Structural and electronic tunability of Ruddlesden–Popper oxyfluorides through nickel–copper substitution in La₂Ni₁₋ₓCuₓO₂.₅F₃ (0 ≤ x ≤ 1)

Title data

Jacobs, Jonas ; Ritter, Clemens ; Xu, Ke ; Schmedt auf der Günne, Jörn ; Wang, Hai-Chen ; Marques, Miguel A. L. ; Hofmann, Anja ; Marschall, Roland ; Ebbinghaus, Stefan G.:
Structural and electronic tunability of Ruddlesden–Popper oxyfluorides through nickel–copper substitution in La₂Ni₁₋ₓCuₓO₂.₅F₃ (0 ≤ x ≤ 1).
In: Journal of Materials Chemistry A. Vol. 13 (2025) Issue 38 . - pp. 32539-32550.
ISSN 2050-7496
DOI: https://doi.org/10.1039/D5TA05605E

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Abstract in another language

In this contribution we report on the synthesis, structure and optical characterization of Ruddlesden–Popper oxyfluorides La2Ni1−xCuxO2.5F3 (0 ≤ x ≤ 1) obtained by topochemical low-temperature fluorination of La2Ni1−xCuxO4 with polyvinylidene fluoride (PVDF). Our study reveals that the anionic ordering in the tetragonal unit cell of La2NiO2.5F3 persists even at high Cu substitution levels (x = 0.9), with minimal change in unit cell volume. This observation is contrary to expectations based on Jahn–Teller induced unit cell distortions, which were previously reported for the oxides La2Ni1−xCuxO4, as well as for the closely related oxyfluorides La2Ni1−xCuxO3F2. The pure copper-containing compound La2CuO2.5F3 crystallizes in a triclinic version of the same structure, and the symmetry lowering is attributed to the enhanced space requirements of the Jahn–Teller elongated CuO4F2 octahedra. The structural investigations based on XRD and ND Rietveld refinements are supported by low-field 19F MAS NMR experiments. We also report the results of diffuse reflectance UV-Vis measurements, which are complemented by DFT calculations. Here, we demonstrate a strong impact of the Cu substitution on the electronic structure of the oxyfluorides, resulting in band gap energies in the range of 3.4 eV to 1.3 eV, spanning the whole visible spectrum. Notably, first photocatalytic water splitting tests reveal a considerable hydrogen evolution activity for x = 0.2, highlighting the potential of Ruddlesden–Popper oxyfluorides for solar energy applications.

Further data

Item Type:	Article in a journal
Refereed:	Yes
Institutions of the University:	Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Physical Chemistry III - Sustainable Materials for Solar Energy Conversion Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Physical Chemistry III - Sustainable Materials for Solar Energy Conversion > Chair Physical Chemistry III - Sustainable Materials for Solar Energy Conversion - Univ.-Prof. Dr. Roland Marschall
Result of work at the UBT:	Yes
DDC Subjects:	500 Science > 540 Chemistry
Date Deposited:	13 Oct 2025 06:48
Last Modified:	13 Oct 2025 06:48
URI:	https://eref.uni-bayreuth.de/id/eprint/94879