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Surface Limited Redox Replacement Deposition of Platinum Ultrathin Films on Gold:Thickness and Structure Dependent Activity towards the Carbon Monoxide and Formic Acid Oxidation reactions

机译:铂超薄膜在金上的表面有限氧化还原置换沉积:厚度和结构对一氧化碳和甲酸氧化反应的活性

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摘要

The Surface Limited Redox Replacement (SLRR) method in one-cell configuration has been used to grow Pt ultra-thin films on Au using two different sacrificial underpotentially deposited (UPD) layers: Cu and Pb. The Pt films grown by multiple Pb UPD-SLRR cycles (1-10) exhibit comparable roughness as determined by integration of the H UPD charge. In contrast to that, due to the 2:1 stoichiometry of the replacement between Cu UPD layer and PtCl ions, the Pt films grown by Cu UPD-SLRR show a steady increase of the roughness with the number of deposition cycles (1-10). The differences in the structure of the films have been used as a platform to study the stripping of pre-adsorbed CO and the formic acid oxidation (FAO) reaction as a function of their thickness. On Pt films of comparable roughness grown by SLRR of Pb UPD, the CO stripping peak shows no significant changes in the onset potential and a small peak maximum shift of ∼ 7 mV between the film of lowest (1 ML) and all higher thicknesses (2-10 ML). However, Pt films grown by SLRR of Cu UPD show a larger potential window of differences of ∼ 26 mV over which the peak maximum potentials shift more negative with the number of deposition cycles. The most positive CO stripping potential obtained for a sub-ML Pt (∼ 0.56 ML) grown by a single SLRR cycle suggests CO is more strongly bonded than on films grown by multiple replacements that completely cover the Au substrate. The measured activity toward FAO is in agreement with the CO electro-oxidation results. No significant differences in the activity for FAO have been observed on Pt films of comparable roughness grown by SLRR of Pb UPD which show activity close to that of pure Pt. However, a more significant change of FAO reactivity has been measured for Pt films grown via SLRR of Cu UPD with the highest activity measured for a sub-ML Pt deposit. Following subsequent replacements, the FAO activity tends towards that of pure Pt. The observed differences in the catalytic behaviour of Pt films grown by SLRR are the result of the differences in their morphology and the nanocluster structure of the films. On sub-monolayer Pt films, the behaviour is dominated by nanocluster size and coverage of the deposit. For a completely covered surface of Au, the effect of roughness of Pt films and nanocluster nature of the deposit has a dominant role in the behaviour and activity.
机译:使用单单元配置的表面受限氧化还原置换(SLRR)方法已使用两个不同的牺牲性欠电位沉积(UPD)层:Cu和Pb在Au上生长Pt超薄膜。通过H UPD电荷的积分确定,通过多个Pb UPD-SLRR循环(1-10)生长的Pt膜表现出相当的粗糙度。与此相反,由于Cu UPD层和PtCl离子之间的化学计量比为2:1,因此Cu UPD-SLRR生长的Pt膜随着沉积循环次数的增加而显示出粗糙度的稳定增长(1-10) 。薄膜结构的差异已用作研究预吸附CO的汽提和甲酸氧化(FAO)反应随厚度变化的平台。在Pb UPD的SLRR所生长的粗糙度相当的Pt膜上,CO剥离峰在最低(1 ML)膜和所有更高厚度的膜之间显示出开始电势无明显变化,并且最大峰值的小位移约为7 mV(2 -10毫升)。但是,通过Cu UPD的SLRR生长的Pt膜显示出较大的电位差窗口,约为26 mV,在该窗口上,最大峰值电势随沉积循环数的增加而向负方向移动。通过单个SLRR循环生长的亚ML Pt(约0.56 ML)获得的最强的CO剥离潜力表明,与通过多次覆盖完全覆盖Au基材的替代膜生长的膜相比,CO的结合力更强。测得的对粮农组织的活动与一氧化碳电氧化结果一致。在由铅UPD的SLRR生长的粗糙度相当的Pt膜上,未观察到FAO活动的显着差异,其活性接近纯Pt。但是,对于通过Cu UPD的SLRR生长的Pt膜,测量到的FAO反应性发生了更为显着的变化,而对于次ML Pt沉积而言,其活性最高。在随后的替换之后,粮农组织的活动趋向于纯铂。观察到的通过SLRR生长的Pt薄膜的催化行为的差异是其形态和薄膜纳米簇结构差异的结果。在亚单层Pt膜上,其行为主要由纳米簇的大小和沉积物的覆盖范围决定。对于完全覆盖的金表面,Pt膜的粗糙度和沉积物的纳米簇性质的影响在行为和活性中起主要作用。

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