Optimizing the Distance between Upconversion Thin Films and Silver Nanoprisms for the Design of a High-Performance Plasmonic Triplet-Triplet Annihilation Upconversion System.

While the distance dependence of metal-enhanced fluorescence has been extensively studied for composite systems comprising fluorophores and metal nanoparticles, the corresponding distance dependence of triplet-triplet annihilation upconversion (TTA-UC) systems remains unexplored. Herein, we investigated the influence of the spatial distance between Ag nanoprisms (AgPRs) and TTA-UC thin films consisting of a palladium octaethylporphyrin (PdOEP) sensitizer and a 9,10-diphenylanthracene (DPA) emitter, aiming at enhancing the upconverted (UC) emission as efficiently as possible. Results indicated that the optimal distance for the examined system was significantly longer (12.6 nm) than those of typical metal-enhanced fluorescence systems (about 2 nm). We demonstrated that the UC emission enhancement factor can be expressed as a product including factors of the PdOEP photoexcitation rate, triplet-triplet energy transfer (TTET) efficiency from PdOEP to DPA, triplet excited DPA lifetime, and fluorescence efficiency of singlet excited DPA. We discovered that the AgPRs play a beneficial role in enhancing the PdOEP photoexcitation, whereas they exert detrimental effects on the other three factors. Among these three factors, quenching contributions by the decrease of the triplet excited DPA lifetime and DPA fluorescence efficiency were significant, making these the primary and secondary factors, respectively, for the UC emission quenching, particularly at short distances. These results demonstrate that the characteristic distance dependence of the UC emission enhancement is determined by the competing effects of beneficial PdOEP photoexcitation enhancement and the detrimental localized surface plasmon (and/or AgPR)-induced nonradiative decay of the triplet- and singlet excited DPA molecules. The findings offer valuable guidelines for the design of high-performance plasmonic TTA-UC systems.

A Light-Harvesting/Charge-Separation Model with Energy Gradient Made of Assemblies of meta-Pyridyl Zinc Porphyrins.

Self-assembly of porphyrins is a fascinating topic, not only for mimicking chlorophyll assemblies in photosynthetic organisms, but also for the potential of creating molecular-level devices. Herein, zinc porphyrin derivatives bearing a meta-pyridyl group at the meso position were prepared and their assemblies studied in chloroform. Among the porphyrins studied, one with a carbamoylpyridyl moiety gave a distinct 1 H NMR spectrum in CDCl3 , which allowed the supramolecular structure in solution to be probed in detail. Ring-current-induced chemical-shift changes in the 1 H NMR spectrum, together with vapor-pressure osmometry and diffusion-ordered NMR spectroscopy, among other evidence, suggested that the porphyrin molecules form a trimer with a triangular cone structure. Incorporation of a directly linked porphyrin-ferrocene dyad with the same assembling properties in the assemblies led to a rare example of a light-harvesting/charge-separation system in which an energy gradient is incorporated and reductive quenching occurs.

Performance Improvement of Triplet-Triplet Annihilation-Based Upconversion Solid Films through Plasmon-Induced Backward Scattering of Periodic Arrays of Ag and Al.

The performance improvement of solid-state triplet-triplet annihilation-based photon upconversion (TTA-UC) systems is required for the application to various solar devices. The performance can be improved by making use of the local strong electric field generated through the excitation of localized surface plasmon (LSP) resonance of metal nanostructures. However, since the improvement is effective only within the limited nanospace around nanoparticles (i.e., the near-field effect), a methodology for improving the performance over a wider spatial region is desirable. In this study, a significant improvement in the threshold light excitation intensity (Ith) (77% decrease) as the figure of merit and the upconverted emission intensity (6.3 times enhancement) in a solid-state TTA-UC film with a thickness of 3 µm was achieved by stacking the film with periodic Ag half-shell arrays. The highest-enhanced upconverted emission was obtained by tuning the diffuse reflectance peak, which results from the excitation of LSP resonance of the Ag half-shell arrays, to overlap well with the photoexcitation peak of the sensitizer in the TTA-UC film. The intensity of the enhanced upconverted emission was independent of the distance between the lower edge of the TTA-UC film and the surface of half-shell arrays in the nanometer order. These results suggest that the performance improvement was attributed to the photoexcitation enhancement of the sensitizer by elongating the excitation light path length inside the TTA-UC film, which was achieved through a strong backward scattering of the incident light based on the LSP resonance excitation (i.e., the far-field effect). In addition, the upconverted emission was improved using half-shell arrays comprising low-cost Al, although the enhancement factor was 3.5, which was lower than that of Ag half-shell arrays. The lower enhancement may be attributed to a decrease in the backward scattering of the excitation light owing to the intrinsic strong interband transition of Al at long visible wavelengths.

