Synthesis and spectroscopic identification of nickel and cobalt layered hydroxides and hydroxynitrates
The formation of different nickel and cobalt layered hydroxide phases by a variety of solution and solid-state synthesis methods have been investigated. Initially, the preparative conditions were refined to generate single-phase products from metal(II) nitrate hexahydrate starting materials and were characterised by powder X-ray diffraction, vibrational spectroscopy and thermogravimetric analysis. As well as the brucite type β-M(OH)2 and the hydrotalcite-like [M(OH)2-x(H2O)x]x+ alpha-phases (where M = Ni, Co), two different hydroxynitrate phases were isolated with the generic formula M(OH)2-x(NO3)x with x = 0.67 and 1.0 (where M = Ni, Co). The reduction of symmetry of the nitrate anion from D3h to C2v allows the alpha-phases to be distinguished from the two different layered hydroxynitrate phases by both infrared and Raman spectroscopy through the loss of symmetry and concomitant splitting of the degenerate bands. The symmetric N-O stretch enables the two hydroxynitrate phases to be distinguished from one another through the sharp absorption bands at ca. 1000 cm-1 (x = 0.67) and ca. 1050 cm-1 (x = 1.0). The thermogravimetric analysis data of the phases showed key differences between the layered hydroxides, with anhydrous phases having singular weight losses over short temperature ranges and hydrated phases having multiple losses over more extended temperature ranges.
Funding
COG3: The geology, geometallurgy and geomicrobiology of cobalt resources leading to new product streams
Natural Environment Research Council
Find out more...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...History
School
- Science
Department
- Chemistry
Published in
Dalton TransactionsVolume
51Issue
47Pages
18010-18023Publisher
Royal Society of ChemistryVersion
- VoR (Version of Record)
Rights holder
© The AuthorsPublisher statement
This is an Open Access Article. It is published by the 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
2022-11-08Publication date
2022-11-08Copyright date
2022ISSN
1477-9226eISSN
1477-9234Publisher version
Language
- en