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用电化学针尖增强拉曼光谱技术对氧还原反应过程中酞菁铁失活的原位表征。

Operando Characterization of Iron Phthalocyanine Deactivation during Oxygen Reduction Reaction Using Electrochemical Tip-Enhanced Raman Spectroscopy.

出版信息

J Am Chem Soc. 2019 Oct 2;141(39):15684-15692. doi: 10.1021/jacs.9b07979. Epub 2019 Sep 18.

Abstract

Electrochemical tip-enhanced Raman spectroscopy (EC-TERS) has been implemented to investigate the structure and activity of iron(II) phthalocyanine (FePc)-a model catalyst for the oxygen reduction reaction (ORR). Using EC-TERS, both reversible change and irreversible degradation to FePc have been observed during ORR. The reversible change in the Raman spectrum of FePc can be related to the FePc molecules that adapt a nonplanar geometry during catalysis. In contrast, the irreversible degradation of FePc is a consequence of FePc demetalation, leading to the subsequent formation of free base phthalocyanine. This observation affirms that FePc demetalation during ORR proceeds via a direct loss of Fe and that carbon corrosion is not the operative mechanism. Importantly, the FePc demetalation process can be correlated with a loss of ORR activity suggesting that Fe-containing sites are essential for FePc to achieve high catalytic activity. This study establishes EC-TERS as a promising technique for the operando characterization of electrocatalytic reactions at the molecular scale.

摘要

电化学尖端增强拉曼光谱(EC-TERS)已被用于研究铁(II)酞菁(FePc)的结构和活性,FePc 是氧还原反应(ORR)的模型催化剂。通过 EC-TERS,在 ORR 过程中观察到 FePc 的可逆变化和不可逆降解。FePc 拉曼光谱的可逆变化可归因于催化过程中 FePc 分子适应非平面几何形状。相比之下,FePc 的不可逆降解是 FePc 脱金属的结果,导致随后形成自由碱酞菁。这一观察结果证实,ORR 过程中 FePc 的脱金属是通过 Fe 的直接损失进行的,而不是通过碳腐蚀进行的。重要的是,FePc 的脱金属过程与 ORR 活性的丧失相关,这表明含 Fe 位点对于 FePc 实现高催化活性是必不可少的。这项研究确立了 EC-TERS 作为在分子尺度上对电催化反应进行原位表征的有前途的技术。

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