Controlled growth and interaction of NiCo2S4 on conductive substrate for enhanced electrochemical performance
The controlled nanostructure growth and its strong coupling with the current collector are key factors to achieve good electrochemical performance of faradaic-dominant electroactive materials. In this work, we demonstrate binder-less and additive-free hydrothermal and physical vapor doping methods f...
Saved in:
Published in: | Journal of power sources Vol. 451; p. 227763 |
---|---|
Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
01-03-2020
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The controlled nanostructure growth and its strong coupling with the current collector are key factors to achieve good electrochemical performance of faradaic-dominant electroactive materials. In this work, we demonstrate binder-less and additive-free hydrothermal and physical vapor doping methods for the synthesis of nickel cobalt sulfide (NiCo2S4) deposited on different conductive substrates such as pristine nickel foam (NF), reduced graphene oxide coated on NF (rGO/NF), and N-doped rGO coated on NF (N-rGO/NF). The size and density of NiCo2S4 nanosheets are controlled through the strong coupling with N-rGO/NF and rGO/NF. This controllable synthesis allows N-rGO/NF to achieve better electrochemical performance such as high capacity of 623.5 mAh g−1 at 4 mA cm−2, energy efficiency of 59.4% at 120 mA cm−2, and cycling stability of 57% after 10,000 cycles than those of pristine NF and rGO/NF. These results are attributed to the synergy of controllably structured NiCo2S4 nanosheets and strong interaction with conductive substrate.
•Surface energy of the conductive substrate affects nanostructure growth.•The functional groups of conductive substrates strongly interact with nanosheets.•NiCo2S4 nanosheets on N-rGO/NF substrate exhibits high areal capacity.•The hybrid interaction is related to superior rate and cyclic capabilities. |
---|---|
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2020.227763 |