Upconversion System Research Articles

Photochemical Upconversion in Solution: The Role of Oxygen and Magnetic Field Response

Upconversion processes effectively convert two or more low energy photons into one higher energy photon, and they have diverse prospective applications in photovoltaics and biomedicine. We focus on two specific mechanisms for photochemical upconversion in solution: triplet-triplet annihilation (TTA) and singlet oxygen mediated energy transfer (SOMET). TTA is spin-selective, whereas SOMET is not, so the interplay between these two upconversion mechanisms can be examined via their different magnetic field responses. A kinetic model is developed and applied to explain the different photoluminescence profiles of oxygenated versus deoxygenated systems. From the magnetic field response, the triplet-triplet annihilation rate constant is estimated. The conditions required to maximize upconversion photoluminescence intensity in oxygenated solution are determined, providing a set of design principles to guide molecule choices for robust and air-stable upconversion systems in the future.

Highly Efficient Triplet–Triplet Annihilation Upconversion with a Thermally Activated Delayed Fluorescence Molecule as Triplet Photosensitizer

Thermally activated delayed fluorescence (TADF) molecules have great potential for practical applications as triplet photosensitizers, owing to their long triplet lifetimes, almost negligible energy loss in intersystem crossing, and excellent light-harvesting ability. Recently, several triplet–triplet annihilation (TTA) upconversion systems using the TADF photosensitizer have been reported. To provide comprehensive dynamic information for designing an optimized system in the future, more experiments with the new TADF photosensitizers are necessary. Herein, we conducted a new TTA upconversion system with a recently developed TADF molecule, DMACPDO, as the triplet photosensitizer and 9,10-diphenylanthracene (DPA) as the annihilator. The overall upconversion yield was determined to be relatively high, e.g., 22.3% in toluene, 21.9% in benzene, and 8.1% in chlorobenzene. By examining elementary photophysical and photochemical processes with time-resolved transient absorption and fluorescence emission spectroscopy, we revealed the influence of solvent polarity and viscosity on each step. Our conclusion highlights the elusive solvent effect in TTA upconversion application of the TADF photosensitizer.

Photochemical Upconversion.

Photochemical upconversion is a process whereby two lower-energy photons are converted into a higher-energy photon by sensitized triplet-triplet annihilation. While recent interest in this process has been motivated by improving the efficiencies of solar cells, many applications are being explored. In this review, we address the underlying physicochemical phenomena that are responsible for photochemical upconversion. We review their kinetics, and the requirements for annihilators and sensitizers to design efficient upconversion systems. We discuss the spin physics of the bi-excitonic interactions and how the spin character of the triplet pairs can fundamentally limit the upconversion efficiency and give rise to the magnetic field effect on delayed photoluminescence. Finally, we address light-matter coupling phenomena that could be employed to enhance photochemical upconversion.

Boosting Photo Upconversion in Electropolymerised Thin Film with Yb/Er Complexes

AbstractUpconversion luminescence (UCL) in organometallic complexes has attracted great interest in photovoltaics and biological applications due to their fascinating energy transfer mechanism from low‐energy photon to high‐energy photon. However, photon‐upconversion operating in a single discrete entity remains a challenge caused by low‐absorption cross section of the luminescent lanthanide element. Here, a novel upconversion system is reported combining Yb (Ytterbium) sensitizers and Er (Erbium) activators in the film by electropolymerization, which leads to excited‐state absorption (ESA) and energy transfer upconversion (ETU) processes. For the first time, the UCL has been achieved in the thin films upon near‐infrared laser irradiation, and the upconversion intensity exhibits up to 30‐fold enhancement with the variation of Yb/Er ratio.

A new green-to-blue upconversion system with efficient photoredox catalytic properties.

The design and development of new triplet-triplet annihilation upconversion (TTA-UC) systems combining triplet sensitizers with acceptor compounds have attracted considerable interest. In this vein, sensitizers made from purely organic dyes rather than transition-metal complexes appear to be more convenient from an environmental point of view. BODIPYs are a very well-known class of dyes with applications in a widespread range of scientific areas. Owing to the versatility of BODIPYs, we present herein a new asymmetric BODIPY with excellent photophysical properties to be used as an appropriate sensitizer in a bimolecular TTA-UC system. Detailed spectroscopic measurements demonstrated the ability of this new design to sensitize TTA-UC by combination with a suitable acceptor such as 2,5,8,11-tetra-tert-butylperylene (TBPe), allowing a successful conversion of green to blue light. The singlet-excited TBPe so obtained is capable of activating aryl chlorides reductively which initiated the functionalization of N-methylpyrrole (Meerwein-type arylation) and formation of both substituted triarylethylenes (Mizoroki-Heck reaction) and heteroarene phosphonates (photo-Arbuzov reaction). Product yields reveal that our TTA-UC system behaved as a highly efficient photocatalytic entity.

