Fe‐Incorporated Ni3S4/NiS2 Nanocomposite as an Efficient Electrocatalyst for Alkaline Water Oxidation. Issue 9 (13th July 2022)

• Record Type: Journal Article
• Authors: Tudu, Gouri; Ghosh, Sourav; Inta, Harish Reddy; Koppisetti, Heramba V. S. R. M.; Ganguli, Sagar; Mahato, Ashok Kumar; Mahalingam, Venkataramanan
• Is Part Of: ChemNanoMat. Volume 8:Issue 9(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-07-13
• Subjects: iron incorporation -- nickel hydroxide -- nickel sulfide -- oxygen evolution reaction -- sulfurization -- water electrolysis; Nanochemistry -- Periodicals; Nanostructured materials -- Periodicals; Nanochemistry; Nanostructured materials; Periodicals; 541.2
• DOI: 10.1002/cnma.202200199
• Languages: English
• ISSNs: 2199-692X

Abstract

Abstract: We report the development of iron‐incorporated nickel sulfide (Fe−Ni3 S4 /NiS2 ) nanocomposite through sulfurization of iron incorporated nickel hydroxide precursor by using simple solvothermal method. The formation of Ni3 S4 /NiS2 mixed‐phase material was confirmed by PXRD analysis and the presence of multiple oxidation states of Ni (II and III) and incorporated Fe (III) was revealed by XPS studies. The electrochemical studies demonstrated that Fe−Ni3 S4 /NiS2 electrocatalyst has a high catalytic activity towards alkaline OER, as it requires only 280 mV overpotential to achieve the benchmark current density of 10 mA/cm 2 geo . The superiority of the catalyst was exhibited by low charge transfer resistance of about 6 Ohms, along with low Tafel slope of 43 mV dec −1 . Further, the observed long‐term stability for 72 h and remarkable Faradaic efficiency with 99% indicate good durability and excellent selectivity towards OER, respectively. The superior activity of Fe−Ni3 S4 /NiS2 is attributed to fast kinetics and low charge transfer resistance of the material facilitating the generation of active catalyst. Abstract : The Fe−Ni3 S4 /NiS2 nanocomposite was synthesized from sulfurization of Fe−(NiOH)2 nanosheets which displays excellent electrocatalytic activity towards alkaline OER compared to its hydroxide analogue.