Acta Chimica Sinica ›› 2007, Vol. 65 ›› Issue (15): 1437-1442. Previous Articles     Next Articles

Original Articles

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

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