Ultrathin NiO nanosheets anchored to a nitrogen-doped dodecahedral carbon framework for aqueous potassium-ion hybrid capacitors

Abstract

Hierarchical porous structures and well-modulated interfacial interactions are essential for the performance of electrode materials. The energy storage performance can be promoted by regulating the diffusion behavior of the electrolyte and constructing a coupled interaction at heterogeneous interfaces. Herein, we have synthesized ultrathin NiO nanosheets anchored to nitrogen-doped hierarchical porous carbon (NiO/N-HPC) and applied it to construct aqueous potassium ion hybrid capacitors (APIHCs). The abundant and interconnected porous architecture promotes electrolyte penetration/diffusion and shortens the ion transport path, thereby accelerating storage reaction kinetics. The nitrogen-doped carbon support can achieve optimized metal oxides–carbon interaction and enhance the adsorption ability for the electrolyte ions, leading to earning higher storage capacity. Consequently, the prepared NiO/N-HPC exhibits a superior capacitance of 126.4 F g−1 at a current density of 0.5 A g−1, and the as-fabricated NiO/N-HPC//N-HPC APIHC achieves an ultra-high capacitance retention of 91.6% over 8000 cycles at a current density of 2 A g−1. Meanwhile, the APIHC device shows an excellent energy density of 21.95 W h kg−1 and a power density of 9000 W kg−1.

Graphical abstract: Ultrathin NiO nanosheets anchored to a nitrogen-doped dodecahedral carbon framework for aqueous potassium-ion hybrid capacitors

Supplementary files

Article information

Article type
Paper
Submitted
09 ⵎⴰⵕ 2024
Accepted
18 ⵢⵓⵏ 2024
First published
25 ⵢⵓⵏ 2024
This article is Open Access
Creative Commons BY-NC license

J. Mater. Chem. A, 2024, Advance Article

Ultrathin NiO nanosheets anchored to a nitrogen-doped dodecahedral carbon framework for aqueous potassium-ion hybrid capacitors

T. Wang, W. Zong, J. Yang, L. Zhang, J. Meng, J. Ge, G. Yang, J. Ren, P. He, E. Debroye, J. Gohy, T. Liu and F. Lai, J. Mater. Chem. A, 2024, Advance Article , DOI: 10.1039/D4TA01608D

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