AVS 66th International Symposium & Exhibition
    Thin Films Division Monday Sessions
       Session TF+2D+AP+EL+SS-MoA

Paper TF+2D+AP+EL+SS-MoA5
Controlling the Nucleation of CVD Cobalt Films on SiO2 : Combining an Amido-based Nucleation Promotor with an Amine-based Growth Inhibitor to Afford Atomically-smooth Surfaces

Monday, October 21, 2019, 3:00 pm, Room A124-125

Session: ALD and CVD: Nucleation, Surface Reactions, Mechanisms, and Kinetics
Presenter: Zhejun Zhang, University of Illinois at Urbana-Champaign
Authors: Z. Zhang, University of Illinois at Urbana-Champaign
G.S. Girolami, University of Illinois at Urbana-Champaign
J.R. Abelson, University of Illinois at Urbana-Champaign
Correspondent: Click to Email

Cobalt films are of interest for the back-end metallization and transistor contact in microelectronics because cobalt has a greater electromigration resistance and a lower diffusion rate in dielectrics compared with copper. However, few-nanometer thick Co films deposited by CVD on dielectrics are usually non-continuous – they consist of islands with pinholes and significant roughness – which renders them unsuitable for nanoscale device fabrication. A nucleation layer, such as TiN, can be pre-deposited to improve the area density of Co nuclei; this approach eliminates the problem of islanding, but it subtracts cross-sectional area from the plug or line, thus increasing the electrical resistance.

Here, we solve the Co nucleation problem in CVD using a two-pronged approach. First we expose the SiO2 surface to a tetrakis(dimethylamido)(transition metal) precursor at low temperature. This affords a self-limiting, submonolayer coverage of an intermediate, similar to the behavior of such molecules in ALD processes. The adsorbate layer then enhances the nucleation of cobalt from the Co2(CO)8 precursor, such that a large area density of nanoscale islands forms with essentially no nucleation delay. Using this approach, the rms surface roughness for a 1.5-nm-thick Co film decreases from 2.5 to 1.0 nm.

Second, we further improve the surface morphology by adding a co-flow of ammonia together with the carbonyl precursor; this serves as a growth inhibitor that reduces the steady-state growth rate of Co films by 50 %. The presence of the inhibitor does not alter the nucleation rate, however, the rms roughness of a 1.5-nm-thick film is further reduced to only 0.4 nm. We suggest that the roughness is due to a better valley-filling at low precursor reaction probability, consistent with the literature. In summary, our approach enables the use of CVD to afford excellent Co films for nanofabrication.