Issue 8, 2025

High-performance hybrid supercapacitors enabled by CoTe@CoFeTe double-shelled nanocubes

Abstract

Metal tellurides, known for their superior electrical conductivity and excellent electrochemical properties, are promising candidates for supercapacitor applications. This study introduces a novel method involving a metal–organic framework hybrid to synthesize CoTe@CoFeTe double-shelled nanocubes. Initially, zeolitic imidazolate framework-67 (ZIF67) and CoFe Prussian blue analog (PBA) nanocubes are synthesized through an anion-exchange reaction with [Fe(CN)6]3− ions. Subsequent annealing treatment converts these structures into Co3O4@CoFe2O4 double-shelled nanocubes. These are then subjected to a tellurization process to form CoTe@CoFeTe, which exhibits outstanding supercapacitive performance. Notably, the CoTe@CoFeTe based-electrode demonstrates superior supercapacitive properties compared to their oxide counterparts, mainly due to the introduction of tellurium ions. These nanocubes show an impressive specific capacity of 1312 C g−1 at a current density of 1 A g−1 and maintain 92.35% of their capacity after 10 000 charging cycles, highlighting their durability and the synergistic effect of the mixed metals and their hollow structure. Furthermore, when used as the positive electrode material in a hybrid supercapacitor with activated carbon (AC), the device achieves an energy density of 64.66 W h kg−1 and retains 88.25% of its capacity after 10 000 cycles. These results confirm the potential of the developed material for advanced supercapacitor applications.

Graphical abstract: High-performance hybrid supercapacitors enabled by CoTe@CoFeTe double-shelled nanocubes

Supplementary files

Article information

Article type
Paper
Submitted
29 Sep 2024
Accepted
29 Dec 2024
First published
30 Dec 2024

Nanoscale, 2025,17, 4591-4602

High-performance hybrid supercapacitors enabled by CoTe@CoFeTe double-shelled nanocubes

H. Gholami Shamami, A. Mohammadi Zardkhoshoui and S. S. Hosseiny Davarani, Nanoscale, 2025, 17, 4591 DOI: 10.1039/D4NR03996C

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