Monitoring the Activation of Open Metal Sites in [Fe x M 3– x (μ 3 -O)] Cluster-Based Metal–Organic Frameworks by Single-Crystal X-ray Diffraction
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The Bardeen–Cooper–Schrieffer theory of superconductivity and the Landau–Fermi liquid theory form the basis of our current understanding of conventional superconductors and their parent non-superconducting phases. However, some exotic superconductors do not conform to this physical picture but instead feature an unusual ‘normal’ state that is not a Fermi liquid. One explanation of this unusual behaviour is that pre-formed pairs of electrons are established above the superconducting temperature T c . Here, we highlight recent experiments that show the likely existence of these pre-formed pairs in two rather different materials—a high-temperature cuprate superconductor and strontium titanate. Moreover, in both materials the normal state from which superconductivity emerges has other shared properties, including a pseudogap and electronic nematicity—rotational symmetry breaking in the electron fluid that is not expected in Fermi liquid theory nor more generally from the crystal lattice symmetry. These experimental findings should provoke more interaction between the communities working on these materials and new insights into the underlying mechanism of the creation of pre-formed pairs.
When protons and neutrons (nucleons) are bound into atomic nuclei, they are close enough to feel significant attraction, or repulsion, from the strong, short-distance part of the nucleon-nucleon interaction. These strong interactions lead to hard collisions between nucleons, generating pairs of highly energetic nucleons referred to as short-range correlations (SRCs). SRCs are an important but relatively poorly understood part of nuclear structure, and mapping out the strength and the isospin structure (neutron-proton (np) versus proton-proton (pp) pairs) of these virtual excitations is thus critical input for modelling a range of nuclear, particle and astrophysics measurements. Two-nucleon knockout or 'triple coincidence' reactions have been used to measure the relative contribution of np-SRCs and pp-SRCs by knocking out a proton from the SRC and detecting its partner nucleon (proton or neutron). These measurements have shown that SRCs are almost exclusively np pairs, but they had limited statistics and required large model-dependent final-state interaction corrections. Here we report on measurements using inclusive scattering from the mirror nuclei hydrogen-3 and helium-3 to extract the np/pp ratio of SRCs in systems with a mass number of three. In this work we obtain a measure of the np/pp SRC ratio that is an order of magnitude more precise than previous experiments, and find a marked deviation from the near-total np dominance observed in heavy nuclei. This result implies an unexpected structure in the high-momentum wavefunction for hydrogen-3 and helium-3. Understanding these results will improve our understanding of the short-range part of the nucleon-nucleon interaction.
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The Mott metal-insulator transition arises from electron-electron interactions determined by the ratio of Coulomb to kinetic energy scales (U/t). While temperature, pressure, and doping can induce Mott transitions, direct control of U in solid-state systems remains largely unexplored, particularly in the inhomogeneous environments of emerging neuromorphic devices, where conductive filaments create complex gradients of local properties. Here we show that interface-induced screening can continuously tune the electron-electron interaction strength U to drive an isothermal Mott transition. Using thickness-graded LaTiO3/SrTiO3 heterostructures, we used diffraction and photoemission spectroscopy to reveal a continuous, isothermal quantum phase transition from a Fermi liquid quasiparticle with incoherent excitations to a Mott insulator with Hubbard bands. The primary determinant of the transition is the enhanced local screening environment, which directly influences the interaction strength U, driving the system metallic. This demonstrates that interface engineering of the local screening environment provides a promising approach to manipulate Mott physics through correlation control, beyond traditional bandwidth or filling approaches.
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The existence of bridging domains in the vicinity of morphotropic phase boundaries brings an insight into the interplay of phase and domain and explains the excellent piezoelectric performance.
Graphic illustrating the chemical reactions that occur during sintering of LLZTO pellets up to 1100 °C.
Tetravalent praseodymium in a homoleptic imidophosphorane complex is identified and characterized in solution via UV-vis-NIR, cyclic voltammetry, theoretical calculations, and X-band EPR.
Transition metal silicon arsenide with Ir–Si and Ir–As covalent bonding exhibits remarkable non-linear optical properties: high second harmonic generation activity and a large laser damage threshold.
Cation off-centering is crystallography frustrated in the pyrochlore but exhibits local ordering.
Encapsulation of a ferric tris-anilate complex engenders inequivalence of the two spin crossover Fe( ii ) centers of an otherwise symmetric coordination helical host.
The bonding, non-covalent interactions, vibrational features, and formation reactions were explored with Np(v) Cl - compounds. DFT calculated ΔH r of chain formation showed the thermodynamic favorability of reactions forming the molecular components.
We calculate the energetics of protonation in proton-conducting oxides, as well as defect concentrations and mobility under electrolysis conditions.
The gas-phase reaction of two resonantly stabilized radicals synthesizes the 10π Hückel aromatic azulene and naphthalene – which can be embedded into saddle-shaped carbonaceous nanostructures exhibiting positive and negative curvatures.
The PIN–0.36PT relaxor ferroelectric at the MPB exhibits reversible phase transformation and relatively flexible M structure, which enable large lattice strain and domain switching, and are responsible for the enhanced piezoelectric properties.
Recent advances enabled the discovery of heterometallic molecules for many metals: main group, d-block, lanthanides, and some actinides (U, Th).