Electrolyte‐Dependent Charge Storage in ZnFe 2 O 4 : Insights Into Fe Mixed‐Valence Electronic Structure via Near‐Edge X‐Ray Absorption Fine Structure ( NEXAFS ) and Symmetric Supercapacitor Performance

ABSTRACT This study establishes a direct correlation between Fe mixed‐valence electronic structure and electrolyte‐dependent charge‐storage behavior in ZnFe 2 O 4 . ZnFe 2 O 4 were synthesized via a co‐precipitation route and systematically investigated for their structural, electronic, and electrochemical properties. Near‐edge X‐ray absorption fine structure (NEXAFS) spectroscopy at the Fe L 3,2 ‐ and O K‐edges revealed a partially inverse spinel structure with mixed Fe 2+ /Fe 3+ valence states, where linear combination fitting indicated ~74.4% Fe 3+ and ~25.6% Fe 2+ . The enhanced Fe‐O hybridization arising from this mixed‐valence configuration is beneficial for charge transport. Electrochemical performance of the ZnFe 2 O 4 electrode was evaluated in a three‐electrode configuration using cyclic voltammetry, galvanostatic charge–discharge, and electrochemical impedance spectroscopy in 1.0 M KOH and 1.0 M Na 2 SO 4 electrolytes. The ZnFe 2 O 4 electrode exhibited significantly superior capacitive behavior in Na 2 SO 4 , delivering a high specific capacitance of 692.2 F/g at 1 A/g and an energy density of 96.13 Wh/kg. Kinetic analysis revealed a mixed charge‐storage mechanism dominated by surface‐controlled capacitive processes. Furthermore, the electrode demonstrated excellent cyclic stability with ~91% capacitance retention after 2000 charge–discharge cycles. The enhanced electrochemical performance in Na 2 SO 4 is attributed to improved ion transport, reduced interfacial resistance, and greater electrochemical stability. When employed as an electrode in a symmetric supercapacitor device, ZnFe 2 O 4 delivered a maximum specific capacitance of 201.28 F/g at a current density of 0.25 A/g, along with a high energy density of 71.57 Wh/kg at a power density of 400 W/kg. Furthermore, the SSCD exhibited notable cycling stability, retaining 46.93% of its initial capacitance after 10 000 galvanostatic charge–discharge cycles at a current density of 2.5 A/g. These results highlight ZnFe 2 O 4 as a promising electrode material for high‐performance supercapacitor applications, particularly in neutral electrolytes.

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Journal
Energy Storage
Published
2026-08-25
DOI
https://doi.org/10.1002/est2.70501
Primary Topic
Supercapacitor Materials and Fabrication
Type
article
Field-Weighted Citation Impact
0.00

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Electrolyte‐Dependent Charge Storage in ZnFe 2 O 4 : Insights Into Fe Mixed‐Valence Electronic Structure via Near‐Edge X‐Ray Absorption Fine Structure ( NEXAFS ) and Symmetric Supercapacitor Performance

Adil Ahmed Alshoaibi, Nagih M. Shaalan, Shalendra Kumar, Keun Hwa Chae et al.
Energy Storage
Supercapacitor Materials and Fabrication
article

Electrolyte‐Dependent Charge Storage in ZnFe 2 O 4 : Insights Into Fe Mixed‐Valence Electronic Structure via Near‐Edge X‐Ray Absorption Fine Structure ( NEXAFS ) and Symmetric Supercapacitor Performance

Adil Ahmed Alshoaibi, Nagih M. Shaalan, Shalendra Kumar, Keun Hwa Chae, Najla Khaled Almulhem, Manas Nasit
article en

Abstract

ABSTRACT This study establishes a direct correlation between Fe mixed‐valence electronic structure and electrolyte‐dependent charge‐storage behavior in ZnFe 2 O 4 . ZnFe 2 O 4 were synthesized via a co‐precipitation route and systematically investigated for their structural, electronic, and electrochemical properties. Near‐edge X‐ray absorption fine structure (NEXAFS) spectroscopy at the Fe L 3,2 ‐ and O K‐edges revealed a partially inverse spinel structure with mixed Fe 2+ /Fe 3+ valence states, where linear combination fitting indicated ~74.4% Fe 3+ and ~25.6% Fe 2+ . The enhanced Fe‐O hybridization arising from this mixed‐valence configuration is beneficial for charge transport. Electrochemical performance of the ZnFe 2 O 4 electrode was evaluated in a three‐electrode configuration using cyclic voltammetry, galvanostatic charge–discharge, and electrochemical impedance spectroscopy in 1.0 M KOH and 1.0 M Na 2 SO 4 electrolytes. The ZnFe 2 O 4 electrode exhibited significantly superior capacitive behavior in Na 2 SO 4 , delivering a high specific capacitance of 692.2 F/g at 1 A/g and an energy density of 96.13 Wh/kg. Kinetic analysis revealed a mixed charge‐storage mechanism dominated by surface‐controlled capacitive processes. Furthermore, the electrode demonstrated excellent cyclic stability with ~91% capacitance retention after 2000 charge–discharge cycles. The enhanced electrochemical performance in Na 2 SO 4 is attributed to improved ion transport, reduced interfacial resistance, and greater electrochemical stability. When employed as an electrode in a symmetric supercapacitor device, ZnFe 2 O 4 delivered a maximum specific capacitance of 201.28 F/g at a current density of 0.25 A/g, along with a high energy density of 71.57 Wh/kg at a power density of 400 W/kg. Furthermore, the SSCD exhibited notable cycling stability, retaining 46.93% of its initial capacitance after 10 000 galvanostatic charge–discharge cycles at a current density of 2.5 A/g. These results highlight ZnFe 2 O 4 as a promising electrode material for high‐performance supercapacitor applications, particularly in neutral electrolytes.

Energy StorageVol. 8(6)
Advanced Analysis Center (JP), King Faisal University (SA), University of Petroleum and Energy Studies (IN)
King Faisal University
Affordable and clean energy
Openalex Percentile: Top 27%
Supercapacitor Materials and Fabrication
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