Knowing the underlying photophysics of thermally activated delayed fluorescence (TADF) allows proper design of high efficiency organic light-emitting diodes. We have proposed a model to describe reverse intersystem crossing (rISC) in donor–acceptor charge transfer molecules, where spin–orbit coupling between singlet and triplet states is mediated by one of the local triplet states of the donor (or acceptor). This second order, vibronically coupled mechanism describes the basic photophysics of TADF. Through a series of measurements, whereby the energy ordering of the charge transfer (CT) excited states and the local triplet are tuned in and out of resonance, we show that TADF reaches a maximum at the resonance point, substantiating our model of rISC. Moreover, using photoinduced absorption, we show how the populations of both singlet and triplet CT states and the local triplet state change in and out of resonance. Our vibronic coupling rISC model is used to predict this behaviour and describes how rISC and TADF are affected by external perturbation.
Thermally activated delayed fluorescence (TADF)1,2,3 is a phenomenon of great potential and interest in the organic light-emitting diode (OLED) research community due to the potential for high external quantum efficiencies without the use of heavy metals. In the past, high external quantum efficiencies have been achieved through the use of phosphorescent iridium complexes, where rapid intersystem crossing achieves 100% internal quantum efficiency from triplet states4,5,6,7. However, phosphors often suffer from degradation, especially blue phosphors due to intrinsic issues related to the population of higher-lying 3dd* metal orbitals8,9,10. Triplet–triplet annihilation is another way of retrieving singlets, at the cost of two triplets for each singlet11,12,13, but these materials are also subject to instability issues14. TADF, with its ability to produce an emissive singlet from a triplet state, is the only known mechanism that can achieve a fully fluorescent internal quantum efficiency of 100% (ref. 15).
A typical chemical structure used in effective TADF materials is often that of donor–acceptor (D–A)16, or donor–acceptor–donor (D–A–D)17 (Fig. 1a), a structure that promotes the formation of intramolecular charge-transfer (CT) states between the donor and acceptor units. Initially, it was proposed that cyclic intersystem crossing within the CT singlet and triplet manifolds gave rise to TADF1,2, but with the two uncoupled electrons, on the donor and acceptor, being so far apart and in orthogonal orbitals, the spin–orbit interaction between them must be very small, making this scenario unrealistic18. However, our recent experimental19 and quantum dynamics studies20 suggest that the intersystem crossing (ISC) and reverse intersystem crossing (rISC) between 1CT singlet and 3CT triplet states is a more complicated second order process. This second order process is mediated by vibronic coupling of the 3CT to the local exciton triplet (3LE) states to allow spin–orbit coupling to the 1CT state18,20,21. These results are also in line with the previous findings of Lim et al.22 and Dance et al.23
This model predicts that the energy gaps between both 3LE–3CT and 3LE–1CT states are critical activation barriers and so the relative energy ordering between the CT states and 3LE, along with the magnitude of each barrier controls ISC, rISC and hence TADF efficiency. Here we give spectroscopic evidence from measurements with further theoretical modelling that clearly shows how rISC is affected by the relative energy ordering of the CT and 3LE states, substantiating our model and how the predicted changes due to the relative energy ordering affects rISC and TADF. A scheme outlining the ways in which the CT states may move in and out of resonance with a local exciton triplet state is given, controlled by external factors such as host/solvent polarity, and give rise to three distinct types of TADF (Fig. 1b). This work demonstrates the roles played by the 1CT, 3CT and 3LE states in controlling rISC and that all experimental observations are explained by our spin–vibronic coupling mechanism of rISC and thus TADF.
Previous theoretical work on CT states shows that spin–orbit coupling between 1CT singlet and 3CT triplet states is forbidden22. This is because, within the one electron approximation, the spin–orbit operator operates upon both the spin magnetic quantum number of the electron and its spatial angular momentum quantum number. Consequently, coupling between singlet and triplet states with the same spatial orbital occupation are formally zero as any change in spin cannot be compensated by a corresponding change in angular momentum, and so total angular momentum is not conserved. For organic TADF emitters, this was confirmed by recent quantum chemical calculations18. Therefore:
However, ISC between energetically close 1CT and a local triplet state, 3LE, can efficiently mediate ISC by a spin–orbit charge transfer mechanism with an overlap represented by,
where πD and πA are the highest filled electronic orbitals of the donor and acceptor respectively.
