Suppression of lattice doubling in quasi-skutterudite La3Rh4Sn13: a comparison of temperature and hydrostatic pressure routes.

We present structural properties at different temperatures and high-pressure (HP) of La3Rh4Sn13 which is one of the interesting systems in the Remika phase RE3Rh4Sn13 (RE = Sr, Ca, La, Pr, Ce) quasi-skutterudite series using synchrotron diffraction. Data at ambient conditions revealed the presence of several weak reflections, which could be accounted only with a superlattice I* structure (I4132) with lattice parameter a ~19.457 Å. However, above 350 K, a complete suppression of the weak superlattice reflections of the I*  structure is observed. Data at higher temperatures is found to be well described by the I structure (Pm-3n) having half the lattice parameter compared to the I* structure. HP-XRPD at ambient temperature showed that pressures greater than 7.5 GPa result in similar suppression of the weak I* superlattice reflections. Data at higher pressures is found to be well described by the I structure (Pm-3n), similar to the high-temperature phase. HP Raman measurements demonstrated changes that seem to be consistent with a locally more ordered structure as in the case of the I* à I transition. Our findings on La3Rh4Sn13 open up new avenues to study unexplored HP phenomena, especially the superconductivity in these Remika phase quasi-skutterudites.

Raman Evidence of Multiple Adsorption Sites and Structural Transformation in ZIF-4.

The zeolitic imidazolate framework, ZIF-4, exhibits soft porosity and is known to show pore volume changes with temperatures, pressures, and guest adsorption. However, the mechanism and adsorption behavior of ZIF-4 are not completely understood. In this work, we report an open to narrow pore transition in ZIF-4 around T ∼ 253 K upon lowering the temperature under vacuum (10-6 Torr) conditions, facilitated by C-H···π interactions. In the gaseous environment of N2 and CO2 around the framework, characteristic Raman peaks of adsorbed gases were observed under ambient conditions of 293 K and 1 atm. A guest-induced transition at ∼153 K resulting in the opening of new adsorption sites was inferred from the Raman spectral changes in the C-H stretching modes and low-frequency modes (<200 cm-1). In contrast to a single vibrational mode generally reported for entrapped N2, we show three Raman modes of adsorbed N2 in ZIF-4. The adsorption is facilitated by dispersive and quadrupolar interactions. From our temperature-dependent Raman results and theoretical analysis based on the density functional tight-binding approach, we conclude that the C-Hs are the preferred adsorption sites on ZIF-4 in the following order: C4-H, C5-H > C2-H > center of the Im ring (interacting with C-H centers) > center of the cavity. We also show that with an increasing concentration of N2 adsorbed at low temperatures, the ZIF-4 structure undergoes shear distortion of the window formed by 4-imidazole rings and consequent volumetric expansion. Our results have immediate implications in the field of porous materials and could be vital in identifying subtle structural transformations that may favor or hinder guest adsorption.

Entanglement between Muon and I>1/2 Nuclear Spins as a Probe of Charge Environment.

We report on the first example of quantum coherence between the spins of muons and quadrupolar nuclei. We reveal that these entangled states are highly sensitive to a local charge environment and thus, can be deployed as a functional quantum sensor of that environment. The quantum coherence effect was observed in vanadium intermetallic compounds which adopt the A15 crystal structure, and whose members include all technologically pertinent superconductors. Furthermore, the extreme sensitivity of the entangled states to the local structural and electronic environments emerges through the quadrupolar interaction with the electric field gradient due to the charge distribution at the nuclear (I>1/2) sites. This case study demonstrates that positive muons can be used as a quantum sensing tool to also probe structural and charge-related phenomena in materials, even in the absence of magnetic degrees of freedom.

Measurement of Spin Dynamics in a Layered Nickelate Using X-Ray Photon Correlation Spectroscopy: Evidence for Intrinsic Destabilization of Incommensurate Stripes at Low Temperatures.

