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Assembling organic-inorganic building blocks for high-capacity electrode design.

Authors :
Zhao X
Hu Z
Li Y
Wang Y
Song E
Zhang L
Liu J
Source :
Materials horizons [Mater Horiz] 2021 Jun 01; Vol. 8 (6), pp. 1825-1834. Date of Electronic Publication: 2021 Apr 26.
Publication Year :
2021

Abstract

Metal-organic electrode materials have exhibited extraordinary promise for green and sustainable electrochemical energy storage devices, but usually suffer from low specific capacity, and poor cycling stability and rate capability because of limited active sites at organic functional groups. To address this issue, activating transition metals and carbon conjugate rings has become significantly effective to make transferred electrons dispersed in the whole molecule. In this work, we demonstrate that assembling inorganic-organic building blocks into "local" composite metal-organic materials could synergistically activate transition metal ions and carbon conjugate rings to operate cationic and anionic redox, respectively. Based on first-principles calculations, the composite inorganic-organic material FeF <subscript>3</subscript> (4,4'-bpy) generates 8-electron transfer redox processes of Fe <superscript>3+</superscript> + 2e <superscript>-</superscript> → Fe <superscript>+</superscript> and 2 -C[double bond, length as m-dash]N- + 2e <superscript>-</superscript> → 2 (-C-N-) <superscript>-</superscript> and 4 -C[double bond, length as m-dash]C- + 4e <superscript>-</superscript> → 4 (-C-C-) <superscript>-</superscript> , achieving a high specific capacity of 796.7 mA h g <superscript>-1</superscript> , maintaining structural stability, and reducing the band gap. The strongly electronegative F-ions in inorganic structure [FeF <subscript>4</subscript> ] <superscript>2-</superscript> play an important role in making highly oxidized Fe <superscript>3+</superscript> through forming a strong ligand field and electrochemically activating -C[double bond, length as m-dash]C-via electrostatic interaction with Li <superscript>+</superscript> . In addition, electrochemical measurements also reveal that the central metal Fe, and -C[double bond, length as m-dash]C and -C[double bond, length as m-dash]N bonds of the FeF <subscript>3</subscript> (4,4'-bpy) electrode are the active sites for Li-ion storage to deliver a high reversible capacity (793.1 mA h g <superscript>-1</superscript> at 50 mA g <superscript>-1</superscript> ) and excellent rate capability, which are echoes of the DFT calculations. Through this design principle, we found a series of high-capacity metal organic electrode materials such as MnF <subscript>3</subscript> (4,4'-bpy) (799.6 mA h g <superscript>-1</superscript> ) and VF <subscript>3</subscript> (4,4'-bpy) (811.7 mA h g <superscript>-1</superscript> ).

Details

Language :
English
ISSN :
2051-6355
Volume :
8
Issue :
6
Database :
MEDLINE
Journal :
Materials horizons
Publication Type :
Academic Journal
Accession number :
34846511
Full Text :
https://doi.org/10.1039/d1mh00128k