AVS 61st International Symposium & Exhibition | |
Thin Film | Monday Sessions |
Session TF+PS-MoA |
Session: | ALD Surface Reactions and Precursors |
Presenter: | Brent Sperling, NIST |
Authors: | B.A. Sperling, NIST J.E. Maslar, NIST W.A. Kimes, NIST |
Correspondent: | Click to Email |
In situ Fourier transform infrared (FT-IR) spectroscopy has provided many valuable insights into various chemistries used for atomic layer deposition (ALD). Frequently, it is used to observe the molecular fragments remaining on a surface after exposure to each precursor or the phonon modes of films as they are deposited layer-by-layer. The limitations of FT-IR spectroscopy, however, have restricted it to quasi-static conditions that differ dramatically from most growth studies. Spectra cannot easily be obtained with the temporal resolution needed to keep pace with typical ALD cycle times. We have developed a method that signal averages time-resolved spectra over multiple ALD cycles to improve the rate of data acquisition to around 150 ms. Additionally, by using external reflection from a metal surface, absorption by surfaces species is enhanced; alternating polarization states allows the surface to be differentiated from gas-phase species and deposition on the windows. We apply this method to La(iPrCp)3/H2O chemistry (iPrCp = isopropyl-cyclopentadienyl), which has proved to be difficult to understand from growth studies. We present our attempts to recreate literature conditions in our laminar flow reactor with in situ FT-IR spectroscopy to observe surface and gas-phase species.