Structural change dynamics of heteroleptic Cu(I) complexes observed by ultrafast emission spectroscopy.

[Cu(I)(dmp)(P)2]+ (dmp = 2,9-dimethyl-1,10-phenanthroline derivatives; P = phosphine ligand) is one of the most promising photosensitizers used in a photo-catalytic system for reducing CO2, for which the quantum yield is as high as 57%. In this work, time-resolved emission spectra of Cu(I) complexes in solutions were investigated using femtosecond fluorescence up-conversion and nanosecond time-resolved emission spectroscopic systems. The temporal profiles of emission intensities less than 10 ps in acetonitrile solution were reproduced using a tri-exponential function with three-time constants of 0.040 ps, 0.78 ps and 8.0 ps. We found that only the second time constant is dependent on the solvent (acetonitrile: 0.78 ps, butyronitrile: 1.4 ps), indicating that the 0.78 ps spectral change is attributed to the structural change of the Cu(I) complex. The oscillator strengths of transition species are derived from the intensities in the time-resolved emission spectra (species-associated spectra). Based on the oscillator strengths, we concluded that the 0.040 ps process is the Sn → S1 internal conversion and the 0.78 ps process is a structural change in the S1 state. The final time constant of 8.0 ps is assigned to the S1 → T1 intersystem crossing because the 3MLCT state (τT1 = 97 ns) is generated after the decay. The DFT calculation showed that the 0.78 ps spectral change (∼600 cm-1 redshift) is attributed to Jahn-Teller distortion around the metal center, and there is a large structural change in the ligand, which results in a large Stokes shift in the Sn state (7.3 × 103 cm-1).

Gd–Er interaction promotes NaGdF4:Yb, Er as a new candidate for high-power density applications

Efficient Gd–Er bidirectional energy transfer in NaGdF4:Yb, Er nanoparticles makes this upconversion system relevant for high-power density applications.

Truxene-linked coumarin-corrole triad: Synthesis, photophysical properties and application in Triplet−Triplet annihilation upconversion

It is crucial to develop organic triplet photosensitizers (PSs) with excellent performance for upconversion applications. Herein, we synthesized a novel truxene-linked coumarin-corrole triads (C-Trux-Corr) and investigated the photophysical properties by steady-state UV–Vis absorption and fluorescence spectroscopies as well as nanosecond time-resolved transient absorption spectroscopy. The triad displays an efficient intramolecular singlet energy transfer from coumarin moiety to the corrole moiety. Nanosecond time-resolved transient difference absorption spectra indicate that the triplet excited states of C-Trux-Corr are distributed on the corrole moiety. The triplet lifetimes of C-Trux-Corr and Trux-C are 195.2 μs and 45.9 μs, respectively. The triplet state lifetime of C-Trux-Corr is significantly prolonged and it was applied as an organic triplet photosensitizer in the triplet-triplet upconversion system with an upconversion quantum yield of 2.93%, which is higher than that the corrole itself (1.27%) by more than 2-fold.

Photon Upconversion with a Low Threshold Excitation Intensity in Plain Water.

A triplet-triplet annihilation-based photon upconversion (TTA-UC) system with a low threshold excitation intensity (Ith) in plain water was developed. Water-soluble anionic porphyrin (PdTPPS4-) and diphenylanthracene (DCDPA2-) derivatives were used as light absorbers and emitter molecules, respectively, and no additives such as surfactants were required. The phosphorescence emission from PdTPPS4- under an excitation wavelength of 528 nm was quenched by DCDPA2-, resulting in triplet energy transfer, whereas fluorescence from DCDPA2- was observed in a short wavelength region (400-500 nm). Three independent emission studies utilizing different excitation light sources validated the TTA-UC process in a simple aqueous solution. TTA occurred after the triplet energy transfer, according to the time profiles of phosphorescence and fluorescence detected following pulse laser excitation. The Ith for TTA-UC was estimated to be lower than 6 mW cm-2, although it could not be exactly determined due to the sensitivity limit of the experimental setup. The upper limit of Ith for the aqueous solution of DCDPA2- and PdTPPS4- is the smallest value obtained to date for aqueous systems and comparable to that of high-performance TTA-UC systems in organic solutions.

