催化作用
材料科学
石墨烯
选择性
镍
可逆氢电极
光化学
化学工程
无机化学
过氧化氢
电催化剂
电极
电解质
纳米技术
化学
电化学
物理化学
工作电极
有机化学
冶金
工程类
作者
Xiaozhe Song,Ning Li,Huan Zhang,Li Wang,Yanjun Yan,Hui Wang,Linyuan Wang,Zhaoyong Bian
标识
DOI:10.1021/acsami.0c01278
摘要
Hydrogen peroxide (H2O2) production by electrocatalytic two-electron oxygen reduction shows promise as a replacement for energy-intensive anthraquinone oxidation or H2/O2 direct synthesis. Here, we report on graphene-supported Ni single-atom (SA) electrocatalysts, which are synthesized by a simple surfactant-free reduction process with enhanced electrocatalytic activity and stability. Unlike conventional Ni nanoparticles or alloy catalysts, the well-dispersed Ni-SA sites lack adjacent Ni atoms. This structure promotes H2O2 production by a two-electron oxygen reduction pathway under an alkaline condition (pH = 13). This catalyst exhibited enhanced H2O2 selectivity (>94%) with a considerable mass activity (2.11 A mgNi-1 at 0.60 V vs reversible hydrogen electrode), owing to the presence of oxygen functional groups and isolated Ni sites. Density functional theory calculations provide insights into the role of this catalyst in optimizing the two-electron oxygen reduction reaction pathway with high H2O2 selectivity. This work suggests a new method for controlling reaction pathways in atomically dispersed non-noble catalysts.
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