When the energy gap between 1CT and 3CT becomes very small (effectively <<1 meV), hyperfine coupling between them may become active as well24, but the resulting rISC rate is five orders of magnitude too small to account for the experimental rISC rate. Recently Gibson et al.20 showed that the mechanism for efficient rISC, involves non-adiabatic coupling between the lowest triplet states, 3LE–3CT. This coupling, which is much larger than spin–orbit coupling leads to the rapid formation of an equilibrium between the two triplet states via reverse internal conversion. The 3CT is then coupled to the 1CT state via coupling elements derived from second order perturbation theory, mediated by the 3LE state:
This latter second-order term, which includes the non-adiabatic and spin–orbit coupling terms, is very efficient because of the good vibrational overlap between the almost degenerate initial and final states, 3CT and 1CT, respectively (Supplementary Methods). Either the donor or acceptor local triplet can take this mediator role25.
The ISC rate has also been found to be very sensitive to the position of the local exciton triplet state in polymer:fullerene systems that contain CT states26. Here we develop a technique to measure the effect of changing the relative energy separations and orderings between the CT and 3LE manifolds to explicitly test our model and clearly show that the second order vibronic coupling mechanism is the driving force for efficient rISC, and hence TADF, in D–A systems.
Excited states photoinduced absorption
Figure 2 shows the photoinduced absorption (PIA) for DPTZ-DPTPO2 and the pure phenothiazine donor unit as a reference (PTZ)27,28,29 at room temperature and 20 K in a host matrix of zeonex. In PIA measurements, all excited state populations are sampled, both emissive and non-emissive states. Signals in-phase with the modulation signal relate to fast decaying signals commensurate to the timescale of the prompt CT emission, typically 10 μs (ref. 30), and the out-of-phase signal is generally related to long lived species. It is apparent, through comparison with the reference PTZ spectra that both the in and out-of-phase PIA of the DPTZ-DPTO2 is dominated by the triplet absorption (T1→TN) of the local phenothiazine triplet at 20 K. This induced triplet absorption of PTZ has been reported at 460 nm in the literature27,28,29 and is confirmed independently in these measurements. The PIA of the dibenzothiophene acceptor has not been reproduced here but in the literature31 it is at higher energies than phenothiazine and thus not relevant for these measurements. At room temperature the in-phase PIA spectrum of DPTZ-DPTO2 (Fig. 2a) shows marked differences from the PTZ spectrum with the appearance of a broad induced absorption between 500 and 800 nm. This absorption is attributed to the 1CT states as it is in-phase and thus has a similar lifetime to the 1CT emission. A broad band similar to this has been observed in photoexcited PTZ solution and assigned to solvated electrons, created from absorption of the stabilized phenothiazine radical anion in solution analogous to the 1CT states here27,28. This broad CT absorption is less prominent at lower temperatures due to the thermally activated nature of the rISC, which reduces the 1CT population with decreasing temperature. Thus the 3LE and 1CT states can be differentiated in the D–A–D system. In the out-of-phase measurement (long-lived species, Fig. 2b) at room temperature, the DPTZ-DPTO2 spectrum is dominated by the broad visible to NIR PIA (450–800 nm) of the long-lived 3CT species, identified as having much longer lifetime than the 1CT emission. Again, these states are not observed in the pure donor unit.
The host, zeonex, has a similar polarity to non-polar solvents such as methyl cyclohexane (ɛ=2.02) and also has a very high glass transition temperature (375 K) meaning that there is no ‘solvent’ reorientation and the CT energy and the molecular structure of the guest are fixed. At this polarity the CT states will lie above the local triplet, found at 2.58 eV, found from previously measured phosphorescence of DPTZ-DPTO2 (refs 16, 19). This places this arrangement as an example of Type I TADF in Fig. 1b.
Effects of polarity on emission and photoinduced absorption
To investigate the effect of energy ordering of the excited states, by observing the polarity dependence emission and PIA spectra, 20 μM solutions of DPTZ-DPTO2 in toluene (ɛ=2.38) and 2-methyl tetrahydrofuran (MeTHF) (ɛ=6.97) were studied and compared with films made in the host polyethylene oxide (PEO) which is more polar than zeonex. More significantly, PEO enables us to study polarity dependences in the solid state as it has a temperature dependent dielectric coefficient. At room temperature the dielectric constant of PEO is quoted as ɛ=5. However, this polarity is measured at microwave frequencies32 but at optical frequencies we observe that PEO has a similar polarity to toluene at room temperature (ɛ=2.38) given by the energy position of the DPTZ-DPTO2 emission (Fig. 3a). Furthermore, the glass transition temperature (Tg) of PEO is 220 K, much lower than that of zeonex32,33,34, which causes the dielectric to decrease as the temperature decreases.
