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Redox Properties of Hexagonal and Cubic Sr 0.4 Ba 0.6 Mn 0.94 Ti 0.06 O 3−δ Investigated by In Situ Neutron Powder Diffraction
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Structure, Spin Correlations, and Magnetism of the S = 1/2 Square-Lattice Antiferromagnet Sr 2 CuTe 1– x W x O 6 (0 ≤ x ≤ 1)
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Expanding the Rich Crystal Chemistry of Ruthenium(V) Oxides via the Discovery of BaRu[subscript 2]O[subscript 6], Ba[subscript 5]Ru[subscript 4]O[subscript 15], Ba[subscript 2]Ru[subscript 3]O[subscript 10], and Sr[subscript 2]Ru[subscript 3]O[subscript 9](OH) by pH-Controlled Hydrothermal Synthesis
Abstract not provided
Role of Adsorbate Coverage on the Oxygen Dissociation Rate on Sr-Doped LaMnO 3 Surfaces in the Presence of H 2 O and CO 2
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Influence of Alkaline-Earth-Metal Substitutions on the Bismuth Ruthenate Structure: Bi[subscript 2-x]A;#8242;[subscript x]Ru[subscript 2]O[subscript 6]O;#8242;[subscript 1-y] (A;#8242; = Mg, Ca, Sr)
Abstract not provided
Correction to “Interplay of Crystal Structure and Magnetic Properties of the Eu 5.08– x Sr x Al 3 Sb 6 Solid Solution”
Correction to the funding acknowledgment: This work was supported by the National Science Foundation (NSF), DMR-2307231 (instead of DMR-2335203).
New Insights into the Bonding Properties of [Ag[subscript 25](SR)[subscript 18]][superscript -] Nano
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Modifying Metastable Sr 1– x BO 3−δ (B = Nb, Ta, and Mo) Perovskites for Electrode Materials
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Doping- and Strain-Dependent Electrolyte-Gate-Induced Perovskite to Brownmillerite Transformation in Epitaxial La 1– x Sr x CoO 3–δ Films
Much recent attention has focused on the voltage-driven reversible topotactic transformation between the ferromagnetic metallic perovskite (P) SrCoO 3-δ and oxygen-vacancy-ordered antiferromagnetic insulating brownmillerite (BM) SrCoO 2.5 . This is emerging as a paradigmatic example of the power of electrochemical gating (using, e.g., ionic liquids/gels), the wide modulation of electronic, magnetic, and optical properties generating clear application potential. SrCoO 3 films are challenging with respect to stability, however, and there has been little exploration of alternate compositions. Here, we present the first study of ion-gel-gating-induced P. BM transformations across almost the entire La 1-x SrxCoO 3 phase diagram (0 ≤ x ≤ 0.70), under both tensile and compressive epitaxial strain. Electronic transport, magnetometry, and operando synchrotron X-ray diffraction establish that voltage-induced P → BM transformations are possible at essentially all x, including x ≤ 0.50, where both P and BM phases are highly stable. Under small compressive strain, the transformation threshold voltage decreases from approximately +2.7 V at x = 0 to negligible at x = 0.70. Both larger compressive strain and tensile strain induce further threshold voltage lowering, particularly at low x. The P → BM threshold voltage is thus tunable, via both composition and strain. At x = 0.50, voltage-controlled ferromagnetism, transport, and optical transmittance are then demonstrated, achieving Curie temperature and resistivity modulations of similar to 220 K and at least 5 orders of magnitude, respectively, and enabling estimation of the voltage-dependent Co valence. The results are analyzed in the context of doping- and strain-dependent oxygen vacancy formation energies and diffusion coefficients, establishing that it is thermodynamic factors, not kinetics, that underpin the decrease in the threshold voltage with x, that is, with increasing formal Co valence. These findings substantially advance the practical and mechanistic understanding of this voltage-driven transformation, with fundamental and technological implications.
Reversible Hydrogen-Induced Phase Transformations in La 0.7 Sr 0.3 MnO 3 Thin Films Characterized by In Situ Neutron Reflectometry
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