resource
    ISSN: 1071-1023 , 1520-8567
    RVK:
    Language: English
    Publisher: American Vacuum Society
    Publication Date: 1993
    detail.hit.zdb_id: 3117331-7
    detail.hit.zdb_id: 3117333-0
    detail.hit.zdb_id: 1475429-0
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    American Vacuum Society ; 1996
    In:  Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena Vol. 14, No. 5 ( 1996-09-01), p. 3299-3304
    In: Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena, American Vacuum Society, Vol. 14, No. 5 ( 1996-09-01), p. 3299-3304
    Abstract: The process induced surface microroughness of both the silicon substrate and top surface of 15 nm gate oxide were investigated by atomic force microscopy. Varying degrees of surface microroughness on the Si and on the gate oxide were induced by timed wet silicon etch (750:1 HNO3:HF solution). The Rms roughness of the initial silicon substrate was & lt;0.2 nm, while the value increased to 0.65 nm after extended etch. For short etch times, the initial Si surface roughness was reproduced at the gate oxide surface. The average electrical field strength required to maintain a fixed current density of 1.5×10−5 A/cm2 was found to increase with decrease of the gate oxide surface roughness.
    Type of Medium: Online Resource
    ISSN: 1071-1023 , 1520-8567
    RVK:
    Language: English
    Publisher: American Vacuum Society
    Publication Date: 1996
    detail.hit.zdb_id: 3117331-7
    detail.hit.zdb_id: 3117333-0
    detail.hit.zdb_id: 1475429-0
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    American Vacuum Society ; 1993
    In:  Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films Vol. 11, No. 4 ( 1993-07-01), p. 1692-1695
    In: Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films, American Vacuum Society, Vol. 11, No. 4 ( 1993-07-01), p. 1692-1695
    Abstract: We report for the first time the characteristics of the early growth of chemical vapor deposition (CVD) TiN films on Si (100) in the surface reaction limited regime, using total reflection x-ray fluorescence (TXRF), atomic force microscopy (AFM), and Auger electron spectroscopy (AES). Small amounts of CVD TiN from TiCl4 and NH3 reactants were deposited on Si (100) at 650 °C using a rapid thermal CVD system, at a total pressure of 155 mTorr. We examined these small amounts of CVD TiN by introducing TXRF as a tool for observing the initial stages of growth, and AFM for characterizing changes in the overall surface morphology. The nucleation and growth of the resulting CVD TiN films as determined by TXRF, AFM, and AES will be discussed.
    Type of Medium: Online Resource
    ISSN: 0734-2101 , 1520-8559
    RVK:
    Language: English
    Publisher: American Vacuum Society
    Publication Date: 1993
    detail.hit.zdb_id: 1475424-1
    detail.hit.zdb_id: 797704-9
    Location Call Number Limitation Availability
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