电化学发光
化学
电子转移
离子
氧化铟锡
电化学
电极
阳极
光化学
分析化学(期刊)
兴奋剂
佩多:嘘
鲁米诺
联轴节(管道)
阴极
发光
光电子学
电子
氧化还原
超氧化物
电子传输链
无机化学
铟
导电聚合物
化学物理
激进的
氧化物
离子流
作者
Wan Zhong,Mengxi Guo,Shihao Sun,Peng Li,Hui Xi,Yingjie Fu,Xueqian Chen,C. K. L. LU
标识
DOI:10.1021/acs.analchem.5c06203
摘要
Electrochemiluminescence (ECL) intensity is simultaneously influenced by both the electron-transfer and mass transport processes. However, the current concerns with ECL amplification focus on either electron transfer or ion transport. In this contribution, luminol–dissolved O 2 ECL amplification from coupled electron and ion transport properties of conductive polymers (CPs) was investigated in detail by employing poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as a model CP. The anodic ECL of luminol–dissolved O 2 at a PEDOT:PSS-modified indium tin oxide (ITO) electrode exhibited a 15-fold signal amplification in comparison to that of bare ITO. Further mechanistic investigations revealed that PEDOT could facilitate the electron-transfer process and promote both the conversion of O 2 into superoxide radicals and the transition of luminol anions to anion radicals. Additionally, the porous structure and electrochemical doping of the swollen PEDOT:PSS film enabled the transport of luminol anions, synergistically increasing the ECL intensity. This work provides a basis for designing CP-based ECL amplification platforms by leveraging the coupled electron and ion transport to govern ECL emission in the luminol–dissolved O 2 system.
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