We study the temporal stability of stripe-type spin order in a layered nickelate with x-ray photon correlation spectroscopy and observe fluctuations on timescales of tens of minutes over a wide temperature range. These fluctuations show an anomalous temperature dependence: they slow down at intermediate temperatures and speed up on both heating and cooling. This behavior appears to be directly connected with spatial correlations: stripes fluctuate slowly when stripe correlation lengths are large and become faster when spatial correlations decrease. A low-temperature decay of nickelate stripe correlations, reminiscent of what occurs in cuprates as a result of a competition between stripes and superconductivity, hence occurs via loss of both spatial and temporal correlations.

Evaluation of the Defect Cluster Content in Singly and Doubly Doped Ceria through In Situ High-Pressure X-ray Diffraction.

Defect aggregates in doped ceria play a crucial role in blocking the movement of oxygen vacancies and hence in reducing ionic conductivity. Nevertheless, evaluation of their amount and the correlation between domain size and transport properties is still an open issue. Data derived from a high-pressure X-ray diffraction investigation performed on the Ce1-x(Nd0.74Tm0.26)xO2-x/2 system are employed to develop a novel approach aimed at evaluating the defect aggregate content; the results are critically discussed in comparison to the ones previously obtained from Sm- and Lu-doped ceria. Defect clusters are present even at the lowest considered x value, and their content increases with increasing x and decreasing rare earth ion (RE3+) size; their amount, distribution, and spatial correlation can be interpreted as a complex interplay between the defects' binding energy, nucleation rate, and growth rate. The synoptic analysis of data derived from all of the considered systems also suggests that the detection limit of the defects by X-ray diffraction is correlated to the defect size rather than to their amount, and that the vacancies' flow through the lattice is hindered by defects irrespective of their size and association degree.

Structural Metastability and Fermi Surface Topology of SrAl2Si2.

SrAl2Si2 crystallizes into either a semimetallic, CaAl2Si2-type, α phase or a superconducting, BaZn2P2-type, ß phase. We explore possible α→Pc,⁡Tcß transformations by employing pressure- and temperature-dependent free-energy calculations, vibrational spectral calculations, and room-temperature synchrotron powder X-ray diffraction (PXRD) measurements up to 14 GPa using a diamond anvil cell. Our theoretical and empirical analyses together with all reported baric and thermal events on both phases allow us to construct a preliminary P-T diagram of transformations. Our calculations show a relatively low critical pressure for the α-to-ß transition (4.9 GPa at 0 K, 5.0 GPa at 300 K, and 5.3 GPa at 900 K); nevertheless, our nonequilibrium analysis indicates that the low-pressure low-temperature α phase is separated from a metastable ß phase by a relatively high activation barrier. This analysis is supported by our PXRD data at ambient temperature and P ≤ 14 GPa, which shows an absence of the ß phase even after a compression involving three times the critical pressure. Finally, we briefly consider the change in the Fermi surface topology when atomic rearrangement takes place via either transformations among SrAl2Si2 dimorphs or total chemical substitution of Ca by Sr in the isomorphous CaAl2Si2 α phase; empirically, the manifestation of such a topology modification is evident upon comparison of the evolution of the (magneto)transport properties of members of SrAl2Si2 dimorphs and α isomorphs.

Metavalent Bonding in GeSe Leads to High Thermoelectric Performance.