Figure 3a shows the effect of polarity on the steady state emission spectra of DPTZ-DPTO2 in toluene and MeTHF (whereas the emission spectra of PTZ remains invariant, see Supplementary Fig. 1) alongside that of DPTZ-DPTO2 films made in zeonex and PEO at different temperatures. The emission peak of DPTZ-DPTO2 in toluene and MeTHF is redshifted compared with that in zeonex by 0.2 and 0.4 eV respectively and the intensity of emission reduces as the emission red shifts, in line with the polarity of the solvents. At room temperature PEO acts very much like the toluene solution and by 150 K it is close to zeonex.
This polarity effect on the photophysics of DPTZ-DPTO2 is further emphasized in the PIA investigated in the aforementioned solvents (Fig. 3b) at concentrations of 10 mM. The in-phase spectra show that the 1CT emission dominates and that in toluene it is stronger than in MeTHF, a result mirrored in the steady state PL (Fig. 3a). However, the out-of-phase spectra for both solvent systems are dominated by a broad, long-lived CT state induced absorption. This is attributed to the fact that the energy of the CT states are stabilized in the more polar environments such that they now lie below the 3LE which is unaffected by host polarity30. This provides an extra decay pathway, internal conversion, from 3LE to 3CT, since interconversion from 3CT to 1CT is forbidden, making 3CT an effective triplet reservoir. This PIA is identified as the 3CT state due to it being dominant only in the out-of-phase measurement, concomitant with it having a much longer lifetime than the emissive 1CT state (in-phase signal). This is an example of Type III TADF, Fig. 1b and confirms that the PIA spectra can identify the energetic ordering of excited states in the TADF system.
Figure 4a shows how the properties of the DPTZ-DPTO2 in PEO change as a function of temperature, especially around Tg. The 1CT energy (measurement of these energies are detailed in Supplementary Figs 2–6 and detailed in Supplementary Methods) of the molecule blue shifts as the Tg is approached from above and then stabilizes when the PEO becomes rigid below Tg. With this increase in 1CT energy the intensity of the emission also increases before reducing again at low temperatures. Energetically this relates to the 1CT energy level shifting from below the 3LE state (Type III), passing through resonance at 220 K (Type II) and then increasing further and stabilizing above the 3LE state (Type I), as depicted in Fig. 1b. The shift in the 1CT energy onset is from 2.50 to 2.60 eV bringing the states into resonance and then out of resonance with the 3LE state (again unaffected by temperature). This is shown in the shape of the intensity curve (Fig. 4a). The decrease in intensity at lower temperatures will also be the result of the thermally activated nature of TADF, a phenomenon already well documented in literature1,3,35,36. The exchange energy between 1CT and 3CT in DPTZ-DPTO2 is very small given its near perfect orthogonal D–A–D structure, even in very low polarity medium19. Thus throughout the thermal range used here 1CT and 3CT states will remain nearly isoenergetic. From these measurements it is clear that 1CT emission is maximized when the gap between the CT states and the local triplet state (of the donor in this case) is minimized and that rISC and TADF depend critically on these energy gaps.
Figure 4b shows the relative rate of reverse intersystem crossing as a function of temperature obtained from model quantum dynamics20 using the energetics reported in Fig. 4a. Each point represents a different quantum dynamics simulation with slightly different energy splitting between the 1,3CT–3LE states as shown in Fig. 4a. The full details of these simulations are provided in the Supplementary Methods and Supplementary Tables 1 and 2. The results show strong qualitative agreement with the temperature dependence in Fig. 4a, which as expected points to a strong correlation between the rate of rISC and 1CT emission intensity. A peak in the rISC rate at 225 K is observed because at this temperature in PEO all three states are isoenergetic. The rate rapidly decays either side of this resonance, but this decay is quicker to higher temperatures, because although higher temperatures should promote TADF, the separation between the 1,3CT–3LE states exhibits greater increases at temperatures above 225 K, than below. One deviation of note between Fig. 4a,b is that the rISC is almost completely quenched at lower temperature, while the emission intensity is not (Fig. 4a). This deviation arises from the contribution of prompt 1CT fluorescence and from reductions in non-radiative decay arising from increased rigidity of the matrix, neither of which are included in the model quantum dynamics simulations.
