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Electrochemical Reduction of CO2 on Compositionally Variant Au-Pt Bimetallic Thin Films

机译:组分变化au-pt双金属薄膜上CO2的电化学还原

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摘要

The electrocatalytic reduction of CO2 on Au-Pt bimetallic catalysts with different compositions was evaluated, offering a platform for uncovering the correlation between the catalytic activity and the surface composition of bimetallic electrocatalysts. The Au-Pt alloy films were synthesized by a magnetron sputtering co-deposition technique with tunable composition. It was found that the syngas ratio (CO:H2) on the Au-Pt films is able to be tuned by systematically controlling the binary composition. This tunable catalytic selectivity is attributed to the variation of binding strength of COOH and CO intermediates, influenced by the surface electronic structure (d-band center energy) which is linked to the surface composition of the bimetallic films. Notably, a gradual shift of the d-band center away from the Fermi level was observed with increasing Au content, which correspondingly reduces the binding strength of the COOH and CO intermediates, leading to the distinct catalytic activity for the reduction of CO2 on the compositionally variant Au-Pt bimetallic films. In addition, the formation of formic acid in the bimetallic systems at reduced overpotentials and higher yield indicates that synergistic effects can facilitate reaction pathways for products that are not accessible with the individual components.
机译:评价了在具有不同组成的Au-Pt双金属催化剂上电催化还原CO2的方法,为揭示双金属电催化剂的催化活性和表面组成之间的相关性提供了平台。采用磁控溅射共沉积技术制备了具有可调组成的Au-Pt合金薄膜。发现可以通过系统地控制二元组成来调节Au-Pt膜上的合成气比率(CO∶H 2)。这种可调节的催化选择性归因于受与双金属膜表面组成有关的表面电子结构(d带中心能)影响的COOH和CO中间体结合强度的变化。值得注意的是,随着Au含量的增加,观察到d波段中心逐渐偏离费米能级,这相应地降低了COOH和CO中间体的结合强度,从而导致了明显的催化活性,从而降低了成分上的CO2。变体Au-Pt双金属膜。此外,双金属体系中甲酸的形成以降低的过电势和更高的收率表明协同作用可以促进单个成分无法获得的产物的反应途径。

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