Re-Thinking Dimer Design Principles with Indolonaphthyridine Intramolecular Singlet Fission.

Singlet fission is a phenomenon that could significantly improve the efficiency of photovoltaic devices. Indolonaphthyridine thiophene (INDT) is a photostable singlet fission material that could potentially be utilised in singlet fission-based photovoltaic devices. This study investigates the intramolecular singlet fission (i-SF) mechanism of INDT dimers linked via para-phenyl, meta-phenyl and fluorene bridging groups. Using ultra-fast spectroscopy the highest rate of singlet fission is found in the para-phenyl linked dimer. Quantum calculations show the para-phenyl linker encourages enhanced monomer electronic coupling. Increased rates of singlet fission were also observed in the higher polarity o-dichlorobenzene, relative to toluene, indicating that charge-transfer states have a role in mediating the process. The mechanistic picture of polarisable singlet fission materials, such as INDT, extends beyond the traditional mechanistic landscape.

Aza-Cibalackrot: Turning on Singlet Fission Through Crystal Engineering.

Singlet fission is a photophysical process that provides a pathway for more efficient harvesting of solar energy in photovoltaic devices. The design of singlet fission candidates is non-trivial and requires careful optimization of two key criteria: (1) correct energetic alignment and (2) appropriate intermolecular coupling. Meanwhile, this optimization must not come at the cost of molecular stability or feasibility for device applications. Cibalackrot is a historic and stable organic dye which, although it has been suggested to have ideal energetics, does not undergo singlet fission due to large interchromophore distances, as suggested by single crystal analysis. Thus, while the energetic alignment is satisfactory, the molecule does not have the desired intermolecular coupling. Herein, we improve this characteristic through molecular engineering with the first synthesis of an aza-cibalackrot and show, using ultrafast transient spectroscopy, that singlet fission is successfully "turned on."

Soluble Diphenylhexatriene Dimers for Intramolecular Singlet Fission with High Triplet Energy.

Intramolecular singlet fission (iSF) facilitates single-molecule exciton multiplication, converting an excited singlet state to a pair of triplet states within a single molecule. A critical parameter in determining the feasibility of SF-enhanced photovoltaic designs is the triplet energy; many existing iSF materials have triplet energies too low for efficient transfer to silicon via a photon multiplier scheme. In this work, a series of six novel dimers based upon the high-triplet-energy, SF-active chromophore, 1,6-diphenyl-1,3,5-hexatriene (DPH) [E(T1) ∼ 1.5 eV], were designed, synthesized, and characterized. Transient absorption spectroscopy and fluorescence lifetime studies reveal that five of the dimers display iSF activity, with time constants for singlet fission varying between 7 ± 2 ps and 2.2 ± 0.2 ns and a high triplet yield of 163 ± 63% in the best-performing dimer. A strong dependence of the rate of fission on the coupling geometry is demonstrated. For optimized iSF behavior, close spatial proximity and minimal through-bond communication are found to be crucial for balancing the rate of SF against the reverse recombination process.

Quantitative Singlet Fission in Solution-Processable Dithienohexatrienes.

Singlet fission (SF) is a promising strategy to overcome thermalization losses and enhance the efficiency of single junction photovoltaics (PVs). The development of this field has been strongly material-limited, with a paucity of materials able to undergo SF. Rarer still are examples that can produce excitons of sufficient energy to be coupled to silicon PVs (>1.1 eV). Herein, we examine a series of a short-chain polyene, dithienohexatriene (DTH), with tailored material properties and triplet (T1) energy levels greater than 1.1 eV. We find that these highly soluble materials can be easily spin-cast to create thin films of high crystallinity that exhibit ultrafast singlet fission with near perfect triplet yields of up to 192%. We believe that these materials are the first solution-processable singlet fission materials with quantitative triplet formation and energy levels appropriate for use in conjunction with silicon PVs.

Quantifying Exciton Transport in Singlet Fission Diblock Copolymers.

Singlet fission (SF) is a mechanism of exciton multiplication in organic chromophores, which has potential to drive highly efficient optoelectronic devices. Creating effective device architectures that operate by SF critically depends on electronic interactions across multiple length scales─from individual molecules to interchromophore interactions that facilitate multiexciton dephasing and exciton diffusion toward donor-acceptor interfaces. Therefore, it is imperative to understand the underpinnings of multiexciton transport and interfacial energy transfer in multichromophore systems. Interestingly, block copolymers (BCPs) can be designed to control multiscale interactions by tailoring the nature of the building blocks, yet SF dynamics are not well understood in these macromolecules. Here, we designed diblock copolymers comprising an inherent energy cleft at the interface between a block with pendent pentacene chromophores and an additional block with pendent tetracene chromophores. The singlet and triplet energy offset between the two blocks creates a driving force for exciton transport along the BCP chain in dilute solution. Using time-resolved optical spectroscopy, we have quantified the yields of key energy transfer steps, including both singlet and triplet energy transfer processes across the pentacene-tetracene interface. From this modular BCP architecture, we correlate the energy transfer time scales and relative yields with the length of each block. The ability to quantify these energy transfer processes provides valuable insights into exciton transport at critical length scales between bulk crystalline systems and small-molecule dimers─an area that has been underexplored.