Quasi-steady state photoinduced absorption
The temperature dependence of the PIA of DPTZ-DPTO2 in PEO was measured and is shown in Fig. 5. The in-phase component (Fig. 5a) again shows the increase in intensity of the CT emission, which peaks around Tg. More interestingly, when 1CT emission is a maximum at around 220 K, we also observe strong simultaneous 3LED and 1CT induced absorption, clearly indicating that at this point the populations of both these states are maximized. Below Tg the emission falls off and the PIA becomes dominated by the local triplet (3LED) induced absorption, similar to that observed in zeonex (Fig. 2). This again is consistent with the fact that at lower temperatures the 1CT has shifted above the 3LED state opening up the energy gap between the two, and TADF becomes less efficient as the thermal energy decreases and the long-lived triplet states dominate.
In the out-of-phase signal (Fig. 5b) near Tg, especially 200 K, both triplet absorption and 3CT absorption are seen. Again, this is due to the PEO host bringing the CT states into resonance with 3LE, that is, Type II arrangement achieved. At 220 K, 3CT and 3LED absorption and weak (out-of-phase) emission are observed, a result of TADF being extremely efficient with the large transient 3CT and 3LED states population being in thermal equilibrium and producing emissive 1CT states. This clearly demonstrates the very small magnitude of the energy barriers between the 3LE and CT states that must be reached to achieve efficient TADF and how sensitive rISC is to these gaps. As the temperature is increased and Tg exceeded the polarity of the PEO increases, the 1CT state moves below the local triplet, opening up these gaps and TADF is reduced, shown by the reduction in in-phase emission. These temperature dependent effects are not observed in zeonex as the Tg is so high that the zeonex is a rigid matrix at all analysed temperatures and so its polarity always remains constant.
Figure 6a shows the transient photoluminescence of DPTZ-DBTO2 in PEO across a range of temperatures. Similar to the resonance observed in Fig. 4, the largest amount of rISC occurs around 200 K, when the CT manifold is in resonance with the 3LE. This is indicated by the higher intensity region beyond 102 ns, delayed 1CT emission. Below 200 K, the rISC rate is observed to decrease again, with the fall off of the delayed emission component, emphasizing the resonant behaviour of this phenomenon, with the intensity beyond 102 ns at 80 K being similar to the 275 K values. This peak in the DF, rISC and as a result TADF is emphasized in the estimation of the DF/PF ratio, which is shown in Fig. 6b, where the integrated intensity of the delayed fluorescence is divided by the prompt fluorescence. The peak in the values of these DF/PF ratios also occurs around 200 K and is thus in good agreement with the transient spectra (Fig. 6a) and the experimental intensity resonance and theoretical rISC resonance (Fig. 4). In these efficient TADF molecules the non-radiative decay rates are slow and the PF does not change greatly with temperature as a result of this (see first 100 ns of the temperature dependent decay data, Fig. 6a). This means that DF/PF is to good approximation linearly dependent on the rISC rate in these systems. The values for these ratios are shown in Supplementary Table 3. The temperature dependence of the DF for DPTZ-DBTO2 in zeonex has recently been included in the Supplementary Information of work by Dias et al.19 Here it is seen that the DF monotonically decreases with decreasing temperature and that no resonant behaviour is observed. This is as a result of the non-polar nature of zeonex and its high glass transition temperature.