Development of Plasmonic Cu2O/Cu Composite Arrays as Visible- and Near-Infrared-Light-Driven Plasmonic Photocatalysts.

We describe efficient visible- and near-infrared (vis/NIR) light-driven photocatalytic properties of hybrids of Cu2O and plasmonic Cu arrays. The Cu2O/Cu arrays were prepared simply by allowing a Cu half-shell array to stand in an oxygen atmosphere for 3 h, which was prepared by depositing Cu on two-dimensional colloidal crystals with a diameter of 543 or 224 nm. The localized surface plasmon resonances (LSPRs) of the arrays were strongly excited at 866 and 626 nm, respectively, at which the imaginary part of the dielectric function of Cu is small. The rate of photodegradation of methyl orange was 27 and 84 times faster, respectively, than that with a Cu2O/nonplasmonic Cu plate. The photocatalytic activity was demonstrated to be dominated by Cu LSPR excitation. These results showed that the inexpensive Cu2O/Cu arrays can be excellent vis/NIR-light-driven photocatalysts based on the efficient excitation of Cu LSPR.

Cyclic Tetramers of Zinc Chlorophylls as a Coupled Light-Harvesting Antenna-Charge-Separation System.

A coupled light-harvesting antenna-charge-separation system, consisting of self-assembled zinc chlorophyll derivatives that incorporate an electron-accepting unit, is reported. The cyclic tetramers that incorporated an electron acceptor were constructed by the co-assembly of a pyridine-appended zinc chlorophyll derivative, ZnPy, and a zinc chlorophyll derivative further decorated with a fullerene unit, ZnPyC60 . Comprehensive steady-state and time-resolved spectroscopic studies were conducted for the individual tetramers of ZnPy and ZnPyC60 as well as their co-tetramers. Intra-assembly singlet energy transfer was confirmed by singlet-singlet annihilation in the ZnPy tetramer. Electron transfer from the singlet chlorin unit to the fullerene unit was clearly demonstrated by the transient absorption of the fullerene radical anion in the ZnPyC60 tetramer. Finally, with the co-tetramer, a coupled light-harvesting and charge-separation system with practically 100 % quantum efficiency was demonstrated.

Development of highly thermoresponsive fluorescent sensors consisting of plasmonic silver nanoprisms and poly(N-isopropylacrylamide)-fluorophore composites.

We developed a new hybrid consisting of Ag nanoprisms, poly(N-isopropylacrylamide) (PNIPAm), and fluorophores via layer-by-layer assembly. The fluorescence intensity below the lower critical solution temperature (LCST) of PNIPAm was 6.4 times stronger than that above the LCST, meaning that the hybrids can function as nanosized highly thermoresponsive fluorescent sensors.

Particle size dependence of the surface-enhanced Raman scattering properties of densely arranged two-dimensional assemblies of Au(core)-Ag(shell) nanospheres.

We investigated the dependence of the surface-enhanced Raman scattering (SERS) activity of densely arranged two-dimensional assemblies of spherical Au(core)-Ag(shell) nanoparticles (Au/AgNSs) on the nanoparticle diameter. The size-controlled Au/AgNSs were synthesized using the Au nanosphere seed-mediated growth method without any bulky stabilizers. The diameters of the Au/AgNSs were 38, 53, and 90 nm and the ratio of the total diameter to the Au core diameter was adjusted to ca. 2.0. Extinction spectra of the colloidal solutions of these nanoparticles exhibited the prominent peak of the localized surface plasmon resonance (LSPR) of Ag and therefore the Au/AgNSs exhibited LSPR properties almost the same as Ag nanospheres. It was confirmed from SEM observation that the organic solvent-mediated liquid-liquid interface assembly technique easily generated densely arranged two-dimensional assemblies of the nanospheres. The extinction spectra of all the assemblies exhibited a prominent broad peak ranging from 500 nm to the near-infrared region, which is assigned to the longitudinal LSPR mode of the coupling nanospheres. The extinction intensity increased with increasing nanosphere diameter. The SERS activities of these assemblies were investigated using p-aminothiophenol as a probe molecule. The result revealed that the enhancement factor (EF) of the Raman signal dramatically increased upon increasing the particle diameter. The maximum EF obtained with a laser excitation wavelength of 785 nm was 1.90 × 10(6) for a nanosphere diameter of 90 nm. This renders the two-dimensional assemblies of the plasmonic Au/AgNSs promising for the development of highly sensitive SERS sensor platforms due to their strong electromagnetic effect.

