Long-range Exciton Transport Research Articles

Highly Ordered Supramolecular Materials of Phase-Separated Block Molecules for Long-Range Exciton Transport.

Efficient energy transport over long distances is essential for optoelectronic and light-harvesting devices. Although self-assembled nanofibers of organic molecules have been shown to exhibit long exciton diffusion lengths, alignment of these nanofibers into films with large, organized domains with similar properties remains a challenge. Here, we show how the functionalization of C3 -symmetric carbonyl-bridged triarylamine trisamide (CBT) oligodimethylsiloxane (oDMS) sidechains with discrete length leads to fully covered surfaces with aligned domains up to 125 × 70 μm2 in which long-range exciton transport takes place. The nanoscale morphology within the domains consists of highly ordered nanofibers with discrete intercolumnar spacings within a soft amorphous oDMS matrix. The oDMS prevents bundling of the CBT fibers, reducing the number of defects within the CBT columns. As a result, the columns have a high degree of coherence, leading to exciton diffusion lengths of a few hundred nanometers with exciton diffusivities (∼0.05 cm2 s-1 ) that are comparable to those of a crystalline tetracene. These findings represent the next step towards fully covered surfaces of highly aligned nanofibers through functionalization with oDMS. This article is protected by copyright. All rights reserved.

A New Frontier in Exciton Transport: Transient Delocalization.

Efficient exciton transport is crucial to the application of organic semiconductors (OSCs) in light-harvesting devices. While the physics of exciton transport in highly disordered media is well-explored, the description of transport in structurally and energetically ordered OSCs is less established, despite such materials being favorable for devices. In this Perspective we describe and highlight recent research pointing toward a highly efficient exciton transport mechanism which occurs in ordered OSCs, transient delocalization. Here, exciton–phonon couplings play a critical role in allowing localized exciton states to temporarily access higher-energy delocalized states whereupon they move large distances. The mechanism shows great promise for facilitating long-range exciton transport and may allow for improved device efficiencies and new device architectures. However, many fundamental questions on transient delocalization remain to be answered. These questions and suggested next steps are summarized.

Eliminating Radiative Losses in Long-Range Exciton Transport

We demonstrate that it is possible to effectively eliminate radiative losses during excitonic energy transport in systems with an intrinsic energy gradient. By considering chain-like systems of repeating `unit' cells which can each consist of multiple sites, we show that tuning a single system parameter (the intra-unit-cell coupling) leads to efficient and highly robust transport over relatively long distances. This remarkable transport performance is shown to originate from a partitioning of the system's eigenstates into energetically-separated bright and dark subspaces, allowing long range transport to proceed efficiently through a `dark chain' of eigenstates. Finally, we discuss the effects of intrinsic dipole moments, which are of particular relevance to molecular architectures, and demonstrate that appropriately-aligned dipoles can lead to additional protection against other (non-radiative) loss processes. Our dimensionless open quantum systems model is designed to be broadly applicable to a range of experimental platforms.

Efficient Long-Range Triplet Exciton Transport by Metal-Metal Interaction at Room Temperature.

Efficient and long-range exciton transport is critical for photosynthesis and opto-electronic devices, and for triplet-harvesting materials, triplet exciton diffusion length ( ) and coefficient ( ) are key parameters in determining their performances. Herein, we observed that PtII and PdII organometallic nanowires exhibit long-range anisotropic triplet exciton LD of 5-7 μm along the M-M direction using direct photoluminescence (PL) imaging technique by low-power continuous wave (CW) laser excitation. At room temperature, via a combined triplet-triplet annihilation (TTA) analysis and spatial PL imaging, an efficient triplet exciton diffusion was observed for the PtII and PdII nanowires with extended close M-M contact, while is absent in nanowires without close M-M contact. Two-dimensional electronic spectroscopy (2DES) and calculations revealed a significant contribution of the delocalized 1/3 [dσ*(M-M)→π*] excited state during the exciton diffusion modulated by the M-M distance.

Efficient Energy Funneling in Spatially Tailored Segmented Conjugated Block Copolymer Nanofiber-Quantum Dot or Rod Conjugates.

