4.8 Article

NiCoFe-Layered Double Hydroxides/N-Doped Graphene Oxide Array Colloid Composite as an Efficient Bifunctional Catalyst for Oxygen Electrocatalytic Reactions

期刊

ADVANCED ENERGY MATERIALS
卷 8, 期 9, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.201701905

关键词

array-like structures; bifunctional catalysts; in situ growth; layered double hydroxide; N-doped graphene

资金

  1. National Natural Science Foundation of China (NSFC) [21676022]
  2. Program for Changjiang Scholars and Innovative Research Team in the University [IRT1205]
  3. Fundamental Research Funds for the Central Universities [JD1701, JD 1612, YS1406]
  4. Long-Term Subsidy Mechanism from the Ministry of Finance
  5. Ministry of Education of PRC
  6. National Key Research and Development Project [2016YFF0204402]

向作者/读者索取更多资源

Ternary NiCoFe-layered double hydroxide ((NiCoFe)-Fe-III-LDH) with Co3+ is grafted on nitrogen-doped graphene oxide (N-GO) by an in situ growth route. The array-like colloid composite of (NiCoFe)-Fe-III-LDH/N-GO is used as a bifunctional catalyst for both oxygen evolution/reduction reactions (OER/ORR). The (NiCoFe)-Fe-III-LDH/N-GO array has a 3D open structure with less stacking of LDHs and an enlarged specific surface area. The hierarchical structure design and novel material chemistry endow high activity propelling O-2 redox. By exposing more amounts of Ni and Fe active sites, the (NiCoFe)-Fe-III-LDH/N-GO illustrates a relatively low onset potential (1.41 V vs reversible hydrogen electrode) in 0.1 mol L-1 KOH solution under the OER process. Furthermore, by introducing high valence Co3+, the onset potential of this material in ORR is 0.88 V. The overvoltage difference is 0.769 V between OER and ORR. The key factors for the excellent bifunctional catalytic performance are believed to be the Co with a high valence, the N-doping of graphene materials, and the highly exposed Ni and Fe active sites in the array-like colloid composite. This work further demonstrates the possibility to exploit the application potential of LDHs as OER and ORR bifunctional electrochemical catalysts.

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