Electrochemical corrosion of a glassy carbon electrode

被引:406
|
作者
Yi, Youngmi [1 ]
Weinberg, Gisela [2 ]
Prenzel, Marina [1 ]
Greiner, Mark [1 ,2 ]
Heumann, Saskia [1 ]
Becker, Sylvia [1 ]
Schloegl, Robert [1 ,2 ]
机构
[1] Max Planck Inst Chem Energy Convers, Stiftstr 34-36, D-45470 Mulheim, Germany
[2] Max Planck Gesell, Fritz Haber Inst, Faradayweg 4-6, D-14195 Berlin, Germany
关键词
Carbon corrosion; Carbon electrode; Glassy carbon; Electrochemical oxidation; Acid catalyzed addition/substitution; Radical substitution; Local selective oxidation; FUNCTIONAL-GROUPS; OXYGEN EVOLUTION; SPECTROSCOPIC CHARACTERIZATION; ELECTROCATALYTIC ACTIVITY; NITROGEN; ELECTROREDUCTION; ELLIPSOMETRY; ACTIVATION; BLACK;
D O I
10.1016/j.cattod.2017.07.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Glassy carbon is widely used in electrochemistry due to its properties of high temperature resistance, hardness, low density and low electrical resistance. The present study focuses on the chemical resistance under electrochemical oxidative conditions, which occur under oxygen-involving reactions like oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The electrochemical performance of glassy carbon investigated in alkaline, neutral and acidic media reveal the same chemical processes during the OER but showing different degradation mechanism. The electrochemical signature of the corrosion in different media could be directly associated with the formation of oxygen functional groups determined by spectroscopic methods like Raman, infrared (IR) and x-ray photoelectron spectroscopy (XPS). The morphology change of the carbon surface caused by carbon oxidation was investigated by microscopy. A rough surface was obtained in the acidic case, whereas dents were seen in alkaline media. It is assumed that the glassy carbon electrode in acidic media degrades by forming surface oxides by acid catalyzed process leading to ring opening in the graphitic structure and therefore oxidation in the bulk. In alkaline media OH radicals preferentially react with alkyl site chains, leading to oxidation of the edges of carbon layers until they become hydrophilic and dissolve.
引用
收藏
页码:32 / 40
页数:9
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