Optical Sciences

Biomolecules and nanostructures

The Optical Sciences group studies the interaction of light and matter at the nanoscale. We do this by exploring ways to shape light and its environment. It's what we call active and passive control. Our current focus is on the interaction of light with biomolecules and nanostructures. We are part of Twente University's Department of Science and Technology and member of the MESA+ institute.
We participate in the EU-COST actions MP1102: Coherent Raman microscopy (MicroCor) and CM1202: Supramolecular photocatalytic water splitting (PERSPECT-H2O)


Photophysics of molecular plasmonics

  • Florian Sterl - Former member
  • David van Duinen - Former member
  • Annemarie Huijser - Former member

  • The fascinating feature of plasmonic metal nanoantennas of being able to confine light far beyond the diffraction limit is attracting rapidly increasing attention in solar applications, nanoimaging, ultrasensitive detectors and nonlinear processes. An intriguing unexplored question is whether the plasmonic antenna alters the photodynamics of the molecule in the vicinity.

    We are studying the photophysics of plasmonic antennas coated with Ru[(dpp)3]2+ (tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride) molecules, a well-known model system for Ru-ligand-metal based H2-evolving photocatalysts. The phosphorescence of Ru[(dpp)3]2+ in water shows a decay which is well described by a mono-exponential function with a time constant of 746 +/- 1 ns (black curve in Figure 1). We found that electrostatic attachment of a monolayer of Ru[(dpp)3]2+ molecules on the surface of an antenna (Ag sphere with a radius of 50 nm and 8 nm silica shell) alters the phosphorescence decay (red curve), with the appearance of a 15 +/- 1 ns decay (38 % amplitude). This fast decay may correspond to molecules in the field-enhanced regions of the antenna, while the long-lived component is assigned to molecules outside this region for which the decay is slowed down slightly as compared to the aqueous environment. Ultrafast transient absorption measurements are underway to establish the nature of this fast excited state deactivation.

    Phosphorescence decay
    figure 1. Phosphorescence decay of Ru[(dpp)3]2+ in H2O, and electrostatically attached to a plasmonic antenna. Fits to mono- and bi-exponential decay functions and resulting time constants are included.
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