Hybrid systems composed of conjugated polymers and inorganic semiconductor nanocrystals such as quantum dots (QDs) and nanorods (QRs) represent highly desirable multifunctional materials for applications from energy harvesting to light emission and sensing. Herein, we describe energy transfer studies between low-dispersity segmented conjugated polymer micellar nanofibers integrated with quantum dots that are spatially confined to discrete regions in the hybrid assembly via noncovalent interactions. The nanofibers were prepared from diblock copolymers with a crystallizable poly(di-n-hexylfluorene) (PDHF) core-forming block and different corona-forming blocks using the seeded-growth "living" crystallization-driven self-assembly method. The highly ordered crystalline PDHF core in the fibers functions as a donor and permits long-range exciton transport (>200 nm). Energy can therefore be funneled through the fiber core to QDs and QRs that function as acceptor materials and which are noncovalently bound to spatially defined coronal regions of poly(2-vinylpyridine) (P2VP) or quaternized polyfluorene (QPF). Using steady-state and time-resolved spectroscopy, we demonstrate that efficient energy transfer (over 70%) occurs from the crystalline PDHF donor core to the acceptor CdSe QRs attached at the fiber termini. The emission of the PDHF donor in the hybrid conjugate was extensively quenched (by 84%), and a subsequent 4-fold enhancement of the QR emission in solution was observed. These results indicate that the conjugates prepared in this work show promise for potential applications in fields such as light-emitting diodes, photovoltaics, chemical sensors, and photocatalysis.

Anisotropy in fifth-order exciton-exciton-interaction two-dimensional spectroscopy.

Exciton-exciton-interaction two-dimensional (EEI2D) spectroscopy is a fifth-order variant of 2D electronic spectroscopy. It can be used to probe biexciton dynamics in molecular systems and to observe exciton diffusion in extended systems such as polymers or light-harvesting complexes. The exciton transport strongly depends on the geometrical and energetic landscape and its perturbations. These can be of both local character, such as molecular orientation and energetic disorder, and long-range character, such as polymer kinks and structural domains. In the present theoretical work, we investigate the anisotropy in EEI2D spectroscopy. We introduce a general approach for how to calculate the anisotropy by using the response-function formalism in an efficient way. In numerical simulations, using a Frenkel exciton model with Redfield-theory dynamics, we demonstrate how the measurement of anisotropy in EEI2D spectroscopy can be used to identify various geometrical effects on exciton transport in dimers and polymers. Investigating a molecular heterodimer as an example, we demonstrate the utility of anisotropy in EEI2D spectroscopy for disentangling dynamic localization and annihilation. We further calculate the annihilation in extended systems such as conjugated polymers. In a polymer, a change in the anisotropy provides a unique signature for exciton transport between differently oriented sections. We analyze three types of geometry variations in polymers: a kink, varying geometric and energetic disorder, and different geometric domains. Our findings underline that employing anisotropy in EEI2D spectroscopy provides a way to distinguish between different geometries and can be used to obtain a better understanding of long-range exciton transport.

Long-range exciton transport and slow annihilation in two-dimensional hybrid perovskites

Two-dimensional hybrid organic-inorganic perovskites with strongly bound excitons and tunable structures are desirable for optoelectronic applications. Exciton transport and annihilation are two key processes in determining device efficiencies; however, a thorough understanding of these processes is hindered by that annihilation rates are often convoluted with exciton diffusion constants. Here we employ transient absorption microscopy to disentangle quantum-well-thickness-dependent exciton diffusion and annihilation in two-dimensional perovskites, unraveling the key role of electron-hole interactions and dielectric screening. The exciton diffusion constant is found to increase with quantum-well thickness, ranging from 0.06 ± 0.03 to 0.34 ± 0.03 cm2 s−1, which leads to long-range exciton diffusion over hundreds of nanometers. The exciton annihilation rates are more than one order of magnitude lower than those found in the monolayers of transition metal dichalcogenides. The combination of long-range exciton transport and slow annihilation highlights the unique attributes of two-dimensional perovskites as an exciting class of optoelectronic materials.

Interplay between structural hierarchy and exciton diffusion in artificial light harvesting

Unraveling the nature of energy transport in multi-chromophoric photosynthetic complexes is essential to extract valuable design blueprints for light-harvesting applications. Long-range exciton transport in such systems is facilitated by a combination of delocalized excitation wavefunctions (excitons) and exciton diffusion. The unambiguous identification of the exciton transport is intrinsically challenging due to the system’s sheer complexity. Here we address this challenge by employing a spectroscopic lab-on-a-chip approach: ultrafast coherent two-dimensional spectroscopy and microfluidics working in tandem with theoretical modeling. We show that at low excitation fluences, the outer layer acts as an exciton antenna supplying excitons to the inner tube, while under high excitation fluences the former converts its functionality into an exciton annihilator which depletes the exciton population prior to any exciton transfer. Our findings shed light on the excitonic trajectories across different sub-units of a multi-layered artificial light-harvesting complex and underpin their great potential for directional excitation energy transport.

Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals

Long-range exciton diffusion facilitates efficient exciton harvesting in a lightly-doped organic semiconductor crystal.

Long-range exciton transport in conjugated polymer nanofibers prepared by seeded growth.