(Keynote) Rational Design of Quantum Dot/Mediator Interfaces for Triplet Energy Transfer and Photon Upconversion

Photon upconversion, where two or more low energy photons are converted into one high energy photon, shows great potential in bioimaging, catalysis and solar energy conversion. Photon upconversion has traditionally been realized with lanthanide-doped nanoparticles, or organic dye sensitized triplet-triplet annihilation (TTA) based upconversion platforms. In recent years, QD sensitized triplet-triplet annihilation based upconversion systems have achieved impressive upconversion quantum efficiency and demonstrated many unique advantages, including high photostability, large extinction coefficient, high spectral coverage and tunability, and low singlet-triplet energy gap. In this talk, we discuss our recent work in developing and understanding QD/mediator interface for efficient QD-sensitized photon upconversion. We summarize the main results of time-resolved spectroscopic studies of various factors affecting the rate of triplet energy transfer (TET) from the QD to the surface attached mediator (TET1) and from the mediator to the emitter in solution (TET2). To identify the key design rules, we compare three PbS sensitized upconversion systems using three mediator molecules with the same tetracene triplet acceptor at different distances from the QD. Our results show that the mediator triplet state is mostly formed by direct TET from quantum dot. With increasing distance between the mediator and PbS QD, the efficiency of the TET1 from the QD to the mediator decreases due to a decrease in the rate of this triplet energy transfer step, while the efficiency of the TET2 from the mediator to emitter increases due to a reduction in the QD induced mediator triplet state decay (via the external heavy atom effect). The rate constant of TET2 is three orders of magnitude slower than the diffusion limited value. We show that the effect of QD/mediator on the total unconversion efficiency measured under CW illumination conditions can be well accounted for by the independently determined efficiencies of TET1 and TET2 steps, providing important insight on the design and rational improvement of efficient photon upconversion systems. Ongoing detailed mechanistic studies of the TET1 process shows that both QD bright and dark exciton states contribute to the TET process and higher lying bridge states play significant role in enhancing TET from core/shell QDs.

Excited-State Transient Chemistry of Rubrene: A Whole Story.

The ability to manipulate low-energy triplet excited states into higher-energy emissive singlet states, a process known as photon upconversion (UC), has potential applications in bioimaging, photocatalysis, and in increasing the efficiency of solar cells. However, the overall UC mechanism is complex and can involve many intermediate states, especially when semiconductors such as lead halide perovskites are used to sensitize the required triplet states. Using a combination of pulse radiolytic and electrochemical techniques, we have now explored the transient features of rubrene─a commonly employed triplet annihilator in UC systems. The rubrene triplet, radical anion, and radical cation species yield unique spectra that can serve as spectral fingerprints to distinguish between transient species formed during UC processes. Using detailed kinetic studies, we have succeeded in establishing that the rubrene triplets are susceptible to self-quenching (kquench = 3.6 × 108 M-1 s-1), and as the triplets decay, an additional transient feature is observed in the transient absorption spectra. This new feature indicates a net electron transfer process occurs to form the radical cation and anion as the triplets recombine. Taken together, this work provides a comprehensive picture of the excited state and transient features of rubrene and will be crucial for understanding the mechanism(s) of photon upconversion systems.

Achieving Photon Upconversion in Mononuclear Lanthanide Molecular Complexes at Room Temperature.

Photon upconversion luminescence at the molecule scale is a rarely observed phenomenon despite possessing colossal potential for basic research and reality applications. Here we show that the eight-coordinate erbium molecular complex composed of Er3+ ion, dibenzoylmethane, and 2,2'-bipyridine exhibits upconversion emission. Under direct excitation at the absorption band of Er3+ ion at 980 nm, the complex shows upconverted green emissions of Er3+ ion at 525 and 545 nm at room temperature. Noticeably, upon the introduction of fluoride ions into this complex, an additional upconverted red emission at 667 nm appears as well, and the luminescence intensities of both the green and red emissions increase by a factor of 13 at most. This study not only provides a strategy to adjust the green and red emissions in mononuclear erbium complexes but also broadens the horizons of designing lanthanide-based molecular upconversion systems.

