Metal‐Organic‐Framework‐Derived Nitrogen‐Doped Hybrid Nickel‐Iron‐Sulfide Architectures on Carbon Cloth as Efficient Electrocatalysts for the Oxygen Evolution Reaction. Issue 10 (20th May 2019)

• Record Type: Journal Article
• Authors: Shen, Yirui; Wang, Ling; Jiang, Pingping; Lee, Wee Siang Vincent; Xue, Junmin
• Is Part Of: ChemElectroChem. Volume 6:Issue 10(2019)
• Page Start: 2741
• Page End: 2747
• Publication Date: 2019-05-20
• Subjects: metal-organic frameworks -- nickel-iron-sulfides -- nitrogen doping -- oxygen evolution reaction -- electrocatalysts; Electrochemistry -- Periodicals; 541.37
• DOI: 10.1002/celc.201900481
• Languages: English
• ISSNs: 2196-0216

Abstract

Abstract: Metal‐organic framework (MOF)‐derived nitrogen‐doped NiFe‐sulfides/carbon hybrid architectures were successfully constructed on carbon cloth (CC) with different n (Ni)/ n (Fe) ratios through a simultaneous carbonization and sulfurization procedure from the corresponding bimetal NiFe‐based MOFs. The samples were directly utilized as the working electrodes for the oxygen evolution reaction (OER). The optimal sample N‐NiFe‐S/C‐8/2@CC possessed superior OER electrocatalytic activity with a remarkably low overpotential of 232 mV at a current density of 10 mA cm −2 in 1 M KOH aqueous solution. At the same time, a small Tafel slope of 58 mV dec −1 was achieved and excellent durability was also demonstrated. Such superior OER activity and durability of N‐NiFe‐S/C@CC may originate from a synergetic effect between Fe and Ni, the nitrogen‐doped carbon matrix derived from MOFs, and the direct growth of active materials on CC. This facile approach of preparing bimetal sulfide compounds derived from MOFs may be a viable method for designing and preparing high‐performing electrocatalytic materials for wider applications. Abstract : Stable and productive : Metal‐organic‐framework‐derived nitrogen‐doped nickel−iron−sulfide/carbon hybrid electrocatalysts are successfully synthesized through a simple strategy and exhibited superior oxygen evolution reaction activity and stability.