Indolonaphthyridine: A Versatile Chromophore for Organic Electronics Inspired by Natural Indigo Dye.

Organic electronics is an exciting field of research offering innovative technologies from roll-to-roll inkjet-printed solar cells to foldable displays for cellphones and televisions. These functional devices exploit the flexible nature of conjugated organic materials, both polymeric and molecular, to absorb and emit light and to facilitate transport of charge carriers. A major driving force of development within the field is the creation of novel high-performance building blocks, providing a fruitful and ever-growing library of materials for tailored applications. Most of these building blocks contain chromophores that are entirely synthetic, yet there exist many naturally occurring building blocks, which have been relatively overlooked, despite their innate high stability and inexpensive nature. Indigo is the most produced dye worldwide and has one of the richest histories of all known textile dyes, dating before 4000 BC. Indigo's superior photostability has been linked to fast, favorable deactivation pathways following light absorption. But through one straightforward reaction, the chromophore of indigo can be transformed to a new chromophore with remarkable optoelectronic properties.In this Account, we discuss this chromophore, indolonaphthyridine, and give an overview of our research into the synthesis and optoelectronics properties of functional organic electronic materials derived from it. The unit's strong, fused planar construction contains bis-imide functional groups in similarity to the field-favorite diketopyrrolopyrrole, and similarly requires solubilizing with long alkyl chains, the installation of which is nontrivial and achieved using a protecting group strategy. Our solubilized indolonaphthyridine monomer allows us to copolymerize it with simple archetypal comonomers (thiophene, benzothiadiazole, etc.), in contrast to the other research groups working on the chromophore, who employ complex alkylated comonomer units. We discovered materials with extraordinary performance in organic photovoltaics, affording power conversion efficiencies up to 4.1% in the near-IR region of the spectrum. In organic field-effect transistors, the copolymers exhibited ambipolar transport and notable n-type mobilities up to 3.1 cm2/(V s), well above the benchmark set by silicon (1 cm2/(V s)). The strong absorption in the near-IR allowed us to explore the use of the polymers as contrast agents in photoacoustic imaging, an emerging technique capable of achieving deep tissue penetration without the need for ionizing radiation, while maintaining high contrast and high accuracy responses. Finally, we discuss an exciting aspect of the photophysics of molecular indolonaphthyridine: its ability to undergo singlet fission. Moreover, most singlet fission materials exhibit poor ambient stability; however our molecular indolonaphthyridines exhibit superior stability. It is our hope that this Account showcases the remarkable potential of this relatively unexplored, versatile chromophore and leads to wider adoption in the future.

Molecular Engineering of Chromophores to Enable Triplet-Triplet Annihilation Upconversion.

Triplet-triplet annihilation upconversion (TTA-UC) is an unconventional photophysical process that yields high-energy photons from low-energy incident light and offers pathways for innovation across many technologies, including solar energy harvesting, photochemistry, and optogenetics. Within aromatic organic chromophores, TTA-UC is achieved through several consecutive energy conversion events that ultimately fuse two triplet excitons into a singlet exciton. In chromophores where the singlet exciton is roughly isoergic with two triplet excitons, the limiting step is the triplet-triplet annihilation pathway, where the kinetics and yield depend sensitively on the energies of the lowest singlet and triplet excited states. Herein we report up to 40-fold improvements in upconversion quantum yields using molecular engineering to selectively tailor the relative energies of the lowest singlet and triplet excited states, enhancing the yield of triplet-triplet annihilation and promoting radiative decay of the resulting singlet exciton. Using this general and effective strategy, we obtain upconversion yields with red emission that are among the highest reported, with remarkable chemical stability under ambient conditions.

Manipulating molecules with strong coupling: harvesting triplet excitons in organic exciton microcavities.