Photophysical and electrochemical properties of thienylnaphthalimide dyes with excellent photostability.

The development of robust dyes is a highly important theme for any applications of dyes. Here we present photophysical and electrochemical characterization of a set of robust dyes based on the thienylnaphthalimide unit. The set is comprised of the thienylnaphthalimide derivatives with phenyl- (Ph-), 4-nitrophenyl- (NO2Ph-), and 4-(diphenylamino)phenyl (Ph2NPh-) substituents as exemplars covering electron-withdrawing to electron-donating groups. The fluorescence quantum yields of the Ph-TNI increases as the solvent polarity increases, while that of Ph2NPh-TNI showed the opposite trend. Changes in the rates of nonradiative decay were found to be a major factor for these contrasting behaviors. Cyclic voltammetry showed that the substituent effects were more apparent for the HOMO energies rather than the LUMO energies. Density functional theory calculations showed that the first singlet excited state of these compounds is a (1)π,π* state with a significant charge transfer character. Ph-TNI and Ph2NPh-TNI are much more stable against photodegradation than coumarin and fluorescein dyes.

Development of Au Nanoparticle Two-Dimensional Assemblies Dispersed with Au Nanoparticle-Nanostar Complexes and Surface-Enhanced Raman Scattering Activity.

We recently found that polyvinylpyrrolidone (PVP)-protected metal nanoparticles dispersed in water/butanol mixture spontaneously float to the air/water interface and form two-dimensional assemblies due to classical surface excess theory and Rayleigh-Bénard-Marangoni convection induced by butanol evaporation. In this study, we found that by leveraging this principle, a unique structure is formed where hetero gold nanospheres (AuNPs)/gold nanostars (AuNSs) complexes are dispersed within AuNP two-dimensional assemblies, obtained from a mixture of polyvinylpyrrolidone-protected AuNPs and AuNSs that interact electrostatically with the AuNPs. These structures were believed to form as a result of AuNPs/AuNSs complexes formed in the water/butanol mixture floating to the air/water interface and being incorporated into the growth of AuNP two-dimensional assemblies. These structures were obtained by optimizing the amount of mixed AuNSs, with excessive addition resulting in the formation of random three-dimensional network structures. The AuNP assemblies dispersed with AuNPs/AuNSs complexes exhibited significantly higher Raman (surface-enhanced resonance Raman scattering: SERRS) activity compared to simple AuNP assemblies, while the three-dimensional network structure did not show significant SERRS activity enhancement. These results demonstrate the excellent SERRS activity of AuNP two-dimensional assemblies dispersed with hetero AuNPs/AuNSs complexes.

Development of excitation power-responsive anti-stokes emission wavelength switching and their energy saving induced by localized surface plasmon resonance.

We designed an external stimulus-responsive anti-Stokes emission switching using dual-annihilator-based triplet-triplet annihilation upconversion systems. This system, which was constructed by incorporating a palladium porphyrin derivative as a sensitizer and 9,10-diphenylanthracene (DPA) and 9,10-bis(triisopropylsilyl)ethynylanthracene (TIPS) as annihilators into polymer thin films, produced TIPS- and DPA-based anti-Stokes emission under low and high excitation powers, respectively. The mechanism involves the following: under low excitation power, triplet energy transfer from triplet-excited PdOEP to DPA is induced, followed by relay to TIPS. This results in the generation of triplet-excited TIPS, and the subsequent triplet-triplet annihilation between them produces TIPS-based anti-Stokes emission. Conversely, under high excitation power, the high-density triplet-excited DPA, generated through triplet energy transfer from PdOEP, undergoes triplet-triplet annihilation among themselves, resulting in the generation of DPA-based anti-Stokes emission. Additionally, we achieved energy savings by reducing the required excitation power for switching through the utilization of plasmonic metal nanoparticles. The strong local electromagnetic fields associated with the localized surface plasmon resonance of metal nanoparticles enhance the photoexcitation efficiency of PdOEP, subsequently increasing the density of triplet-excited DPA. As a result, anti-Stokes emission switching becomes feasible at lower excitation powers.

