Ce(OH)2Cl and lanthanide-substituted variants as precursors to redox-active CeO2 materials. Issue 42 (19th October 2020)

• Record Type: Journal Article
• Authors: Dunn, Alexander J. A.; Annis, James W.; Fisher, Janet M.; Thompsett, David; Walton, Richard I.
• Is Part Of: Dalton transactions. Volume 49:Issue 42(2020)
• Page Start: 14871
• Page End: 14880
• Publication Date: 2020-10-19
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d0dt03435e
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Lanthanide hydroxide-chlorides Ce1− x Ln x (OH)2 Cl for Ln = La, Pr, Gd, Tb crystallise from poly(ethylene) glycol ( M n = 400) at 240 °C. Subsequent thermal decomposition yields oxides Ce1− x Ln x O2− δ with redox properties suited for heterogeneous catalysis. Abstract : The cerium(iii ) hydroxide chloride Ce(OH)2 Cl crystallises directly as a polycrystalline powder from a solution of CeCl3 ·7H2 O in poly(ethylene) glycol ( M n = 400) heated at 240 °C and is found to be isostructural with La(OH)2 Cl, as determined from high-resolution synchrotron powder X-ray diffraction ( P 21 / m, a = 6.2868(2) Å, b = 3.94950(3) Å, c = 6.8740(3) Å, β = 113.5120(5)°). Replacement of a proportion of the cerium chloride in synthesis by a second lanthanide chloride yields a set of materials Ce1− x Ln x (OH)2 Cl for Ln = La, Pr, Gd, Tb. For La the maximum value of x is 0.2, with an isotropic expansion of the unit cell, but for the other lanthanides a wider composition range is possible, and the lattice parameters show an isotropic contraction with increasing x . Thermal decomposition of the hydroxide chlorides at 700 °C yields mixed-oxides Ce1− x Ln x O2− δ that all have cubic fluorite structures with either expanded (Ln = La, Gd) or contracted (Ln = Pr, Tb) unit cells compared to CeO2 . Scanning electron microscopy shows a shape memory effect in crystal morphology upon decomposition, with clusters of anisotropic sub-micron crystallites being seen in the precursor and oxide products. The Pr- and Tb-substituted oxides contain the substituent in a mixture of +3 and +4 oxidation states, as seen by X-ray absorption near edge structure spectroscopy at the lanthanide LIII edges. The mixed oxide materials are examined using temperature programmed reduction in 10%H2 in N2, which reveals redox properties suitable for heterogeneous catalysis, with the Pr-substituted materials showing the greatest reducibility at lower temperature.