Precise Characterization of the Rich Structural Landscape Induced by Pressure in Multifunctional FeVO4.

We have studied the high-pressure behavior of FeVO4 by means of single-crystal X-ray diffraction (XRD) and density functional theory (DFT) calculations. We have found that the structural sequence of FeVO4 is different from that previously assumed. In particular, we have discovered a new high-pressure phase at 2.11(4) GPa (FeVO4-I'), which was not detected by previous powder XRD studies. We have determined that FeVO4, under compression (at room temperature), first transforms at 2.11(4) GPa from the ambient-pressure triclinic structure (FeVO4-I) to a second previously unknown triclinic structure (FeVO4-I'), which experiences a subsequent phase transition at 4.80(4) GPa to a monoclinic structure (FeVO4-II'), which was also previously detected in powder XRD experiments. Single-crystal XRD has enabled these novel findings as well as an accurate determination of the crystal structure of FeVO4 polymorphs under high-pressure conditions. The crystal structure of all polymorphs has been accurately solved at all measured pressures. The pressure dependence of the unit-cell parameters and polyhedral coordination have been obtained and are discussed. The room-temperature equation of state and the principal axes of the isothermal compressibility tensor of FeVO4-I and FeVO4-I' have also been determined. The structural phase transition observed here between these two triclinic structures at 2.11(4) GPa implies abrupt coordination polyhedra modifications, including coordination number changes. DFT calculations support the conclusions extracted from our experiments.

Phase Behavior of TmVO4 under Hydrostatic Compression: An Experimental and Theoretical Study.

We present a structural and optical characterization of magnetoelastic zircon-type TmVO4 at ambient pressure and under high pressure. The properties under high pressure have been determined experimentally under hydrostatic conditions and theoretically using density functional theory. By powder X-ray diffraction we show that TmVO4 undergoes a first-order irreversible phase transition to a scheelite structure above 6 GPa. We have also determined (from powder and single-crystal X-ray diffraction) the bulk moduli of both phases and found that their compressibilities are anisotropic. The band gap of TmVO4 is found to be Eg = 3.7(2) eV. Under compression the band gap opens linearly, until it undergoes a huge collapse following the structural phase transition (ΔEg = 1.15 eV). Ab initio structural and free energy calculations support our findings. Moreover, calculations of the band structure and density of states reveal that for both zircon and scheelite TmVO4 the band gap is entirely determined by the V 3d and O 2p states of the VO43- ion. The behavior of the band gap can thus be understood entirely in terms of the structural modifications of the VO4 units under compression. Additionally, we have calculated the evolution of the infrared and Raman phonons of both phases upon compression. The presence of soft modes is related to the dynamic instability of the low-pressure phase and to the phase transition.

PrVO4 under High Pressure: Effects on Structural, Optical, and Electrical Properties.

In the pursuit of a systematic characterization of rare-earth vanadates under compression, in this work we present a multifaceted study of the phase behavior of zircon-type orthovanadate PrVO4 under high-pressure conditions, up to 24 GPa. We have found that PrVO4 undergoes a zircon to monazite transition at around 6 GPa, confirming previous results found by Raman experiments. A second transition takes place above 14 GPa, to a BaWO4-II type structure. The zircon to monazite structural sequence is an irreversible first-order transition, accompanied by a volume collapse of about 9.6%. The monazite phase is thus a metastable polymorph of PrVO4. The monazite-BaWO4-II transition is found instead to be reversible and occurs with a similar volume change. Here we report and discuss the axial and bulk compressibility of all phases. We also compare our results with those for other rare-earth orthovanadates. Finally, by means of optical-absorption experiments and resistivity measurements, we determined the effect of pressure on the electronic properties of PrVO4. We found that the zircon-monazite transition produces a collapse of the band gap and an abrupt decrease in the resistivity. The physical reasons for this behavior are discussed. Density functional theory simulations support our conclusions.

Pressure-Induced Hexagonal to Monoclinic Phase Transition of Partially Hydrated CePO4.

We present a study of the pressure dependence of the structure of partially hydrated hexagonal CePO4 up to 21 GPa using synchrotron powder X-ray diffraction. At a pressure of 10 GPa, a second-order structural phase transition is observed, associated with a novel polymorph. The previously unknown high-pressure phase has a monoclinic structure with a similar atomic arrangement as the low-pressure phase, but with reduced symmetry, belonging to space group C2. Group-subgroup relations hold for the space symmetry groups of both structures. There is no detectable volume discontinuity at the phase transition. Here we provide structural information on the new phase and determine the axial compressibility and bulk modulus for both phases. They are found to have an anisotropic behavior and to be much more compressible than the denser monazite-like polymorph of CePO4. In addition, the isothermal compressibility tensor for the high-pressure structure is reported at 10 GPa and the direction of maximum compressibility described. Finally, the possible role of water and the pressure medium in the high-pressure behavior is discussed. The results are compared with those from other rare-earth orthophosphates.

