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Register a new userSimultaneous investigation of shear modulus and torsional resonance of solid 4He
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We investigate the origin of a resonant period drop of a torsional oscillator (TO) containing solid ${}^{4}$He by inspecting its relation to a change in elastic modulus. To understand this relationship directly, we measure both phenomena simultaneously using a TO with a pair of concentric piezoelectric transducers inserted in its annulus. Although the temperature, ${}^{3}$He concentration, and frequency dependence are essentially the same, a marked discrepancy in the drive amplitude dependence is observed. We find that this discrepancy originates from the anisotropic response of polycrystalline solid ${}^{4}$He connected with low-angle grain boundaries by studying the shear modulus parallel to and perpendicular to the driving direction.
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In these torsional oscillator experiments the samples of solid $^4$He were characterized by measuring their thermal conducitvity. Polycrystalline samples of helium of either high isotopic purity or natural concentration of $^3$He were grown in an annular container by the blocked-capillary method and investigated before and after annealing. No correlation has been found between the magnitude of the low-temperature shift of the torsional oscillator frequency and the amount of crystalline defects as measured by the thermal conductivity. In samples with the natural $^3$He concentration a substantial excess thermal conductivity over the usual $T^3$ dependence was observed below 120 mK.
X-ray diffraction experiments show that solid 4He grown in aerogel is highly polycrystalline, with a hcp crystal structure (as in bulk) and a crystallite size of approximately 100 nm. In contrast to the expectation that the highly disordered solid will have a large supersolid fraction, torsional oscillator measurements show a behavior that is strikingly similar to high purity crystals grown from the superfluid phase. The low temperature supersolid fraction is only ~3x10-4 and the onset temperature is ~ 100 mK.
The changes that vacancies produce in the properties of hcp solid 4He are studied by means of quantum Monte Carlo methods. Our results show that the introduction of vacancies produces significant changes in the behavior of solid 4He, even when the vacancy concentration is very small. We show that there is an onset temperature where the properties of incommensurate 4He change significantly. Below this temperature, we observe the emergence of off-diagonal long range order and a complete spatial delocalization of the vacancies. This temperature is quite close to the temperature where non-classical rotational inertia has been experimentally observed. Finally, we report results on the influence of vacancies in the elastic properties of hcp 4He at zero temperature.
The ground state of solid $^4$He is studied using the diffusion Monte Carlo method and a new trial wave function able to describe the supersolid. The new wave function is symmetric under the exchange of particles and reproduces the experimental equation of state. Results for the one-body density matrix show the existence of off-diagonal long-range order with a very small condensate fraction $sim 10^{-4}$. The superfluid density of the commensurate system is below our resolution threshold, $rho_s/rho < 10^{-5}$. With a 1% concentration of vacancies the superfluid density is manifestly larger, $rho_s/rho=3.2(1) cdot 10^{-3}$.
We study the zero-temperature equation of state (EOS) of solid 4He in the hexagonal closed packet (hcp) phase over the 0-57 GPa pressure range by means of the Diffusion Monte Carlo (DMC) method and the semi-empirical Aziz pair potential HFD-B(HE). In the low pressure regime (P ~ 0-1 GPa) we assess excellent agreement with experiments and we give an accurate description of the atomic kinetic energy, Lindemann ratio and Debye temperature over a wide range of molar volumes (22-6 cm^{3}/mol). However, on moving to higher pressures our calculated P-V curve presents an increasingly steeper slope which ultimately provides differences within ~40 % with respect to measurements. In order to account for many-body interactions arising in the crystal with compression which are not reproduced by our model, we perform additional electronic density-functional theory (DFT) calculations for correcting the computed DMC energies in a perturbative way. We explore both generalized gradient and local density approximations (GGA and LDA, respectively) for the electronic exchange-correlation potential. By proceeding in this manner, we show that discrepancies with respect to high pressure data are reduced to 5-10 % with few computational extra cost. Further comparison between our calculated EOSs and ab initio curves deduced for the perfect crystal and corrected for the zero-point motion of the atoms enforces the reliability of our approach.
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