Recent Advances in Understanding Triplet States in Metal Nanoclusters: Their Formation, Energy Transfer, and Applications in Photon Upconversion.

Recent experimental findings, rapidly accumulating over the past few years, has revealed that in the electronic excited states of metal nanoclusters (MNCs) composed of noble metal atoms (e.g., Cu, Ag, or Au), triplet states are generated with remarkably high efficiency, exerting a pivotal influence over the photophysical properties of the MNCs, notably their photoluminescence characteristics.

Tailoring sensitization properties and improving near-infrared photon upconversion performance through alloying in superatomic molecular Au nanoclusters.

Noble-metal nanoclusters (NCs) protected by organic ligands have recently come to the forefront as potent triplet sensitizers for photon upconversion (UC) triplet-triplet annihilation (TTA), owing to their capacity for atomic-level photophysical property customization. Among these, the rod-shaped bi-icosahedral [Au(PPh)(S-CHPh)Cl] (Au-rod) NC is a particularly iconic superatomic molecular NC, recently identified as a near-infrared (NIR)-absorbing sensitizer for TTA-UC. In this study, we synthesized Cu-doped NCs, [AuCu(PPh)(S-CHPh)Cl] (AuCu-rod), and paired them with 9,10-bis(phenylethynyl)anthracene (BPEA) annihilator/emitter to explore the impact of Cu-doping on the triplet sensitization and NIR-UC performance.

Triplet-Mediator Ligand-Protected Metal Nanocluster Sensitizers for Photon Upconversion.

Triplet-triplet annihilation photon upconversion (TTA-UC) is attracting a great deal of attention as a viable approach to exploit unutilized wavelengths of light in solar-driven devices. Recently, ligand-protected metal nanoclusters have emerged as a compelling platform for serving as triplet sensitizers for TTA-UC. In this study, we developed an atomically precise, triplet-mediator ligand (TL)-protected metal nanocluster, AuCu(S-Adm)[P(DPA)] (; S-Adm = 1-adamanthanethiolate, DPA = 9,10-diphenylanthracene).

Triplet properties and intersystem crossing mechanism of PtAg28 nanocluster sensitizers achieving low threshold and efficient photon upconversion.

Ligand-protected metal nanoclusters have emerged as a promising platform for providing sensitizers for triplet-triplet annihilation upconversion (TTA-UC). Herein, we report [PtAg28(BDT)] (PtAg28; BDT = 1,3-benzenedithiolate) as a sensitizer enabling TTA-UC at low excitation intensities. PtAg28 exhibits a long-lived triplet state (approximately 7 μs) generated with a 100% intersystem crossing (ISC) quantum yield.

Dissecting the Triplet-State Properties and Intersystem Crossing Mechanism of the Ligand-Protected Au Superatom.

Icosahedral Au nanoclusters are among the most typical superatoms and are of great interest as promising building blocks for nanocluster-assembled materials. Herein, the key parameters involved in the intersystem crossing (ISC) process of [Au(dppe)Cl] (; dppe = 1,2-bis(diphenylphosphino)ethane) were characterized. Quenching experiments using aromatic compounds revealed that the T energy of is 1.

Nested Keplerian architecture of [CuH(SPr)(PPh)] nanoclusters.

This article explores the challenges in synthesizing highly symmetric Cu(I)-thiolate nanoclusters and reports a nested Keplerian architecture of [CuH(SPr)(PPh)] (Pr = CHCHCH). The structure is made up of five concentric polyhedra of Cu(I) atoms, which create enough space to accommodate five ligand shells all within a range of 2 nm. This fascinating structural architecture is also linked to the unique photoluminescence properties of the nanoclusters.

Structurally Flexible Au-Cu Alloy Nanoclusters Enabling Efficient Triplet Sensitization and Photon Upconversion.