Controlling the mode of operation of organic transistors through side-chain engineering.

Electrolyte-gated organic transistors offer low bias operation facilitated by direct contact of the transistor channel with an electrolyte. Their operation mode is generally defined by the dimensionality of charge transport, where a field-effect transistor allows for electrostatic charge accumulation at the electrolyte/semiconductor interface, whereas an organic electrochemical transistor (OECT) facilitates penetration of ions into the bulk of the channel, considered a slow process, leading to volumetric doping and electronic transport. Conducting polymer OECTs allow for fast switching and high currents through incorporation of excess, hygroscopic ionic phases, but operate in depletion mode. Here, we show that the use of glycolated side chains on a thiophene backbone can result in accumulation mode OECTs with high currents, transconductance, and sharp subthreshold switching, while maintaining fast switching speeds. Compared with alkylated analogs of the same backbone, the triethylene glycol side chains shift the mode of operation of aqueous electrolyte-gated transistors from interfacial to bulk doping/transport and show complete and reversible electrochromism and high volumetric capacitance at low operating biases. We propose that the glycol side chains facilitate hydration and ion penetration, without compromising electronic mobility, and suggest that this synthetic approach can be used to guide the design of organic mixed conductors.

Effect of High Pressure on the Crystal Structure and Vibrational Properties of Olivine-Type LiNiPO4.

In this work, we present an experimental and theoretical study of the effects of high pressure and high temperature on the structural properties of olivine-type LiNiPO4. This compound is part of an interesting class of materials primarily studied for their potential use as electrodes in lithium-ion batteries. We found that the original olivine structure (α-phase) is stable up to ∼40 GPa. Above this pressure, the onset of a new phase is observed, as put in evidence by the X-ray diffraction (XRD) experiments. The structural refinement shows that the new phase (known as ß-phase) belongs to space group Cmcm. At room temperature, the two phases coexist at least up to 50 GPa. A complete conversion to the ß-phase was only obtained at high-pressure and high-temperature conditions (973 K, 6.5 GPa), as confirmed by both XRD and Raman spectroscopy. Ab initio calculations support the same structural sequence. The need of high-temperature conditions to obtain the complete transformation of the α-phase into the ß-phase is indicative of the existence of a kinetic barrier for the phase transition. Here, we report the evolution of crystallographic parameters as a function of pressure for both phases, comparing them with the theoretical predictions. We also discuss the influence of pressure on the polyhedral units and report room-temperature equations of state. The dependence of the Raman phonons of both phases on pressure is also studied, assigning to each phonon its respective symmetry by comparison with the results of the ab initio simulations.

Molecular Design of Semiconducting Polymers for High-Performance Organic Electrochemical Transistors.

The organic electrochemical transistor (OECT), capable of transducing small ionic fluxes into electronic signals in an aqueous environment, is an ideal device to utilize in bioelectronic applications. Currently, most OECTs are fabricated with commercially available conducting poly(3,4-ethylenedioxythiophene) (PEDOT)-based suspensions and are therefore operated in depletion mode. Here, we present a series of semiconducting polymers designed to elucidate important structure-property guidelines required for accumulation mode OECT operation. We discuss key aspects relating to OECT performance such as ion and hole transport, electrochromic properties, operational voltage, and stability. The demonstration of our molecular design strategy is the fabrication of accumulation mode OECTs that clearly outperform state-of-the-art PEDOT-based devices, and show stability under aqueous operation without the need for formulation additives and cross-linkers.

Operational mechanism of conjugated polyelectrolytes.

Conjugated polyelectrolytes (CPEs) are versatile materials used in a range of organic optoelectronic applications. Because of their ionic/electronic nature, characterizing these materials is nontrivial, and their operational mechanism is not fully understood. In this work we use a methodology that combines constant-voltage-driven current-density transient measurements with fast current vs voltage scans to allow decoupling of ionic and electronic phenomena. This technique is applied to diodes prepared with cationic CPEs having different charge-compensating anions. Our results indicate that the operational mechanism of these devices is governed by electrochemical doping of the CPE. On the basis of the notion that the saturated depletion layer for the anions consists of the same π-conjugated backbone material, we discern how the extent and speed of formation of the doped region depend on the anion structure. Apart from addressing fundamental transport questions, this work provides a tool for future characterization of different CPEs and other similar systems.

Exploring the crystal structure and properties of ytterbium orthoantimonate under high pressure.

The crystal structure of YbSbO4 was determined from powder X-ray diffraction data using the Rietveld method. YbSbO4 is found to be monoclinic and isostructural to α-PrSbO4. We have also tested the influence of pressure on the crystal structure up to 22 GPa by synchrotron powder X-ray diffraction. No phase transition was found. The P-V equation of state and axial compressibilities were determined. Experiments were combined with density-functional theory calculations, which provided information on the elastic constants and the influence of pressure in the crystal structure and Raman/infrared phonons. Results are compared with those from other orthoantimonates. Reasons for the difference in the high-pressure behaviour of YbSbO4 compared with most antimony oxides will be discussed.

