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Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis

机译:杂质离子络合增强二氧化碳还原催化作用

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摘要

Herein, we show that group 11 CO[subscript 2] reduction catalysts are rapidly poisoned by progressive deposition of trace metal ion impurities present in high purity electrolytes. Metal impurity deposition was characterized by XPS and in situ stripping voltammetry and is coincident with loss of catalytic activity and selectivity for CO[subscript 2] reduction, favoring hydrogen evolution on poisoned surfaces. Metal deposition can be suppressed by complexing trace metal ion impurities with ethylenediaminetetraacetic acid or solid-supported iminodiacetate resins. Metal ion complexation allows for reproducible, sustained catalytic activity and selectivity for CO[subscript 2] reduction on Au, Ag, and Cu electrodes. Together, this study establishes the principal mode by which group 11 CO[subscript 2] reduction catalysts are poisoned and lays out a general approach for extending the lifetime of electrocatalysts subject to impurity metal deposition.
机译:在本文中,我们表明第11组CO [下标2]还原催化剂会因高纯度电解质中存在的痕量金属离子杂质的逐步沉积而迅速中毒。金属杂质的沉积通过XPS和原位溶出伏安法进行了表征,并且与催化活性的丧失和对CO [下标2]还原的选择性降低,有利于在有毒表面上析出氢气。通过将痕量金属离子杂质与乙二胺四乙酸或固体负载的亚氨基二乙酸酯树脂络合,可以抑制金属沉积。金属离子络合可以在Au,Ag和Cu电极上实现可再生的,持续的催化活性和CO [下标2]还原的选择性。总之,这项研究建立了第11组CO [下标2]还原催化剂被毒化的主要模式,并提出了一种通用的方法来延长遭受杂质金属沉积的电催化剂的寿命。

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