催化作用
氧还原
化学
氧还原反应
Atom(片上系统)
还原(数学)
氧气
氧原子
材料科学
纳米技术
有机化学
物理化学
分子
计算机科学
电化学
几何学
电极
数学
嵌入式系统
作者
Ergui Luo,Wang Xian,Liqin Gao,Liyuan Gong,Tuo Zhao,Junjie Ge,Zheng Jiang,Changpeng Liu
标识
DOI:10.1002/ange.201906289
摘要
Abstract Single‐atom catalysts (SACs) are attracting widespread interest for the catalytic oxygen reduction reaction (ORR), with Fe−N x SACs exhibiting the most promising activity. However, Fe‐based catalysts suffer serious stability issues as a result of oxidative corrosion through the Fenton reaction. Herein, using a metal‐organic framework as an anchoring matrix, we for the first time obtained pyrolyzed Cr/N/C SACs for the ORR, where the atomically dispersed Cr is confirmed to have a Cr−N 4 coordination structure. The Cr/N/C catalyst exhibits excellent ORR activity with an optimal half‐wave potential of 0.773 V versus RHE. More excitingly, the Fenton reaction is substantially reduced and, thus, the final catalysts show superb stability. The innovative and robust active site for the ORR opens a new possibility to circumvent the stability issue of the non‐noble metal ORR catalysts.
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