Orthorhombic GeSe is a promising thermoelectric material. However, large band gap and strong covalent bonding result in a low thermoelectric figure of merit, zT≈0.2. Here, we demonstrate a maximum zT≈1.35 at 627 K in p-type polycrystalline rhombohedral (GeSe)0.9 (AgBiTe2 )0.1 , which is the highest value reported among GeSe based materials. The rhombohedral phase is stable in ambient conditions for x=0.8-0.29 in (GeSe)1-x (AgBiTe2 )x . The structural transformation accompanies change from covalent bonding in orthorhombic GeSe to metavalent bonding in rhombohedral (GeSe)1-x (AgBiTe2 )x . (GeSe)0.9 (AgBiTe2 )0.1 has closely lying primary and secondary valence bands (within 0.25-0.30 eV), which results in high power factor 12.8 µW cm-1 K-2 at 627 K. It also exhibits intrinsically low lattice thermal conductivity (0.38 Wm-1 K-1 at 578 K). Theoretical phonon dispersion calculations reveal vicinity of a ferroelectric instability, with large anomalous Born effective charges and high optical dielectric constant, which, in concurrence with high effective coordination number, low band gap and moderate electrical conductivity, corroborate metavalent bonding in (GeSe)0.9 (AgBiTe2 )0.1 . We confirmed the presence of low energy phonon modes and local ferroelectric domains using heat capacity measurement (3-30 K) and switching spectroscopy in piezoresponse force microscopy, respectively.

Mesoporous Metal-Organic Framework MIL-101 at High Pressure.

The chromium terephthalate MIL-101 is a mesoporous metal-organic framework (MOF) with unprecedented adsorption capacities due to the presence of giant pores. The application of an external pressure can effectively modify the open structure of MOFs and its interaction with guest molecules. In this work, we study MIL-101 under pressure by synchrotron X-ray diffraction and infrared (IR) spectroscopy with several pressure transmitting media (PTM). Our experimental results clearly show that when a solid medium as NaCl is employed, an irreversible amorphization of the empty structure occurs at about 0.4 GPa. Using a fluid PTM, as Nujol or high-viscosity silicone oil, results in a slight lattice expansion and a strong modification of the peak frequency and shape of the MOF hydroxyl vibration below 0.1 GPa. Moreover, the framework stability is enhanced under pressure with the amorphization onset shifted to about 7 GPa. This coherent set of results points out the insertion of the fluid inside the MIL-101 pores. Above 7 GPa, concomitantly to the nucleation of the amorphous phase, we observe a peculiar medium-dependent lattice expansion. The behavior of the OH stretching vibrations under pressure is profoundly affected by the presence of the guest fluid, showing that OH bonds are sensitive vibrational probes of the host-guest interactions. The present study demonstrates that even a polydimethylsiloxane silicone oil, although highly viscous, can be effectively inserted into the MIL-101 pores at a pressure below 0.2 GPa. High pressure can thus promote the incorporation of large polymers in mesoporous MOFs.

Single-crystal diffraction at the high-pressure Indo-Italian beamline Xpress at Elettra, Trieste.

In this study the first in situ high-pressure single-crystal X-ray diffraction experiments at Xpress, the Indo-Italian beamline of the Elettra synchrotron, Trieste (Italy), are reported. A description of the beamline experimental setup and of the procedures for single-crystal centring, data collection and processing, using diamond anvil cells, are provided. High-pressure experiments on a synthetic crystal of clinoenstatite (MgSiO3), CaCO3 polymorphs and a natural sample of leucophoenicite [Mn7Si3O12(OH)2] validated the suitability of the beamline experimental setup to: (i) locate and characterize pressure-induced phase transitions; (ii) solve ab initio the crystal structure of high-pressure polymorphs; (iii) perform fine structural analyses at the atomic scale as a function of pressure; (iv) disclose complex symmetry and structural features undetected using conventional X-ray sources.

Covalent Organic Framework (COF-1) under High Pressure.

COF-1 has a structure with rigid 2D layers composed of benzene and B3 O3 rings and weak van der Waals bonding between the layers. The as-synthesized COF-1 structure contains pores occupied by solvent molecules. A high surface area empty-pore structure is obtained after vacuum annealing. High-pressure XRD and Raman experiments with mesitylene-filled (COF-1-M) and empty-pore COF-1 demonstrate partial amorphization and collapse of the framework structure above 12-15 GPa. The ambient pressure structure of COF-1-M can be reversibly recovered after compression up to 10-15 GPa. Remarkable stability of highly porous COF-1 structure at pressures at least up to 10 GPa is found even for the empty-pore structure. The bulk modulus of the COF-1 structure (11.2(5) GPa) and linear incompressibilities (k[100] =111(5) GPa, k[001] =15.0(5) GPa) were evaluated from the analysis of XRD data and cross-checked against first-principles calculations.

