<p>Precise measurement of the particle number, spatial distribution and internal state is fundamental to all proposed experiments with ultracold molecules both in bulk gases and optical lattices. Here, we demonstrate in-situ detection of individual molecules in a bulk sample of <sup>87</sup>Rb<sup>133</sup>Cs molecules. Extending techniques from atomic quantum gas microscopy, we pin the molecules in a deep two-dimensional optical lattice and, following dissociation, collect fluorescence from the constituent atoms using a high-numerical-aperture objective. This enables detection of individual molecules up to the resolution of the sub-micron lattice spacing. Our approach provides direct access to the density distribution of small samples of molecules, allowing us to obtain precise measurements of density-dependent collisional losses. Further, by mapping two internal states of the molecule to different atomic species, we demonstrate simultaneous detection of the position and rotational state of individual molecules. Finally, we implement local addressing of the sample using a focused beam to induce a spatially-dependent light shift on the rotational transitions of the molecules.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Multi-state detection and spatial addressing in a microscope for ultracold molecules

  • Jonathan M. Mortlock,
  • Adarsh P. Raghuram,
  • Benjamin P. Maddox,
  • Philip D. Gregory,
  • Simon L. Cornish

摘要

Precise measurement of the particle number, spatial distribution and internal state is fundamental to all proposed experiments with ultracold molecules both in bulk gases and optical lattices. Here, we demonstrate in-situ detection of individual molecules in a bulk sample of 87Rb133Cs molecules. Extending techniques from atomic quantum gas microscopy, we pin the molecules in a deep two-dimensional optical lattice and, following dissociation, collect fluorescence from the constituent atoms using a high-numerical-aperture objective. This enables detection of individual molecules up to the resolution of the sub-micron lattice spacing. Our approach provides direct access to the density distribution of small samples of molecules, allowing us to obtain precise measurements of density-dependent collisional losses. Further, by mapping two internal states of the molecule to different atomic species, we demonstrate simultaneous detection of the position and rotational state of individual molecules. Finally, we implement local addressing of the sample using a focused beam to induce a spatially-dependent light shift on the rotational transitions of the molecules.