石墨烯
电化学
材料科学
酞菁
循环伏安法
层状结构
聚合物
化学工程
电极
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/anie.202301642
摘要
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 O2 -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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