Thermally Activated Delayed Photoluminescence: Deterministic Control of Excited-State Decay.

Thermally activated photophysical processes are ubiquitous in numerous organic and metal-organic molecules, leading to chromophores with excited-state properties that can be considered an equilibrium mixture of the available low-lying states. Relative populations of the equilibrated states are governed by temperature. Such molecules have been devised as high quantum yield emitters in modern organic light-emitting diode technology and for deterministic excited-state lifetime control to enhance chemical reactivity in solar energy conversion and photocatalytic schemes. The recent discovery of thermally activated photophysics at CdSe nanocrystal-molecule interfaces enables a new paradigm wherein molecule-quantum dot constructs are used to systematically generate material with predetermined photophysical response and excited-state properties. Semiconductor nanomaterials feature size-tunable energy level engineering, which considerably expands the purview of thermally activated photophysics beyond what is possible using only molecules. This Perspective is intended to provide a nonexhaustive overview of the advances that led to the integration of semiconductor quantum dots in thermally activated delayed photoluminescence (TADPL) schemes and to identify important challenges moving into the future. The initial establishment of excited-state lifetime extension utilizing triplet-triplet excited-state equilibria is detailed. Next, advances involving the rational design of molecules composed of both metal-containing and organic-based chromophores that produce the desired TADPL are described. Finally, the recent introduction of semiconductor nanomaterials into hybrid TADPL constructs is discussed, paving the way toward the realization of fine-tuned deterministic control of excited-state decay. It is envisioned that libraries of synthetically facile composites will be broadly deployed as photosensitizers and light emitters for numerous synthetic and optoelectronic applications in the near future.

Energy Migration Processes in Re(I) MLCT Complexes Featuring a Chromophoric Ancillary Ligand.

We present the synthesis, structural characterization, electronic structure calculations, and ultrafast and supra-nanosecond photophysical properties of a series of five Re(I) bichromophores exhibiting metal to ligand charge transfer (MLCT) excited states based on the general formula fac-[Re(N∧N)(CO)3(PNI-py)]PF6, where PNI-py is 4-piperidinyl-1,8-naphthalimidepyridine and N∧N is a diimine ligand (Re1-5), along with their corresponding model chromophores where 4-ethylpyridine was substituted for PNI-py (Mod1-5). The diimine ligands used include 1,10-phenanthroline (phen, 1), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (bcp, 2), 4,4'-di-tert-butyl-2,2'-bipyridine (dtbb, 3), 4,4'-diethyl ester-2,2'-bipyridine (deeb, 4), and 2,2'-biquinoline (biq, 5). In these metal-organic bichromophores, structural modification of the diimine ligand resulted in substantial changes to the observed energy transfer efficiencies between the two chromophores as a result of the variation in 3MLCT excited-state energies. The photophysical properties and energetic pathways of the model chromophores were investigated in parallel to accurately track the changes that arose from introduction of the organic chromophore pendant on the ancillary ligand. All relevant photophysical and energy transfer processes were probed and characterized using time-resolved photoluminescence spectroscopy, ultrafast and nanosecond transient absorption spectroscopy, and time-dependent density functional theory calculations. Of the five bichromophores in this study, four (Re1-4) exhibited a thermal equilibrium between the 3PNI-py and the 3MLCT excited state, drastically extending the lifetimes of the parent model chromophores.

Energy Transfer Dynamics in Triplet-Triplet Annihilation Upconversion Using a Bichromophoric Heavy-Atom-Free Sensitizer.

A heavy-atom-free triplet sensitizer suitable for triplet-triplet annihilation-based photon upconversion was developed from the thermally activated delayed fluorescence (TADF) molecule 4CzPN by covalently tethering a pyrene derivative (DBP) as a triplet acceptor. The triplet exciton produced by 4CzPN is captured by the intramolecular pyrenyl acceptor and subsequently transferred via intermolecular triplet-triplet energy transfer (TTET) to freely diffusing pyrenyl acceptors in toluene. Transient absorption and time-resolved photoluminescence spectroscopy were employed to examine the dynamics of both the intra- and intermolecular TTET processes, and the results indicate that the intramolecular energy transfer from 4CzPN to DBP is swift, quantitative, and nearly irreversible. The reverse intersystem crossing is suppressed while intersystem crossing remains efficient, achieving high triplet yield and long triplet lifetime simultaneously. The ultralong excited state lifetime characteristic of the DBP triplet was shown to be crucial for enhancing the intermolecular TTET efficiency and the subsequent triplet-triplet annihilation photochemistry. It was also demonstrated that with the long triplet lifetime of the tethered DBP, TTET was enabled under low free acceptor concentrations and/or with sluggish molecular diffusion in polymer matrixes.

