石墨烯
酞菁
电化学
循环伏安法
材料科学
层状结构
聚合物
化学工程
化学
电极
无机化学
纳米技术
物理化学
复合材料
工程类
作者
Longbin Li,Xiannong Tang,Senhe Huang,Chenbao Lu,Dirk Lützenkirchen‐Hecht,Kai Yuan,Xiaodong Zhuang,Yiwang Chen
标识
DOI:10.1002/ange.202301642
摘要
Abstract Iron phthalocyanine‐based polymers (PFePc) are attractive noble‐metal‐free candidates for catalyzing oxygen reduction reaction (ORR). However, the low site‐exposure degree and poor electrical conductivity of bulk PFePc restricted their practical applications. Herein, laminar PFePc nanosheets covalently and longitudinally linked to graphene (3D‐G‐PFePc) was prepared. Such structural engineering qualifies 3D‐G‐PFePc with high site utilization and rapid mass transfer. Thence, 3D‐G‐PFePc demonstrates efficient ORR performance with a high specific activity of 69.31 μA cm −2 , a high mass activity of 81.88 A g −1 , and a high turnover frequency of 0.93 e s −1 site −1 at 0.90 V vs. reversible hydrogen electrode in O 2 ‐saturated 0.1 M KOH, outperforming the lamellar PFePc wrapped graphene counterpart. Systematic electrochemical analyses integrating variable‐frequency square wave voltammetry and in situ scanning electrochemical microscopy further underline the rapid kinetics of 3D‐G‐PFePc towards ORR.
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