AVS 63rd International Symposium & Exhibition
    Plasma Science and Technology Wednesday Sessions
       Session PS+TF-WeA

Paper PS+TF-WeA8
Plasma Assisted Atomic Layer Deposition of SiCxNy Films with Methylamine as the Carbon Source

Wednesday, November 9, 2016, 4:40 pm, Room 104B

Session: Plasma Deposition and Plasma Assisted ALD
Presenter: Rafaiel Ovanesyan, Colorado School of Mines
Authors: R.A. Ovanesyan, Colorado School of Mines
N. Leick, Colorado School of Mines
R.J. Gasvoda, Colorado School of Mines
K.M. Kelchner, Lam Research Corporation
D.M. Hausmann, Lam Research Corporation
S. Agarwal, Colorado School of Mines
Correspondent: Click to Email

The introduction of 3-D device architectures in integrated circuits has created a need for atomic layer deposition (ALD) of highly conformal ultra-thin films. In particular, ALD of low-dielectric-constant, carbon-containing silicon nitride (SiCxNy) films at temperatures ≤400 °C is required. However, controlled incorporation of C atoms into SiNx during ALD remains challenging.

In this work, we report the C incorporation mechanism during two plasma-enhanced SiCxNy ALD processes. The first ALD process consisted of three steps, Si2Cl6/thermal CH3NH2/N2 plasma, while the second process consists of two steps, Si2Cl6/CH3NH2 plasma. In both ALD processes, we have determined the film composition, reactive sites, and adsorbed surface species using in situ attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. In addition, the growth per cycle (GPC) and refractive index were determined using in situ four-wavelength ellipsometry.

Our IR spectra show that in the first ALD process, the CH3NH2 thermally reacts with –SiClx surface species created after the Si2Cl6 half-cycle to form -CHx terminated surface amides. During the subsequent N2 plasma half-cycle, in addition to nitridation of Si, a fraction of the surface CHx groups were incorporated into the SiCxNy film as -N=C=N- species, which appear as a strong vibrational mode at ~2170 cm-1. The composition of the SiNx films in the two-step ALD process was very similar, with C incorporated primarily as -N=C=N- groups created during the CH3NH2 plasma half-cycle. We find that during the exposure of the film to Si2Cl6 following an CH3NH2 plasma half-cycle, surface carbodiimides (-N=C=NH) rearrange to nitriles (-NH-C≡N), while most of the surface is terminated with –SiClx species. The subsequent CH3NH2 plasma half-cycle, shows that the-NH-C≡N species formed during the Si2Cl6 half-cycle are removed, and the N=C=NH surface species are restored along with –NHx groups. For the Si2Cl6/CH3NH2 plasma ALD process, SiNx films grown at 400 °C show a carbon content of ~4 at.% as measured through Rutherford backscattering spectroscopy combined with hydrogen forward scattering. Transmission electron microscopy shows a conformality of >95% for the SiCxNy films. The GPC for both processes was ~0.9 Å, with a refractive index of 1.95 and 1.86 for the N2 plasma and CH3NH2 plasma ALD processes, respectively.