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Adsorption and Reaction Pathways of 1H-Pyrazole on Cu(100) and O/Cu(100)
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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 WangYaw-Wen Yang
Journal of Physical Chemistry C, 卷.122(11), 頁碼.6195-6208
03/2018

摘要

Electronic Optical and Magnetic Materials Energy (all) Physical and Theoretical Chemistry Surfaces Coatings and Films
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 H 2 (∼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 4 C-H, is the main origin for the H 2 formation from the pyrazolate. In the ring-opening process of the pyrazolate, cleavage of the two C-N bonds produces N 2 , while concomitant dissociation of the N-N and 3 C- 4 C bonds leads to the formation of HCN and CH 3 CN. 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 H 2 O and dehydrogenated 1H-pyrazole species. Further reaction of the dehydrogenated species at 480 K produces adsorbed NCO and pyrazolate and gaseous H 2 , H 2 O, HCN, CO, and CO 2 , with other products of CH 2 â•CHNH 2 at 515 K and NH 3 at 535 K. The remaining pyrazolate decomposes at 550 K to generate H 2 , N 2 , HCN, and CH 3 CN.

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