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π⋯π interaction directed 2D FeNi-LDH nanosheets from 2D Hofmann-MOFs for the oxygen evolution reaction.

Authors :
Huo, Jia-Min
Wang, Ying
Meng, Jie
Zhao, Xin-Yi
Zhai, Quan-Guo
Jiang, Yu-Cheng
Hu, Man-Cheng
Li, Shu-Ni
Chen, Yu
Source :
Journal of Materials Chemistry A; 1/28/2022, Vol. 10 Issue 4, p1815-1820, 6p
Publication Year :
2022

Abstract

Layered double hydroxides (LDHs) have attracted much attention for the oxygen evolution reaction (OER) in electrochemical water splitting. In this work, we use a two-dimensional (2D) MOF transformation strategy to synthesize FeNi layered double hydroxides (FeNi LDHs). 2D FeNi Hofmann MOFs ([Fe(L)<subscript>2</subscript>Ni(CN)<subscript>4</subscript>]) with a similar structure but different ligands (L = py, ISOQ) are synthesized as precursors. Accordingly, hydrolysis transformation assisted by NaBH<subscript>4</subscript> leads to the growth of 2D FeNi-LDH nanosheets from 2D Hofmann-MOFs. During hydrolysis, OH<superscript>−</superscript> ions preferentially attack the coordination bond of [Fe(L)<subscript>2</subscript>Ni(CN)<subscript>4</subscript>], which allows FeNi-LDHs to form quickly on the surface of 2D MOFs. This rapid conversion process can effectively avoid the self-accumulation of LDHs. The hydrogen bubbles produced by NaBH<subscript>4</subscript> can also inhibit the self-stacking of LDHs, which expose ample active species for the OER. Meanwhile, the synergistic effect between Fe and Ni contributes to the outstanding OER performance of FeNi-py-LDH, which shows an overpotential of 238 mV at 10 mA cm<superscript>−2</superscript>, a Tafel slope of 22 mV dec<superscript>−1</superscript> and an excellent stability for 15 h. This work provides a universal synthesis method for ultra-thin FeNi-LDHs, which avoids the self-stacking of nanosheets and offers new insights into the OER. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
10
Issue :
4
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
154889788
Full Text :
https://doi.org/10.1039/d1ta09921c