Electrochemical Screening of Au/Pt Catalysts for the Thermocatalytic Synthesis of Hydrogen Peroxide Based on Their Oxygen Reduction and Hydrogen Oxidation Activities Probed via Voltammetric Scanning Electrochemical Microscopy

扫描电化学显微镜 催化作用 线性扫描伏安法 电化学 过氧化氢 氧化还原 化学 循环伏安法 化学工程 无机化学 材料科学 纳米技术 电极 有机化学 物理化学 工程类
作者
Yuanya Zhao,Jason S. Adams,Aravind Baby,Matthew L. Kromer,David W. Flaherty,Joaquín Rodríguez‐López
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:10 (51): 17207-17220 被引量:9
标识
DOI:10.1021/acssuschemeng.2c05120
摘要

Electrochemical analysis provides a convenient way to screen active materials for thermocatalytic processes involving implicit electrochemical redox mechanisms. Here, we show how a combinatorial method based on scanning electrochemical microscopy (SECM) rapidly screens multiple catalysts for hydrogen peroxide direct synthesis reaction by independently analyzing their hydrogen oxidation and oxygen reduction reactivities on the same chip. We present a reproducible and quantifiable procedure to fabricate catalyst spot array samples using photolithography and microdispensing. This procedure enables the exploration of up to 10 catalysts with three replicates each on one chip, allowing us to study 30 compositions to identify reactive trends in a vast compositional space. SECM imaging with linear sweep voltammetry improved the accuracy and efficiency of data collection. Kinetic parameters of both half-reactions for each catalyst were extracted from experimental data with the help of established analytical theory and finite element analysis simulation. A library of AuxPty catalysts with a range of Au/Pt ratios from 1200:1 to 120:12 were examined. For the synthesized AuxPty catalysts, the rate constants of oxygen reduction and hydrogen reduction increase as Pt content increases and then level off beyond Au120Pt7. Therefore, to achieve the highest activity while keeping the cost low, Au120Pt7 would be a promising composition to further investigate. We believe this SECM-based technique will expedite the catalyst design and discovery process for classes of thermochemical reactions involving underlying heterolytic electrochemical mechanisms, thus assisting in the synthesis and utilization of sustainable fuels and commodity chemicals.
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