Engineering Papers⌕ Search

DOE OSTI · 1048693

Tiny Bubbles in my BEC

Abstract

Ultracold atomic gases provide a unique way for exploring many-body quantum phenomena that are inaccessible to conventional low-temperature experiments. Nearly two decades ago the Bose-Einstein condensate (BEC) - an ultracold gas of bosons in which almost all bosons occupy the same single-particle state - became experimentally feasible. Because a BEC exhibits superfluid properties, it can provide insights into the behavior of low-temperature helium liquids. We describe the case of a single distinguishable atom (an impurity) embedded in a BEC and strongly coupled to the BEC bosons. Depending on the strength of impurity-boson and boson-boson interactions, the impurity self-localizes into two fundamentally distinct regimes. The impurity atom can behave as a tightly localized 'polaron,' akin to an electron in a dielectric crystal, or as a 'bubble,' an analog to an electron bubble in superfluid helium. We obtain the ground state wavefunctions of the impurity and BEC by numerically solving the two coupled Gross-Pitaevskii equations that characterize the system. We employ the methods of imaginary time propagation and conjugate gradient descent. By appropriately varying the impurity-boson and boson-boson interaction strengths, we focus on the polaron to bubble crossover. Our results confirm analytical predictions for the polaron limit and uncover properties of the bubble regime. With these results we characterize the polaron to bubble crossover. We also summarize our findings in a phase diagram of the BEC-impurity system, which can be used as a guide in future experiments.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Blinova, Alina A. 2012-08-01. Tiny Bubbles in my BEC. https://www.osti.gov/biblio/1048693

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related reports

Cyclic moisture reactivation of calcium sorbents for long duration thermochemical energy storage

The transition to a flexible and reliable energy infrastructure, using electro-thermal energy generation technologies such as geothermal, concentrated solar power, and nuclear, usually demands simultaneous advancement of thermal energy storage (TES) to support on-demand electricity generation and industrial applications while mitigating the inherent intermittency of renewable energy sources and power outages from direct energy generation. Among TES technologies, thermochemical energy storage (TCES) based on calcium looping emerges as a compelling high-power energy storage candidate due to its high reaction enthalpy, compatibility with elevated operating temperatures, and abundance of low-cost materials. However, the long-term durability of calcium-based sorbents for TCES is hindered by surface sintering and particle aggregation, leading to performance degradation over repeated thermal cycles. This study explores a moisture hydration-based strategy to regenerate a degraded calcium sorbent and mitigate performance degradation for long duration TCES. The addition of moisture transforms calcium oxide into calcium hydroxide and produces intercalation water layers, associated with a regenerated surface area and reduced calcium oxide crystallite size. Both these effects are beneficial in restoring the sorbents' reactivity for carbonization. Additionally, an optimized hydration-assisted reactivation protocol balances the recovered energy storage capacity with heating penalty required for moisture removal from hydrated samples, resulting in an enhanced energy storage capacity up to 176% compared to benchmark sorbents that undergo cycling without reactivation after 60 cycles. In conclusion, these results highlight the potential of hydration-assisted reactivation to enhance the long-term performance of TCES, providing an effective pathway to advancing electro-thermal storage technologies.

36 MATERIALS SCIENCE↗