Home > Press > Reaction Mechanisms during Plasma-assisted Atomic Layer Deposition
Figure 1: Schematic concept of the different diagnostics implemented in situ to obtain a fundamental understanding of the reaction mechanism of plasma-assisted ALD |
Abstract:
Dr Erik Langereis and Prof Erwin Kessels
Department of Applied Physics, Eindhoven University of Technology, The Netherlands
Atomic layer deposition (ALD) is considered the primary candidate for growth of conformal films with thickness control on the atomic level. The technique derives its growth control by alternating (two) self-limiting adsorption reactions in order to ensure that a submonolayer of film is deposited per so-called ALD cycle. By selecting the appropriate amount of deposition cycles, the film thickness can be controlled with ultimate precision.
A novel ALD concept is to use a plasma to activate one of the reactants in the gas phase in order to provide additional reactivity to the surface chemistry. These plasma-assisted ALD processes are researched to allow for deposition at reduced temperatures, to realize improved and tunable film properties, and to increase the choice in chemistry and precursors. To obtain a fundamental understanding of the surface reactions taking place and to evaluate the merits of the use of a plasma, a systematic study on the reaction mechanism of plasma-assisted ALD has been carried out for the deposition of metaloxides, metal-nitrides, and noble metals (Fig. 1).
Especially at reduced substrate temperatures, plasma-assisted ALD of metal-oxides distinguishes itself by providing good quality films due to the reactivity delivered by an O2 plasma. By determination of the surface groups by transmission infrared (IR) spectroscopy [1] and the reaction by-products by the combination of mass spectrometry and optical emission spectroscopy (OES) [2], it has been established that the Al2O3 growth is driven by a combustion-like surface chemistry. This chemistry proceeds for depositions down to room temperature. At this low temperature, it is observed that the plasma exposure time is an effective means to optimize the film quality.
For plasma-assisted ALD of metal-nitrides, the reducing power of an H2 plasma is found to be key in depositing conductive films. Using a plasma provides, moreover, the opportunity to tailor the material properties of the film by controlling the plasma condition. For example, by varying the plasma exposure time and plasma gas composition, the TaNx film properties can be controlled from conductive TaN to semiconductive Ta3N5 as evident from spectroscopic ellipsometry [3,4].
Furthermore, for ALD of noble metals such as Pt and Ru, the nucleation and film closure can be improved considerably using a plasma, which can result in smoother and thinner applicable metal films [5]. The mechanisms and growth observations deduced from these studies are expected to be generic for equivalent plasma-assisted ALD processes.
[1] Langereis et al., Appl. Phys. Lett. 92, 231904 (2008).
[2] Heil et al., J. Appl. Phys. 103, 103302 (2008).
[3] Langereis et al., J. Appl. Phys. 102, 083517 (2007).
[4] Langereis et al., topical review in J. Phys. D.: Appl. Phys. 42, 073001 (2009)
[5] Knoops et al., Electrochem. Solid-State Lett. 12, G34 (2009).
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