用于增强异质电催化活性的噻吩基桥接融合卟啉带

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Hadi Ghahramanzadehasl, Deepak Bansal, Drialys Cardenas Morcoso, Nicolas D. Boscher
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引用次数: 0

摘要

开发高度共轭的金属卟啉组件是提高其催化活性以优化能源转换过程的关键步骤。在本文中,二噻吩基取代的镍(II)卟啉被用来形成高度共轭的卟啉结构。在碱性 pH 条件下,卟啉基共轭聚合物催化剂具有 266 mV 的低起始过电位和高反应动力学(Tafel 斜率为 69.9 mV/dec),电流密度达到 4.5 mA/cm2。卟啉基共轭聚合物催化剂显著的 OER 催化活性归功于共轭作用的增强,这种共轭作用是通过一个独特的过程发生的,其中包括卟啉的直接融合,然后是融合卟啉带的噻吩桥接,最终导致建立一个高度交联的卟啉网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thienyl-Bridged Fused Porphyrin Tapes for Enhanced Heterogeneous Electrocatalytic Activity

Thienyl-Bridged Fused Porphyrin Tapes for Enhanced Heterogeneous Electrocatalytic Activity

Thienyl-Bridged Fused Porphyrin Tapes for Enhanced Heterogeneous Electrocatalytic Activity

The development of highly conjugated metalloporphyrin assemblies is a crucial step to improve their catalytic activity for optimal energy conversion processes. Herein, di-thienyl substituted nickel(II) porphyrin is used to form a highly conjugated porphyrin structure. The resulting porphyrin-based conjugated polymer catalyst exhibited exceptional oxygen evolution reaction “OER” performances, featuring a low onset overpotential of 266 mV and high reaction kinetics (Tafel slope of 69.9 mV/dec) under alkaline pH conditions, achieving a current density of 4.5 mA/cm2. The remarkable OER catalytic activity of porphyrin-based conjugated polymer catalyst is attributed to the enhancement of the conjugation, which occurs through a unique process involving direct fusion of the porphyrins followed by thienyl bridging of the fused porphyrin tapes, ultimately leading to the establishment of a highly cross-linked porphyrinic network.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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