Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Bulletin of the American Physical Society

Ultracold Fermionic gases of Li atoms and LiNa molecules

Caleb A. Christensen, Jae Hyuk Choi, Ye-Ryoung Lee, Gyu-Boong Jo, Wolfgang Ketterle, David E. Pritchard

Published May 27, 2010• 0 citations
OpenAlex

Related papers

Cold and ultracold reactive collisions of Li with LiNa

Brian K. Kendrick

Bulletin of the American Physical Society•Jun 1, 2021•0 citations

Ultracold Gas of Fermionic Molecules in the Triplet Ground State

Juliana Park, Timur M. Rvachov, Hyungmok Son +3 more

Bulletin of the American Physical Society•May 29, 2018•0 citations

A neural network potential energy surface for the Li + LiNa → Li 2 + Na reaction and quantum dynamics study from ultracold to thermal energies

Bayaer Buren

, 124303), which indicates that the dynamics of the ultracold Li + LiNa reaction can be well described by the SQM approach. The time-dependent wave packet calculations are performed for the Li + LiNa reaction at thermal energies, and the characteristic of differential cross-sections confirms that the reaction follows the complex-forming reaction mechanism.

Physical Chemistry Chemical Physics•Jan 1, 2023•3 citations

Non-adiabatic quantum interference in the ultracold Li + LiNa → Li 2 + Na reaction

Brian K. Kendrick, Hui Li, Ming Li +3 more

Electronically non-adiabatic effects play an important role in many chemical reactions. However, how these effects manifest in cold and ultracold chemistry remains largely unexplored. Here for the first time we present from first principles the non-adiabatic quantum dynamics of the reactive scattering between ultracold alkali-metal LiNa molecules and Li atoms. We show that non-adiabatic dynamics induces quantum interference effects that dramatically alter the ultracold rotationally resolved reaction rate coefficients. The interference effect arises from the conical intersection between the ground and an excited electronic state that is energetically accessible even for ultracold collisions. These unique interference effects might be exploited for quantum control applications such as a quantum molecular switch. The non-adiabatic dynamics are based on full-dimensional ab initio potential energy surfaces for the two electronic states that includes the non-adiabatic couplings and an accurate treatment of the long-range interactions. A statistical analysis of rotational populations of the Li2 product reveals a Poisson distribution implying the underlying classical dynamics are chaotic. The Poisson distribution is robust and amenable to experimental verification and appears to be a universal property of ultracold reactions involving alkali metal dimers.

Physical Chemistry Chemical Physics•Jan 1, 2021•48 citations

Exploring a quantum degenerate, ultracold gas of fermionic atoms

Brian DeMarco, D. S. Jin

Physical Review A•Jan 1, 1998•2 citations

Non-universal behavior in the ultracold Li + LiNa $\to$ Li$_2$ + Na reaction

Brian K. Kendrick, James F. E. Croft, N. Balakrishnan +3 more

Bulletin of the American Physical Society•May 30, 2019•0 citations
Electronically non-adiabatic effects play an important role in many chemical reactions. However, how these effects manifest in cold and ultracold chemistry remains largely unexplored. Here for the first time we present from first principles the non-adiabatic quantum dynamics of the reactive scattering between ultracold alkali-metal LiNa molecules and Li atoms. We show that non-adiabatic dynamics induces quantum interference effects that dramatically alter the ultracold rotationally resolved reaction rate coefficients. The interference effect arises from the conical intersection between the ground and an excited electronic state that is energetically accessible even for ultracold collisions. These unique interference effects might be exploited for quantum control applications such as a quantum molecular switch. The non-adiabatic dynamics are based on full-dimensional ab initio potential energy surfaces for the two electronic states that includes the non-adiabatic couplings and an accurate treatment of the long-range interactions. A statistical analysis of rotational populations of the Li2 product reveals a Poisson distribution implying the underlying classical dynamics are chaotic. The Poisson distribution is robust and amenable to experimental verification and appears to be a universal property of ultracold reactions involving alkali metal dimers.
Non-universal behavior in the ultracold Li + LiNa →\to→ Li2_22​ + Na reaction