Nature's highly efficient light-harvesting antennae, such as those found in green sulfur bacteria, consist of supramolecular building blocks that self-assemble into a hierarchy of close-packed structures. In an effort to mimic the fundamental processes that govern nature's efficient systems, it is important to elucidate the role of each level of hierarchy: from molecule, to supramolecular building block, to close-packed building blocks. Here, we study the impact of hierarchical structure. We present a model system that mirrors nature's complexity: cylinders self-assembled from cyanine-dye molecules. Our work reveals that even though close-packing may alter the cylinders' soft mesoscopic structure, robust delocalized excitons are retained: Internal order and strong excitation-transfer interactions-prerequisites for efficient energy transport-are both maintained. Our results suggest that the cylindrical geometry strongly favors robust excitons; it presents a rational design that is potentially key to nature's high efficiency, allowing construction of efficient lightharvesting devices even from soft, supramolecular materials. supramolecular assembly | self-assembled excitonic nanoscale systems | photosynthesis | exciton theory | light-harvesting antennae systems T he most remarkable materials that demonstrate the ability to capture solar energy are natural photosynthetic systems such as those found in primitive marine algae and bacteria (1-10). Their light-harvesting (LH) antennae are crucial components, because they absorb the light and direct the resulting excitation energy efficiently to a reaction center, which then converts these excitations (excitons) into charge-separated states (1,4,11,12). Although the noncovalent interactions that link the individual molecules within the LH antennae are weak, the excitation transfer interactions between the molecules are relatively strong; new excited states, so-called Frenkel excitons (13), are generated that are delocalized over a number of molecules (1). These delocalized excitons are key to nature's efficiency and are therefore of high interest (14)(15)(16)(17)(18)(19)(20).To create such efficient LH systems, nature assembles molecular subunits into individual supramolecular structures, which are then further assembled into close-packed superstructures (1, 4, 7-10, 12, 21). This hierarchical assembly is a generic motif of nature's photosynthetic systems. As with natural systems, assembling artificial LH devices from supramolecular structures will require close packing into hierarchical assemblies to maximize the amount of absorbed light (19). Therefore, key to our ability to tune materials properties for efficient LH applications is a basic understanding of the role of each level of the hierarchy: from the individual molecule, to the individual supramolecular building block, to the close-packed assembly. Whereas the role of the individual molecules in the excitonic properties of the building blocks is well-studied (1, 7-10, 20, 22-37), the effect of structural hierar...

Photosynthetic antennae and organic electronic materials use topological, structural, and molecular control of delocalized excitons to enhance and direct energy transfer. Interactions between the transition dipoles of individual chromophore units allow for coherent delocalization across multiple molecular sites. This delocalization, for specific geometries, greatly enhances the transition dipole moment of the lowest energy excitonic state relative to the chromophore and increases its radiative rate, a phenomenon known as superradiance. In this study, we show that ordered, self-assembled light-harvesting nanotubes (LHNs) display excitation-induced photobrightening and photodarkening. These changes in quantum yield arise due to changes in energetic disorder, which in turn increases/decreases excitonic superradiance. Through a combination of experiment and modeling, we show that intense illumination induces different types of chemical change in LHNs that reproducibly alter absorption and fluorescence properties, indicating control over excitonic delocalization. We also show that changes in spectral width and shift can be sensitive measures of system dimensionality, illustrating the mixed 1-2D nature of LHN excitons. Our results demonstrate a path forward for mastery of energetic disorder in an excitonic antenna, with implications for fundamental studies of coherent energy transport.

Long-lived exciton coherences have been recently observed in photosynthetic complexes via ultrafast spectroscopy, opening exciting possibilities for the study and design of coherent exciton transport. Yet, ambiguity in the spectroscopic signals has led to arguments for interpreting them in terms of the exciton dynamics, demanding more stringent tests. We propose a novel strategy, Quantum Process Tomography (QPT) for ultrafast spectroscopy, to reconstruct the evolving quantum state of excitons in double-walled supramolecular light-harvesting nanotubes at room temperature. The protocol calls for eight transient grating experiments with varied pulse spectra. Our analysis reveals unidirectional energy transfer from the outer to the inner wall excitons, absence of nonsecular processes, and an unexpected coherence between those two states lasting about 150 femtoseconds, indicating weak electronic coupling between the walls. Our work constitutes the first experimental QPT in a "warm" and complex system, and provides an elegant scheme to maximize information from ultrafast spectroscopy experiments.Recently, there has been great excitement about the detection of long-lived coherent dynamics in natural lightharvesting photosynthetic complexes via two-dimensional spectroscopy [1][2][3]. This long-lived coherence has generated interest and debate about its role in the efficient design of light-harvesting and exciton transport in biological and artificial settings [4][5][6][7]. These discussions have highlighted the importance of correctly interpreting the spectroscopic signals in terms of the microscopic dynamics in the material. The interplay between excitonic dynamics and vibrational dynamics can produce complex and potentially ambiguous spectroscopic signals, which can make extraction of information about exciton transport challenging [8][9][10]. Therefore, it is essential to develop methods to reliably extract the quantum dynamics of the interrogated material. In this article, we demonstrate the systematic characterization of the quantum dynamics of a condensed phase molecular system, namely, the excitons originating from the inner and outer walls of supramolecular light-harvesting nanotubes, via ultrafast Quantum Process Tomography (QPT) [11][12][13]. This manuscript is organized as follows: First, we briefly sketch the QPT formalism as a general method to maximize information from a quantum system interacting with its environment. Then, we describe the nanotubes and the optical setup, and explain how these two are ideally suited for the QPT protocol. Finally, we present the experimental data and its analysis, yielding a full characterization of the quantum dynamics of the excitonic system. To our knowledge, this article constitutes the first experimental realization of QPT on a molecular system in condensed phase, and provides general guidelines to adapt standard spectroscopic experiments to carry out QPT.The time evolution of the excited state of an open quantum system (a system interacting with its environme...

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