4.8 Article

Boosted Oxygen Evolution Reactivity via Atomic Iron Doping in Cobalt Carbonate Hydroxide Hydrate

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 36, 页码 40220-40228

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c07260

关键词

atomically doped Fe; intrinsic activity; single atom catalysts; in-situ electrochemical transformation; oxygen evolution reaction

资金

  1. Beijing Natural Science Foundation [JQ18005]
  2. National Natural Science Foundation of China [51671003, 21427811, 21721003]
  3. Instrument Foundation CAS [YJ-KYYQ20180028]
  4. MOST, China [2016YFA0203200, 2017YFA0205700]
  5. Youth Innovation Promotion Association CAS [2016208]
  6. Jilin Province Science Technology Development Plan Project [20170101194JC]

向作者/读者索取更多资源

Cobalt carbonate hydroxide hydrate (CCHH) has long been functioning merely as a precursor to prepare compound catalysts; however, its intrinsic potential for the oxygen evolution reaction (OER) is quite limited due to its poor catalytic activity. Herein, a concept has been proposed to solve this issue by doping Fe into CCHH nanowires grown on nickel foam (denoted as Fe-CCHH/NF) for achieving efficient OER catalysis by electro-chemical transformation. The obtained Fe-CCHH/NF-30 exhibits OER catalytic performance with an overpotential of only 200 mV versus the reversible hydrogen electrode (vs. RHE) at a current density of 10 mA cm(-2) and small Tafel slope of 50 mV dec(-1) in 1 M KOH. Moreover, it displays stability for over 130 h at a large current density of 55 mA cm(-2), and no activity decline is observed after the 3000 cycle test. The performance of Fe-CCHH/NF-30 renders it one of the most promising OER catalysts. The density functional theory calculation reveals that the doped Fe can greatly enhance the OER activity by lowering the reactive energy barrier.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据