Phase transitions in N—n-propylpyridinium-TCNQ2 and N—n-butylpyridinium-TCNQn at high pressures

The electrical resistivity of N-n-propylpyridinium-TCNQ₂ (NPPy-TCNQ₂) and N-n-butylpyridinium-TCNQ_n (NBPy-TCNQ_n) has been measured as a function of temperature and pressure. Phase transitions in these salts have been studied at high pressures. The transition temperature (T_c) in NPPy-TCNQ₂ at atmospheric pressure increased with increasing pressure at the rate of dT_c/dP = + 12.0 degkbar^?1. The value of volume change calculated from the Clapeylon-Clausius relation was + 4.4 cm³ mol^?1. The electrical resistivity along the a- and c-axis increased with increasing pressure below 7 kbar. This anomalous electrical behaviour is closely related to the crystal structure of NPPy-TCNQ₂. The resistivity dropped sharply at about 11 kbar. This abrupt change may be due to a new pressure induced phase transition.The T_c of the NBPy-TCNQ_n increased remarkably with increasing pressure up to 0.7 kbar, above which the phase transition disappeared. The phase transitions of N-n-alkyl-substituted pyridinium TCNQ salts depend strongly on the nature of cations.     

Phase transformations in equiatomic alloy TiZr at pressure up to 70 kbar

The effect of pressure on the α ? β and ω ? β transformations in the equiatomic alloy TiZr is studied by the differential thermal analysis (DTA) and calorimetric technique. The α-β equilibrium at atmospheric pressure occurs at a temperature of 579°C, and the heat of transition ΔH is 40.9±2.0 J/g. As the pressure increases up to 28 kbar, the temperature of the α-β equilibrium linearly decreases, dT/dP=?2.2±0.3 K/kbar. In the pressure range 28–48 kbar, the β-phase undergoes a transition to the two-phase (α + ω) state upon cooling to room temperature. At pressures above the triple point with the coordinates P=49±3 kbar and T=460±30°C, the cooling of the β-phase gives rise to only the hexagonal ω-phase with the unit cell parameters a=4.843 Å, c=2.988 Å, and c/a=0.617 under normal conditions. The slope of the ω-β equilibrium boundary is positive at pressures up to 70 kbar, dT/dP≈0.46 K/kbar. The ω → α transformation at atmospheric pressure proceeds in the temperature range T=425–470°C with the enthalpy of transition ΔH=2.8 J/g.     

High pressure study of BaPb0.7Bi0.3O3 films

The resistance R, the superconducting transition temperature T_c and the energy gap Δ(T) have been measured on the BaPb_0.7Bi_0.3O₃ films up to 14 kbar. We have found that up to 14 kbar: (1) pressure suppresses T_c and Δ(T) while enhances R, (2) the value of 2Δ(0)/kT_c is 3.8±0.1, independent of pressure, and (3) the Δ(T)/Δ(0) varies with T/T_c in a BCS fashion but only for T/T_c<0.75 and independent of pressure. The results show that BaPb_1?xBi_xO₃ is a weak-coupling superconductor, but fail to provide information about the cause for the high T_c of the compound.     

压力对NH4IO3及其固溶体相变的影响

在流体静压力到10kbar范围内,采用DTA技术研究了压力对NH₄IO₃及其固溶体K_x(NH₄)_1-xIO₃的相变温度(T_c)的影响。实验结果表明,虽然固溶体的相变温度T_c随K⁺组分的增加而减小,但是dT_c/dP值却同K⁺组分无关。这意味着在压力下IO₃^-离子的伸长对T_c随压力增加起主要作用。 关键词：     

Superconductivity in α- and ω-Zirconium under high pressure

The pressure dependence of the superconducting transition temperatureT _c (p) of α-Zr has been investigated in both solid and liquid pressure transmitting media. Up to about 45 kbardT _c /dp was measured to be + 3.5 × 10^?6 K/bar. Cold working at 4.2 K produced a strong irreversible effect onT _c . The superconductivity of the high pressure phase, ω-Zr, has been studied in its region of stability, i.e. above 60 kbar. For ω-Zr,dT _c /dp=+7.7 × 10^?6K/bar, andT _c (0)=0.72 K (by extrapolation).     

Hydrostatic pressure effect on the metal-insulator transition in LaO0.7Ca0.3Mn1−x(Fe/Ge)xO3 perovskites

Abstract

The temperature dependences of the resistivity of La_0.7Ca_0.3Mn_1?xFe_xO₃ and La_0.7Ca_0.3Mn_1?xFe_xO₃ (0 < × < 0.04) mixed crystals were studied under hydrostatic pressures up to 15kbar. The substitution of Fe for Mn results in an increase of the resistivity and a continuous decrease of the metal-insulator transition temperature T_mi while the substitution of Ge for Mn leads to a more complicated T_mi(x)-curve. In all cases T_mi shifts under pressure with a rate between 1.6 and 2.9K/kbar and a correlation between T_mi and its pressure derivative dT_mi/dP is observed which is in accordance with the general trend of dT_mi/dP versus T_mi as derived for other manganites and is discussed in terns of a competition between superexchange and double exchange.     