Electrochemical Synthesis of Binary and Ternary Niobium-Containing Oxide Electrodes Using the p-Benzoquinone/Hydroquinone Redox Couple.

New electrochemical synthesis methods have been developed to obtain layered potassium niobates, KNb3O8 and K4Nb6O17, and perovskite-type KNbO3 as film-type electrodes. The electrodes were synthesized from aqueous solutions using the redox chemistry of p-benzoquinone and hydroquinone to change the local pH at the working electrode to trigger deposition of desired phases. In particular, the utilization of electrochemically generated acid via the oxidation of hydroquinone for inorganic film deposition was first demonstrated in this study. The layered potassium niobates could be converted to (H3O)Nb3O8 and (H3O)4Nb6O17 by cationic exchange, which, in turn, could be converted to Nb2O5 by heat treatment. The versatility of the new deposition method was further demonstrated for the formation of CuNb2O6 and AgNbO3, which were prepared by the deposition of KNb3O8 and transition metal oxides, followed by thermal and chemical treatments. Considering the lack of solution-based synthesis methods for Nb-based oxide films, the methods reported in this study will contribute greatly to studies involving the synthesis and applications of Nb-based oxide electrodes.

Controlling Thermally Activated Delayed Photoluminescence in CdSe Quantum Dots through Triplet Acceptor Surface Coverage.

Quantum-dot/molecule composites (QD/mol) have demonstrated useful photochemical properties for many photonic and optoelectronic applications; however, a comprehensive understanding of these materials remains elusive. This work introduces a series of cadmium(II) selenide/1-pyrenecarboxylic acid (CdSe/PCA) nanomaterials featuring bespoke PCA surface coverage on CdSe585 (coded by the peak of the first exciton absorption band) to glean insight into the QD/mol photophysical behavior. Tailoring the energy gap between the CdSe585 first exciton band (2.1 eV) and the lowest PCA triplet level (T1 = 2.0 eV) to be nearly isoenergetic, strong thermally activated delayed photoluminescence (TADPL) is observed resulting from reverse triplet-triplet energy transfer. The resultant average decay time constant (τobs) of the photoluminescence emanating from CdSe585 is deterministically controlled with surface-bound PCAn chromophores (n = average number of adsorbed PCA molecules) by shifting the triplet excited state equilibrium from the CdSe585 to the PCA molecular triplet reservoir as a function of n.

TIPS-pentacene triplet exciton generation on PbS quantum dots results from indirect sensitization.

Many fundamental questions remain in the elucidation of energy migration mechanisms across the interface between semiconductor nanomaterials and molecular chromophores. The present transient absorption study focuses on PbS quantum dots (QDs) of variable size and band-edge exciton energy (ranging from 1.15 to 1.54 eV) post-synthetically modified with a carboxylic acid-functionalized TIPS-pentacene derivative (TPn) serving as the molecular triplet acceptor. In all instances, selective excitation of the PbS NCs at 743 nm leads to QD size-dependent formation of an intermediate with time constants ranging from 2-13 ps, uncorrelated to the PbS QD valence band potential. However, the rate constant for the delayed formation of the TPn triplet excited state markedly increases with increasing PbS conduction band energy, featuring a parabolic Marcus free energy dependence in the normal region. These observations provide evidence of an indirect triplet sensitization process being inconsistent with a concerted Dexter-like energy transfer process. The collective data are consistent with the generation of an intermediate resulting from hole trapping of the initial PbS excited state by midgap states, followed by formation of the TPn triplet excited state whose rate constant and yield increases with decreasing quantum dot size.