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Quantifying the density and utilization of active sites in non-precious metal oxygen electroreduction catalysts

机译:量化非贵金属氧电还原催化剂中活性位的密度和利用

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摘要

Carbon materials doped with transition metal and nitrogen are highly active, non-precious metal catalysts for the electrochemical conversion of molecular oxygen in fuel cells, metal air batteries, and electrolytic processes. However, accurate measurement of their intrinsic turn-over frequency and active-site density based on metal centres in bulk and surface has remained difficult to date, which has hampered a more rational catalyst design. Here we report a successful quantification of bulk and surface-based active-site density and associated turn-over frequency values of mono- and bimetallic Fe/N-doped carbons using a combination of chemisorption, desorption and 57Fe Mössbauer spectroscopy techniques. Our general approach yields an experimental descriptor for the intrinsic activity and the active-site utilization, aiding in the catalyst development process and enabling a previously unachieved level of understanding of reactivity trends owing to a deconvolution of site density and intrinsic activity.
机译:掺杂有过渡金属和氮的碳材料是高活性的非贵金属催化剂,用于燃料电池,金属空气电池和电解过程中分子氧的电化学转化。然而,至今仍难以根据散装和表面的金属中心准确测量其固有的翻转频率和活性位密度,这阻碍了更合理的催化剂设计。在这里,我们报告了结合化学吸附,解吸和 57 的单/双金属Fe / N掺杂碳的体积和基于表面的活性位点密度以及相关的转换频率值的成功量化FeMössbauer光谱技术。我们的通用方法为内在活性和活性位利用提供了实验性描述,有助于催化剂的开发过程,并且由于位密度和内在活性的去卷积,使得人们对反应趋势的理解达到了前所未有的水平。

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