Effect of H2O on the Pressure-Induced Amorphization of Hydrated AlPO4-17.

The incorporation of guest species in zeolites has been found to strongly modify their mechanical behavior and their stability with respect to amorphization at high pressure (HP). Here we report the strong effect of H2O on the pressure-induced amorphization (PIA) in hydrated AlPO4-17. The material was investigated in-situ at HP by synchrotron X-ray powder diffraction in diamond anvil cells by using non- and penetrating pressure transmitting media (PTM), respectively, silicone oil and H2O. Surprisingly, in non-penetrating PTM, its structural response to pressure was similar to its anhydrous phase at lower pressures up to ~1.4 GPa, when the amorphization was observed to start. Compression of the structure of AlPO4-17 is reduced by an order of magnitude when the material is compressed in H2O, in which amorphization begins in a similar pressure range as in non-penetrating PTM. The complete and irreversible amorphization was observed at ~9.0 and ~18.7 GPa, respectively, in non- and penetrating PTM. The present results show that the insertion of guest species can be used to strongly modify the stability of microporous material with respect to PIA, by up to an order of magnitude.

Determination of the local structure of Sr2-xMxIrO4 (M = K, La) as a function of doping and temperature.

The local structure of correlated spin-orbit insulator Sr2-xMxIrO4 (M = K, La) has been investigated by Ir L3-edge extended X-ray absorption fine structure measurements. The measurements were performed as a function of temperature for different dopings induced by substitution of Sr with La or K. It is found that Ir-O bonds have strong covalency and they hardly show any change across the Néel temperature. In the studied doping range, neither Ir-O bonds nor their dynamics, measured by their mean square relative displacements, show any appreciable change upon carrier doping, indicating the possibility of nanoscale phase separation in the doped system. On the other hand, there is a large increase of the static disorder in Ir-Sr correlation, larger for K doping than La doping. Similarities and differences with respect to the local lattice displacements in cuprates are briefly discussed.

CH3NH3PbI3, A Potential Solar Cell Candidate: Structural and Spectroscopic Investigations.

Hybrid organic-inorganic metal halides of the type CH3NH3PbX3 have emerged as potential materials for photovoltaic applications. In this paper we discuss structural, electronic, and optical spectroscopy investigations performed on high quality single crystals of CH3NH3PbI3. Our results conclusively suggest that CH3NH3PbI3 crystallizes in centrosymmetric space group and the methylammonium moiety exhibits disordered packing at room temperature. Extracted values of the exciton binding energy, the electron-phonon coupling constant, and the schematic energy level diagram constructed from the emission broadening, Raman, and photoemission spectroscopy measurements clearly show the potential of this system in photovoltaic applications.

Strongly Modified Mechanical Properties and Phase Transition in AlPO4-17 Due to Insertion of Guest Species at High Pressure.

The porous aluminophosphate AlPO4-17 with a hexagonal erionite structure, exhibiting very strong negative thermal expansion, anomalous compressibility, and pressure-induced amorphization, was studied at high pressure by single-crystal and powder X-ray diffraction in the penetrating pressure transmitting media N2, O2, and Ar. Under pressure, these guest species were confirmed to enter the pores of AlPO4-17, thus completely modifying its behavior. Pressure-induced collapse in the xy plane of AlPO4-17 no longer occurred, and this plane exhibited close to zero area compressibility. Pressure-induced amorphization was also suppressed as the elastic instability in the xy plane was removed. Crystal structure refinements at a pressure of 5.5 GPa indicate that up to 28 guest molecules are inserted per unit cell and that this insertion is responsible for the reduced compressibility observed at high pressure. A phase transition to a new hexagonal structure with cell doubling along the a direction was observed above 4.4 GPa in fluid O2.