Equations of State and Crystal Structures of KCaPO4, KSrPO4, and K2Ce(PO4)2 under High Pressure: Discovery of a New Polymorph of KCaPO4.

We have studied by means of angle-dispersive powder synchrotron X-ray diffraction the structural behavior of KCaPO4, SrKPO4, and K2Ce(PO4)2 under high pressure up to 26, 25, and 22 GPa, respectively. For KCaPO4, we have also accurately determined the crystal structure under ambient conditions, which differs from the structure previously reported. Arguments supporting our structural determination will be discussed. We have found that KCaPO4 undergoes a reversible phase transition. The onset of the transition is at 5.6 GPa. It involves a symmetry decrease. The low-pressure phase is described by space group P3̅m1 and the high-pressure phase by space group Pnma. For KSrPO4 and K2Ce(PO4)2, no evidence of phase transitions has been found up to the highest pressure covered by the experiments. For the three compounds, the linear compressibility for the different crystallographic axes and the pressure-volume equation of states are reported and compared with those of other phosphates. The three studied compounds are among the most compressible phosphates. The results of the study improve the knowledge about the high-pressure behavior of complex phosphates.

Synthesis and Characterization of Novel Nanoparticles of Lithium Aluminum Iodate LiAl(IO3)4, and DFT Calculations of the Crystal Structure and Physical Properties.

Here we report on the non-hydrothermal aqueous synthesis and characterization of nanocrystalline lithium aluminum iodate, LiAl(IO3)4. Morphological and compositional analyses were carried out by using scanning electron microscopy (SEM) and energy-dispersive X-ray measurements (EDX). The optical and vibrational properties of LiAl(IO3)4 have been studied by UV-Vis and IR spectroscopy. LiAl(IO3)4 is found to crystallize in the non-centrosymmetric, monoclinic P21 space group, contrary to what was reported previously. Theoretical simulations and Rietveld refinements of crystal structure support this finding, together with the relatively high Second Harmonic Generation (SGH) response that was observed. Electronic band structure calculations show that LiAl(IO3)4 crystal has an indirect band gap Egap=3.68 eV, in agreement with the experimental optical band gap Egap=3.433 eV. The complex relative permittivity and the refraction index of LiAl(IO3)4 have also been calculated as a function of energy, as well as its elastic constants and mechanical parameters. LiAl(IO3)4 is found to be a very compressible and ductile material. Our findings imply that LiAl(IO3)4 is a promising material for optoelectronic and non -linear optical applications.

Author Correction: Thermal equation of state of ruthenium characterized by resistively heated diamond anvil cell.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

In situ characterization of the high pressure - high temperature melting curve of platinum.

In this work, the melting line of platinum has been characterized both experimentally, using synchrotron X-ray diffraction in laser-heated diamond-anvil cells, and theoretically, using ab initio simulations. In the investigated pressure and temperature range (pressure between 10 GPa and 110 GPa and temperature between 300 K and 4800 K), only the face-centered cubic phase of platinum has been observed. The melting points obtained with the two techniques are in good agreement. Furthermore, the obtained results agree and considerably extend the melting line previously obtained in large-volume devices and in one laser-heated diamond-anvil cells experiment, in which the speckle method was used as melting detection technique. The divergence between previous laser-heating experiments is resolved in favor of those experiments reporting the higher melting slope.

Thermal equation of state of ruthenium characterized by resistively heated diamond anvil cell.

The high-pressure and high-temperature structural and chemical stability of ruthenium has been investigated via synchrotron X-ray diffraction using a resistively heated diamond anvil cell. In the present experiment, ruthenium remains stable in the hcp phase up to 150 GPa and 960 K. The thermal equation of state has been determined based upon the data collected following four different isotherms. A quasi-hydrostatic equation of state at ambient temperature has also been characterized up to 150 GPa. The measured equation of state and structural parameters have been compared to the results of ab initio simulations performed with several exchange-correlation functionals. The agreement between theory and experiments is generally quite good. Phonon calculations were also carried out to show that hcp ruthenium is not only structurally but also dynamically stable up to extreme pressures. These calculations also allow the pressure dependence of the Raman-active E2g mode and the silent B1g mode of Ru to be determined.

Ion-selective organic electrochemical transistors.

Ion-selective organic electrochemical transistors with sensitivity to potassium approaching 50 µA dec(-1) are demonstrated. The remarkable sensitivity arises from the use of high transconductance devices, where the conducting polymer is in direct contact with a reference gel electrolyte and integrated with an ion-selective membrane.