化学
铂金
催化作用
过氧化氢
吸附
单原子离子
无机化学
氢
氧气
过氧化物
光化学
物理化学
有机化学
作者
Rubén Rizo,Juan M. Feliú,Enrique Herrero
标识
DOI:10.1016/j.jcat.2021.04.018
摘要
The hydrogen peroxide reduction reaction (HPRR) is investigated at pH = 13 on the Pt basal planes and stepped surfaces with (1 1 1) terraces separated by either monatomic (1 0 0) or (1 1 0) steps. A quantitative analysis of the surface structure effect revealed that Pt(1 1 1) is the most active surface and its activity progressively decreases when steps are introduced. Additionally, inhibition of the HPRR is observed at low potentials, which onset potential is governed by the OHads and the point of maximum entropy (pme) of the interphase. Experiments with different rotation rates suggest the formation of an HPRR intermediate linked to the inhibition process, which is more strongly adsorbed on (1 1 0) than (1 0 0) steps. Finally, a comparison of the HPRR and ORR (oxygen reduction reaction) illustrated the important differences for both reactions, which are dependent on the step density. These divergences have been discussed based on adsorbed intermediates and O2 interactions with the Pt surface.
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