Exciton-polaritons are quasiparticles with mixed photon and exciton character that demonstrate rich quantum phenomena, novel optoelectronic devices and the potential to modify chemical properties of materials. Organic materials are of current interest as active materials for their ability to sustain exciton-polaritons even at room temperature. However, within organic optoelectronic devices, it is often the 'dark' spin-1 triplet excitons that dominate operation. These triplets have been largely ignored in treatments of polaritons, which instead only consider the role of states that directly and strongly interact with light. Here we demonstrate that these 'dark' states can also play a major role in polariton dynamics, observing polariton population transferred directly from the triplet manifold via triplet-triplet annihilation. The process leads to polariton emission that is longer-lived (>µs) even than exciton emission in bare films. This enhancement is directly linked to spin-2 triplet-pair states, which are formed in films and microcavities by singlet fission or triplet-triplet annihilation. Such high-spin multiexciton states are generally non-emissive and cannot directly couple to light, yet the formation of polaritons creates for them entirely new radiative decay pathways. This is possible due to weak mixing between singlet and triplet-pair manifolds, which - in the strong coupling regime - enables direct interaction between the bright polariton states and those that are formally non-emissive. Our observations offer the enticing possibility of using polaritons to harvest or manipulate population from states that are formally dark.

Exploiting Excited-State Aromaticity To Design Highly Stable Singlet Fission Materials.

Singlet fission, the process of forming two triplet excitons from one singlet exciton, is a characteristic reserved for only a handful of organic molecules due to the atypical energetic requirement for low energy excited triplet states. The predominant strategy for achieving such a trait is by increasing ground state diradical character; however, this greatly reduces ambient stability. Herein, we exploit Baird's rule of excited state aromaticity to manipulate the singlet-triplet energy gap and create novel singlet fission candidates. We achieve this through the inclusion of a [4n] 5-membered heterocycle, whose electronic resonance promotes aromaticity in the triplet state, stabilizing its energy relative to the singlet excited state. Using this theory, we design a family of derivatives of indolonaphthyridine thiophene (INDT) with highly tunable excited state energies. Not only do we access novel singlet fission materials, they also exhibit excellent ambient stability, imparted due to the delocalized nature of the triplet excited state. Spin-coated films retained up to 85% activity after several weeks of exposure to oxygen and light, while analogous films of TIPS-pentacene showed full degradation after 4 days, showcasing the excellent stability of this class of singlet fission scaffold. Extension of our theoretical analysis to almost ten thousand candidates reveals an unprecedented degree of tunability and several thousand potential fission-capable candidates, while clearly demonstrating the relationship between triplet aromaticity and singlet-triplet energy gap, confirming this novel strategy for manipulating the exchange energy in organic materials.

Discerning Bulk and Interfacial Polarons in a Dual Electron Donor/Acceptor Polymer.

The active layer of organic solar cells typically possesses a complex morphology, with amorphous donor/acceptor mixed domains present in addition to purer, more crystalline domains. These crystalline domains may represent an energy sink for free charges that aids charge separation and suppresses bimolecular recombination. The first step in exploiting this behavior is the identification and characterization of charges located in these different domains. Herein, the generation and recombination of both bulk and interfacial polarons are demonstrated in the dual electron donor/acceptor polymer XIND using transient absorption spectroscopy. The absorption spectra of XIND bulk polarons, present in pristine polymer domains, are clearly distinguishable from those of polarons present at the donor/acceptor interface. Furthermore, it is shown that photogenerated polarons are transferred from the interface to the bulk. These findings support the energy sink hypothesis and offer a way to maximize morphology relationships to enhance charge generation and suppress recombination.

Persistent Multiexcitons from Polymers with Pendent Pentacenes.

Singlet fission has emerged as a key mechanism of exciton multiplication in organic chromophores, generating two triplet excitons from a single photon. Singlet fission is typically studied in crystalline films or in isolated dimers. Here, we investigate an intermediate regime where through-space interactions mediate singlet fission and triplet pair recombination within isolated polymer chains. Specifically, we investigate how appending pentacenes to a polynorbornene backbone can lead to macromolecules that take advantage of through-space π-π interactions for fast singlet fission and rapid triplet pair dissociation. Singlet fission in these systems is affected by molecular dynamics, and triplet-triplet recombination is a geminate process where the rate of recombination scales with molecular-weight. We find that these pendent pentacene polymers yield free triplets with lifetimes that surpass those of crystalline chromophores in both solution as isolated polymers and in thin films.

Singlet fission in a hexacene dimer: energetics dictate dynamics.

Singlet fission (SF) is an exciton multiplication process with the potential to raise the efficiency limit of single junction solar cells from 33% to up to 45%. Most chromophores generally undergo SF as solid-state crystals. However, when such molecules are covalently coupled, the dimers can be used as model systems to study fundamental photophysical dynamics where a singlet exciton splits into two triplet excitons within individual molecules. Here we report the synthesis and photophysical characterization of singlet fission of a hexacene dimer. Comparing the hexacene dimer to analogous tetracene and pentacene dimers reveals that excess exoergicity slows down singlet fission, similar to what is observed in molecular crystals. Conversely, the lower triplet energy of hexacene results in an increase in the rate of triplet pair recombination, following the energy gap law for radiationless transitions. These results point to design rules for singlet fission chromophores: the energy gap between singlet and triplet pair should be minimal, and the gap between triplet pair and ground state should be large.

