首页> 外文期刊>Electrochimica Acta >Electrocatalytic reduction of dioxygen at a modified glassy carbon electrode based on Nafion-dispersed single-walled carbon nanotubes and cobalt-porphyrin with palladium nanoparticles in acidic media
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Electrocatalytic reduction of dioxygen at a modified glassy carbon electrode based on Nafion-dispersed single-walled carbon nanotubes and cobalt-porphyrin with palladium nanoparticles in acidic media

机译:基于Nafion分散的单壁碳纳米管和钴卟啉与钯纳米粒子在酸性介质中的修饰玻碳电极上电催化还原双氧

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摘要

Cathodic dioxygen (O_2) reduction was performed at a modified glassy carbon electrode (GCE) by single-walled carbon nanotubes (SWCNT)/Nafion (NF) film with cobalt (II) tetra (2-amino-phenyl) porphyrin (CoTAPP) and palladium (Pd) nanoparticles incorporated and employed as doping agents. Both the electrochemical behavior of SWCNT with a P(CoTAPP)-Pd nanoparticle matrix and the electrocatalytic reduction of O_2 were investigated using transmission electron microscopy (TEM), cyclic voltammetry (CV) and rotating ring-disk electrode (RRDE) techniques in 0.1 mol l~(-1) H_2SO_4 aqueous solutions. The electrocatalytic reduction of O_2 at the SWCNT/NF/P(CoTAPP)-Pd composite film established a pathway of four-electron transfer reductions into H_2O. Hydrodynamic voltammetry revealed that the modified electrode was catalyzed effectively by the four-electron transferred reduction of dioxygen into H_2O with minimal generation of H_2O_2. The SWCNT/NF/P(CoTAPP)-Pd composite film showed a highly efficient electrocatalytic performance. P(CoTAPP)-Pd was an effective mediator for the reduction of dioxygen and was responsible for the enhanced catalytic activity.
机译:阴极双氧(O_2)还原是在修饰的玻碳电极(GCE)上通过单壁碳纳米管(SWCNT)/ Nafion(NF)膜与钴(II)四(2-氨基-苯基)卟啉(CoTAPP)和掺入并用作掺杂剂的钯(Pd)纳米颗粒。使用透射电子显微镜(TEM),循环伏安法(CV)和旋转环盘电极(RRDE)技术在0.1 mol中研究了具有P(CoTAPP)-Pd纳米粒子基质的SWCNT的电化学行为和O_2的电催化还原。 1〜(-1)H_2SO_4水溶液。 OCNT在SWCNT / NF / P(CoTAPP)-Pd复合膜上的电催化还原建立了四电子转移还原为H_2O的途径。流体动力学伏安法表明,修饰的电极被四电子转移的双氧还原成H_2O有效地催化,生成的H_2O_2最少。 SWCNT / NF / P(CoTAPP)-Pd复合膜表现出高效的电催化性能。 P(CoTAPP)-Pd是一种有效的介体,可减少双氧,并负责增强催化活性。

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