English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 6507/11669
造訪人次 : 29935290      線上人數 : 512
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 進階搜尋

請使用永久網址來引用或連結此文件: http://ir.ncue.edu.tw/ir/handle/987654321/16814

題名: Comparison of Vacuum-Annealed and Electrochemically Cycled Electrodes in Adsorption and Electrocatalysis: Aromatic Compounds at Platinum(111) and Polycrystalline Platinum
作者: Gui, John Y.;Kahn, Bruce E.;Laarni Laguren-Davidson;Lin, Chiu-Hsun;Lu, Frank;Ghaleb N. Salaita;Stern, Donald A.;Arthur T. Hubbard
貢獻者: 化學系
日期: 1989-05
上傳時間: 2013-06-05T09:35:57Z
出版者: American Chemical Society
摘要: These studies compare adsorbed layer vibrational spectra and packing densities of various aromatic compounds at annealed Pt( 111) and polycrystalline Pt surfaces (Pt(po1y)) with the behavior of surfaces pretreated by “electrochemical cycling” (the oxidation-reduction procedure commonly employed to pretreat electrodes prior to use). Surface structural changes produced by cycling exert a profound effect upon each of the properties studied. Adsorbates studied represent various types of surface attachment: hydroquinone (HQ), which displays a-bonding to Pt surfaces (horizontal orientation) when adsorbed from sufficiently dilute aqueous solutions; 2,2’,5,5’-tetrahydroxybiphenyl (THBP), which adopts a mixture of horizontal and vertical orientations; 3-thiophenecarboxylic acid (3TCA), (3-pyridy1)hydroquinone (BPHQ), and nicotinic acid (NA), which exhibit primarily a-bonding (tilted vertical orientation); and benzyl mercaptan (BM) and 2,5-dihydroxy-4-methylbenzylm ercaptan (DMBM), for which attachment occurs through a sulfur atom to form a benzyl pendant. Packing densities (moles adsorbed per unit area) were measured for each compound at each surface by Auger spectroscopy. Surface vibrational spectra were obtained by electron energy loss spectroscopy (EELS) and were assigned by comparison with the IR spectra of the pure compounds. Substrate surfaces were characterized by LEED. Cycling the Pt(ll1) surface affects the adsorbate packing density by up to 50%, while smaller effects are observed for Pt(po1y). Cycling causes the LEED pattern of the Pt(ll1) substrate to become diffuse. Cyclic voltammetry, where applicable, confirms the changes in packing density observed by Auger spectroscopy. Cycling of the Pt(ll1) surface greatly decreases the elastic specular reflection intensity of EELS electrons, while Pt(po1y) exhibits low reflectivity after either pretreatment. EELS spectra of adsorbed HQ and THBP display profound intensity changes as a result of cycling. That is, interaction of the aromatic ring system with the cycled surface is very different from that with the annealed (atomically smooth) Pt(ll1) surface. Spectra of adsorbates at the Pt(po1y) surface are similar to cycled Pt(ll1); cycling of the Pt(po1y) has little additional effect. Adsorbed layers in which the aromatic ring is attached to the surface primarily through a single heteroatom (3TCA, NA, and 3PHQ) are less strongly influenced by the cycling pretreatment. Adsorbates for which the aromatic ring is pendant from the surface through a benzyl mercaptan sulfur atom (BM and DMBM) are affected relatively slightly by surface structure.
關聯: Langmuir, 5(3): 819-828
顯示於類別:[化學系] 期刊論文

文件中的檔案:

檔案 大小格式瀏覽次數
index.html0KbHTML635檢視/開啟


在NCUEIR中所有的資料項目都受到原著作權保護.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