Abstract

The reaction between adsorbed trimethylaluminum (TMA) and water was studied on Pt(111) and Pd(111) surfaces. Upon exposure to TMA at approximately 10–5 mbar, C- and Al-containing species appeared on both surfaces, as observed by X-ray photoelectron spectroscopy (XPS). On both surfaces, the adsorbed Al oxidation state observed by XPS was closest to metallic. Density functional theory (DFT) calculations suggest that decomposition to methyl aluminum (Al-CH3; “MMA”) or atomic Al is thermodynamically favorable. The formation of a Pd–Al alloy was observed on Pd(111), but Pt–Al alloy formation was not observed on Pt(111). Following TMA adsorption, each surface was exposed to water vapor at 400 °C either at a pressure of 7 × 10–6 mbar (UHV-XPS) or at 0.1 mbar (in situ XPS). The substrate and water dosing conditions determined the ability of each surface to remove residual carbon: on Pt(111), carbon from the TMA precursor was removed from Pt(111) during 0.1 mbar water exposure at 400 °C, whereas carbon was not rem...

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