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Asymmetric reaction pathway of Na+-ion during fast cycling in α- and γ-Fe2O3 thin film anode for sodium-ion battery.

Authors :
Nayak, Debasis
Puravankar, Sreeraj
Ghosh, Sudipto
Adyam, Venimadhav
Source :
Ionics; Dec2019, Vol. 25 Issue 12, p5857-5868, 12p
Publication Year :
2019

Abstract

This study aims to evaluate various polymorphs of Fe<subscript>2</subscript>O<subscript>3</subscript> (γ- and α-types) as anode material for sodium-ion batteries and their conversion mechanisms. In this work, pulsed laser deposition (PLD) was used to successfully fabricate Fe<subscript>2</subscript>O<subscript>3</subscript> (both γ- and α-types) thin film followed by the electrochemical investigation as anode material for a sodium-ion battery. The γ-Fe<subscript>2</subscript>O<subscript>3</subscript> shows high reversibility than α-Fe<subscript>2</subscript>O<subscript>3</subscript> while discharging at a deep discharge voltage of 0.01 V. The α-Fe<subscript>2</subscript>O<subscript>3</subscript> changes to Fe<subscript>3</subscript>O<subscript>4</subscript> during sodium extraction, while the γ-Fe<subscript>2</subscript>O<subscript>3</subscript> remains unaltered upon cycling. The γ-Fe<subscript>2</subscript>O<subscript>3</subscript> shows high electrochemical performance regarding cycle life and discharge capacity than α-Fe<subscript>2</subscript>O<subscript>3</subscript> (considering up to 80 cycles). The discharge capacity of γ-Fe<subscript>2</subscript>O<subscript>3</subscript> is 335.2 mAh g<superscript>−1</superscript> and of α-Fe<subscript>2</subscript>O<subscript>3</subscript> is 248.7 mAh g<superscript>−1</superscript> for the 1st cycle at a current rate of 475 mA g<superscript>−1</superscript>. The achieved superior performance of γ-Fe<subscript>2</subscript>O<subscript>3</subscript> is credited to the reversible reaction path and binder-free nature of the thin film. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09477047
Volume :
25
Issue :
12
Database :
Complementary Index
Journal :
Ionics
Publication Type :
Academic Journal
Accession number :
139692153
Full Text :
https://doi.org/10.1007/s11581-019-03112-3