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Exploring High-Energy Li-I(r)on Batteries and Capacitors with Conversion-Type Fe3O4-rGO as the Negative Electrode.

Authors :
Kim, Hyun‐Kyung
Aravindan, Vanchiappan
Roh, Ms. Ha‐Kyung
Lee, Kyujoon
Jung, Myung‐Hwa
Madhavi, Srinivasan
Roh, Kwang Chul
Kim, Kwang‐Bum
Source :
ChemElectroChem; Oct2017, Vol. 4 Issue 10, p2626-2633, 8p
Publication Year :
2017

Abstract

We report a microwave-assisted solvothermal process for the preparation of magnetite (Fe<subscript>3</subscript>O<subscript>4</subscript>, ca. 5 nm)-anchored reduced graphene oxide (rGO). It has been examined as a prospective conversion-type negative electrode for multiple energy storage applications, such as Li-ion batteries (LIBs) and Li-ion capacitors (LICs). A LiFePO<subscript>4</subscript>/Fe<subscript>3</subscript>O<subscript>4</subscript>-rGO cell is constructed and capable of delivering an energy density of approximately 139 Wh kg<superscript>−1</superscript> with a notable cyclability (ca. 76 %) after 500 cycles. Prior to the fabrication of a LIB, the Fe<subscript>3</subscript>O<subscript>4</subscript>-rGO is electrochemically pretreated to eliminate the irreversible capacity loss. In addition to the LIB, a high-energy LIC is also fabricated by using the pre-lithiated Fe<subscript>3</subscript>O<subscript>4</subscript>-rGO composite as the anode and commercial activated carbon as the cathode. This LIC registered a maximum energy density of approximately 114 Wh kg<superscript>−1</superscript> with good cyclability. For both the LIB and LIC, the mass loading between the electrodes was adjusted based on the performance with metallic Li. The improved electrochemical performance of Fe<subscript>3</subscript>O<subscript>4</subscript>-rGO over existing materials is a promising development in the quest for novel, fast, low cost, and efficient energy storage systems without compromising the eco-friendliness [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21960216
Volume :
4
Issue :
10
Database :
Complementary Index
Journal :
ChemElectroChem
Publication Type :
Academic Journal
Accession number :
125690702
Full Text :
https://doi.org/10.1002/celc.201700484