Easily processed materials with the ability to transport excitons over length scales of more than 100 nanometers are highly desirable for a range of light-harvesting and optoelectronic devices. We describe the preparation of organic semiconducting nanofibers comprising a crystalline poly(di-n-hexylfluorene) core and a solvated, segmented corona consisting of polyethylene glycol in the center and polythiophene at the ends. These nanofibers exhibit exciton transfer from the core to the lower-energy polythiophene coronas in the end blocks, which occurs in the direction of the interchain π-π stacking with very long diffusion lengths (>200 nanometers) and a large diffusion coefficient (0.5 square centimeters per second). This is made possible by the uniform exciton energetic landscape created by the well-ordered, crystalline nanofiber core.

On the Long-Range Exciton Transport in Molecular Systems: The Application to H-Aggregated Heterotriangulene Chains

Self-assembled aggregates of pigment molecules are potential building blocks for excitonic circuits that find their application in energy conversion and optical signal processing. Recent experimental studies of one-dimensional heterotriangulene supramolecular aggregates suggested that singlet excitons in these structures can propagate on several micron distances. We explore this possibility theoretically by combining electronic structure calculations with microscopic models for exciton transport. A detailed characterization of the structural disorder and exciton decoherence is provided. We argue that advanced, well-established exciton transport models, used in our study, give about one order of magnitude shorter estimates for the exciton propagation length which suggest that there are other possible explanations of the experimental results.

Direct Imaging of Exciton Transport in Tubular Porphyrin Aggregates by Ultrafast Microscopy.

Long-range exciton transport is a key challenge in achieving efficient solar energy harvesting in both organic solar cells and photosynthetic systems. Self-assembled molecular aggregates provide the potential for attaining long-range exciton transport through strong intermolecular coupling. However, there currently lacks an experimental tool to directly characterize exciton transport in space and in time to elucidate mechanisms. Here we report a direct visualization of exciton diffusion in tubular molecular aggregates by transient absorption microscopy with ∼200 fs time resolution and ∼50 nm spatial precision. These direct measurements provide exciton diffusion constants of 3-6 cm2 s-1 for the tubular molecular aggregates, which are 3-5 times higher than a theoretical lower bound obtained by assuming incoherent hopping. These results suggest that coherent effects play a role, despite the fact that exciton states near the band bottom crucial for transport are only weakly delocalized (over <10 molecules). The methods presented here establish a direct approach for unraveling the mechanisms and main parameters underlying exciton transport in large molecular assemblies.

Direct Imaging of Long-Range Exciton Transport in Quantum Dot Superlattices by Ultrafast Microscopy.

Long-range charge and exciton transport in quantum dot (QD) solids is a crucial challenge in utilizing QDs for optoelectronic applications. Here, we present a direct visualization of exciton diffusion in highly ordered CdSe QDs superlattices by mapping exciton population using ultrafast transient absorption microscopy. A temporal resolution of ∼200 fs and a spatial precision of ∼50 nm of this technique provide a direct assessment of the upper limit for exciton transport in QD solids. An exciton diffusion length of ∼125 nm has been visualized in the 3 ns experimental time window and an exciton diffusion coefficient of (2.5 ± 0.2) × 10(-2) cm(2) s(-1) has been measured for superlattices constructed from 3.6 nm CdSe QDs with center-to-center distance of 6.7 nm. The measured exciton diffusion constant is in good agreement with Förster resonance energy transfer theory. We have found that exciton diffusion is greatly enhanced in the superlattices over the disordered films with an order of magnitude higher diffusion coefficient, pointing toward the role of disorder in limiting transport. This study provides important understandings on energy transport mechanisms in both the spatial and temporal domains in QD solids.

Delocalization-Enhanced Long-Range Energy Transfer between Cryptophyte Algae PE545 Antenna Proteins

We study the dynamics of interprotein energy transfer in a cluster, consisting of four units of phycoerythrin 545 (PE545) antenna proteins via a hybrid quantum-classical approach. Long-range exciton transport is viewed as a random walk in which the hopping probabilities are determined from a quantum theory. We apply two different formulations of the exciton transport problem to obtain the hopping probabilities, and find that a theory that regards energy transfer as relaxations among the excitonic eigenstates mediated by the vibrational bath, predicts the fastest dynamics. Our results indicate that persistent exciton delocalization is an important implication of the quantum nature of energy transfer on a multiprotein length scale, and that a hybrid quantum-classical approach is a viable starting point in studies of long-range energy transfer in condensed phase biological systems.

Long-Range Exciton Transport by Dynamic Strain Fields in a GaAs Quantum Well

We present a novel approach for the microscopic confinement and transport of excitons in GaAs quantum wells (QWs) using the moving strain field of a surface acoustic wave (SAW). We demonstrate that the band-gap modulation induced by the SAW strain field traps long-living indirect excitons in a double QW structure within sub-$\ensuremath{\mu}\mathrm{m}$-wide stripes parallel to the acoustic wave fronts and transports them over several hundreds of $\ensuremath{\mu}\mathrm{m}$.