Polydopamine functionalized graphene/NiFe2O4 nanocomposite with improving Li storage performances
Polydopamine (PDA) functionalized graphene/NiFe2O4 (GNSs–PDA–NiFe2O4) nanocomposite has been successfully synthesized through an in-situ ultrasonic method. The obtained GNSs–PDA–NiFe2O4 nanocomposite shows a reversible capacity up to 947mAhg−1 and much improved rate capability, e.g. delivering a cap...
Saved in:
Published in | Nano energy Vol. 6; pp. 51 - 58 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Ltd
01.05.2014
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Polydopamine (PDA) functionalized graphene/NiFe2O4 (GNSs–PDA–NiFe2O4) nanocomposite has been successfully synthesized through an in-situ ultrasonic method. The obtained GNSs–PDA–NiFe2O4 nanocomposite shows a reversible capacity up to 947mAhg−1 and much improved rate capability, e.g. delivering a capacity of 562mAhg−1 at 5Ag−1, about 7 times higher than that of graphene/NiFe2O4 nanocomposite. The improvement in the rate capability of the obtained GNSs–PDA–NiFe2O4 nanocomposite can be attributed to the improved interactions between graphene and NiFe2O4 derived from PDA, and a high conductive network fabricated by PDA functionalized graphene, which can be supported by TEM images and EIS measurements. Further studies reveal the strong graphene–NiFe2O4 interactions are also beneficial for retaining the high conductive network after the charge–discharge processes, and further beneficial for its cyclic stability.
[Display omitted]
•GNSs–PDA–NiFe2O4 synthesized by in-situ ultrasonic process shows 838mAhg−1 at 1Ag−1 after 100 cycles.•The enhanced lithium storage performances can be attributed to the nature of PDA interlayers.•PDA interlayers can enhance the mechanical connections between GNSs/NiFe2O4 and build a conductive network.•Covalent nature of PDA can improve the wettability of composite in organic electrolyte and decrease charge transfer resistance. |
---|---|
ISSN: | 2211-2855 |
DOI: | 10.1016/j.nanoen.2014.03.006 |