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Instruments / Technical Area	Publication Details	Published
I09-Surface and Interface Structural Analysis I11-High Resolution Powder Diffraction	Complex magnetic order in topochemically reduced Rh(I)/Rh(III) LaM0.5Rh0.5O2.25 (M = Co, Ni) phases Zheying Xu , Pardeep K. Thakur , Tien-Lin Lee , Anna Regoutz , Emmanuelle Suard , Inés Puente-Orench , Michael A. Hayward Inorganic Chemistry 2 DOI: 10.1021/acs.inorgchem.2c02747 Diamond Proposal Number(s): [29451] Open Access Show Abstract ▼ Abstract: Topochemical reduction of the cation-disordered perovskite oxides LaCo0.5Rh0.5O3 and LaNi0.5Rh0.5O3 with Zr yields the partially anion-vacancy ordered phases LaCo0.5Rh0.5O2.25 and LaNi0.5Rh0.5O2.25, respectively. Neutron diffraction and Hard X-ray photoelectron spectroscopy (HAXPES) measurements reveal that the anion-deficient phases contain Co1+/Ni1+ and a 1:1 mixture of Rh1+ and Rh3+ cations within a disordered array of apex-linked MO4 square-planar and MO5 square-based pyramidal coordination sites. Neutron diffraction data indicate that LaCo0.5Rh0.5O2.25 adopts a complex antiferromagnetic ground state, which is the sum of a C-type ordering (mM5 +) of the xy-components of the Co spins and a G-type ordering (mΓ1 +) of the z-components of the Co spins. On warming above 75 K, the magnitude of the mΓ1 + component declines, attaining a zero value by 125 K, with the magnitude of the mM5 + component remaining unchanged up to 175 K. This magnetic behavior is rationalized on the basis of the differing d-orbital fillings of the Co1+ cations in MO4 square-planar and MO5 square-based pyramidal coordination sites. LaNi0.5Rh0.5O2.25 shows no sign of long-range magnetic order at 2 K − behavior that can also be explained on the basis of the d-orbital occupation of the Ni1+ centers.	Sep 2022
I11-High Resolution Powder Diffraction	Hole and electron doping of topochemically reduced Ni(I)/Ru(II) insulating ferromagnetic oxides Zheying Xu , Lun Jin , Julius-Konstantin Backhaus , Felicity Green , Michael A. Hayward Inorganic Chemistry 2 DOI: 10.1021/acs.inorgchem.1c02265 Diamond Proposal Number(s): [13284] Show Abstract ▼ Abstract: LaxSr2–xNiRuO6, LaxSr4–xNiRuO8, and LaxSr3–xNiRuO7 are, respectively, the n = ∞, 1, and 2 members of the (Lax/2Sr1–(x/2))nSr(Ni0.5Ru0.5)nO3n+1 compositional series. Reaction with CaH2, in the case of the LaxSr2–xNiRuO6 perovskite phases, or Zr oxygen getters in the case of the LaxSr4–xNiRuO8 and LaxSr3–xNiRuO7 Ruddlesden–Popper phases, yields the corresponding topochemically reduced (Lax/2Sr1–(x/2))nSr(Ni0.5Ru0.5)nO3n–1 compounds (LaxSr2–xNiRuO4, LaxSr4–xNiRuO6, and LaxSr3–xNiRuO5), which contain Ni and Ru cations in square-planar coordination sites. The x = 1 members of each series (LaSrNiRuO4, LaSr3NiRuO6, and LaSr2NiRuO5) exhibit insulating ferromagnetic behavior at low temperature, attributable to exchange couplings between the Ni1+ and Ru2+ centers they contain. Increasing the La3+ concentration (x > 1) leads to a reduction of some of the Ru2+ centers to Ru1+ centers and a suppression of the ferromagnetic state (lower Tc, reduced saturated ferromagnet moment). In contrast, increasing the Sr2+ concentration (x < 1) oxidizes some of the Ru2+ centers to Ru3+ centers and enhances the ferromagnetic coupling (increased Tc, increased saturated ferromagnet moment) for the n = ∞ and n = 2 samples but appears to have no influence on the magnetic ordering temperature of the n = 1 samples. The magnetic couplings and influence of doping are discussed on the basis of superexchange and direct exchange couplings between the square-planar Ni and Ru centers.	Sep 2021
I11-High Resolution Powder Diffraction	LaSrCo0.5Rh0.5O3.25 and LaSrNi0.5Rh0.5O3.25: topochemically reduced, mixed valence Rh(I)/Rh(III) oxides Zheying Xu , Robert G. Palgrave , Michael A. Hayward Inorganic Chemistry DOI: 10.1021/acs.inorgchem.0c02131 Diamond Proposal Number(s): [13284] Show Abstract ▼ Abstract: Topochemical reduction of the n = 1 Ruddlesden–Popper phases LaSrCo0.5Rh0.5O4 and LaSrNi0.5Rh0.5O4 with Zr yields LaSrCo0.5Rh0.5O3.25 and LaSrNi0.5Rh0.5O3.25, respectively. Magnetization and XPS data reveal that while the rhodium centers in LaSrCo0.5Rh0.5O3.25 and LaSrNi0.5Rh0.5O3.25 have an average oxidation state of Rh2+, these are actually mixed valence Rh(I,III) compounds, with the disproportionation of Rh2+ driven by the favorability of locating d8 Rh1+ and d6 Rh3+ cations within square-planar and square-based pyramidal coordination sites, respectively.	Sep 2020

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