Ligand-protected noble-metal nanoclusters exhibit an innately triplet nature and have been recently recognized as emerging platforms for triplet sensitizers of photon upconversion (UC) via triplet-triplet annihilation. Herein, we report that a structurally flexible Au-Cu alloy nanocluster, [AuCu(S-Adm)(DPPM)] (; S-Adm = 1-adamantanethiolate, DPPM = bis(diphenylphosphino)methane), exhibited favorable sensitizer properties and superior UC performance. Contrary to the structurally rigid AuCu(S-Adm)(TPP) (, TPP = triphenylphosphine), exhibited significantly better sensitizer characteristics, such as a near-unity quantum yield for intersystem crossing (ISC), long triplet lifetime (ca.

Charge-Transfer-Mediated Mechanism Dominates Oxygen Quenching of Ligand-Protected Noble-Metal Cluster Photoluminescence.

Photoluminescence (PL) quenching of ligand-protected noble-metal clusters (NMCs) by molecular oxygen is often used to define whether the PL of NMC is fluorescent or phosphorescent, and only energy transfer has been always considered as the quenching mechanism. Herein, we performed the Rehm-Weller analysis of the O-induced PL quenching of 13 different NMCs and found that the charge-transfer (CT)-mediated mechanism dominates the quenching process. The quenching rate constant showed a clear dependence on the CT driving force, varied markedly from 10 to 10 Ms.

Evidence for triplet-state-dominated luminescence in biicosahedral superatomic molecular Au clusters.

In photoluminescence (PL) quenching and triplet fusion upconversion experiments with fluorescent organic-molecule quenchers, it was revealed that a rod-shaped, phosphine- and thiolate-protected biicosahedral Au cluster (a representative di-superatomic molecule) exhibits only phosphorescence, not fluorescence, at room temperature with an intersystem crossing quantum yield of almost 100%. By virtue of these photophysical properties, this cluster can be used as a triplet sensitizer that undergoes direct singlet-triplet transitions in the near-infrared (NIR) region (730-900 nm), inducing photon upconversion from NIR to visible light.

Excited-State Symmetry Breaking in a Multiple Multipolar Chromophore Probed by Single-Molecule Fluorescence Imaging and Spectroscopy.

Excited-state symmetry breaking (ESB) has attracted much attention because it is often observed in symmetric multipolar chromophores designed as two-photon absorption/emission materials. Herein, we report an ensemble and single-molecule fluorescence imaging and spectroscopy investigation of ESB in hexakis[4-(-dioctylaminostyryl)phenylethynyl]benzene(), a two-photon absorber possessing a -symmetric π-D structure (π = hexaethynylbenzene, D = (-dioctylaminostyryl)phenyl group) consisting of three equivalent D-π-D moieties. Ensemble and single-molecule measurements and theoretical calculations revealed that undergoes a photoabsorption process with two orthogonal transition dipole moments, whereas it fluoresces with a single transition dipole moment after one- or two-step ESB upon photoexcitation, depending on the environmental polarity.

Starburst-Shaped D-π-A Chromophores Possessing a Hexaethynylbenzene Core for Dye-Sensitized Solar Cells.

Two starburst-shaped organic chromophores, incorporating a hexaethynylbenzene core modified by five donor branches (D-branches) of (-dioctylaminostyryl)benzene and one acceptor/anchoring branch (A-branch) of either carboxylic acid-terminated phenylethynylbenzene () or cyanoacrylic acid-terminated diketopyrrolopyrrole (DPP)-thiophene (), were synthesized and applied to dye-sensitized solar cells (DSSCs). In these chromophores, the common donor moiety, five (-dioctylaminostyryl)phenyl groups, exhibits excellent optical absorption in the visible region (molar absorption coefficient ε > 10 M cm below 500 nm). The A-branch of does not possess strong electron-accepting properties; however, the A-branch of , the DPP-thiophene moiety, serves as a strong electron acceptor site.

Single Platinum Atom Doping to Silver Clusters Enables Near-Infrared-to-Blue Photon Upconversion.

Photon upconversion (UC) from near-infrared (NIR) to visible has been realized using singlet-to-triplet absorption of sensitizers, which are currently limited to osmium complexes and semiconductor nanocrystals. Motivated by the atomically precise tunability of electronic structure and photophysical properties of noble metal clusters, which often possess absorption bands that extend into the NIR region, we investigated MAg (SR) (M=Ag, Pt; SR=2,4-dimethylbenzenethiolate) clusters as a new NIR-absorbing sensitizer for triplet-triplet annihilation UC. Combined with a blue light emitter, the NIR excitation (λ =785 nm) of Ag (SR) results in no UC emission, while PtAg (SR) exhibits strong UC emission.

