Electrochemical synthesis of hydrogen peroxide: Rotating disk electrode and fuel cell studies

被引:78
作者
Lobyntseva, Elena
Kallio, Tanja [1 ]
Alexeyeva, Nadezda
Tammeveski, Kaido
Kontturi, Kyoesti
机构
[1] Aalto Univ, Phys Chem & Electrochem Lab, FI-02015 Helsinki, Finland
[2] Univ Tartu, Inst Phys Chem, EE-51014 Tartu, Estonia
关键词
oxygen reduction; electrocatalysis; peroxide synthesis; rotating disk electrode; fuel cell;
D O I
10.1016/j.electacta.2007.05.076
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical reduction of oxygen on various catalysts was studied using the thin-layer rotating disk electrode (RDE) method. High-surface-area carbon was modified with an anthraquinone derivative and gold nanoparticles. Polytetrafluoroethylene (PTFE) and cationic polyelectrolyte (FAA) were used as binders in the preparation of thin-film electrodes. Our primary goal was to find a good electrocatalyst for the two-electron reduction of oxygen to hydrogen peroxide. All electrochemical measurements were carried out in 0.1 M KOH. Cyclic voltammetry was used in order to characterise the surface processes of the modified electrodes in O-2-free electrolyte. The RDE results revealed that the carbon-supported gold nanoparticles are active catalysts for the four-electron reduction of oxygen in alkaline solution. Anthraquinone-modified high-area carbon catalyses the two-electron reduction at low overpotentials, which is advantageous for hydrogen peroxide production. In addition, the polymer electrolyte fuel cell technology was used for the generation of hydrogen peroxide. The cell was equipped with a bipolar membrane which consisted of commercial Nafion 117 as a cation-exchange layer and FT-FAA as an anion-exchange layer. The bipolar membranes were prepared by a hot pressing method. Use of the FAA ionomer as a binder for the anthraquinone-modified carbon catalyst resulted in production of hydrogen peroxide. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7262 / 7269
页数:8
相关论文
共 61 条
[1]   Electrogeneration of hydroperoxide ion using an alkaline fuel cell [J].
Alcaide, F ;
Brillas, E ;
Cabot, PL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3444-3449
[2]   Limiting behaviour during the hydroperoxide ion generation in a flow alkaline fuel cell [J].
Alcaide, F ;
Brillas, E ;
Cabot, PL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 566 (01) :235-240
[3]   The removal of low level organics via hydrogen peroxide formed in a reticulated vitreous carbon cathode cell, Part 1. The electrosynthesis of hydrogen peroxide in aqueous acidic solutions [J].
Alvarez-Gallegos, A ;
Pletcher, D .
ELECTROCHIMICA ACTA, 1998, 44 (05) :853-861
[4]   The removal of low level organics via hydrogen peroxide formed in a reticulated vitreous carbon cathode cell. Part 2: The removal of phenols and related compounds from aqueous effluents [J].
Alverez-Gallegos, A ;
Pletcher, D .
ELECTROCHIMICA ACTA, 1999, 44 (14) :2483-2492
[5]   RING-DISK ELECTRODE STUDY OF REDUCTION OF OXYGEN ON ACTIVE-CARBON IN ALKALINE-SOLUTION [J].
APPEL, M ;
APPLEBY, AJ .
ELECTROCHIMICA ACTA, 1978, 23 (11) :1243-1246
[6]   KINETICS OF OXYGEN REDUCTION ON CARBON MATERIALS IN ALKALINE-SOLUTION [J].
APPLEBY, AJ ;
MARIE, J .
ELECTROCHIMICA ACTA, 1979, 24 (02) :195-202
[7]   PREPARATION AND CHARACTERIZATION OF CARBON TITANIUM-DIOXIDE SURFACES - THE REDUCTION OF OXYGEN [J].
BAEZ, VB ;
PLETCHER, D .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 382 (1-2) :59-64
[8]  
BREZINA M, 1973, COLLECT CZECH CHEM C, V38, P985
[9]   A small-scale flow alkaline fuel cell for on-site production of hydrogen peroxide [J].
Brillas, E ;
Alcaide, F ;
Cabot, PL .
ELECTROCHIMICA ACTA, 2002, 48 (04) :331-340
[10]   Hydrogen peroxide synthesis: An outlook beyond the anthraquinone process [J].
Campos-Martin, Jose M. ;
Blanco-Brieva, Gema ;
Fierro, Jose L. G. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (42) :6962-6984