4.7 Article

Electronic Structure Modulation and Phase Transformation of Nickel-Cobalt Carbonate Hydroxide Caused by Halogen Doping and Its Effect on Supercapacitor Performance

Journal

ACS APPLIED ENERGY MATERIALS
Volume 5, Issue 1, Pages 469-480

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c02995

Keywords

doping; halogen; electronic structure; phase transition; supercapacitor; energy storage; layered double hydroxide

Funding

  1. National Natural Science Foundation of China [11972195]

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This study investigates the effect of halogen anion modification on nickel-cobalt carbonate hydroxides (NiCo-CHs) and its impact on the electrochemical properties for supercapacitor applications. The results show that halogen doping changes the morphology of NiCo-CHs and influences the metal valence. Fluorine (F) doping, in particular, leads to the formation of a different phase of NiCo-LDH due to its high electronegativity. The study also demonstrates a strong correlation between the performance of NiCo-CHs as supercapacitors and the electronegativity of the doped halogen. Furthermore, density functional theory calculations reveal that F doping improves the reaction kinetics and conductivity. The assembled asymmetric devices showed promising energy density and cycle performance.
Nickel-cobalt layered double hydroxides (NiCo-LDHs) have been widely used as supercapacitor materials, and their performance can also be improved by doping engineering. However, the systematic study of halogen anion (X-)-modified NiCo-LDH has rarely been reported. In this study, X- were used to modify nickel-cobalt carbonate hydroxides (NiCo-CHs) via hydrothermal preparation. The halogen doping resulted in changes to the morphology of NiCo-CH. In particular, the electronegativity and electron-withdrawing ability of the halogen were found to be the key to the changes in the metal valence in the NiCo-CHs. Due to the high electronegativity of F, after 12 h of hydrothermal treatment, F-doped NiCo-CH (named F-NCCH12) caused the formation of high-valent M3+ sites, resulting in the production of a NiCo-LDH phase different from other halogen dopings. By varying the hydrothermal reaction time, we identified the mechanism of the structural and phase transition. In addition, by testing the electrochemical properties of NiCo-CHs for their applications as supercapacitors, we found a strong correlation with the doped halogen. Specifically, the supercapacitor performance improved with an increase in the electronegativity of the halogen. Furthermore, density functional theory calculations showed that F doping accelerates the reaction kinetics and improves the conductivity. Finally, we assembled NF@F-NCCH12//AC asymmetric devices, which exhibited an energy density of 35.3 W h kg(-1) at a power density of 375 W kg(-1). Crucially, the stable phase structure resulted in improved cycle performance of the F-NCCH12 electrode material, which showed an initial specific capacitance retention of 91.6% after 10,000 cycles.

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