4.8 Article

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

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 36, Pages 40220-40228

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c07260

Keywords

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

Funding

  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]

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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.

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