Superconducting transition temperature,its pressure dependence and structural transformation in (La,Ce)Ru2 alloys

The superconducting transition temperature and its dependence on hydrostatic pressure to 22 kbar have been determined for a series of (La, Ce)Ru₂ alloys. The variations of these quantities with composition are found to be generally related; however, specific irregularities in the curve of dT_c/dp versus composition are not reflected in the smooth variation of the transition temperature T_c. Some features of dT_c/dp may be correlated with the occurrence of a cubic-tetragonal transformation at low temperatures.     

Pressure dependence of the superconducting transition temperature of a (Mo0.6Ru0.4)86B14 metallic glass

We have studied the pressure dependence of the superconducting transition temperature of amorphous (Mo_0.6Ru_0.4)₈₆B₁₄ for hydrostatic pressures up to P ～ 9 kbar. The transition temperature T_c decreases with pressure at a rate dT_c/dP=-(9±1) mK kbar^-1. We estimate the Grüneisen parameter and the volume dependence of the electron-phonon coupling constant.     

Onset of superconductivity at 107K in YBa2Cu3O7 − δ at high pressure

Electrical resistivity measurements under pressure have been carried out on the high-temperature superconductor YBa₂Cu₃O_{7 –} as a function of temperature T between 1 and 300 K at various pressures between 8 kbar and 149 kbar. The superconducting transition temperature T_c increases almost linearly with pressure at the rate dT_c/dP - 0.13 K/kbar. The onset of T_c, defined as the temperature at which(T) drops to 90% of its extrapolated normal state value, increases from 95 K at 8 kbar to 107 K at 149 kbar. These results suggest that higher pressures will yield yet higher values of T_c.     

Pressure-induced diffusion effects in the intercalation complex TaS2:NH3-AN NMR study

Nuclear spin-lattice relaxation times (T₁) for protons in the intercalation complex TaS₂:NH₃ have been measured as a function of temperature (27 ≤ T ≤ 300 K) and pressure (0 ≤ P ≤ 4 kbar). Dipolar fluctuations associated with translation and reorientation of the NH₃ molecules are the dominant T₁ mechanism for T > 100 K. A one parameter diffusion model analysis yields an activation energy (E) of 0.13 eV for these motions. The rate of change of E with pressure is estimated at d$\text{l}$nE/dP = 2.3%/kbar, much larger than expected from the compressibility of most solids. A sign reversal of dT₁/dP occurs at temperatures near the T₁ minimum, observable in the present case because of the large pressure response of these materials.     

The pressure dependence of the superconducting transition temperature of LaT4P12(T = Fe,Ru, Os)

The superconducting transition temperature, T_c, of the LaT₄P₁₂ compounds with T = Fe, Ru, or Os has been measured under hydrostatic pressure P up to 1.8 GPa. The T = Fe compound exhibits a substantial increase of T_c from T_c (P = 0) = 4.1 K at a rate (dT_c/dP)_P=0= +7.2 x 10^-1 K/GPa. In contrast, the Ru and Os compounds exhibit only weak decreases of T_c from T_c (P = 0) = 7.2 K and 1.8 K with (dT_c/dP)_P=0= -1.6 x 10^-1 K/GPa and -9.5 x 10^-2 K/GPa, respectively. An analysis of this strikingly divergent behavior of T_c(P) in terms of the structural characteristics of the RT₄X₁₂ class of compounds where R = rare earth element, T = Fe, Ru, or Os, and X = P, As, or Sb suggests that T_c(P) for these materials consists of two competing contributions: a depression of T_c due to the compression of the lattice (i.e., decrease in volume), and an enhancement of T_c due to the effect of pressure on La itself.     

Pressure dependence of the superconducting transition temperature of the stage-2 potassium mercurographitide intercalation compound

Measurements of the pressure (P) dependence of the superconducting transition temperature T_c of stage-two KHgC₈ are reported. T_c is found to decrease with applied pressure from a room pressure value of 1.85K at a rate dT_c/dP=-6.5 × 10^-5K/bar, similar to typical superconducting elements such as Sn. No superconductivity was detected for stage-one KHgC₄ or K_0.5Hg_0.5 amalgam to a limiting temperature T = 1.3K and a limiting pressure P = 22 kbar. These results are discussed in reference to the possible occurence of structural and charge density wave transitions in these materials and recent theoretical models of superconducting graphire intercalation compounds.     

