Unusual polymerization in the Li4C60 fulleride

Li4C60, one of the best representatives of lithium intercalated fullerides, features a novel type of 2D polymerization. Extensive investigations, including laboratory x-ray and synchrotron radiation diffraction, 13C NMR, MAS and Raman spectroscopy, show a monoclinic I2/m structure, characterized by chains of [2+2]-cycloaddicted fullerenes, sideways connected by single C-C bonds. This leads to the formation of polymeric layers, whose insulating nature, deduced from the NMR and Raman spectra, denotes the complete localization of the electrons involved in the covalent bonds.Comment: 7 pages, 6 figures, RevTex4, submitted to Phys. Rev.

Pressure tuning of light-induced superconductivity in K3C60

Optical excitation at terahertz frequencies has emerged as an effective means to manipulate complex solids dynamically. In the molecular solid K3C60, coherent excitation of intramolecular vibrations was shown to transform the high temperature metal into a non-equilibrium state with the optical conductivity of a superconductor. Here we tune this effect with hydrostatic pressure, and we find it to disappear around 0.3 GPa. Reduction with pressure underscores the similarity with the equilibrium superconducting phase of K3C60, in which a larger electronic bandwidth is detrimental for pairing. Crucially, our observation excludes alternative interpretations based on a high-mobility metallic phase. The pressure dependence also suggests that transient, incipient superconductivity occurs far above the 150 K hypothesised previously, and rather extends all the way to room temperature.Comment: 33 pages, 17 figures, 2 table

Recovering Metallicity in A4C60: The Case of Monomeric Li4C60

The restoration of metallicity in the high-temperature, cubic phase of Li4C60 represents a remarkable feature for a member of the A4C60 family (A = alkali metal), invariably found to be insulators. Structural and resonance technique investigations on Li4C60 at T > 600 K, show that its fcc structure is associated with a complete (4e) charge transfer to C60 and a sparsely populated Fermi level. These findings not only emphasize the crucial role played by lattice symmetry in fulleride transport properties, but also re-dimension the role of Jahn-Teller effects in band structure determination. Moreover, they suggest the present system as a potential precursor to a new class of superconducting fullerides.Comment: 4 pages, 3 figure

Superconducting fluctuations observed far above T_c in the isotropic superconductor K₃C₆₀

Alkali-doped fullerides are strongly correlated organic superconductors that exhibit high transition temperatures, exceptionally large critical magnetic fields and a number of other unusual properties. The proximity to a Mott insulating phase is thought to be a crucial ingredient of the underlying physics, and may also affect precursors of superconductivity in the normal state above T$_\text{c}$. We report on the observation of a sizeable magneto-thermoelectric (Nernst) effect in the normal state of K$_3$C$_{60}$, which displays the characteristics of superconducting fluctuations. The anomalous Nernst effect emerges from an ordinary quasiparticle background below a temperature of 80K, far above T$_\text{c}$ = 20K. At the lowest fields and close to T$_\text{c}$, the scaling of the effect is captured by a model based on Gaussian fluctuations. The temperature up to which we observe fluctuations is exceptionally high for a three-dimensional isotropic system, where fluctuation effects are usually suppressed

Giant resonant enhancement for photo-induced superconductivity in K3_3C60_{60}

Photo-excitation at terahertz and mid-infrared frequencies has emerged as a new way to manipulate functionalities in quantum materials, in some cases creating non-equilibrium phases that have no equilibrium analogue. In K$_3$C$_{60}$, a metastable zero-resistance phase was documented with optical properties and pressure dependences compatible with non-equilibrium high temperature superconductivity. Here, we report the discovery of a dominant energy scale for this phenomenon, along with the demonstration of a giant increase in photo-susceptibility near 10 THz excitation frequency. At these drive frequencies a metastable superconducting-like phase is observed up to room temperature for fluences as low as ~400 $\mu J/cm^2$. These findings shed light on the microscopic mechanism underlying photo-induced superconductivity. They also trace a path towards steady state operation, currently limited by the availability of a suitable high-repetition rate optical source at these frequencies.Comment: 35 pages, 13 figures, including supplementar

Absence of giant spin splitting in the two-dimensional electron liquid at the surface of SrTiO3 (001)

We reinvestigate the putative giant spin splitting at the surface of SrTiO3 reported by Santander-Syro et al. [Nature Mat. 13, 1085 (2014)]. Our spin- and angle-resolved photoemission experiments on fractured (001) oriented surfaces supporting a two-dimensional electron liquid with high carrier density show no detectable spin polarization in the photocurrent. We demonstrate that this result excludes a giant spin splitting while it is consistent with the unconventional Rashba-like splitting seen in band structure calculations that reproduce the experimentally observed ladder of quantum confined subbands.PostprintPeer reviewe

An optically stimulated superconducting-like phase in K3C60 far above equilibrium Tc

The control of non-equilibrium phenomena in complex solids is an important research frontier, encompassing new effects like light induced superconductivity. Here, we show that coherent optical excitation of molecular vibrations in the organic conductor K3C60 can induce a non-equilibrium state with the optical properties of a superconductor. A transient gap in the real part of the optical conductivity and a low-frequency divergence of the imaginary part are measured for base temperatures far above equilibrium Tc=20 K. These findings underscore the role of coherent light fields in inducing emergent order.Comment: 40 pages, 23 figure

The structural and electronic evolution of Li4C60 through the polymer–monomer transformation

In this paper, we combine synchrotron powder x-ray diffraction, 7Li nuclear magnetic resonance (NMR) and electron paramagnetic resonance (EPR) experiments to study the structural evolution of Li4C60 and how its electronic ground state depends on the crystal symmetry. The compound in the two-dimensional polymer phase with mixed interfullerene bonding motifs is a band gap insulator. EPR, however, reveals the presence of intrinsic centers originating from broken C60–C60 bonds and local Li off-stoichiometry that create states in the band gap and account for the complex temperature dependence of the spin susceptibility as well as the residual temperature dependence of the 7Li NMR shift. At low temperatures, the Li+ ions are statically disordered on the 7Li NMR timescale. The observed 7Li NMR line narrowing at T>200 K is ascribed to the Li+ diffusion dynamics and above room temperature the polymer phase is already a good ionic conductor. Heating the sample to temperatures above ~470 K results in gradual depolymerization to the metallic monomer fcc high temperature structure. The transformation is first order and polymer as well as monomer phases coexist over a broad temperature interval (130 K)

Innovative Optoeletronic Approaches to Biomolecular Analysis with Arrays of Silicon Devices

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