A Sensitizer of Purpose: Generating Triplet Excitons with Semiconductor Nanocrystals.

The process of photon upconversion promises importance for many optoelectronic applications, as it can result in higher efficiencies and more effective photon management. Upconversion via triplet-triplet annihilation (TTA) occurs at low incident powers and at high efficiencies, requirements for integration into existing optoelectronic devices. Semiconductor nanocrystals are a diverse class of triplet sensitizers with advantages over traditional molecular sensitizers such as energetic tunability and minimal energy loss during the triplet sensitization process. In this Perspective, we review current progress in semiconductor nanocrystal triplet sensitization, specifically focusing on the nanocrystal, the ligand shell which surrounds the nanocrystal, and progress in solid-state sensitization. Finally, we discuss potential areas of improvement which could result in more efficient upconversion systems sensitized by semiconductor nanocrystals. Specifically, we focus on the development of solid-state TTA upconversion systems, elucidation of the energy transfer mechanisms from nanocrystal to transmitter ligand which underpin the upconversion process and propose novel configurations of nanocrystal-sensitized systems.

Interfacial charge transfer states enable efficient solid-state upconversion

While high-efficiency upconversion is widely demonstrated in solution, solid-state upconversion has lagged significantly behind. Recently, Hiramoto et al. reported a novel solid-state upconversion system based on organic semiconductor heterojunctions, leading to more than 10-fold improvement in efficiency.

Recent Advances in the Photoreactions Triggered by Porphyrin-Based Triplet-Triplet Annihilation Upconversion Systems: Molecular Innovations and Nanoarchitectonics.

Triplet–triplet annihilation upconversion (TTA-UC) is a very promising technology that could be used to convert low-energy photons to high-energy ones and has been proven to be of great value in various areas. Porphyrins have the characteristics of high molar absorbance, can form a complex with different metal ions and a high proportion of triplet states as well as tunable structures, and thus they are important sensitizers for TTA-UC. Porphyrin-based TTA-UC plays a pivotal role in the TTA-UC systems and has been widely used in many fields such as solar cells, sensing and circularly polarized luminescence. In recent years, applications of porphyrin-based TTA-UC systems for photoinduced reactions have emerged, but have been paid little attention. As a consequence, this review paid close attention to the recent advances in the photoreactions triggered by porphyrin-based TTA-UC systems. First of all, the photochemistry of porphyrin-based TTA-UC for chemical transformations, such as photoisomerization, photocatalytic synthesis, photopolymerization, photodegradation and photochemical/photoelectrochemical water splitting, was discussed in detail, which revealed the different mechanisms of TTA-UC and methods with which to carry out reasonable molecular innovations and nanoarchitectonics to solve the existing problems in practical application. Subsequently, photoreactions driven by porphyrin-based TTA-UC for biomedical applications were demonstrated. Finally, the future developments of porphyrin-based TTA-UC systems for photoreactions were briefly discussed.

Micellar Ratiometric Fluorescent Blood pH Probe Based on Triplet-Sensitized Upconversion and Energy-Transfer Behaviors.

The measurement of pH is greatly significant in monitoring physiological and biochemical states. In this work, a novel micellar ratiometric fluorescent probe featuring sophisticated energy-transfer (ET) behaviors with p-nitrophenol (PNP) as the energy acceptor and a triplet-triplet annihilation upconversion (TTA-UC) system as the energy donor was designed. The pH-induced molecular configuration of PNP determined the process for the transfer of energy from TTA-UC to PNP. The introduction of the TTA-UC system enabled probe excitation under a long wavelength and afforded a ratiometric signal for pH detection with excellent reliability over diverse interfering factors. This TTA-UC/ET pH probe demonstrated a high sensitivity to hydronium below nanomolar concentrations and an excellent anti-interference ability in serum samples, which provided a novel significant strategy for rapid and accurate detection of blood pH in vitro.

