Enhancing Long-Range Energy Transport in Supramolecular Architectures by Tailoring Coherence Properties

Efficient long-range energy transport along supramolecular architectures of functional organic molecules is a key step in nature for converting sunlight into a useful form of energy. Understanding and manipulating these transport processes on a molecular and supramolecular scale is a long-standing goal. However, the realization of a well-defined system that allows for tuning morphology and electronic properties as well as for resolution of transport in space and time is challenging. Here we show how the excited-state energy landscape and thus the coherence characteristics of electronic excitations can be modified by the hierarchical level of H-type supramolecular architectures. We visualize, at room temperature, long-range incoherent transport of delocalized singlet excitons on pico- to nanosecond time scales in single supramolecular nanofibers and bundles of nanofibers. Increasing the degree of coherence, i.e., exciton delocalization, via supramolecular architectures enhances exciton diffusivities up to 1 order of magnitude. In particular, we find that single supramolecular nanofibers exhibit the highest diffusivities reported for H-aggregates so far

Real-Time Observation of Iodide Ion Migration in Methylammonium Lead Halide Perovskites

Organic-inorganic metal-halide perovskites (e.g. CH3NH3PbI3-xClx) emerged as a promising opto-electronic material. However, the Shockley–Queisser Limit for the power conversion efficiency (PCE) of perovskite-based photovoltaic devices has still not been reached, which was attributed to non-radiative recombination pathways, as suggested by photoluminescence (PL) inactive (or dark) areas on perovskite films. Although these observations have been related to the presence of ions/defects, the underlying fundamental physics and detailed microscopic processes, concerning trap/defect status, ion migration, etc., still remain poorly understood. Here we utilize correlated wide-field PL microscopy and impedance spectroscopy (IS) on perovskite films to in-situ investigate both the spatial and temporal evolution of these PL inactive areas under external electrical fields. We attribute the formation of PL inactive domains to the migration and accumulation of iodine ions under external fields. Hence we are able to characterize the kinetic processes and determine the drift velocities of these ions. In addition, we show that I2 vapor directly affects the PL quenching of a perovskite film, which provides evidence that the migration/segregation of iodide ions plays an important role in the PL quenching and consequently limits the PCE of organometal halide based perovskite photovoltaic devices

pH dependent photocatalytic hydrogen evolution by self-assembled perylene bisimides

There is growing interest in the design of supramolecular structures that are photocatalytically active. Perylene bisimides can be self-assembled to produce structures for photocatalytic hydrogen evolution. Herein we explore the role of pH in controlling self-assembly and photocatalysis. It is shown that self-assembly, which occurs as the pH of the system is decreased, is required for hydrogen evolution to occur

3D visualization of additive occlusion and tunable full-spectrum fluorescence in calcite

From biomineralization to synthesis, organic additives provide an effective means of controlling crystallization processes. There is growing evidence that these additives are often occluded within the crystal lattice. This promises an elegant means of creating nanocomposites and tuning physical properties. Here we use the incorporation of sulfonated fluorescent dyes to gain new understanding of additive occlusion in calcite (CaCO3), and to link morphological changes to occlusion mechanisms. We demonstrate that these additives are incorporated within specific zones, as defined by the growth conditions, and show how occlusion can govern changes in crystal shape. Fluorescence spectroscopy and lifetime imaging microscopy also show that the dyes experience unique local environments within different zones. Our strategy is then extended to simultaneously incorporate mixtures of dyes, whose fluorescence cascade creates calcite nanoparticles that fluoresce white. This offers a simple strategy for generating biocompatible and stable fluorescent nanoparticles whose output can be tuned as required

Synergy of Axial and Point Chirality to Construct Helical N

We report on the cooperative supramolecular polymerization of a series of N-heterotriangulenes that aggregate into helical columnar stacks by the operation of H-bonding interactions between the peripheral amide groups and π-stacking of the central aromatic moieties. The helical outcome of the highly stable supramolecular polymers stems from the joint effect of the point chirality dictated by the stereogenic centers at the side chains that, in turn, conditions the molecular atropisomerism generated by the restricted rotation of the peripheral benzamide moieties affording a propeller-like geometry. To the best of our knowledge, this is the first example in which two different elements of asymmetry act together to bias the helicity of chiral supramolecular polymers.MINECO of SpainDepto. de Química OrgánicaFac. de Ciencias QuímicasTRUEpu

Highly circularly polarized broad-band emission from chiral naphthalene diimide-based supramolecular aggregates

We report off-white circularly polarized luminescence (CPL) from supramolecular aggregates formed by a chiral carboxylic acid-functionalized naphthalene diimide. The self-assembly behaviour and the stability of the aggregates in solution were assessed by variable-temperature UV-Vis and electronic circular dichroism experiments. The observed 200 nm-wide emission band is unusual for a single chromophore and is a consequence of the supramolecular ordering due to a combination of π-stacking and H-bonding interactions, leading to excimer formation. High emission anisotropy factors glum, around |1-2| × 10-2, were observed over the whole spectrum in chlorinated/hydrocarbon solvent mixtures, as well as in thin films. These values are one order of magnitude higher than those of most chiral self-assembled fluorophores and other common small organic emitters