Metallorganic Chemical Vapor Deposition of Ru and RuO2 Using Ruthenocene Precursor and Oxygen Gas

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© 2000 ECS - The Electrochemical Society
, , Citation Sung‐Eon Park et al 2000 J. Electrochem. Soc. 147 203 DOI 10.1149/1.1393175

1945-7111/147/1/203

Abstract

Thin films of Ru and were deposited using ruthenocene and oxygen as a precursor and reaction gas, respectively. Two phases, Ru and , could be deposited using the same source and reaction gas. The phase of the as‐deposited film was found to be critically dependent on the deposition process parameters such as precursor partial pressure, oxygen partial pressure, and substrate temperature. A decrease in precursor partial pressure by either reducing carrier gas flow rate or bubbler temperature led to formation while a decrease in oxygen partial pressure resulted in Ru formation. It was also identified that there exists a substrate temperature range in which a Ru film is deposited at a given processing condition. When the temperature is either higher or lower than this temperature range, film deposition results. From careful analysis of the film deposition rate in conjunction with the evolution of the film phase, we conclude that film deposition occurs by two independent processes. One is the source gas decomposition process resulting in Ru film deposition, and the other is the oxidation of the Ru film resulting in deposition. © 2000 The Electrochemical Society. All rights reserved.

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