Achieving low-power single-wavelength-pair nanoscopy with NIR-II continuous-wave laser for multi-chromatic probes

Stimulated emission depletion (STED) microscopy is a powerful diffraction-unlimited technique for fluorescence imaging. Despite its rapid evolution, STED fundamentally suffers from high-intensity light illumination, sophisticated probe-defined laser schemes, and limited photon budget of the probes. Here, we demonstrate a versatile strategy, stimulated-emission induced excitation depletion (STExD), to deplete the emission of multi-chromatic probes using a single pair of low-power, near-infrared (NIR), continuous-wave (CW) lasers with fixed wavelengths. With the effect of cascade amplified depletion in lanthanide upconversion systems, we achieve emission inhibition for a wide range of emitters (e.g., Nd3+, Yb3+, Er3+, Ho3+, Pr3+, Eu3+, Tm3+, Gd3+, and Tb3+) by manipulating their common sensitizer, i.e., Nd3+ ions, using a 1064-nm laser. With NaYF4:Nd nanoparticles, we demonstrate an ultrahigh depletion efficiency of 99.3 ± 0.3% for the 450 nm emission with a low saturation intensity of 23.8 ± 0.4 kW cm−2. We further demonstrate nanoscopic imaging with a series of multi-chromatic nanoprobes with a lateral resolution down to 34 nm, two-color STExD imaging, and subcellular imaging of the immunolabelled actin filaments. The strategy expounded here promotes single wavelength-pair nanoscopy for multi-chromatic probes and for multi-color imaging under low-intensity-level NIR-II CW laser depletion.

Heavy atom-free triplet photosensitizer based on thermally activated delayed fluorescence material for NIR-to-blue triplet-triplet annihilation upconversion

Triplet-triplet annihilation (TTA) upconversion-based materials have potential application in the broad range of research areas, including photocatalysis and life sciences. However, near-infrared (NIR)-to-blue upconverted emission is preferred for most of the practical applications, but developing a NIR-to-blue TTA upconversion system is a challenging task in photochemistry. In this work, a thermally activated delayed fluorescence (TADF) material with intense visible-to-NIR absorption is demonstrated that shows a longer triplet state lifetime (32 µs) and high triplet state energy (ET = 1.55 eV). For the first time, a heavy atom-free NIR (λex > 650 nm) to blue (λem< 460 nm) TTA upconversion system was devised, employing the dimeric borondifluoride curcuminoid TADF material as triplet photosensitizer (PS) and a large anti-Stokes shift (0.88 eV) along with moderate upconversion yield was achieved. Our work provides the solution and guidance for the future development of purely organic heavy atom-free NIR activating TTA upconversion system for a wide array of applications.

Photon Upconversion Systems Based on Triplet-Triplet Annihilation as Photosensitizers for Chemical Transformations.

Photon upconversion (UC) based on triplet-triplet annihilation (TTA) is considered one of the most attractive methodologies for switching wavelengths from lower to higher energy. This two-photon process, which requires the involvement of a bimolecular system, has been widely used in numerous fields such as bioimaging, solar cells, displays, drug delivery, and so on. In the last years, we have witnessed the harnessing of this concept by the organic community who have developed new strategies for synthetic purposes. Interestingly, the generation of high-energetic species by this phenomenon has provided the opportunity not only to photoredox activate compounds with high-energy demanding bonds, expanding the reactivity window that lies outside the energy window of the initial irradiation wavelength, but also to sensitized conventional photocatalysts through energy transfer processes even employing infrared irradiation. Herein, an overview of the principal examples found in literature is described where TTA-UC systems are found to be suitable photosensitizers for several chemical transformations.

White up-conversion luminescence and highly-sensitive optical temperature sensing in Na3La(VO4)2:Yb,Er,Tm,Ho phosphors

In this work, tunable white up-conversion luminescence was achieved in the Yb3+, Er3+, Tm3+, Ho3+ co-doped Na3La(VO4)2 phosphors under 980 nm excitation. The emissions of three primary colors are mainly attributed to the 2H11/2/4S3/2 → 4I15/2 transitions of Er3+, 1G4→3H6 transition of Tm3+, and 5F5→5I8 transition of Ho3+. White luminescence characteristics and mechanisms of up-conversion system were investigated in detail. In addition, the temperature sensing behaviors of multiple levels emission combinations for Na3La(VO4)2:Yb3+,Er3+,Tm3+,Ho3+ were analyzed by employing thermally coupled and non-thermally coupled energy levels. Based on the emissions of 3F2,3/1G4 energy levels, the maximum relative and absolute sensitivities were obtained to be 2.20%/K and 0.279 K–1. The design of up-conversion luminescence materials with high-quality white luminescence and excellent sensitivity performance is critical in the field of optical applications.