Thiol-Anchored TIPS-Tetracene Ligands with Quantitative Triplet Energy Transfer to PbS Quantum Dots and Improved Thermal Stability.

Triplet energy transfer between inorganic quantum dots (QDs) and organic materials plays a fundamental role in many optoelectronic applications based on these nanocomposites. Attaching organic molecules to the QD as transmitter ligands has been shown to facilitate transfer both to and from QDs. Here we show that the often disregarded thiol anchoring group can achieve quantitative triplet energy transfer yields in a PbS QD system with 6,11-bis[(triisopropylsilyl)ethynyl]tetracene-2-methylthiol (TET-SH) ligands. We demonstrate efficient triplet transfer in a singlet fission-based photon multiplication system with 5,12-bis[(triisopropylsilyl)ethynyl]tetracene generating triplets in solution that transfer to the PbS QDs via the thiol ligand TET-SH. Importantly, we demonstrate the increased thermal stability of the PbS/TET-SH system, compared to the traditional carboxylic acid counterpart, allowing for higher photoluminescence quantum yields

Singlet Fission and Triplet Transfer to PbS Quantum Dots in TIPS-Tetracene Carboxylic Acid Ligands.

Singlet exciton fission allows for the generation of two triplet excitons for each photon absorbed within an organic semiconductor. Efficient harvesting of these triplets could allow for the Shockley-Queisser limit on the power conversion efficiency of single-junction photovoltaics to be broken. Here, we show that singlet fission molecules bound directly to PbS quantum dots as ligands can undergo singlet fission with near unity efficiency and can transfer triplets sequentially into the PbS with near unity efficiency. Within the PbS, the excitations recombine, giving rise of the emission of photons. This allows for the doubling of the quantum dot photoluminescence quantum efficiency when photons are absorbed by the singlet fission ligand, as compared to when directly absorbed in the quantum dot. Our approach demonstrates that it is possible to convert the exciton multiplication process of singlet fission into a photon multiplication process and provides a new path to harness singlet fission with photovoltaics

Engineering Molecular Ligand Shells on Quantum Dots for Quantitative Harvesting of Triplet Excitons Generated by Singlet Fission.

Singlet fission is an exciton multiplication process in organic molecules in which a photogenerated spin-singlet exciton is rapidly and efficiently converted to two spin-triplet excitons. This process offers a mechanism to break the Shockley-Queisser limit by overcoming the thermalization losses inherent to all single-junction photovoltaics. One of the most promising methods to harness the singlet fission process is via the efficient extraction of the dark triplet excitons into quantum dots (QDs) where they can recombine radiatively, thereby converting high-energy photons to pairs of low-energy photons, which can then be captured in traditional inorganic PVs such as Si. Such a singlet fission photon multiplication (SF-PM) process could increase the efficiency of the best Si cells from 26.7% to 32.5%, breaking the Shockley-Queisser limit. However, there has been no demonstration of such a singlet fission photon multiplication (SF-PM) process in a bulk system to date. Here, we demonstrate a solution-based bulk SF-PM system based on the singlet fission material TIPS-Tc combined with PbS QDs. Using a range of steady-state and time-resolved measurements combined with analytical modeling we study the dynamics and mechanism of the triplet harvesting process. We show that the system absorbs >95% of incident photons within the singlet fission material to form singlet excitons, which then undergo efficient singlet fission in the solution phase (135 ± 5%) before quantitative harvesting of the triplet excitons (95 ± 5%) via a low concentration of QD acceptors, followed by the emission of IR photons. We find that in order to achieve efficient triplet harvesting it is critical to engineer the surface of the QD with a triplet transfer ligand and that bimolecular decay of triplets is potentially a major loss pathway which can be controlled via tuning the concentration of QD acceptors. We demonstrate that the photon multiplication efficiency is maintained up to solar fluence. Our results establish the solution-based SF-PM system as a simple and highly tunable platform to understand the dynamics of a triplet energy transfer process between organic semiconductors and QDs, one that can provide clear design rules for new materials.ER

Singlet exciton fission in a modified acene with improved stability and high photoluminescence yield

Abstract: We report a fully efficient singlet exciton fission material with high ambient chemical stability. 10,21-Bis(triisopropylsilylethynyl)tetrabenzo[a,c,l,n]pentacene (TTBP) combines an acene core with triphenylene wings that protect the formal pentacene from chemical degradation. The electronic energy levels position singlet exciton fission to be endothermic, similar to tetracene despite the triphenylenes. TTBP exhibits rapid early time singlet fission with quantitative yield of triplet pairs within 100 ps followed by thermally activated separation to free triplet excitons over 65 ns. TTBP exhibits high photoluminescence quantum efficiency, close to 100% when dilute and 20% for solid films, arising from triplet-triplet annihilation. In using such a system for exciton multiplication in a solar cell, maximum thermodynamic performance requires radiative decay of the triplet population, observed here as emission from the singlet formed by recombination of triplet pairs. Combining chemical stabilisation with efficient endothermic fission provides a promising avenue towards singlet fission materials for use in photovoltaics