Tuning Negative Thermal Expansion in AlPO4-17 by Insertion of Guest Molecules.

The very strong negative thermal expansion in the porous aluminophosphate AlPO4-17 with a hexagonal erionite structure was tuned by the insertion of oxygen molecules at high pressure. The structure of the oxygen-filled material was determined in situ at high pressure by synchrotron, single-crystal X-ray diffraction. The thermal expansion of this material was measured precisely at 0.38 GPa by synchrotron X-ray powder diffraction. Whereas the overall volume thermal expansion only exhibits a small change with respect to empty AlPO4-17 at ambient pressure, the expansion along the a direction decreases almost to zero and the expansion along c increases by a factor of 7. Such highly anisotropic thermal expansion properties are of great interest for mechanical and optical applications as in two directions the dimensions of the material are extremely stable, whereas a very strong linear negative thermal expansion of -2.2 × 10-5 K-1 is observed in the perpendicular direction. Guest insertion is thus a very powerful tool for tuning the thermal expansion properties of porous materials.

Pressure-Induced Structural Behavior of Orthorhombic Mn3(VO4)2: Raman Spectroscopic and X-ray Diffraction Investigations.

The effect of high pressure on the structure of orthorhombic Mn3(VO4)2 is investigated using in situ Raman spectroscopy and X-ray powder diffraction up to high pressures of 26.2 and 23.4 GPa, respectively. The study demonstrates a pressure-induced structural phase transition starting at 10 GPa, with the coexistence of phases in the range of 10-20 GPa. The sluggish first-order phase transition is complete by 20 GPa. Importantly, the new phase could be recovered at ambient conditions. Raman spectra of the recovered new phase indicate increased distortion and as a consequence the lowering of the local symmetry of the VO4 tetrahedra. This behavior is different from that reported for isostructural compounds Zn3(VO4)2 and Ni3(VO4)2 where both show stable structures, although almost similar anisotropic compression of the unit cell is observed. The transition observed in orthorhombic Mn3(VO4)2 could be due to the internal charge transfer between the cations, which favors the structural transition at lower pressures and the eventual recovery of the new phase even upon pressure release in comparison to other isostructural compounds. The experimental equation of state parameters obtained for orthorhombic Mn3(VO4)2 match excellently with empirically calculated values reported earlier.

Pressure-enhanced superconductivity in cage-type quasiskutterudite Sc5Rh6Sn18single crystal.

Sc5Rh6Sn18with a cage-type quasiskutterudite crystal lattice and type II superconductivity, with superconducting transition temperatureTc= 4.99 K, was investigated under hydrostatic high-pressure (HP) using electrical transport, synchrotron x-ray diffraction (XRD) and Raman spectroscopy. Our data show that HP enhance the metallic nature andTcof the system.Tcis found to show a continuous increase reaching to 5.24 K at 2.5 GPa. Although the system is metallic in nature, Raman spectroscopy investigations at ambient pressure revealed the presence of three weak modes at 165.97, 219.86 and 230.35 cm-1, mostly related to the rattling atom Sc. The HP-XRD data revealed that the cage structure was stable without any structural phase transition up to ∼7 GPa. The lattice parameters and volume exhibited a smooth decrease without any anomalies as a function of pressure in this pressure range. In particular, a second order Birch-Murnaghan equation of state can describe the pressure dependence of the unit cell volume well, yielding a bulk modulus of ∼97 GPa. HP Raman investigations revealed a linear shift of all the three Raman modes to higher wavenumbers with increasing pressure up to ∼8 GPa. As the pressure enhances the bond overlap, thus inducing more electronic charges into the system, HP-XRD and Raman results may indicate the possibility of obtaining higherTcwith increasing pressures in this pressure range.

