Mass Transport Influence in the SO2 Oxidation Reaction on Au Electrodes

被引:2
|
作者
De Angelis, Leonardo D. [2 ]
de Torresi, Susana Cordoba I. [2 ]
Dourado, Andre H. B. [1 ]
机构
[1] Univ Sao Paulo, Dept Fisico Quim, Inst Quim Sao Carlos, Ave Trab Sao Carlense 400, BR-13566590 Sao Carlos, SP, Brazil
[2] Univ Sao Paulo, Dept Quim Fundamental, Inst Quim, Ave Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Electrochemistry; Mass transport; Reaction mechanisms; Sulfur dioxide; Water splitting; AQUEOUS SULFUR-DIOXIDE; POLYCRYSTALLINE GOLD ELECTRODES; HOMOGENEOUS CHEMICAL-KINETICS; ROTATING-DISK HMRD; ELECTROCATALYTIC OXIDATION; ELECTROCHEMICAL OXIDATION; SULFITE OXIDATION; ACIDIC MEDIA; CARBON-STEEL; HYDROGEN;
D O I
10.1002/celc.202201032
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The use of fossil fuels as energy source is unsustainable in the long term and net-zero carbon processes need to be implemented to maintain environmental balance. One could make use of assisted water electrolysis to produce clean hydrogen and avoid high overpotentials observed for the oxygen evolution reaction by switching to the SO2 oxidation reaction (SO2OR). This process exhibits a complex mechanism on Au electrodes, which is strongly affected by convection, exhibiting an anti-Levich behavior, in which the limiting current linearly decreases with the square root of the rotation rate. Likewise, the bi-stability region observed in the j/E profiles narrows in a sigmoidal profile with the rotation rate, leading to a non-linear phenomenon with two controlling parameters, mass transport and potential applied. These events were understood to be related to the changing in the reaction mechanism by controlling the electrode rotation, much related to the decrease in the current aforementioned.
引用
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页数:8
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