The surface chemistry of CN and H on Pt(111)

• Published in: Surface science 1996-12, Vol.368 (1), p.354-360
• Main Authors: Jentz, D., Mills, P., Celio, H., Trenary, M.
• Format: Article
• Language: English
• Subjects: Applied sciences; Chemistry; Cyanogen; Exact sciences and technology; General and physical chemistry; Hydrogen cyanide; Infrared absorption spectroscopy; Low index single crystal surfaces; Metals. Metallurgy; Models of surface chemical reactions; Platinum; Solid-gas interface; Surface chemical reaction; Surface physical chemistry; Vibrations of adsorbed molecules
• ISSN: 0039-6028; 1879-2758
• DOI: 10.1016/S0039-6028(96)01075-8

Through a series of studies using reflection absorption infrared spectroscopy (RAIRS), we have observed some common trends in the surface chemistry of CN-containing adsorbates on Pt(111). The molecules that have been studied include azomethane (CH 3N 2CH 3), methylamine (CH 3NH 2), hydrogen cyanide (HCN), cyanogen (C 2N 2), and acetonitrile (CH 3CN). We find that HCN decomposes to yield adsorbed CN, which subsequently hydrogenates to form aminomethylidyne, CNH 2. The aminomethylidyne species also forms from the thermal decomposition of azomethane and methylamine, but not from acetonitrile. Molecularly adsorbed cyanogen, C 2N 2, hydrogenates to form H 2NCCNH 2. Thus, the CNH 2 functionality seems to have high stability on the Pt(111) surface. Detailed interpretation of the various RAIRS results required extensive use of isotopic substitution, normal-mode analyses, and an understanding of the effects of adsorbate-adsorbate interactions on the spectra.