Anchoring stable FeS2 nanoparticles on MXene nanosheets via interface engineering for efficient water splitting. Issue 4 (20th January 2022)

• Record Type: Journal Article
• Authors: Xie, Yaoyi; Yu, Hanzhi; Deng, Liming; Amin, R. S.; Yu, Deshuang; Fetohi, Amani E.; Maximov, Maxim Yu.; Li, Linlin; El-Khatib, K. M.; Peng, Shengjie
• Is Part Of: Inorganic chemistry frontiers. Volume 9:Issue 4(2022)
• Page Start: 662
• Page End: 669
• Publication Date: 2022-01-20
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d1qi01465j
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : Benefiting from an abundant interface with many active sites, robust interaction and synergistic effect between FeS2 and MXene, FeS2 @MXene exhibits remarkable catalytic activity towards water splitting in alkaline electrolytes. Abstract : Exploring highly efficient, economical and environment friendly electrocatalysts for the hydrogen and oxygen evolution reactions (HER and OER) is necessary but challenging for economical water splitting. Herein, FeS2 nanoparticles were anchored on the surface of MXene through a simple adsorption-growth route (FeS2 @MXene). By virtue of the large active surface area of FeS2 and its robust interfacial interaction with conductive and hydrophilic MXene nanosheets, the obtained FeS2 @MXene composite can accelerate the transfer of mass/charge and facilitate contact between water molecules and reactive sites of FeS2 . Specifically, MXene as a support material can not only alter the electrophilicity of the active centers of FeS2 through modulating the electron density but also prevent the aggregation of FeS2, thereby promoting activity and stability. The optimized FeS2 @MXene delivers a 10 mA cm −2 current density at overpotentials of 87 and 240 mV in alkaline solution for the HER and OER, respectively, which is comparable with reported transition metal sulfide (TMS) based catalysts. More importantly, in situ Raman spectroscopy reveals that the FeOOH generated during the OER process as a actual active species enhances the intrinsic activity of the catalyst. This work paves a new way for the interface engineering of TMS-based electrocatalysts towards water splitting.