Collisions of ultracold molecules in bright and dark optical dipole traps

被引:58
作者
Bause, Roman [1 ,2 ]
Schindewolf, Andreas [1 ,2 ]
Tao, Renhao [1 ,2 ]
Duda, Marcel [1 ,2 ]
Chen, Xing-Yan [1 ,2 ]
Quemener, Goulven [3 ]
Karman, Tijs [4 ]
Christianen, Arthur [1 ,2 ]
Bloch, Immanuel [1 ,2 ,5 ]
Luo, Xin-Yu [1 ,2 ]
机构
[1] Max Planck Inst Quantum Opt, D-85748 Garching, Germany
[2] Munich Ctr Quantum Sci & Technol, D-80799 Munich, Germany
[3] Univ Paris Saclay, CNRS, Lab Aime Cotton, F-91405 Orsay, France
[4] Radboud Univ Nijmegen, Inst Mol & Mat, Heijendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands
[5] Ludwig Maximilians Univ Munchen, Fak Phys, D-80799 Munich, Germany
来源
PHYSICAL REVIEW RESEARCH | 2021年 / 3卷 / 03期
关键词
REACTIVE MOLECULES; POLAR-MOLECULES; QUANTUM; GAS;
D O I
10.1103/PhysRevResearch.3.033013
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Understanding collisions between ultracold molecules is crucial for making stable molecular quantum gases and harnessing their rich internal degrees of freedom for quantum engineering. Transient complexes can strongly influence collisional physics, but in the ultracold regime, key aspects of their behavior have remained unknown. To explain experimentally observed loss of ground-state molecules from optical dipole traps, it was recently proposed that molecular complexes can be lost due to photoexcitation. By trapping molecules in a repulsive box potential using laser light near a narrow molecular transition, we are able to test this hypothesis with light intensities three orders of magnitude lower than what is typical in red-detuned dipole traps. This allows us to investigate light-induced collisional loss in a gas of nonreactive fermionic Na-23 K-40 molecules. Even for the lowest intensities available in our experiment, our results are consistent with universal loss, meaning unit loss probability inside the short-range interaction potential. Our findings disagree by at least two orders of magnitude with latest theoretical predictions, showing that crucial aspects of molecular collisions are not yet understood and provide a benchmark for the development of new theories.
引用
收藏
页数:12
相关论文
共 70 条
[41]   Liquid and Crystal Phases of Dipolar Fermions in Two Dimensions [J].
Matveeva, N. ;
Giorgini, S. .
PHYSICAL REVIEW LETTERS, 2012, 109 (20)
[42]   Scattering of ultracold molecules in the highly resonant regime [J].
Mayle, Michael ;
Quemener, Goulven ;
Ruzic, Brandon P. ;
Bohn, John L. .
PHYSICAL REVIEW A, 2013, 87 (01)
[43]   Statistical aspects of ultracold resonant scattering [J].
Mayle, Michael ;
Ruzic, Brandon P. ;
Bohn, John L. .
PHYSICAL REVIEW A, 2012, 85 (06)
[44]   Creation of Ultracold 87Rb133Cs Molecules in the Rovibrational Ground State [J].
Molony, Peter K. ;
Gregory, Philip D. ;
Ji, Zhonghua ;
Lu, Bo ;
Koeppinger, Michael P. ;
Le Sueur, C. Ruth ;
Blackley, Caroline L. ;
Hutson, Jeremy M. ;
Cornish, Simon L. .
PHYSICAL REVIEW LETTERS, 2014, 113 (25)
[45]   Creation of a low-entropy quantum gas of polar molecules in an optical lattice [J].
Moses, Steven A. ;
Covey, Jacob P. ;
Miecnikowski, Matthew T. ;
Yan, Bo ;
Gadway, Bryce ;
Ye, Jun ;
Jin, Deborah S. .
SCIENCE, 2015, 350 (6261) :659-662
[46]   Homogeneous Atomic Fermi Gases [J].
Mukherjee, Biswaroop ;
Yan, Zhenjie ;
Patel, Parth B. ;
Hadzibabic, Zoran ;
Yefsah, Tarik ;
Struck, Julian ;
Zwierlein, Martin W. .
PHYSICAL REVIEW LETTERS, 2017, 118 (12)
[47]   A high phase-space-density gas of polar molecules [J].
Ni, K. -K. ;
Ospelkaus, S. ;
de Miranda, M. H. G. ;
Pe'er, A. ;
Neyenhuis, B. ;
Zirbel, J. J. ;
Kotochigova, S. ;
Julienne, P. S. ;
Jin, D. S. ;
Ye, J. .
SCIENCE, 2008, 322 (5899) :231-235
[48]   Dipolar collisions of polar molecules in the quantum regime [J].
Ni, K. -K. ;
Ospelkaus, S. ;
Wang, D. ;
Quemener, G. ;
Neyenhuis, B. ;
de Miranda, M. H. G. ;
Bohn, J. L. ;
Ye, J. ;
Jin, D. S. .
NATURE, 2010, 464 (7293) :1324-1328
[49]   Dipolar exchange quantum logic gate with polar molecules [J].
Ni, Kang-Kuen ;
Rosenband, Till ;
Grimes, David D. .
CHEMICAL SCIENCE, 2018, 9 (33) :6830-6838
[50]   Quantum-State Controlled Chemical Reactions of Ultracold Potassium-Rubidium Molecules [J].
Ospelkaus, S. ;
Ni, K. -K. ;
Wang, D. ;
de Miranda, M. H. G. ;
Neyenhuis, B. ;
Quemener, G. ;
Julienne, P. S. ;
Bohn, J. L. ;
Jin, D. S. ;
Ye, J. .
SCIENCE, 2010, 327 (5967) :853-857