TY - JOUR
T1 - Temperature controlled cell for in situ infrared spectroelectrochemical measurements and its use in the study of CO isothermal desorption
AU - Huang, Jimin
AU - Korzeniewski, Carol
N1 - Funding Information:
We are grateful to the Office of Naval Research for support of this work and thank Professor M.J. Weaver (Purdue University) for providing a copy of Ref. [34] in advance of publication.
PY - 1999/8/13
Y1 - 1999/8/13
N2 - An infrared spectroelectrochemical cell capable of operation at temperatures between ambient and 70 °C is described. The cell is based on a conventional design with temperature sensing and heating functions built into the working electrode. The cell was applied to study the isothermal desorption of carbon monoxide from a polycrystalline platinum electrode. The measurements indicate CO desorption can be activated by the solvent. In acetonitrile containing 0.1 M tetrabutyl ammonium tetrafluoroborate (TBAF), the lifetime of a CO adlayer decreased progressively from about 6 h to less than 2 h when CO desorption was monitored at constant temperatures in the range 25-45 °C and potentials between 0.0-0.2 V (vs. a Ag|AgCl|KCl (sat) reference electrode). In contrast, CO was stable on platinum electrodes in 0.1 M HClO4 at temperatures between ambient and 40 °C, as long as the electrode was maintained at double layer potentials. In acetonitrile solutions, the addition of chloride, oxygen or one of several organic impurities had little eflect on the CO desorption behavior.
AB - An infrared spectroelectrochemical cell capable of operation at temperatures between ambient and 70 °C is described. The cell is based on a conventional design with temperature sensing and heating functions built into the working electrode. The cell was applied to study the isothermal desorption of carbon monoxide from a polycrystalline platinum electrode. The measurements indicate CO desorption can be activated by the solvent. In acetonitrile containing 0.1 M tetrabutyl ammonium tetrafluoroborate (TBAF), the lifetime of a CO adlayer decreased progressively from about 6 h to less than 2 h when CO desorption was monitored at constant temperatures in the range 25-45 °C and potentials between 0.0-0.2 V (vs. a Ag|AgCl|KCl (sat) reference electrode). In contrast, CO was stable on platinum electrodes in 0.1 M HClO4 at temperatures between ambient and 40 °C, as long as the electrode was maintained at double layer potentials. In acetonitrile solutions, the addition of chloride, oxygen or one of several organic impurities had little eflect on the CO desorption behavior.
UR - http://www.scopus.com/inward/record.url?scp=0032685407&partnerID=8YFLogxK
U2 - 10.1016/S0022-0728(99)00270-3
DO - 10.1016/S0022-0728(99)00270-3
M3 - Article
AN - SCOPUS:0032685407
SN - 0022-0728
VL - 471
SP - 146
EP - 150
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
IS - 2
ER -