X-ray photoelectron spectroscopic study of the activation of molecularly-linked gold nanoparticle catalysts

被引:86
作者
Maye, MM
Luo, J
Lin, YH
Engelhard, MH
Hepel, M
Zhong, CJ [1 ]
机构
[1] SUNY Binghamton, Dept Chem, Binghamton, NY 13902 USA
[2] Pacific NW Natl Lab, Environm & Mol Sci Lab, Richland, WA 99352 USA
[3] SUNY Coll Potsdam, Dept Chem, Potsdam, NY 13676 USA
关键词
D O I
10.1021/la0264116
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper reports the results of a study on the activation of core-shell assembled gold nanoparticle catalysts using X-ray photoelectron spectroscopy (XPS). The goal is to determine the surface reconstitution of the nanostructured catalysts upon electrochemical activation for the electrocatalytic oxidation of methanol. The decanethiolate-capped gold nanoparticles of 2-5 nm core sizes were assembled as catalyst thin films on electrode surfaces using 1,9-nonanedithiol and 11-mercaptoundecanoic acid as model molecular linkers. The XPS results have provided two important insights into the surface reconstitution of the activated nanostructure. First, the capping/linking thiolates or dithiolates are partially removed to produce the catalytic access, with the degree of removal being dependent on the nature of the molecular linker. Second, oxygenated species are detected on the activated gold nanocrystals, demonstrating the formation of surface gold oxide and its participation in the electrocatalytic oxidation of methanol. The findings are also correlated with results from studies of surface microscopic morphology and interfacial mass flux and provide further insights into issues related to the design and preparation of highly active nanostructured gold catalysts.
引用
收藏
页码:125 / 131
页数:7
相关论文
共 40 条
[31]   Two-laser mass spectrometry of thiolate, disulfide, and sulfide self-assembled monolayers [J].
Trevor, JL ;
Lykke, KR ;
Pellin, MJ ;
Hanley, L .
LANGMUIR, 1998, 14 (07) :1664-1673
[32]   Onset of catalytic activity of gold clusters on titania with the appearance of nonmetallic properties [J].
Valden, M ;
Lai, X ;
Goodman, DW .
SCIENCE, 1998, 281 (5383) :1647-1650
[33]  
Wagner C.D., 1978, HDB XRAY PHOTOELECTR
[34]   ELECTROCHEMICAL AND X-RAY PHOTOELECTRON SPECTROSCOPIC EVIDENCE FOR DIFFERENCES IN THE BINDING-SITES OF ALKANETHIOLATE MONOLAYERS CHEMISORBED AT GOLD [J].
WALCZAK, MM ;
ALVES, CA ;
LAMP, BD ;
PORTER, MD .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 396 (1-2) :103-114
[35]   Methanol oxidation and direct methanol fuel cells:: a selective review [J].
Wasmus, S ;
Küver, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 461 (1-2) :14-31
[36]   THE ELECTROCHEMICAL DESORPTION OF N-ALKANETHIOL MONOLAYERS FROM POLYCRYSTALLINE AU AND AG ELECTRODES [J].
WIDRIG, CA ;
CHUNG, C ;
PORTER, MD .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1991, 310 (1-2) :335-359
[37]   Imparting biomimetic ion-gating recognition properties to electrodes with a hydrogen-bonding structured core-shell nanoparticle network [J].
Zheng, WX ;
Maye, MM ;
Leibowitz, FL ;
Zhong, CJ .
ANALYTICAL CHEMISTRY, 2000, 72 (10) :2190-2199
[38]  
Zhong CJ, 2001, ADV MATER, V13, P1507, DOI 10.1002/1521-4095(200110)13:19<1507::AID-ADMA1507>3.0.CO
[39]  
2-#
[40]   Organosulfur monolayers at gold surfaces: Reexamination of the case for sulfide adsorption and implications to the formation of monolayers from thiols and disulfides [J].
Zhong, CJ ;
Brush, RC ;
Anderegg, J ;
Porter, MD .
LANGMUIR, 1999, 15 (02) :518-525