Prof. Stephan Götzinger

  • Professor
  • Room: A.3.230
  • Telephone: +49 9131 7133315
  • E-mail

My research is focused on solid-state quantum optics. In the past few years I have, for example, investigated methods to collect single photons with near-unity efficiency. Another emphasis is on techniques which can be used to enhance the interaction of a single photon with a single emitter.

2012

Single-Photon Spectroscopy of a Single Molecule

Y. L. A. Rezus, S. G. Walt, R. Lettow, A. Renn, G. Zumofen, S. Goetzinger, V. Sandoghdar

Physical Review Letters 108 093601 (2012) | Journal

Efficient interaction of light and matter at the ultimate limit of single photons and single emitters is of great interest from a fundamental point of view and for emerging applications in quantum engineering. However, the difficulty of generating single-photon streams with specific wavelengths, bandwidths, and power as well as the weak interaction probability of a single photon with an optical emitter pose a formidable challenge toward this goal. Here, we demonstrate a general approach based on the creation of single photons from a single emitter and their use for performing spectroscopy on a second emitter situated at a distance. While this first proof of principle realization uses organic molecules as emitters, the scheme is readily extendable to quantum dots and color centers. Our work ushers in a new line of experiments that provide access to the coherent and nonlinear couplings of few emitters and few propagating photons.

Spontaneous emission enhancement of a single molecule by a double-sphere nanoantenna across an interface

K-G. Lee, H. Eghlidi, X-W. Chen, A. Renn, S. Goetzinger, V. Sandoghdar

Optics Express 20 23331-23338 (2012) | Journal

We report on two orders of magnitude reduction in the fluorescence lifetime when a single molecule placed in a thin film is surrounded by two gold nanospheres across the film interface. By attaching one of the gold particles to the end of a glass fiber tip, we could control the modification of the molecular fluorescence at will. We find a good agreement between our experimental data and the outcome of numerical calculations. (C) 2012 Optical Society of America

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