催化作用
离解(化学)
贵金属
材料科学
纳米颗粒
化学工程
金属
电化学
无机化学
碱土金属
氢
氢氧化物
纳米技术
化学
物理化学
电极
冶金
有机化学
工程类
作者
Hanbin Liao,Chao Wei,Jingxian Wang,Adrian C. Fisher,Thirumany Sritharan,Zhenxing Feng,Zhichuan J. Xu
标识
DOI:10.1002/aenm.201701129
摘要
Abstract The hydrogen evolution reaction (HER) on a noble metal surface in alkaline media is more sluggish than that in acidic media due to the limited proton supply. To promote the reaction, it is necessary to transform the alkaline HER mechanism via a multisite catalyst, which has additional water dissociation sites to improve the proton supply to an optimal level. Here, this study reports a top‐down strategy to create a multisite HER catalyst on a nano‐Pd surface and how to further fine‐tune the areal ratio of the water dissociation component to the noble metal surface in core/shell‐structured nanoparticles (NPs). Starting with Pd/Fe 3 O 4 core/shell NPs, electrochemical cycling is used to tune the coverage of iron (oxy)hydroxide on a Pd surface. The alkaline HER activity of the core/sell Pd/FeO x (OH) 2−2 x NPs exhibits a volcano‐shaped correlation with the surface Fe species coverage. This indicates an optimum coverage level where the rates of both the water dissociation step and the hydrogen formation step are balanced to achieve the highest efficiency. This multisite strategy assigns multiple reaction steps to different catalytic sites, and should also be extendable to other core/shell NPs to optimize their HER activity in alkaline media.
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