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The utilization of plasmonic energy in the form of heat, resonance energy, and/or hot carriers offers unique possibilities for various applications, like in catalytic and medical applications, due to their simple recyclability or administration. A common strategy to make this plasmonic energy available to the direct environment is to introduce conductive polymer coatings to transfer the energy and to increase the excitons lifetime. However, their practical use is limited due to the limited spectral match of gold with commonly used polymeric materials and semiconductors, the oxidation vulnerability of silver, and the short range of the required strong plasmonic interactions. To overcome these challenges, we developed the synthesis of conjugated polymer–gold–silver hybrid colloids that simultaneously enable silver as the central plasmonic material and prolong the internal relaxation by a heterojunction with a conductive polymer shell. The introduced thin gold layer focuses the plasmonic energy to the metal surface, enhancing and enabling the photocatalyzed polymerization of polypyrrole (PPy) while maintaining the plasmonic properties of silver. Hence, the introduced hybrid particles allow the foreseeable use of plasmonic energy in real-world applications via the strong plasmonics of silver and compatible conductive polymer shells as mediators.

We review the field of organic–inorganic nanocomposites with a focus on materials that exhibit a significant degree of electronic coupling across the hybrid interface. These nanocomposites undergo a variety of charge and energy transfer processes, enabling optoelectronic applications in devices which exploit singlet fission, triplet energy harvesting, photon upconversion or hot charge carrier transfer. We discuss the physical chemistry of the most common organic and inorganic components. Based on those we derive synthesis and assembly strategies and design criteria on material and device level with a focus on photovoltaics, spin memories or optical upconverters. We conclude that future research in the field should be directed towards an improved understanding of the binding motif and molecular orientation at the hybrid interface. © 2020 The Authors. Published by Wiley-VCH GmbH

Plasmonic waveguides consisting of metal nanoparticle chains can localize and guide light well below the diffraction limit, but high propagation losses due to lithography-limited large interparticle spacing have impeded practical applications. Here, we demonstrate that DNA-origami-based self-assembly of monocrystalline gold nanoparticles allows the interparticle spacing to be decreased to ∼2 nm, thus reducing propagation losses to 0.8 dB per 50 nm at a deep subwavelength confinement of 62 nm (∼ /10). We characterize the individual waveguides with nanometer-scale resolution by electron energy-loss spectroscopy. Light propagation toward a fluorescent nanodiamond is directly visualized by cathodoluminescence imaging spectroscopy on a single-device level, thereby realizing nanoscale light manipulation and energy conversion. Simulations suggest that longitudinal plasmon modes arising from the narrow gaps are responsible for the efficient waveguiding. With this scalable DNA origami approach, micrometer-long propagation lengths could be achieved, enabling applications in information technology, sensing, and quantum optics.