Magnetic properties of NdSb,GdSb, TbSb,DySb, HbSb and ErSb under hydrostatic pressure

The hydrostatic pressure dependence of magnetic properties are reported for antiferromagnetic RSb where R = Nd, Gd, Tb, Dy, HoorEr. Measurements were made for pressures 0 ≤ p ≤ 10 kbar, magnetic fields 0 ≤ H₀ ≤ 60 kG, and temperatures 1.4 K ≤ T ≤ 35 K. dT_N/dP shows no systematic trend and ranges from -0.038 K/kbar for DySb to + 0.21 K/kbar for NdSb. The magnetic properties of DySb are strongly P-dependent, whereas those of HoSb are P-independent, but sample-dependent.     

The pressure dependence of the néel temperature in FeF2

A Mössbauer measurement of the pressure dependence of the Néel temperature in FeF₂ is reported. Up to the maximum pressure of 50 kbar T_N increases at the rate of 0.27 ± 0.03°K/kbar. When this pressure dependence is converted to volume dependence, the result, d In T_N/d In V = 3.2 ± 0.3, is found to obey the $\text{“10}\text{3}$ rule” established by Bloch for a wide variety of antiferromagnetic insulators.     

High pressure effect on the electrical properties of NiS2

A semiconductor-metal transition in the electrical resistance of NiS₂, which has been suggested to be a Mott transition, is observed with decreasing temperature under pressure up to 44 kbar. The transition temperature increases with pressure with a slope of $\text{dT}\text{dP}\text{= 6 ± 1 K/kbar}$. The activation energy in a semiconducting region is found to decrease with increasing pressure and to vanish at about 46 kbar. The critical pressure and temperature are predicted to be 46 ± 2 kbar and 350 ± 20 K.     

Pressure dependence of the Néel temperature of f.c.c. stainless steel

The Néel temperature T_N of f.c.c. stainless steel has been measured as a function of pressure using the Mössbauer effect. A sample with approximately 74 wt.% Fe, doped with ^57Co, and having T_N = 58.4 ± 0.1 K at zero pressure, shows T_N rising with pressure with increasing slope. Our results indicate that T_N is raised to room temperature by a pressure of 175 ± 5 kbar.     

Ferroelastic phase transition and anomalous elastic and thermal properties of betaine borate (CH3)3NCH2COO·H3BO3

The temperature and pressure derivatives of the elastic constants of orthorhombic betaine borate, (CH₃)₃NCH₂COO·H₃BO₃, have been determined by measuring temperature and stress induced shifts of resonance frequencies of thick plates at ca. 15 MHz in the range between 140 and 300 K and 0 and 3 kbar. The elastic ‘shear’ resistance c₄₄ exhibits a value as low as 0.0492×10¹⁰Nm^-2at 293 K. With decreasing temperature c₄₄ approaches zero at ca. 142.5 K, indicating an acoustic soft mode behaviour connected with a ferroelastic phase transition. The softening of c₄₄ is described in a good approximation by c₄₄(T)_p=0 =alogT/T₀ with a=0.0663×10¹⁰Nm^-2 and T₀ = 139.5 K. Further, c₄₄ decreases with increasing pressure according to the linear relation c₄₄(p)_{T=293 K} = 0.0492?0.184×10^-4p (p in bar, c₄₄ in 10¹⁰ Nm^-2). All other elastic constants show a quite normal temperature and pressure dependence. At 293 K the transition is induced by a pressure of 2.65 kbar. The transition temperature T_c depends linearly on pressure according to T_c = 142.5+0.0568 p (pinbar, T_cinK). Passing through the transition no discontinuous change of the lattice constants is observed. The three principal coefficients of thermal expansion and the pressure derivatives of the dielectric constants exhibit discontinuities at the transition. The transition is of strongly second order.     

Influence of hydrostatic pressure on the phase transition in the complex antifluorites and hexammines: Rigid-sphere model interpretation

Abstract

The pressure coefficient of the phase transition temperature T_c, dT_c/dp = -(11⁺-1) K/GPa, has been determined for Ni (NH₃)₆Cl₂ using a new high pressure and low temperature probe. The relations between T_c and dT_c/dp were determined for antifluorite K₂MCl₆ compounds and hexammines applying the rigid-sphere model.     

Pressure effect on the anomalous electrical conductivity of magnetite

The temperature dependence of the electrical conductivity of magnetite was measured under hydrostatic pressure up to 18.4 kbar. It is found that the temperature of the conductivity maximum in the high temperature phase is more rapidly reduced by pressure (dT_m/dP = -4.1 K/kbar) than the Verwey temperature (dT_v/dP = -0.27 K/kbar). The discontinuous change of the conductivity at T_v appears to increase with applied pressure as a result of a lowering of T_m.