部分
氧化还原
电化学
阴极
电极
铂金
电子转移
动力学
石墨
化学
玻璃碳
铜
反应机理
无机化学
化学工程
材料科学
光化学
物理化学
有机化学
循环伏安法
催化作用
物理
量子力学
工程类
作者
Meilin Liu,Steven J. Visco,Lutgard C. De Jonghe
摘要
The electrode kinetics of a diverse group of organodisulfide cathode materials have been systematically investigated. The electrochemical behavior of these redox couples was studied as a function of the organic moiety (R) in the organodisulfide compounds (RSSR). These studies were performed with a variety of working electrodes, including platinum, glassy carbon, graphite, stainless steel, aluminum, and copper. The possible reaction pathways and mechanisms have been hypothetically postulated, theoretically analyzed, and experimentally verified. Observations showed that while electron transfer rate constants varied with organic moiety, the mechanistic details of the redox path were invariant with the R groups of the organodisulfides studied. The reaction mechanism, as determined from experimental observations, can be expressed as
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