We have examined superfluid properties of $^4$He confined to a nano-porous Gelsil glass that has nanopores 2.5 nm in diameter. The pressure-temperature phase diagram was determined by torsional oscillator, heat capacity and pressure studies. The supe
rfluid transition temperature $T_{mathrm c}$ approaches zero at 3.4 MPa, indicating a novel quantum superfluid transition. By heat capacity measurements, the nonsuperfluid phase adjacent to the superfluid and solid phases is identified to be a nanometer-scale, localized Bose condensation state, in which global phase coherence is destroyed. At high pressures, the superfluid density has a $T$-linear term, and $T_{mathrm c}$ is proportional to the zero-temperature superfluid density. These results strongly suggest that phase fluctuations in the superfluid order parameter play a dominant role on the phase diagram and superfluid properties.
We report the measurements of the heat capacity of ^4He confined in nanoporous Gelsil glass that has nanopores of 2.5-nm diameter at pressures up to 5.3 MPa. The heat capacity has a broad peak at a temperature much higher than the superfluid transiti
on temperature obtained using the torsional oscillator technique. The peak provides a definite thermodynamic evidence for the formation of localized Bose-Einstein condensates (LBECs) on nanometer length scales. The temperature dependence of heat capacity is well described by the excitations of phonons and rotons, supporting the existence of LBEC.
We have studied the liquid - solid (L-S) phase transition of ^4He confined in nanoporous glass, which has interconnected nanopores of 2.5 nm in diameter. The L-S boundary is determined by the measurements of pressure and thermal response during slow
cooling and warming. Below 1 K, the freezing pressure is elevated to 1.2 MPa from the bulk freezing pressure, and appears to be independent of temperature. The T-independent L-S boundary implies the existence of a localized Bose-Einstein condensation state, in which long-range superfluid coherence is destroyed by narrowness of the nanopores and random potential.