Ligand-Directed Self-Assembly of Organic-Semiconductor/Quantum-Dot Blend Films Enables Efficient Triplet Exciton-Photon Conversion

Blends comprising organic semiconductors and inorganic quantum dots (QDs) are relevant for many optoelectronic applications and devices. However, the individual components in organic-QD blends have a strong tendency to aggregate and phase-separate during film processing, compromising both their structural and electronic properties. Here, we demonstrate a QD surface engineering approach using electronically active, highly soluble semiconductor ligands that are matched to the organic semiconductor host material to achieve well-dispersed inorganic–organic blend films, as characterized by X-ray and neutron scattering, and electron microscopies. This approach preserves the electronic properties of the organic and QD phases and also creates an optimized interface between them. We exemplify this in two emerging applications, singlet-fission-based photon multiplication (SF-PM) and triplet–triplet annihilation-based photon upconversion (TTA-UC). Steady-state and time-resolved optical spectroscopy shows that triplet excitons can be transferred with near unity efficiently across the organic–inorganic interface, while the organic films maintain efficient SF (190% yield) in the organic phase. By changing the relative energy between organic and inorganic components, yellow upconverted emission is observed upon 790 nm NIR excitation. Overall, we provide a highly versatile approach to overcome longstanding challenges in the blending of organic semiconductors with QDs that have relevance for many optical and optoelectronic applications

Organic-quantum dot hybrid interfaces and their role in photon fission/fusion applications

Solar energy is rapidly becoming a more important aspect in today's energy systems, and solar cells are playing a major role in this shift. However, to further boost the efficiency of conventional solar cells, fundamental thermodynamic limits must be overcome. Photon fission and photon fusion, also known as photon downconversion and photon upconversion, are gaining increasing attention as a means to improve solar energy harvesting in solar cells by overcoming thermalization and transmission losses, respectively. Important developments in these fields include the use of organic–inorganic hybrid materials that can leverage the advantages of each material. In this review, we look at the development of organic–quantum dot (QD) hybrid materials and their use as components of photon fission and fusion systems. We put a particular focus on the triplet energy transfer across these organic–inorganic hybrid interfaces and how this understanding has been developed. In the later part of the review, we focus on the recent examples of these hybrid materials as crucial components in solar energy harvesting applications based on triplet–triplet annihilation photon upconversion or singlet-fission–based photon multiplication. By highlighting the most relevant discoveries toward understanding and designing organic-QD hybrid interfaces for photon fission and fusion applications, we establish a starting point for researchers to continue moving this research field forward toward practical applications.</jats:p

Photon upconversion utilizing energy beyond the band gap of crystalline silicon with a hybrid TES-ADT/PbS quantum dots system

The recent introduction of inorganic semiconductor quantum dots (QDs) as triplet sensitizers for molecular semiconductors has led to significant interest in harvesting low energy photons, which can then be used for photon upconversion (PUC), via triplet-triplet annihilation (TTA). A key goal is the harvesting of photons from below the bandgap of crystalline silicon 1.12 eV (approximate to 1100 nm) and their upconversion into the visible region. In practice, the systems demonstrated so far have been limited to harvesting photons with energies above 1.2 eV (approximate to 1 mu m), due to two reasons: firstly the need to use transmitter ligands which allow efficient energy harvesting from the QD but introduce an energy loss of larger than 200 meV in transmission from the QD to the annihilator, and secondly due to the use of molecules such as tetracene which cannot accept smaller energy than 1.2 eV. Here, we introduce a new strategy to overcome these difficulties by using a low energy triplet annihilator that also harvests excitations efficiently from QDs. Specifically, we show that 5,11-bis(triethylsilylethynyl) anthradithiophene (TES-ADT, triplet energy of 1.08 eV: ca. 1150 nm) functions as a triplet annihilator (20% TTA efficiency) while also rapidly extracting triplet excitons from lead sulfide (PbS) QDs with a rate constant of k = ca. 2 x 10(-8) s(-1) with an excitation at 1064 nm. This rate is consistent with an orbital overlap between TES-ADT and PbS QDs, which we propose is due to the thiophene group of TES-ADT, which enables a close association with the PbS surface, allowing this system to function both as annihilator and transmitter. Our results pave the way for the design of triplet annihilators that can closely associate with the QD surface and harvest low energy excitons with minute losses in energy during the TET process, with the ultimate goal of efficiently utilizing photon energy beyond the bandgap of crystalline silicon

Photon Upconversion from Near-Infrared to Blue Light with TIPS-Anthracene as an Efficient Triplet–Triplet Annihilator

