Co (II) porphyrin adsorbed on SiO2/SnO2/phosphate prepared by the sol-gel method

被引:22
作者
Cardoso, WS
Francisco, MSP
Landers, R
Gushikem, Y
机构
[1] Univ Estadual Campinas, Inst Quim, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Inst Fis Gleb Wataghin, BR-13084971 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
SiO2/SnO2 mixed oxide; carbon paste electrode; dissolved dioxygen sensor; cobalt porphyrin; electrocatalysis;
D O I
10.1016/j.electacta.2005.02.001
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 [应用化学];
摘要
This paper describes the immobilization procedure of 5,10,15,20-tetrakis(1-methyl-4-pyridyl)-21-H,23-H-porphyrin ion on SiO2/SnO2/phosphate, obtained by the sol-gel processing method. P 2p X-ray photoelectron and the P-31 MAS NMR spectra revealed that dihydrogen phosphate is the species present on the surface. The porphyrin was adsorbed on the surface of the modified material and furthermore metallized in situ with Co (H) ion. The porphyrin metallation process was followed with UV-vis spectroscopy by inspecting the Q bands of the free and metallated porphyrin. The free porphyrin presented four Q bands associated to a D-2h local symmetry and the metallated one, two bands related to a D-4h local symmetry. The amount of electroactive species adsorbed on the material was estimated by integrating the area under the peak of Co (II) -> Co (I) reduction by using the pulse differential voltammetric technique. The amount of the metallated porphyrin was 2.3 x 10(-10) Mol cm(-2). A carbon paste electrode of the modified material containing metallated porphyrin was used to study the electrocatalytic reduction of dissolved dioxygen by means of cyclic voltammetry, chronoamperometry and linear sweeping voltammetry. The modified electrode was very stable and exhibited the electrocatalytic reduction of dissolved dioxygen at -180mV versus SCE by a two-electron mechanism, producing hydrogen peroxide at pH 5.4. The electroactive species was strongly retained on the material surface, presumably inside the pores of the material, since in a test of various oxidation-reduction cycles no significant decrease of the current densities was detected, indicating that it was not leached off during the experiment. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4378 / 4384
页数:7
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