Adsorption and thermal reactions of alkanethiols on Pt(111): Dependence on the length of the alkyl chain

被引:21
作者
Lin, TH
Huang, TP
Liu, YL
Yeh, CC
Lai, YH
Hung, WH [1 ]
机构
[1] Natl Taiwan Normal Univ, Dept Chem, Taipei 116, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
关键词
D O I
10.1021/jp058084r
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption and thermal decomposition of alkanethiols (R-SH, where R = CH3, C2H5, and C4H9) on Pt(111) were studied with temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) with synchrotron radiation. Dissociation of sulfhydryl hydrogen (RS-H) of alkanethiol results in the formation of alkanethiolate; the extent of dissociation at an adsorption temperature of 110 K depends on the length of the alkyl chain. At small exposure, all chemisorbed CH3SH, C2H5SH, and C4H9SH decompose to desorb hydrogen below 370 K and yield carbon and sulfur on the surface. Desorption of products containing carbon is observed only at large exposure. In thermal decomposition, alkanethiolate is proposed to undergo a stepwise dehydrogenation: R'-CH2S -> R'-CHS -> R'-CS, R' = H, CH3, and C3H7. Further decomposition of the R'-CS intermediate results in desorption of H-2 at 400-500 K and leaves carbon and sulfur on the surface. On the basis of TPD and XPS data, we conclude that the density of adsorption of alkanethiol decreases with increasing length of the alkyl chain. C4H9SH is proposed to adsorb mainly with a configuration in which its alkyl group interacts with the surface; this interaction diminishes the density of adsorption of alkanethiols but facilitates dehydrogenation of the alkyl group.
引用
收藏
页码:14079 / 14084
页数:6
相关论文
共 36 条
[1]   INFLUENCE OF ACCEPTOR AND DONOR ADSORBATES (CO, K, NH3) ON PT SURFACE CORE-LEVEL SHIFTS [J].
APAI, G ;
BAETZOLD, RC ;
JUPITER, PJ ;
VIESCAS, AJ ;
LINDAU, I .
SURFACE SCIENCE, 1983, 134 (01) :122-134
[2]   Accurate density functional calculations of core electron binding energies on hydrogen-bonded systems [J].
Aplincourt, P ;
Bureau, C ;
Anthoine, JL ;
Chong, DP .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (31) :7364-7370
[3]   FORMATION OF MONOLAYERS BY THE COADSORPTION OF THIOLS ON GOLD - VARIATION IN THE HEAD GROUP, TAIL GROUP, AND SOLVENT [J].
BAIN, CD ;
EVALL, J ;
WHITESIDES, GM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (18) :7155-7164
[4]   Mimicking aspects of heterogeneous catalysis: Generating, isolating, and reacting proposed surface intermediates on single crystals in vacuum [J].
Bent, BE .
CHEMICAL REVIEWS, 1996, 96 (04) :1361-1390
[5]   Urea adsorption on platinum single crystal stepped surfaces [J].
Climent, V ;
Rodes, A ;
Albalat, R ;
Claret, J ;
Feliu, JM ;
Aldaz, A .
LANGMUIR, 2001, 17 (26) :8260-8269
[6]   DEDUCTION OF REACTION-MECHANISMS FOR SURFACE PROCESSES - DESULFURIZATION OF ORGANIC SULFIDES AND THIOLS ON MO(110) [J].
FRIEND, CM ;
ROBERTS, JT .
ACCOUNTS OF CHEMICAL RESEARCH, 1988, 21 (11) :394-400
[7]   Abstraction of sulfur from Pt(111) surfaces with thermal H atoms toward adsorbed and gaseous H2S [J].
Güttler, A ;
Kolovos-Vellianitis, D ;
Zecho, T ;
Küppers, J .
SURFACE SCIENCE, 2002, 516 (03) :219-229
[8]   THE REACTIVITY OF SULFUR-CONTAINING MOLECULES ON NOBLE-METAL SURFACES .3. ETHANETHIOL ON AU(110) AND AG(110) [J].
JAFFEY, DM ;
MADIX, RJ .
SURFACE SCIENCE, 1994, 311 (1-2) :159-171
[9]   Chemisorption site of methanethiol on Pt{111} [J].
Kim, SS ;
Kim, Y ;
Kim, HI ;
Lee, SH ;
Lee, TR ;
Perry, SS ;
Rabalais, JW .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (21) :9574-9582
[10]   OBSERVATION OF NOVEL INTERMEDIATES FROM CH3SH DECOMPOSITION ON PT(111) WITH HREELS AND NEXAFS [J].
KOESTNER, RJ ;
STOHR, J ;
GLAND, JL ;
KOLLIN, EB ;
SETTE, F .
CHEMICAL PHYSICS LETTERS, 1985, 120 (03) :285-291