Double helices of a pyridine-appended zinc chlorophyll derivative.

Self-assembled structures formed from a pyridine-appended zinc chlorophyll derivative are reported. While the zinc complex forms cyclic oligomers in chloroform solution, as indicated by (1)H NMR studies (including diffusion-ordered spectroscopy), vapor pressure osmometry, and cold-spray ionization mass spectrometry, it forms double-stranded helical coordination polymers in the solid state, as revealed by single-crystal X-ray analysis.

Plasmonic Metal Nanostructures Meet Triplet-Triplet Annihilation-Based Photon Upconversion Systems: Performance Improvements and Application Trends.

Improving the performance of upconversion systems based on triplet-triplet annihilation (TTA-UC) can have far-reaching implications for various fields, including solar devices, nano-bioimaging, and nanotherapy. This review focuses on the use of localized surface plasmon (LSP) resonance of metal nanostructures to enhance the performance of TTA-UC systems and explores their potential applications. After introducing the basic driving mechanism of TTA-UC and typical sensitizers used in these systems, we discuss recent studies that have utilized new sensitizers with distinct characteristics. Furthermore, we confirm that the enhancement in upconverted emission can be explained, at least in part, by the mechanism of "metal-enhanced fluorescence", which is attributed to LSP resonance-induced fluorescence enhancement. Next, we describe selected experiments that demonstrate the enhancement in upconverted emission in plasmonic TTA-UC systems, as well as the emerging trends in their application. We present specific examples of studies in which the enhancement in upconverted emission has significantly improved the performance of photocatalysts under both sunlight and indoor lighting. Additionally, we discuss the potential for future developments in plasmonic TTA-UC systems.

Photothermal therapeutic ability of copper open-shell nanostructures that are effective in the second biological transparency window based on symmetry breaking-induced plasmonic properties.

In this study, a photothermal therapy agent that works efficiently in the second biological transparency window was developed based on the localized surface plasmon (LSP) resonance of symmetry-broken open-shell nanostructures of low-cost Cu (CuOSNs). The strong LSP resonance and superior photothermal conversion ability in the second biological transparency window were achieved by generating the dipolar bonding mode due to the plasmon hybridization between the nanoshell dipole and the nanohole dipole at the opening edge in CuOSNs derived from the symmetry breaking of a Cu nanoshell. Oxidative dissolution of CuOSNs in water was significantly suppressed by successive coating with the self-assembled monolayer of 16-mercaptohexadecanoic acid and a thin silica layer. Furthermore, the stability in phosphate buffered saline, which models the biological environment, was attained by further coating the nanoparticles with polyethylene glycol. It was demonstrated from in vitro cell tests using HeLa cells that the cytotoxicity of CuOSNs was effectively suppressed by the surface protection. The viability of HeLa cells incubated with CuOSNs was decreased under the irradiation of low intensity 1060 nm laser with increasing number of CuOSNs. These results demonstrate that low-cost symmetry-broken Cu-based nanostructures can act as an excellent photothermal therapy agent in the second biological transparency window.

Monolayer assemblies of a sandwich-type double-decker porphyrin complex of cerium with an additional pendant porphyrin unit.

We have prepared a novel sandwich-type double-decker porphyrin complex with cerium, in which one of the porphyrins has long alkyl chains and the other has a pendant free-base porphyrin unit. The preparation of the complex was achieved with a Sonogashira coupling reaction between a preformed double-decker complex bearing an ethynyl moiety and an iodophenyl porphyrin. This complex forms moderately ordered self-assembled monolayers at the interface of 1-phenyloctane and highly oriented pyrolytic graphite. STM images with submolecular resolution revealed that the double-decker complexes form monolayers through adsorption of the alkyl-substituted porphyrin unit, presenting the other porphyrin having the additional porphyrin unit to the solution. All molecules are oriented in the same direction within single ordered domains. The double-decker complex and the corresponding free-base porphyrin form mixed monolayers due to their common adsorbing group and the matching unit cell parameters. The high spots for the double-decker cores are accompanied by lower spots, which can be assigned as the pendant free-base porphyrin units, revealing that the double-decker complexes predominantly take perpendicular orientation, in which the additional porphyrin unit orients perpendicular to the molecular row. Both the double-decker complex and the free-base porphyrin adsorb on the surface initially after the mixture was deposited, but the double-decker complex is gradually replaced by free-base porphyrin toward the thermodynamically stable assembly, in which the free-base porphyrin predominates. This behavior is unique to this particular complex among some analogous complexes with the same adsorbing group, which implies that groups not directly involved in adsorption may have profound effects on the adsorption and assembling properties of the molecule.

