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Register a new userMeasurements on Melting Pressure, Metastable Solid Phases, and Molar Volume of Univariant Saturated Helium Mixture
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A concentration-saturated helium mixture at the melting pressure consists of two liquid phases and one or two solid phases. The equilibrium system is univariant, whose properties depend uniquely on temperature. Four coexisting phases can exist on singular points, which are called quadruple points. As a univariant system, the melting pressure could be used as a thermometric standard. It would provide some advantages compared to the current reference, namely pure $^3$He, especially at the lowest temperatures below 1 mK. We have extended the melting pressure measurements of the concentration-saturated helium mixture from 10 mK to 460 mK. The density of the dilute liquid phase was also recorded. The effect of the equilibrium crystal structure changing from hcp to bcc was clearly seen at T=294 mK at the melting pressure P=2.638 MPa. We observed the existence of metastable solid phases around this point. No evidence was found for the presence of another, disputed, quadruple point at around 400 mK. The experimental results agree well with our previous calculations at low temperatures, but deviate above 200 mK.
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Electrons on liquid helium can form different phases depending on density, and temperature. Also the electron-ripplon coupling strength influences the phase diagram, through the formation of so-called ripplonic polarons, that change how electrons are localized, and that shifts the transition between the Wigner solid and the liquid phase. We use an all-coupling, finite-temperature variational method to study the formation of a ripplopolaron Wigner solid on a liquid helium film for different regimes of the electron-ripplon coupling strength. In addition to the three known phases of the ripplopolaron system (electron Wigner solid, polaron Wigner solid, and electron fluid), we define and identify a fourth distinct phase, the ripplopolaron liquid. We analyse the transitions between these four phases and calculate the corresponding phase diagrams. This reveals a reentrant melting of the electron solid as a function of temperature. The calculated regions of existence of the Wigner solid are in agreement with recent experimental data.
We present neutron scattering measurements of the dynamic structure factor, $S(Q,omega)$, of amorphous solid helium confined in 47 $AA$ pore diameter MCM-41 at pressure 48.6 bar. At low temperature, $T$ = 0.05 K, we observe $S(Q,omega)$ of the confined quantum amorphous solid plus the bulk polycrystalline solid between the MCM-41 powder grains. No liquid-like phonon-roton modes, other sharply defined modes at low energy ($omega<$ 1.0 meV) or modes unique to a quantum amorphous solid that might suggest superflow are observed. Rather the $S(Q,omega)$ of confined amorphous and bulk polycrystalline solid appear to be very similar. At higher temperature ($T>$ 1 K), the amorphous solid in the MCM-41 pores melts to a liquid which has a broad $S(Q,omega)$ peaked near $omega simeq$ 0 characteristic of normal liquid $^4$He under pressure. Expressions for the $S(Q,omega)$ of amorphous and polycrystalline solid helium are presented and compared. In previous measurements of liquid $^4$He confined in MCM-41 at lower pressure the intensity in the liquid roton mode decreases with increasing pressure until the roton vanishes at the solidification pressure (38 bars), consistent with no roton in the solid observed here.
There has been a major controversy over the past seven years about the high-pressure melting curves of transition metals. Static compression (diamond-anvil cell: DAC) experiments up to the Mbar region give very low melting slopes dT_m/dP, but shock-wave (SW) data reveal transitions indicating much larger dT_m/dP values. Ab initio calculations support the correctness of the shock data. In a very recent letter, Belonoshko et al. propose a simple and elegant resolution of this conflict for molybdenum. Using ab initio calculations based on density functional theory (DFT), they show that the high-P/high-T phase diagram of Mo must be more complex than was hitherto thought. Their calculations give convincing evidence that there is a transition boundary between the normal bcc structure of Mo and a high-T phase, which they suggest could be fcc. They propose that this transition was misinterpreted as melting in DAC experiments. In confirmation, they note that their boundary also explains a transition seen in the SW data. We regard Belonoshko et al.s Letter as extremely important, but we note that it raises some puzzling questions, and we believe that their proposed phase diagram cannot be completely correct. We have calculated the Helmholtz and Gibbs free energies of the bcc, fcc and hcp phases of Mo, using essentially the same quasiharmonic methods as used by Belonoshko et al.; we find that at high-P and T Mo in the hcp structure is more stable than in bcc or fcc.
The second-layer phase diagrams of $^4$He and $^3$He adsorbed on graphite are investigated. Intrinsically rounded specific-heat anomalies are observed at 1.4 and 0.9 K, respectively, over extended density regions in between the liquid and incommensurate solid phases. They are identified to anomalies associated with the Kosterlitz-Thouless-Halperin-Nelson-Young type two-dimensional melting. The prospected low temperature phase (C2 phase) is a commensurate phase or a $textit{quantum hexatic}$ phase with quasi-bond-orientational order, both containing $textit{zero}$-$textit{point}$ defectons. In either case, this would be the first atomic realization of the $textit{quantum liquid crystal}$, a new state of matter. From the large enhancement of the melting temperature over $^3$He, we propose to assign the observed anomaly of $^4$He-C2 phase at 1.4 K to the hypothetical supersolid or superhexatic transition.
The irrotational nature of superfluid helium was discovered through its decoupling from the container under rotation. Similarly, the resonant period drop of a torsional oscillator (TO) containing solid helium was first interpreted as the decoupling of solid from the TO and appearance of supersolid. However, the resonant period can be changed by mechanisms other than supersolid, such as the elastic stiffening of solid helium that is widely accepted as the reason for the TO response. To demonstrate the irrotational nature more directly, the previous experiments superimposed the dc rotation onto the TO and revealed strong suppression on the TO response without affecting the shear modulus. This result is inconsistent with the simple temperature-dependent elasticity model and supports the supersolid scenario. Here, we re-examine the rotational effect on solid helium with a two-frequency rigid TO to clarify the conflicting observations. Surprisingly, most of the result of previous rotation experiments were not reproduced. Instead, we found a very interesting superfluid-like irrotational response that cannot be explained by elastic models.
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