Deconvoluting HER from CO2RR on an FeN4-Derived Catalyst Using Fourier-Transformed Alternating Current Voltammetry

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2025-04-03 DOI:10.1021/acscatal.4c06850
Nicole Segura-Salas, Rifael Z. Snitkoff-Sol, Danielle Ragonis, Sun-Myung Kim, Jan P. Hofmann, Ulrike I. Kramm, Lior Elbaz
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Abstract

Deciphering electrocatalytic processes with well-defined molecular catalysts is crucial for understanding complex reaction mechanisms. In this study, we investigated iron phthalocyanine (FePc) as a model catalyst for the CO2 reduction reaction (CO2RR). With direct current (dc) voltammetry, we described in detail the redox transitions of the catalyst and emphasized its importance for elucidating the formation of the activated catalytic site. The mechanism for CO2RR and HER was studied with Tafel plot analysis (dc-based) and Fourier-transformed alternating current voltammetry (FTacV). We showed the potential of FTacV as a technique to study catalytic processes vs dc techniques as it allowed us to observe the underlying electron transfer during CO2RR, revealing the formation of *CO2 and defining limiting steps in the reaction. These findings were compared against literature-based spectroscopic results on FePc to propose a possible mechanism. Overall, this work presents FTacV as a powerful tool for mechanistic studies in electrocatalysis, offering more profound insights into electron transfer dynamics during catalytic reactions.

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用傅里叶变换交流伏安法在fen4衍生催化剂上反伏CO2RR中的HER
破译具有明确定义的分子催化剂的电催化过程对于理解复杂的反应机理至关重要。在这项研究中,我们研究了酞菁铁(FePc)作为CO2还原反应(CO2RR)的模型催化剂。利用直流伏安法,我们详细描述了催化剂的氧化还原转变,并强调了其对阐明活化催化位点形成的重要性。采用Tafel图分析(dc-based)和傅立叶变换交流伏安法(FTacV)研究了CO2RR和HER的作用机理。我们展示了FTacV作为一种研究催化过程的技术的潜力,而不是直流技术,因为它允许我们观察CO2RR过程中潜在的电子转移,揭示*CO2 -的形成并确定反应中的限制步骤。将这些发现与基于FePc的文献光谱结果进行比较,以提出可能的机制。总的来说,这项工作将FTacV作为电催化机理研究的有力工具,为催化反应中的电子传递动力学提供了更深刻的见解。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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