催化作用
惰性
兴奋剂
氧还原反应
氢
氧气
可逆氢电极
Atom(片上系统)
材料科学
惰性气体
氧原子
化学
铂金
电极
化学工程
无机化学
纳米技术
物理化学
电化学
光电子学
分子
工作电极
有机化学
嵌入式系统
工程类
计算机科学
作者
Wei‐Hong Lai,Lifu Zhang,Zichao Yan,Weibo Hua,Sylvio Indris,Yaojie Lei,Hanwen Liu,Yunxiao Wang,Zhenpeng Hu,Huan Liu,Shulei Chou,Guoxiu Wang,Shi Xue Dou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-10-04
卷期号:21 (19): 7970-7978
被引量:28
标识
DOI:10.1021/acs.nanolett.1c02013
摘要
The performance of single-atom catalysts strongly depends on their particular coordination environments in the near-surface region. Herein, we discover that engineering extra Pt single atoms in the subsurface (Ptsubsurf) can significantly enhance the catalytic efficiency of surface Pt single atoms toward the oxygen reduction reaction (ORR). We experimentally and theoretically investigated the effects of the Ptsubsurf single atoms implanted in different positions of the subsurface of Co particles. The local environments and catalytic properties of surface Pt1 are highly tunable via Ptsubsurf doping. Specifically, the obtained Pt1@Co/NC catalyst displays a remarkable performance for ORR, achieving mass activity of 4.2 mA μgPt–1 (28 times higher than that of commercial Pt/C) at 0.9 V versus reversible hydrogen electrode (RHE) in 0.1 M HClO4 solution with high stability over 30000 cycles.
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