4.7 Article

Novel Co-doped nickel hydroxyfluorides with rapid electron transfer for high-performance supercapacitors

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 959, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2023.170558

Keywords

Co-doped; Nickel hydroxyfluorides; Defects; High-rate performance; Supercapacitors

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Transition metal electrode materials play a crucial role in high-energy and power-density rechargeable energy devices. In this study, a series of Co-doped nickel hydroxyfluorides (Co-Ni(OH)F) were developed as novel electrode materials with improved charge storage ability at different current densities. The introduction of Co not only regulated the electronic structure and surface morphology but also enhanced the electrochemical activities through abundant redox processes. The optimized Co-Ni(OH)F (Co=20%) electrode exhibited an ultrahigh specific capacity and superior capacity retention rate, making it a promising candidate for advanced energy devices.
Transition metal electrode materials are promising for applications in high-energy and power-density re-chargeable energy devices. However, their poor intrinsic conductivities and limited redox kinetics hinder the rapid energy supply at high current densities. Herein, a series of Co-doped nickel hydroxyfluorides (Co-Ni(OH)F) was constructed as new electrode materials to maximize the charge storage ability at different current densities. The introduction of Co did not only induce abundant defects for regulating the electronic structure but also fine-tuned the surface morphology and shortened the ion/electron diffusion distance. The coexistence of multiple oxidation states of Ni and Co species provided abundant redox processes and ef-fectively enhanced the electrochemical activities. The relationship between Co2+ doping and the increase in conductivity of the system was further confirmed by the calculated density of states (DOS). The optimized Co-Ni(OH)F (Co=20%) electrode material exhibited an ultrahigh specific capacity of 3380.2 F g-1 at a current density of 1 A g-1. Even at an enhanced current density of 20 A g-1, the optimized electrode showed a superior capacity retention rate of 78.4%. After 5000 cycles at a high current density of 30 A g-1, the electrode retained 76.3% of its original capacity. Furthermore, the Co-Ni(OH)F (Co=20%)//Bi2O3 asymmetric device delivered an ultrahigh density of 139.8 Wh kg-1 at a power density of 800 W kg-1, suggesting su-perior energy density than previously reported systems. Overall, new insights into the rational design of novel high-capacity and high-rate electrode materials were provided, promising for the construction of advanced energy devices.(c) 2023 Elsevier B.V. All rights reserved.

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