Photon upconversion (PUC) via triplet–triplet annihilation (TTA) from near-infrared (NIR) to blue photons could have important applications especially to bioimaging and drug delivery accompanied by photochemical reaction. The fundamental challenges in achieving this has been the large anti-Stokes shift combined with the need to efficiently sensitize within the biological transparency window (700–900 nm). This calls for materials combinations with minimal energy losses during sensitization and minimal energy requirements to drive efficient TTA. Here, we demonstrate efficient PUC converting from NIR energy to blue photons using the commercially available material 9,10-bis[((triisopropyl)silyl)ethynyl]anthracene (TIPS-Ac) as the annihilator. With a conventional triplet sensitizing system, TIPS-Ac performed TTA with an efficiency of 77 ± 3% despite a relatively small driving force, compared to conventional TTA material converting from NIR to blue, for the TTA of less than 0.32 eV. Combined with Pt(II) meso-tetraphenyltetrabenzoporphine (PtTPBP), which is a heavy atom triplet sensitizer that directly generates triplets upon NIR photon excitation, the resulting system allowed for an anti-Stokes shift of 1.03 eV. Our results highlight the use of direct triplet generation via NIR excitation as a useful path to achieving large anti-Stokes shift and also show that high TTA efficiencies can be achieved even in the absence of large driving energies for the TTA process.The authors thank the Winton Programme for the Physics of Sustainability and the Engineering and Physical Sciences Research Council for funding. V.G. acknowledges funding from the Swedish Research Council, Vetenskapsrådet 2018-00238. A.P. acknowledges the financial support from the Marie Curie Fellowship (MILORD project, No. 748042). D.B. is an FNRS Research Director

Excimer Formation in Carboxylic Acid-Functionalized Perylene Diimides Attached to Silicon Dioxide Nanoparticles.

The creation of artificial light-harvesting complexes involves the ordered arrangement of chromophores in space. To guarantee efficient energy-transfer processes, organic dyes must be brought into close proximity, often leading to aggregation and the formation of excimer states. In recent years, the attachment of ligand-based chromophores to nanoparticles has also generated interest in relation to improved solar harvesting and spin-dependent electronic interactions such as singlet fission and upconversion. We explore the covalent attachment of two novel perylene-diimide (PDI) carboxylic acid ligands to silicon dioxide nanoparticles. This allows us to study electronic interactions between the ligands when attached to nanoparticles because these cannot couple to the wide band gap silicon dioxide. One of the synthesized PDI ligands has sterically hindering phenols in the bay position and undergoes minimal optical changes upon attachment, but the other forms an excimer state with a red-shifted and long-lived florescence. As such, molecular structure changes offer a method to tune weak and strong interactions between ligand layers on nanocrystal surfaces.European Research Council (670405) Engineering and Physical Sciences Research Council Winton Program for the Physics of Sustainabilit

Direct vs Delayed Triplet Energy Transfer from Organic Semiconductors to Quantum Dots and Implications for Luminescent Harvesting of Triplet Excitons.

Hybrid inorganic-organic materials such as quantum dots (QDs) coupled with organic semiconductors have a wide range of optoelectronic applications, taking advantage of the respective materials' strengths. A key area of investigation in such systems is the transfer of triplet exciton states to and from QDs, which has potential applications in the luminescent harvesting of triplet excitons generated by singlet fission, in photocatalysis and photochemical upconversion. While the transfer of energy from QDs to the triplet state of organic semiconductors has been intensely studied in recent years, the mechanism and materials parameters controlling the reverse process, triplet transfer to QDs, have not been well investigated. Here, through a combination of steady-state and time-resolved optical spectroscopy we study the mechanism and energetic dependence of triplet energy transfer from an organic ligand (TIPS-tetracene carboxylic acid) to PbS QDs. Over an energetic range spanning from exothermic (-0.3 eV) to endothermic (+0.1 eV) triplet energy transfer we find that the triplet energy transfer to the QD occurs through a single step process with a clear energy dependence that is consistent with an electron exchange mechanism as described by Marcus-Hush theory. In contrast, the reverse process, energy transfer from the QD to the triplet state of the ligand, does not show any energy dependence in the studied energy range; interestingly, a delayed formation of the triplet state occurs relative to the quantum dots' decay. Based on the energetic dependence of triplet energy transfer we also suggest design criteria for future materials systems where triplet excitons from organic semiconductors are harvested via QDs, for instance in light emitting structures or the harvesting of triplet excitons generated via singlet fission.We thank the Winton Programme for the Physics of Sustainability and the Engineering and Physical Sciences Research Council for funding. This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement No 758826). VG acknowledges funding from the Swedish research council, Vetenskapsrådet 2018-00238. J. R. A. acknowledges Cambridge Commonwealth European and International Trust for financial support. Z. Z. acknowledges funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie Actions grant (No. 842271 – TRITON project). J. X. acknowledges EPSRC Cambridge NanoDTC, EP/L015978/1 for financial support. JEA and AJP acknowledge the U.S. National Science Foundation (DMREF-1627428) for support of organic semiconductor synthesis