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Tuning Reaction Pathways of Electrochemical Conversion of CO2 by Growing Pd Shells on Ag Nanocubes

机译:在银纳米立方体上生长钯壳层调控CO2电化学转化反应途径

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Y The electrochemical carbon dioxide reduction reaction (CO2RR) has been studied on Ag, Pd, Ag@Pd1-2L nanocubes using a combination of in situ characterization and density functional theory calculations. By manipulating the deposition and diffusion rates of Pd atoms on Ag nanocubes, Ag@Pd core-shell nanocubes with a shell thickness of 1-2 atomic layers have been successfully synthesized for CO2RR. Pd nanocubes produce CO with high selectivity due to the transformation of Pd to Pd hydride (PdH) during CO2RR. In contrast, PdH formation becomes more difficult in Ag@Pd1-2L core-shell nanocubes, which inhibits CO production from the *HOCO intermediate and thus tunes the reaction pathway toward HCOOH. Ag nanocubes exhibit high selectivity toward H-2, and there is no phase transition during CO2RR. The results demonstrate that the CO2RR reaction pathways can be manipulated through engineering the surface structure of Pd-based catalysts by allowing or preventing the formation of PdH.
机译:Y 采用原位表征和密度泛函理论计算相结合的方法,研究了 Ag、Pd Ag@Pd1-2L 纳米立方体上的电化学二氧化碳还原反应 (CO2RR)。通过调控Pd原子在Ag纳米立方体上的沉积和扩散速率,成功合成了壳层厚度为1-2个原子层的Ag@Pd核壳纳米立方体。Pd纳米立方体在CO2RR过程中将Pd转化为Pd氢化物(PdH),从而产生具有高选择性的CO。相比之下,在Ag@Pd1-2L核壳纳米立方体中,PdH的形成变得更加困难,这抑制了*HOCO中间体产生的CO,从而调整了HCOOH的反应途径。Ag纳米立方体对H-2表现出高选择性,并且在CO2RR过程中没有相变。结果表明,通过允许或阻止PdH的形成,可以通过设计Pd基催化剂的表面结构来操纵CO2RR反应途径。

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