Organogel-assisted porous organic polymer embedding Cu NPs for selectivity control in the semi hydrogenation of alkynes.

Heteroatom-rich porous-organic-polymers (POPs) comprising highly cross-linked robust skeletons with high physical and thermal stability, high surface area, and tunable pore size distribution have garnered significant research interest owing to their versatile functionalities in a wide range of applications. Here, we report a newly developed organogel-assisted porous-organic-polymer (POP) supported Cu catalyst (Cu@TpRb-POP). The organogel was synthesized via a temperature induced gelation strategy, employing Schiff-base coupling between 2,4,6-triformylphloroglucinol aldehyde (Tp) and pararosaniline base (Rb). The gel is subsequently transformed to hierarchical porous organic structures without the use of any additive, thereby offering advantageous features including extremely low density, high surface area, a highly cross-linked framework, and a heteroatom-enriched backbone of the polymer. During the semi-hydrogenation of terminal and internal alkynes, the Cu@TpRb-POP-B catalyst with Cu embedded in the TpRb-POP structure consistently demonstrated improved selectivity towards alkenes compared to Cu@TpRb-POP-A, which contains Cu NPs exposed at the exterior surfaces of the POP support. Additionally, Cu@TpRb-POP-B showed higher stability and reusability than Cu@TpRb-POP-A. The superior performance of the Cu@TpRb-POP-B catalyst is attributed to the steric hindrance effect, which controls the product selectivity, as well as the synergistic interaction between the heteroatom-rich POP framework and the embedded Cu NPs. Both the effects are corroborated by experimental characterization of the catalysts and density functional theory (DFT) calculations.

Nanoscale inhomogeneity of charge density waves dynamics in La2-xSrxNiO4.

While stripe phases with broken rotational symmetry of charge density are known to emerge in doped strongly correlated perovskites, the dynamics and heterogeneity of spatial ordering remain elusive. Here we shed light on the temperature dependent lattice motion and the spatial nanoscale phase separation of charge density wave order in the archetypal striped phase in La2-xSrxNiO4+y (LSNO) perovskite using X-ray photon correlation spectroscopy (XPCS) joint with scanning micro X-ray diffraction (SµXRD). While it is known that the CDW in 1/8 doped cuprates shows a remarkable stability we report the CDW motion dynamics by XPCS in nickelates with an anomalous quantum glass regime at low temperature, T < 65 K, and the expected thermal melting at higher temperature 65 < T < 120 K. The nanoscale CDW puddles with a shorter correlation length are more mobile than CDW puddles with a longer correlation length. The direct imaging of nanoscale spatial inhomogeneity of CDW by scanning micro X-ray diffraction (SµXRD) shows a nanoscale landscape of percolating short range dynamic CDW puddles competing with large quasi-static CDW puddles giving rise to a novel form of nanoscale phase separation of the incommensurate stripes order landscape.

Pressure response of decylammonium-containing 2D iodide perovskites.

Manipulation by external pressure of the optical response of 2D Metal Halide Perovskites (MHPs) is a fascinating route to tune their properties and promote the emergence of novel features. We investigate here DA2PbI4 and DA2GeI4 (DA = decylammonium) perovskites in the pressure range up to ∼12 GPa by X-ray powder diffraction, absorption, and photoluminescence spectroscopy. Although the two systems share a similar structural evolution with pressure, the optical properties are rather different and influenced by Pb or Ge. DA2PbI4 shows a progressive red shift from 2.28 eV (P = 0 GPa) to 1.64 eV at 11.5 GPa, with a narrow PL emission, whereas DA2GeI4, changes from a non-PL system at ambient pressure to a clear broadband emitter centered around 730 nm with an intensity maximum at about 3.7 GPa. These results unveil the role of the central atom on the nature of emission under pressure in 2D MHPs containing a long alkyl chain.