Synthesis and Properties of a Cyclohexa-2,7-anthrylene Ethynylene Derivative.

The synthesis of a cyclohexa-2,7-(4,5-diaryl)anthrylene ethynylene (1) was achieved for the first time by using 1,8-diaryl-3,6-diborylanthracene and 1,8-diaryl-3,6-diiodoanthracene as key synthetic intermediates. Macrocycle 1 possesses a planar conformation of approximately D symmetry, because of the triple-bond linker between the anthracene units at the 2,7-positions. It was confirmed that macrocycle 1, bearing bulky substituents at the outer peripheral positions, behaves as a monomeric form in solution without π-stacking self-association.

Geometric and electronic properties of Si-atom doped Al clusters: robustness of binary superatoms against charging.

The geometric and electronic properties of silicon-atom-doped aluminum clusters, AlSi (n = 7-30, m = 0-2), were investigated experimentally. The size dependences of the ionization energy and electron affinity of AlSi show that the stability of AlSi is governed by the total number of valence electrons in the clusters, where Al and Si atoms behave as trivalent and tetravalent atoms, respectively. Together with theoretical calculations, it has been revealed that neutral AlSi and AlSi have a cage-like geometry with central Si atom encapsulation and closed electronic structures of superatomic orbitals (SAOs), and also that they both exhibit geometric robustness against reductive and oxidative changes as cage-like binary superatoms of Si@Al and Si@Al.

Electronic spectra and excited-state dynamics of acridine and its hydrated clusters.

We combine results from several different experiments to investigate the photophysics of acridine (Ac) and its hydrated clusters in the gas phase. Our findings are also compared with results from condensed phase studies. Similar to measurements of Ac dissolved in hydrocarbons, the lifetime of the first electronically excited state of isolated Ac in vacuum is too short for typical resonantly enhanced multiphoton ionization (REMPI) and laser induced fluorescence (LIF) experiments, hence no signal from REMPI and LIF can be attributed to monomeric Ac.

Single-Molecule Fluorescence Spectroscopy of Perylene Diimide Dyes in a γ-Cyclodextrin Film: Manifestation of Photoinduced H-Atom Transfer via Higher Triplet (n, π*) Excited States.

Supramolecular complexation of γ-cyclodextrin (γ-CD) with N,N'-bis(2,6-dimethylphenyl)perylene-3,4,9,10-tetracarboxylic diimide (DMP-PDI) or N,N'-bis(2,6-dioctyl)perylene-3,4,9,10-tetracarboxylic diimide (C8-PDI) dye in an aqueous solution and in a γ-CD solid film were investigated via ensemble and single-molecule fluorescence spectroscopy. These two perylene diimide derivatives possess almost the same electronic structure but have different terminal functional groups. This structural difference leads to formation of an inclusion complex of γ-CD with DMP-PDI but not with C8-PDI in aqueous solution.

Effects of Supramolecular Encapsulation on Photophysics and Photostability of a 9,10-Bis(arylethynyl)anthracene-Based Chromophore Revealed by Single-Molecule Fluorescence Spectroscopy.

The effects of supramolecular encapsulation on the photophysics and photostability of a highly fluorescent dimeric derivative of 2,6-diacetoxy-9,10-bis(arylethynyl)anthracene (G2) were investigated by single-molecule fluorescence spectroscopy (SMFS). The fluorescence properties of free-G2 and its self-assembled boronic ester encapsulation complex, G2@(Cap), were compared in solution and a glassy polymer film. The fluorescence spectral characteristics and theoretical calculations suggest that the environment affects the excited-state conformation and subsequent fluorescence emission of G2@(Cap).

Synthesis and Self-Assembly of Cyclic 2,7-Anthrylene Ethynylene 1,3-Phenylene Ethynylene Trimer with a Planar Conformation.

