Of all known photosynthetic organisms, the green sulfur bacteria are able to survive under the lowest illumination conditions due to highly efficient photon management and exciton transport enabled by their special organelles, the chlorosomes, which consist mainly of self-assembled bacteriochlorophyll c, d, or e molecules. A challenging task is to mimic the principle of self-assembling chromophores in artificial light-harvesting devices. In the present work we have studied exciton transport and dissociation in a bilayer of an electron-accepting semiconductor and an artificial self-assembling zinc porphyrin that mimics natural chlorosomal bacteriochlorophylls using time-resolved microwave conductivity (TRMC). Scanning electron microscopy (SEM) reveals the presence of large domains with dimensions up to several micrometers that consist of self-assembled stacks. In addition to these large self-assembled stacks, absorption and fluorescence spectra reveal the presence of monomers. The fluorescence in the solid state, just as in the chlorosomes, is only partially quenched and its decay shows two components, one with lifetimes of 40 ps stemming from the aggregates and a longer one with 2.5 ns lifetime ascribed to monomeric zinc porphyrins. Predominantly those photons that are absorbed by the monomers lead to the formation of charge-separated states. The rather low contribution of self-assembled stacks to the formation of charge-separated states, most likely, results from their interaction with the semiconductor, combined with the presence of monomers at the semiconductor surface and the energetically unfavorable exciton transfer from a stack to a monomer. However, we prove herein that biomimetic self-assembling porphyrins can be used to photosenzitize wide band gap semiconductors as a 2.2% incident photon to charge separation efficiency could be measured. Realizing an ordered structure of stacks in proper contact with the electron-accepting semiconductor will probably improve their contribution to the formation of charge-separated states. This might pave the way to cost-efficient hybrid solar cells using artificial chlorosome-like antenna architectures, allowing them to work also under dim or diffuse light.

Efforts for building hybrid solar cells which have an antenna system similar to the chlorosomes of green photosynthetic bacteria are reviewed and discussed in the context of the current state-of-the-art.

Being able to control in time and space the positioning, orientation, movement, and sense of rotation of nano- to microscale objects is currently an active research area in nanoscience, having diverse nanotechnological applications. In this paper, we demonstrate unprecedented control and maneuvering of rod-shaped or tubular nanostructures with high aspect ratios which are formed by self-assembling synthetic porphyrins. The self-assembly algorithm, encoded by appended chemical-recognition groups on the periphery of these porphyrins, is the same as the one operating for chlorosomal bacteriochlorophylls (BChl's). Chlorosomes, rod-shaped organelles with relatively long-range molecular order, are the most efficient naturally occurring light-harvesting systems. They are used by green photosynthetic bacteria to trap visible and infrared light of minute intensities even at great depths, e.g., 100 m below water surface or in volcanic vents in the absence of solar radiation. In contrast to most other natural light-harvesting systems, the chlorosomal antennae are devoid of a protein scaffold to orient the BChl's; thus, they are an attractive goal for mimicry by synthetic chemists, who are able to engineer more robust chromophores to self-assemble. Functional devices with environmentally friendly chromophores-which should be able to act as photosensitizers within hybrid solar cells, leading to high photon-to-current conversion efficiencies even under low illumination conditions-have yet to be fabricated. The orderly manner in which the BChl's and their synthetic counterparts self-assemble imparts strong diamagnetic and optical anisotropies and flow/shear characteristics to their nanostructured assemblies, allowing them to be manipulated by electrical, magnetic, or tribomechanical forces.

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