This work shows that the energy separation between the local triplet state 3LE and the CT states of a D–A–D molecule critically controls the efficiency of rISC and hence the TADF process. This supports the second order coupling responsible for rISC20, which invokes the role of an intermediate triplet state. We identify this intermediate state, which can be either the 3CT or 3LE state, depending on the polarity of the host. In both cases, the important factor is the non-adiabatic coupling between them. The presence of an identical PIA peak at 470 nm found in both the PTZ and the D–A–D species analysed here confirms that the lowest energy local triplet resides on the donor. The lower energy, broad induced features are confirmed as induced CT absorption. Furthermore, the rigidity and polarity of the host has a major effect on rISC and hence TADF, also indicates that intramolecular motion of the D–A–D molecule is critical in the TADF process, especially radiative emission37. Three distinct regimes for TADF are identified dependent on the relative energetic positions of the CT and 3LE states. From these results it is clear that both careful molecular design and host environment are critical in controlling the efficiency of TADF and both must be correct to achieve the desired Type II TADF regime. Most importantly, full experimental verification of our model of second order coupling for efficient rISC20 is given, showing the role of all three excited state, 1CT, 3CT and 3LE in rISC and thus TADF. This model is also fully consistent for all CT states, even when 3LE is well below the CT manifolds such that enhanced triplet formation is always observed. This model, in which the coupling between the singlet and triplet states is mediated by non-adiabatic coupling between the 3CT or 3LE states, illustrates the importance of dynamic material design, which explicitly considers the important molecular vibrations that promote this coupling. This understanding may also find application across chemistry, biology and physics to rationalize and manipulate the photophysics of charge transfer/separated states.
Spectroscopic characterization of the excited state populations of the standard TADF emitter, DPTZ-DPTO2 (ref. 19; Fig. 1a), is performed in different hosts and solvents at a range of temperatures, to resolve which excited states control rISC and investigate how the external environment effects TADF. DPTZ-DPTO2 (2,8-di(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene 5,5-dioxide) is a D–A–D material consisting of phenothiazine donor units (D) and dibenzothiophene-S,S-dioxide acceptor units (A)19. Solid state samples were produced by drop casting onto a quartz substrate. The solutions for this process were a 127 mg ml−1 solution of the host in toluene mixed in a 1:1 ratio with DPTZ-DPTO2 (concentration 2.7 mg ml−1 in toluene). Steady state photoluminescence was measured using a Jobin Yvon Fluoromax-3.
Quasi-CW PIA measurements
Measurement of the excited state absorption (and emission) spectra38, where performed using a 375 nm pump beam (Vortran Stradus 375–60) modulated at 73 Hz, with a continuous laser driven white light source (Energetiq EQ-99X) as the probe. The probe beam was then passed through a Bentham TM300 monochromator and incident on a Si detector connected to the Signal Recovery dual channel 7,225 digital lock-in amplifier that also provides the reference frequency modulation for the pump laser. The temperature dependent emission intensities and hence 1CT energies were measured using an Ocean Optics USB4000 spectrograph simultaneously. The intensity of the laser was 305 mW cm−2 for all measurements except for DPTZ-DPTO2 in zeonex where 25 mW cm−2 was used.
Time-resolved emission decay
Photoluminescence decays were recorded using nanosecond gated luminescence and lifetime measurements (from 400 ps to 1 s) using a high energy pulsed Nd:YAG laser emitting at 355 nm (EKSPLA). Emission was focused onto a spectrograph and detected on a sensitive gated iCCD camera (Stanford Computer Optics) having sub-nanosecond resolution3. The laser fluence used was 160 μJ cm−2.
Quantum dynamics simulations probing the mechanism for efficient rISC were performed using the density operator formalism of the multi-configurational time dependent Hartree (MCTDH) method39. Here we adopt a closed quantum system, using the Hamiltonian described in Gibson et al.20. The energy gap between the 1CT–3CT states was as calculated in Gibson et al.20, however the gap between the 3LE–3CT states was as extracted experimentally below. The full details of the simulations and the model Hamiltonians used is provided in the supporting information.
Data supporting this publication is openly available under an ‘Open Data Commons Open Database License’. Additional meta- data are available at: 10.17634/153015–1 (theoretical) and 10.15128/r2jq085j96k (experimental). Please contact Newcastle Research Data Service at email@example.com for access instructions.
How to cite this article: Etherington, M. K. et al. Revealing the spin–vibronic coupling mechanism of thermally activated delayed fluorescence. Nat. Commun. 7, 13680 doi: 10.1038/ncomms13680 (2016).
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A.P.M. acknowledges the EU’s Horizon 2020 for funding the PHEBE project under grant No. 641725 and also the EPSRC for funding under grant number EP/L02621X/1. T.J.P. acknowledges the EPSRC, Project EP/N028511/1 for funding.
The authors declare no competing financial interests.
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Etherington, M., Gibson, J., Higginbotham, H. et al. Revealing the spin–vibronic coupling mechanism of thermally activated delayed fluorescence. Nat Commun 7, 13680 (2016). https://doi.org/10.1038/ncomms13680
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