Cyclic arylene ethynylene hexamer 1, composed of alternating 2,7-anthrylene ethynylene units and meta-phenylene ethynylene units, was synthesized. It shows C symmetry and possesses a flat and rigid conformation with a large equilateral triangle-like cavity. Macrocycle 1 self-associates through π-π stacking interactions between the anthracene-containing macrocyclic aromatic cores with indefinite-association constant K =6980 m in CDCl at 303 K.

Correlations between Photovoltaic Characteristics, Adsorption Number, and Regeneration Kinetics in Dye-Sensitized Solar Cells Revealed by Scanning Photocurrent Microscopy.

Newly developed simultaneous scanning photocurrent and luminescence microscopy was applied to ruthenium-based dye-sensitized solar cells (DSCs) comprising a cover glass photoanode with a 100 nm thick TiO2 layer. Using this, we have investigated the lateral variations of several parameters of these DSCs under short-circuit conditions. Simultaneous measurement of photocurrent and luminescence images for the same area of the DSC demonstrated submicrometric lateral resolution of our photocurrent microscopy, which is approximately 10 times better than the resolution of photocurrent microscopy used in past studies.

Enhanced photostability of an anthracene-based dye due to supramolecular encapsulation: a new type of photostable fluorophore for single-molecule study.

For single-molecule fluorescence studies, highly photostable fluorophores are absolutely imperative, because photo-induced degradation (i.e., photobleaching) limits the observation time of individual molecules.

Formation and electronic structures of organoeuropium sandwich nanowires.

Organoeuropium sandwich clusters, comprising europium (Eu) and 1,3,5,7-cyclooctatetraene (COT) (Eu(n)(COT)(m)), were produced in the gas phase using a laser vaporization synthesis method. Photoionization mass spectra revealed an exclusive Eu(n)(COT)(m) formation with three compositions: m = n + 1, m = n, and m = n - 1, which, we propose, correspond to full-sandwich, half-sandwich, and inverted-sandwich structures, respectively. The charge distributions, metal-ligand bonding characteristics, and electronic structures of the clusters were comprehensively investigated by photoionization measurements of Eu(n)(COT)(m) neutrals and by photoelectron spectroscopy of Eu(n)(COT)(m)(-) and isoelectronic Ba(n)(COT)(m)(-) anions.

Encapsulation with the protrusion of cruciform 9,10-bis(arylethynyl)anthracene derivatives in a self-assembled boronic ester cavitand capsule: photochemical and photophysical properties.

The self-assembled boronic ester cavitand capsule 3 quantitatively and tightly encapsulates 2,6-diacetoxy-9,10-bis(arylethynyl)anthracene derivatives 4 a-4 c as highly fluorescent cruciform guests to form complexes 4 a@3, 4 b@3, and 4 c@(3)2. The structural features of capsule 3, which possesses two polar bowl-shaped aromatic cavity ends and four large equatorial windows connected by dynamic boronic ester bonds, made it possible to encapsulate cruciform 4 with protection of the reactive anthracene core inside the capsule and with two protruding arylethynyl groups, the π-conjugated arms of compound 4, through two of the equatorial windows of the capsule. Thus, complexes 4 a@3, 4 b@3, and 4 c@(3)2 show greater resistance to photochemical reactions in solution and fluorescence quenching in the powder state compared to free guests 4.

Mass spectrometry and photoelectron spectroscopy of o-, m-, and p-terphenyl cluster anions: the effect of molecular shape on molecular assembly and ion core character.

Mass spectrometry and photoelectron spectroscopy of o-, m-, and p-terphenyl cluster anions, (o-TP)n(-) (n = 2-100), (m-TP)n(-) (n = 2-100), and (p-TP)n(-) (n = 1-100), respectively, are conducted to investigate the effect of molecular shape on the molecular aggregation form and the resultant ion core character of the clusters. For (o-TP)n(-) and (m-TP)n(-), neither magic numbers nor discernible isomers are observed throughout the size range. Furthermore, their vertical detachment energies (VDEs) increase up to large n and depend linearly on n(-1/3), implying that they possess a three-dimensional (3D), highly reorganized structure encompassing a monomeric anion core.