Abstract

Films of tantalum oxide, ranging in thickness from 25 to 2000 nm, were successfully deposited on silicon by the electron cyclotron resonance plasma‐enhanced metalorganic chemical vapor deposition (ECR‐MOCVD) process at deposition rates of up to 33 nm/min. The films were produced by decomposition of tantalum pentaethoxide into tantalum oxide in an oxygen ECR microwave plasma. The films were amorphous (but fully dense) since the temperature of the substrate, which was unheated, was estimated to be 76–120°C. The growth of the tantalum oxide films was accompanied by the formation of an interlayer of silicon dioxide at the silicon interface. The tantalum oxide films were oxygen rich (relative to Ta2O5). The effective relative dielectric constant of these dual‐layer dielectrics ranged from ɛef= 8.5 to 24; this range was explained in terms of a bilayer consisting of a 13‐nm‐thick silicon dioxide layer of ɛsx= 4, and a tantalum oxide overgrowth of varying thickness having ɛtx∼ 25. A maximum breakdown strength of the films was 6.9 MV/cm and the leakage current at a field of 1 MV/cm was 3.0 × 10‐8. The breakdown properties were related to the presence of stray particles on the substrate; these properties are expected to improve considerably if the processing is carried out in a clean‐room environment. The silicon dioxide layer is believed to have grown by the diffusion of oxygen through the tantalum oxide overlayer despite the low substrate temperature.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.