Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications
Research Article  ·  Published: 14 August 2026
Issue cover
Journal of Advanced Electronic Materials
Volume 2, Issue 3, 2026: 89-100
Research Article Open Access

Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications

1 Department of Physics, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan
2 Department of Basic and Applied Sciences for Engineering, Sapienza University of Rome, Rome 00185, Italy
* Corresponding Authors: Khizar Hayat, [email protected]; Said Karim Shah, [email protected]
Volume 2, Issue 3

Article Information

Abstract

We report the synthesis of cobalt-based hexacyanoferrate (Co-HCF) via a simple co-precipitation method and its subsequent conversion to a derived oxide through thermal treatment. Comprehensive characterization was performed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). XRD confirms the cubic crystal structure corresponding well to the JCPDS card no. 00-024-0327. FTIR confirms the presence of functional groups in Co-HCF, while the annealing process results in the complete removal of the cyanide ligands, yielding the derived oxide. SEM and EDX analyses confirm the cubic morphology and elemental composition of the prepared samples. Furthermore, electrochemical evaluation using cyclic voltammetry (CV) revealed that Co-HCF delivered a higher specific capacitance (\(C_s\)) of \SI{624}{\farad\per\gram} at \SI{5}{\milli\volt\per\second}, highlighting pseudocapacitive behavior due to its open framework structure and abundant redox-active cobalt centers. In contrast, the annealed sample exhibited comparatively lower \(C_s\) of \SI{143}{\farad\per\gram} under identical conditions, attributed to the partial collapse of the open HCF channels. This work demonstrates a controlled conversion route from Co-HCF to derived oxide, offering a promising pathway for next-generation supercapacitors (SCs) and sustainable energy storage technologies.

Graphical Abstract

Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications

Keywords

cobalt hexacyanoferrates thermal conversion derived oxides pseudocapacitor cyclic voltammetry kinetics

Data Availability Statement

Data will be made available on request.

Funding

This work was supported by the Higher Education Commission (HEC), Islamabad, Pakistan, under Grant 20-140245-75/NRPU/R&ID/HEC/2026.

Conflicts of Interest

The authors declare no conflicts of interest.

AI Use Statement

The authors declare that no generative AI was used in the preparation of this manuscript.

Ethical Approval and Consent to Participate

Not applicable.

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Cite This Article

APA Style
Shah, L., Siddiqa, S. F., Ullah, J., Ullah, A., Sadiq, A., Ahmad, I., Hayat, K., & Shah, S. K. (2026). Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications. Journal of Advanced Electronic Materials, 2(3), 89-100. https://doi.org/10.62762/JAEM.2026.780043
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TY  - JOUR
AU  - Shah, Laiba
AU  - Siddiqa, Syeda Farahat
AU  - Ullah, Javid
AU  - Ullah, Atta
AU  - Sadiq, Adnan
AU  - Ahmad, Ibrar
AU  - Hayat, Khizar
AU  - Shah, Said Karim
PY  - 2026
DA  - 2026/08/14
TI  - Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications
JO  - Journal of Advanced Electronic Materials
T2  - Journal of Advanced Electronic Materials
JF  - Journal of Advanced Electronic Materials
VL  - 2
IS  - 3
SP  - 89
EP  - 100
DO  - 10.62762/JAEM.2026.780043
UR  - https://www.icck.org/article/abs/JAEM.2026.780043
KW  - cobalt hexacyanoferrates
KW  - thermal conversion
KW  - derived oxides
KW  - pseudocapacitor
KW  - cyclic voltammetry
KW  - kinetics
AB  - We report the synthesis of cobalt-based hexacyanoferrate (Co-HCF) via a simple co-precipitation method and its subsequent conversion to a derived oxide through thermal treatment. Comprehensive characterization was performed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). XRD confirms the cubic crystal structure corresponding well to the JCPDS card no. 00-024-0327. FTIR confirms the presence of functional groups in Co-HCF, while the annealing process results in the complete removal of the cyanide ligands, yielding the derived oxide. SEM and EDX analyses confirm the cubic morphology and elemental composition of the prepared samples. Furthermore, electrochemical evaluation using cyclic voltammetry (CV) revealed that Co-HCF delivered a higher specific capacitance (\(C_s\)) of \SI{624}{\farad\per\gram} at \SI{5}{\milli\volt\per\second}, highlighting pseudocapacitive behavior due to its open framework structure and abundant redox-active cobalt centers. In contrast, the annealed sample exhibited comparatively lower \(C_s\) of \SI{143}{\farad\per\gram} under identical conditions, attributed to the partial collapse of the open HCF channels. This work demonstrates a controlled conversion route from Co-HCF to derived oxide, offering a promising pathway for next-generation supercapacitors (SCs) and sustainable energy storage technologies.
SN  - 3070-5649
PB  - Institute of Central Computation and Knowledge
LA  - English
ER  - 
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@article{Shah2026Thermal,
  author = {Laiba Shah and Syeda Farahat Siddiqa and Javid Ullah and Atta Ullah and Adnan Sadiq and Ibrar Ahmad and Khizar Hayat and Said Karim Shah},
  title = {Thermal Conversion of Cobalt Based Hexacyanoferrates into Derived Cobalt Oxides for Supercapacitor Applications},
  journal = {Journal of Advanced Electronic Materials},
  year = {2026},
  volume = {2},
  number = {3},
  pages = {89-100},
  doi = {10.62762/JAEM.2026.780043},
  url = {https://www.icck.org/article/abs/JAEM.2026.780043},
  abstract = {We report the synthesis of cobalt-based hexacyanoferrate (Co-HCF) via a simple co-precipitation method and its subsequent conversion to a derived oxide through thermal treatment. Comprehensive characterization was performed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). XRD confirms the cubic crystal structure corresponding well to the JCPDS card no. 00-024-0327. FTIR confirms the presence of functional groups in Co-HCF, while the annealing process results in the complete removal of the cyanide ligands, yielding the derived oxide. SEM and EDX analyses confirm the cubic morphology and elemental composition of the prepared samples. Furthermore, electrochemical evaluation using cyclic voltammetry (CV) revealed that Co-HCF delivered a higher specific capacitance (\(C\_s\)) of \SI{624}{\farad\per\gram} at \SI{5}{\milli\volt\per\second}, highlighting pseudocapacitive behavior due to its open framework structure and abundant redox-active cobalt centers. In contrast, the annealed sample exhibited comparatively lower \(C\_s\) of \SI{143}{\farad\per\gram} under identical conditions, attributed to the partial collapse of the open HCF channels. This work demonstrates a controlled conversion route from Co-HCF to derived oxide, offering a promising pathway for next-generation supercapacitors (SCs) and sustainable energy storage technologies.},
  keywords = {cobalt hexacyanoferrates, thermal conversion, derived oxides, pseudocapacitor, cyclic voltammetry, kinetics},
  issn = {3070-5649},
  publisher = {Institute of Central Computation and Knowledge}
}

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CC BY Copyright © 2026 by the Author(s). Published by Institute of Central Computation and Knowledge. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.
Journal of Advanced Electronic Materials
Journal of Advanced Electronic Materials
ISSN: 3070-5649 (Online)
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