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Partial sulfur doping induced lattice expansion of NiFe2O4 with enhanced electrochemical capacity for supercapacitor application.

Authors :
Gao, Xicheng
Bi, Jianqiang
Gao, Jian
Meng, Linjie
Xie, Lulin
Liu, Chen
Source :
Electrochimica Acta. Sep2022, Vol. 426, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

• The partial S-doping NiFe 2 O 4 was obtained through a facile hydrothermal method. • The d-spacing of NiFe 2 O 4 was expended caused by partial S-doping. • The impact of partial S-doping to NiFe 2 O 4 is exposed by VASP analysis. • The optimal electrode exhibited the highest specific capacitance of 284 F/g. Nickel ferrite exhibits many advantages as electrode materials in the application of supercapacitor, such as high energy capacity and excellent cycle stability. Whereas, compared with identical-metal sulfides, the specific capacitance of NiFe 2 O 4 is still insufficient. Hence, to combine the superiorities of oxides and sulfides, partial sulfur doping NiFe 2 O 4 is obtained through hydrothermal synthesis method. Analyzed by Vienna Ab-initio Simulation Package (VASP) software and high-resolution transmission electron microscopy, the lattice parameters of NiFe 2 O 4 are confirmed to be expanded by introducing sulfur atoms, which is beneficial to electrochemical performances. At a current density of 1 A/g, the specific capacitance of partial sulfur doping NiFe 2 O 4 is calculated to be 284 F/g, higher than that of the original NiFe 2 O 4 of 182.2 F/g. Moreover, a maximum energy density of 21.14 Wh/kg is achieved at a power density of 375 W/kg. This work shows that partial sulfur doping could improve the electrochemical performance of NiFe 2 O 4. To sum up, this work provides an effective way to enhance the poor electrochemical performance of oxides, greatly encouraging the application of oxides in energy storage field. [Display omitted] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134686
Volume :
426
Database :
Academic Search Index
Journal :
Electrochimica Acta
Publication Type :
Academic Journal
Accession number :
158403006
Full Text :
https://doi.org/10.1016/j.electacta.2022.140739