Determination of layered nickel hydroxide phases in materials disordered by stacking faults and interstratification
The formation of stacking faults and phase interstratification disorder in the layered nickel(II) hydroxides during the chemical precipitation synthesis of the materials using nickel(II) nitrate and potassium hydroxide solutions has been investigated in the temperature range of 5°C to 95°C and time intervals from 1 hour to 1 week. Stacking faulted materials were identified by broadening of the 00l reflections, while interstratified materials were identified through the splitting of the 001 into two lines. In contrast to the disorder concepts presented in previous studies of these materials, this work has shown through vibrational spectroscopy that both the alpha-phase and beta-phase hydroxides are present in materials described with stacking fault disorder, while layered hydroxysalts were additionally present in the materials considered to be interstratified. Standard mixtures of Ni3(OH)4(NO3)2 and β-Ni(OH)2 were prepared to investigate if the intensity of particular vibrational bands could be correlated with the proportion of the particular phases in mixtures. The intensities of the C2v nitrate infrared and Raman bands at 990 cm-1 and 1315 cm-1 were shown to correlate with the amount of layered hydroxynitrate incorporated in the phase, theoretically providing a method to determine the components in mixed compositions. Since disorder and phase impurities in layered nickel hydroxide materials affect both their electroactive stability and performance as cathode materials, this work has important implications in several research fields.
Funding
Development of thin film Ni OH 2 electrochromic materials using in situ microfocus XANES EXAFS and XRD techniques
Science and Technology Facilities Council
Find out more...Sydney Andrew Scholarship
History
School
- Science
Department
- Chemistry
Published in
Journal of Materials Chemistry AVolume
11Issue
2Pages
789 - 799Publisher
Royal Society of ChemistryVersion
- VoR (Version of Record)
Rights holder
© The AuthorsPublisher statement
This is an Open Access Article. It is published by Royal Society of Chemistry under the Creative Commons Attribution 3.0 Unported Licence (CC BY). Full details of this licence are available at: https://creativecommons.org/licenses/by/3.0/Acceptance date
2022-12-05Publication date
2022-12-06Copyright date
2022ISSN
2050-7488eISSN
2050-7496Publisher version
Language
- en