Adsorption and Reaction Pathways of 1H-Pyrazole on Cu(100) and O/Cu(100)

Jyun Yi Jhuang, Szu Han Lee, Shang Wei Chen, Yun Hsien Chen, You Jyun Chen, Jong Liang Lin, Chia Hsin Wang, Yaw Wen Yang

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7 Citations (Scopus)

Abstract

Temperature-programmed reaction/desorption (TPR/D), reflection-absorption infrared spectroscopy (RAIRS), X-ray photoelectron spectroscopy (XPS), and near-edge X-ray absorption fine structure (NEXAFS) have been employed, with the aid of density functional theory calculations, to investigate the adsorption and reaction mechanisms of 1H-pyrazole on Cu(100) and oxygen-precovered Cu(100) (O/Cu(100)). On Cu(100), the adsorbed 1H-pyrazole molecules interact with each other through hydrogen bonding, exhibiting broad infrared absorptions between ∼2750 and ∼3300 cm-1, but without the N-H stretching peak detected. Near a monolayer coverage, heating the surface to ∼200 K induces a change in the adsorption layer structure and generates upright or near upright 1H-pyrazole molecules attaching to the surface through the imine nitrogens. The 1H-pyrazole undergoes N-H bond cleavage first to evolve H2 (∼230 K) and leaves pyrazolate on the surface. This intermediate is proposed to be adsorbed perpendicularly via the two nitrogen atoms, which are close to two surface atop sites. The pyrazolate decomposes by simultaneous C-H bond scission and ring opening with preferential bond breaking steps at ∼550 K. The C-H dissociation, particularly at the 4C-H, is the main origin for the H2 formation from the pyrazolate. In the ring-opening process of the pyrazolate, cleavage of the two C-N bonds produces N2, while concomitant dissociation of the N-N and 3C-4C bonds leads to the formation of HCN and CH3CN. A small amount of the pyrazolate may recombine with hydrogen to evolve 1H-pyrazole. As 1H-pyrazole is adsorbed on O/Cu(100) at 120 K, it dissociates into adsorbed H2O and dehydrogenated 1H-pyrazole species. Further reaction of the dehydrogenated species at 480 K produces adsorbed NCO and pyrazolate and gaseous H2, H2O, HCN, CO, and CO2, with other products of CH2â•CHNH2 at 515 K and NH3 at 535 K. The remaining pyrazolate decomposes at 550 K to generate H2, N2, HCN, and CH3CN.

Original languageEnglish
Pages (from-to)6195-6208
Number of pages14
JournalJournal of Physical Chemistry C
Volume122
Issue number11
DOIs
Publication statusPublished - 2018 Mar 22

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Energy(all)
  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films

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