化学学报 ›› 2007, Vol. 65 ›› Issue (15): 1437-1442. 上一篇    下一篇

研究论文

异烟酸在碱性溶液中金电极上的现场表面增强振动光谱研究

薛晓康1, 霍胜娟1, 严彦刚1, 王金意1, 姚建林2, 蔡文斌*,1   

  1. (1复旦大学化学系上海市分子催化和功能材料重点实验室 上海 200433)
    (2苏州大学化学化工学院 苏州 215006)
  • 投稿日期:2006-10-30 修回日期:2007-03-19 发布日期:2007-08-14
  • 通讯作者: 蔡文斌

In situ Surface-Enhanced Vibrational Spectroscopies on Isonicotinic Acid Adsorbed on Gold Electrodes in Alkaline Solutions

XUE Xiao-Kang1; HUO Sheng-Juan1; YAN Yan-Gang1; WANG Jin-Yi1; YAO Jian-Lin2; CAI Wen-Bin*,1   

  1. (1 Shanghai Key Laboratory for Molecular Catalysis and Innovative Materials and Department of Chemis-try, Fudan University, Shanghai 200433)
    (2 Department of Chemistry, Suzhou University, Suzhou 215006)
  • Received:2006-10-30 Revised:2007-03-19 Published:2007-08-14
  • Contact: CAI Wen-Bin

应用表面增强红外吸收光谱法、循环伏安法和微分电容法研究了0.1 mol•L-1 KClO4和0.1 mol•L-1 KCl碱性化溶液(pH 10)中, 异烟酸(INA)在Au电极表面的吸附取向和结构. 结果表明: -0.5~0.2 V (vs. SCE)间INA阴离子(INA-)通过其羧酸根上的两个氧原子垂直吸附在Au电极表面; 特性吸附Cl-对上述吸附结构无实质影响. 进一步的表面增强拉曼光谱的测试表明即使在-0.8~-0.5 V, 极少量吸附的INA-很可能仍维持上述基本构型.

关键词: 表面增强红外吸收光谱, 异烟酸, Au电极, 吸附构型, 表面增强拉曼光谱

Surface-enhanced infrared absorption spectroscopy (SEIRAS) in conjunction with cyclic voltammetry and differential capacitance measurement has been applied to investigate the adsorption configuration of isonicotinate (INA-) species on Au electrodes in alkalinized 0.1 mol•L-1 KClO4 and 0.1 mol•L-1 KCl solutions (pH 10). The results indicate that INA- is nearly vertically adsorbed on the Au surface through the two oxygen atoms of its carboxylate group between -0.5 and 0.2 V (vs. SCE). The presence of Cl- in a supporting electrolyte dose not change the adsorption configuration of INA- on Au electrodes. Further supporting information from surface-enhanced Raman spectroscopy suggests that at negative potentials from -0.8 to -0.5 V, INA- species adsorbed on Au electrode of a very low coverage is likely to remain the nearly same configuration as that revealed at more positive potentials.

Key words: surface-enhanced infrared absorption spectroscopy, isonicotinic acid, Au electrode, adsorption configuration, surface-enhanced Raman spectroscopy