Effect of Substitution at the Di- and Trivalent Sites of {N[n- C₄H₉]₄]Fe^IIFe^III[C₂O₄]₃]}_∞ on the Nature of Solid State Decomposition Reaction Leading to Various Metal Oxides

Title:Effect of Substitution at the Di- and Trivalent Sites of {N[n- C₄H₉]₄]Fe^IIFe^III[C₂O₄]₃]}_∞ on the Nature of Solid State Decomposition Reaction Leading to Various Metal Oxides

Volume: 12 Issue: 3

Author(s): Debasis Roy, Maciej Zubko, Joachim Kusz and Ashis Bhattacharjee*

Affiliation:

• Department of Physics, Visva-Bharati University, Santiniketan, India

Keywords: Thermal decomposition, oxalate-based molecular materials, thermogravimetry, kinetic calculations, iso-conversional method, XRD.

Abstract:

Background: Oxalate ligand-based metal complexes have long been used for the thermal synthesis of metal oxides. Polymeric homo/heterometallic oxalate-based molecular materials of the general formula, {A]M^IIM^III[C₂O₄]₃]}_∞, [A = organic cation, M^II/M^III: di/trivalent transition metal ion; C₂O₄: oxalate ligand] provides a molecular source to prepare metal oxides through solid state thermal decomposition primarily due to the potential to tune the materials’ outcome by adjusting the molecular stoichiometry and composition.

Objective: The study aims to explore the effect of mixing at the di- and trivalent metal sites of {N[n-C₄H₉]₄]Fe^IIFe^III[C₂O₄]₃]}_∞ which decomposes to hematite, on the nature of thermal decomposition reaction as well as the nature of the obtained decomposed materials.

Methods: Two series of materials {N[n-C₄H₉]₄]Fe^II_1-xZn^II _xFe^III[C₂O₄]₃]}_∞ and {N[n- C₄H₉]₄]Fe^IIFe^III_1-xCr^III_x[C₂O₄]₃]}_∞ were prepared as precursors for non-isothermal thermogravimetry [TG] study. Model-free integral isoconversional method is employed to calculate the activation energy of decomposition, and hence the most probable reaction mechanism, as well as the reaction rate of thermal decomposition, was determined. Based on the kinetic parameters, the important thermodynamic parameters such as the changes of entropy, enthalpy, and Gibbs free energy are estimated for the activated complex formation from the precursors. Powder X-ray diffraction studies were made to identify the decomposed materials.

Results: For materials with 0 < x ≤ 1 well-defined two-step and one-step decomposition process were observed for {N[n-C₄H₉]₄]Fe^II_1-xZn^II _xFe^III[C₂O₄]₃]}_∞ and {N[n- C₄H₉]₄]Fe^IIFe^III_1-xCr^III_x[C₂O₄]₃]}_∞, respectively. For each series of materials, a systematic dependence of the activation energy on the extent of conversion indicates a systematic change in the reactivity. The thermal decomposition strongly depends on the extent of mixing at the di- and trivalent sites and proceeds through different reaction mechanisms at different rates. On the decomposition of these series of materials, a range of metal oxides was obtained. Possibly, during such extent of mixing dependent reactions, the reactant particles go through modifications in their reactivity by several factors.

Conclusion: Present work may invoke interest in solid state synthesis of different metal oxides under controlled thermal decomposition by identifying the rate controlling the process through reaction kinetics study for better synthesis and manoeuvring.

Cite this article as:

Roy Debasis, Zubko Maciej, Kusz Joachim and Bhattacharjee Ashis*, Effect of Substitution at the Di- and Trivalent Sites of {N[n- C₄H₉]₄]Fe^IIFe^III[C₂O₄]₃]}_∞ on the Nature of Solid State Decomposition Reaction Leading to Various Metal Oxides, Current Physical Chemistry 2022; 12 (3) . https://dx.doi.org/10.2174/1877946812666220820162805

DOI https://dx.doi.org/10.2174/1877946812666220820162805	Print ISSN 1877-9468
Publisher Name Bentham Science Publisher	Online ISSN 1877-9476