Tin-doped LuCrO3: A new type of material allowing the location of a 119Sn Mössbauer spectroscopic probe on the gas–solid interface

In situ 119 Sn Mössbauer measurements show that annealing in hydrogen atmosphere of co-precipitated chromium and lutetium hydroxides, doped with 0.2 at.% Sn4+, results in the formation of Sn2+ cations on the surface sites of LuCrO3 microcrystals. Such a distribution of dopant cations is consistent with the anomalously high concentration of tin revealed by X-ray photoelectron spectroscopy (XPS). The 119 Sn spectrum recorded above the Néel point of LuCrO3 attests to the distribution of Sn2+ ions over two kinds of site. For both of them, the isomer shift and quadrupole splitting values agree with those previously reported for 119 Sn 2 + on surface sites of several oxides other than the perovskite-type one. The instantaneous oxidation of tin upon contact with ambient air did not allow us to characterize the cationic surrounding of Sn2+ by measurements involving sample transfer into a liquid-helium cryostat. Relevant information is obtained for the Sn2+→4+ oxidized species located on the sites with unchanged cationic surroundings. The spectrum recorded at 4.2 K shows that nearly two-thirds of the Sn2+→4+ species are spin-polarized to different extents. Comparison with Mössbauer parameters reported for 119 Sn 4 + ions sitting in the regular Cr-substitution site in the bulk of LuCrO3 allows us to ascribe the diffuse magnetic contribution to a distribution of Sn2+→4+ species over Cr-substitution sites with lower (than in the bulk) number of neighboring Cr3+ ions. The presence of an additional non-magnetic component in the spectrum of Sn2+→4+ ions points to the location of the remaining Sn4+ ions and, very likely, the predecessor Sn2+ ones, on Lu-substitution sites with magnetically compensated (2Cr↑+2Cr↓) surroundings.