The butterfly effect in bisfluorenylidene-based dihydroacenes: aggregation induced emission and spin switching.

Linear acenes are a well-studied class of polycyclic aromatic hydrocarbons and their established physical properties have led to their widespread application across the field of organic electronics. However, their quinoidal forms - dihydroacenes - are much less explored and exhibit vastly different photophysical and electronic properties due to their non-planar, cross-conjugated nature. In this work, we present a series of difluorenylidene dihydroacenes which exhibit a butterfly-like structure with a quinoidal skeleton, resulting in comparatively higher optical gaps and lower redox activities than those of their planar analogs. We found that these compounds exhibit aggregation induced emission (AIE), activated through restriction of the "flapping" vibrational mode of the molecules in the solid state. Furthermore, anthracene-containing dihydroacenes exhibit thermally activated ground-state spin switching as evidenced by planarization of the acene core and diradical activity recorded by EPR. These two characteristics in this relatively unexplored class of materials provide new insights for the design of multifunctional materials.

Recent Progress in High-Mobility Organic Transistors: A Reality Check.

Over the past three decades, significant research efforts have focused on improving the charge carrier mobility of organic thin-film transistors (OTFTs). In recent years, a commonly observed nonlinearity in OTFT current-voltage characteristics, known as the "kink" or "double slope," has led to widespread mobility overestimations, contaminating the relevant literature. Here, published data from the past 30 years is reviewed to uncover the extent of the field-effect mobility hype and identify the progress that has actually been achieved in the field of OTFTs. Present carrier-mobility-related challenges are identified, finding that reliable hole and electron mobility values of 20 and 10 cm2 V-1 s-1 , respectively, have yet to be achieved. Based on the analysis, the literature is then reviewed to summarize the concepts behind the success of high-performance p-type polymers, along with the latest understanding of the design criteria that will enable further mobility enhancement in n-type polymers and small molecules, and the reasons why high carrier mobility values have been consistently produced from small molecule/polymer blend semiconductors. Overall, this review brings together important information that aids reliable OTFT data analysis, while providing guidelines for the development of next-generation organic semiconductors.

Synthesis and Exciton Dynamics of Donor-Orthogonal Acceptor Conjugated Polymers: Reducing the Singlet-Triplet Energy Gap.

The presence of energetically low-lying triplet states is a hallmark of organic semiconductors. Even though they present a wealth of interesting photophysical properties, these optically dark states significantly limit optoelectronic device performance. Recent advances in emissive charge-transfer molecules have pioneered routes to reduce the energy gap between triplets and "bright" singlets, allowing thermal population exchange between them and eliminating a significant loss channel in devices. In conjugated polymers, this gap has proved resistant to modification. Here, we introduce a general approach to reduce the singlet-triplet energy gap in fully conjugated polymers, using a donor-orthogonal acceptor motif to spatially separate electron and hole wave functions. This new generation of conjugated polymers allows for a greatly reduced exchange energy, enhancing triplet formation and enabling thermally activated delayed fluorescence. We find that the mechanisms of both processes are driven by excited-state mixing between π-π*and charge-transfer states, affording new insight into reverse intersystem crossing.

Tunable Semiconducting Polymer Nanoparticles with INDT-Based Conjugated Polymers for Photoacoustic Molecular Imaging.

Photoacoustic imaging combines both excellent spatial resolution with high contrast and specificity, without the need for patients to be exposed to ionizing radiation. This makes it ideal for the study of physiological changes occurring during tumorigenesis and cardiovascular disease. In order to fully exploit the potential of this technique, new exogenous contrast agents with strong absorbance in the near-infrared range, good stability and biocompatibility, are required. In this paper, we report the formulation and characterization of a novel series of endogenous contrast agents for photoacoustic imaging in vivo. These contrast agents are based on a recently reported series of indigoid π-conjugated organic semiconductors, coformulated with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, to give semiconducting polymer nanoparticles of about 150 nm diameter. These nanoparticles exhibited excellent absorption in the near-infrared region, with good photoacoustic signal generation efficiencies, high photostability, and extinction coefficients of up to three times higher than those previously reported. The absorption maximum is conveniently located in the spectral region of low absorption of chromophores within human tissue. Using the most promising semiconducting polymer nanoparticle, we have demonstrated wavelength-dependent differential contrast between vasculature and the nanoparticles, which can be used to unambiguously discriminate the presence of the contrast agent in vivo.