4.8 Article

Freestanding 2D NiFe Metal-Organic Framework Nanosheets: Facilitating Proton Transfer via Organic Ligands for Efficient Oxygen Evolution Reaction

期刊

SMALL
卷 18, 期 26, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202201076

关键词

bimetallic metal-organic framework (MOFs); NiFe layered double hydroxides (LDHs); oxygen evolution; two-dimensional materials

资金

  1. New Faculty Start-up Grant of the City University of Hong Kong [9610421]
  2. Innovation and Technology Fund [ITS/095/20, GHP/100/20SZ]
  3. Research Grants Council of Hong Kong [21301319, 11306521]
  4. Guangdong Provincial Science and Technology Plan [2021A0505110003]
  5. Natural Science Foundation of Guangdong Province [2019A1515010761]
  6. Science Technology and Innovation Committee of Shenzhen Municipality [SGDX20210823104002015]

向作者/读者索取更多资源

A novel LDHs-assisted approach is developed to synthesize freestanding bimetallic 2D metal-organic framework nanosheets (2D MOF NSs) with outstanding activities and proton transfer ability in the oxygen evolution reaction (OER).
The oxygen evolution reaction (OER) is crucial to electrochemical hydrogen production. However, designing and fabricating efficient electrocatalysts still remains challenging. By confinedly coordinating organic ligands with metal species in layered double hydroxides (LDHs), an innovative LDHs-assisted approach is developed to facilely synthesize freestanding bimetallic 2D metal-organic framework nanosheets (2D MOF NSs), preserving the metallic components and activities in OER. Furthermore, the research has demonstrated that the incorporation of carboxyl organic ligands coordinated with metal atoms as proton transfer mediators endow 2D MOF NSs with efficient proton transfer during the electrochemical OHads -> O-ads transition. These freestanding NiFe-2D MOF NSs require a small overpotential of 260 mV for a current density of 10 mA cm(-2). When this strategy is applied to LDH nanosheets grown on nickel foam, the overpotential can be reduced to 221 mV. This outstanding OER activity supports the capability of multimetallic organic frameworks for the rational design of water oxidation electrocatalysts. This strategy provides a universal path to the synthesis of 2D MOF NSs that can be used as electrocatalysts directly.

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