Modulation Technique of Localized Surface Plasmon Resonance of Palladium Nanospheres by Coating with Titanium Dioxide Shell for Application to Photothermal Therapy Agent.

Although plasmonic palladium (Pd) nanospheres are thermodynamically stable and have high photothermal conversion due to the free and bound electron coupling associated with the intrinsic high interband transition, they have not attracted attention as a photothermal conversion material for next-generation photothermal cancer therapy. This is because the Pd nanospheres generate the localized surface plasmon resonance (LSPR) intrinsically in the ultraviolet region, which is far away from the biological transparent window (750-900 nm). In this study, we controlled the LSP wavelength of Pd nanospheres by coating with high refractive index TiO2 shells taking advantage of the Pd LSPR which is highly sensitive to changes in the local refractive index around the nanospheres. Our calculations indicated that the absorption cross section at 808 nm (corresponding to the wavelength used for photothermal treatment) was increased by 4.5 times by redshifting the LSPR and increasing the extinction intensity associated with the coating with TiO2 shell. Experiments confirmed the theoretical prediction in that the LSPR of the synthesized Pd nanospheres with a diameter of 81 nm was significantly redshifted by coating with amorphous TiO2 shell, resulting in significant large extinction intensity at 808 nm. The photothermal conversion efficiency was estimated to be 50%. In vitro cell tests, HeLa cells incubated with 100-300 µg/mL TiO2-coated Pd nanospheres were efficiently killed by irradiating 808 nm laser (1.8 W) even though the nanospheres with the same concentrations showed little cytotoxicity. These results indicate that the Pd nanospheres coated with high refractive index shells can be promising as a photothermal therapy agent.

Rotational libration of a double-decker porphyrin visualized.

Scanning tunneling microscopy has revealed the reorientation of one of the macrocyclic rings of the double-decker porphyrin complex [Ce(TPP-Fc)(C(22)OPP)] [TPP-Fc = 5-(4-(4-ferrocenylphenylethynyl)phenyl)-10,15,20-triphenylporphyrin; C(22)OPP = 5,10,15,20-tetrakis(4-docosyloxyphenyl)porphyrin] by 90 degrees between scans when the other ring is fixed on a surface. This libration was evidenced by monitoring the location of the appended ferrocene unit, which functioned as a molecular beacon signaling its position.

Photoisomerization and thermal isomerization of shuttlecock- and bowl-equipped (phenylazo)pyridines.

The photoisomerization and thermal isomerization of sterically hindered (phenylazo)pyridine derivatives with a shuttlecock-shaped (TbetNNPy) or a bowl-shaped framework (BmtNNPy as well as the azoxy counterpart, BmtNN(O)Py) have been investigated. The crystal structures of these compounds revealed a planar conformation of the (phenylazo)pyridine moiety for TbetNNPy and severely distorted conformations for BmtNNPy and BmtNN(O)Py. The quantum yields of the trans-to-cis photoisomerization of TbetNNPy and BmtNNPy is lower than those of unsubstituted (phenylazo)pyridines. The low quantum yields may, to a large part, be attributed to electronic factors rather than steric factors. While the shuttlecock framework in TbetNNPy does not affect the thermal cis-to-trans isomerization, as the activation parameters for TbetNNPy are quite similar to those of azobenzene and azopyridine derivatives, the bowl framework in BmtNNPy renders the thermal isomerization process slower by lowering the frequency factor to an extent that more than compensates for the lowered activation energy. The process is characterized with a large negative activation entropy and a small activation enthalpy, implying that the isomerization proceeds through a limited range of intermediates stabilized by the presence of the bowl framework.

Combined Use of Anisotropic Silver Nanoprisms with Different Aspect Ratios for Multi-Mode Plasmon-Exciton Coupling.

Absorption enhancement based on interaction between the localized surface plasmon (LSP) and molecular exciton is one of the most important phenomena for the development of high-performance solar devices. In this study, hybrids of plasmonic metal nanoparticles and dye molecules have been developed, which exhibit enhanced absorption at precisely tuned wavelengths in a visible region. The hybrids consist of a porphyrin derivative, which has four absorption peaks (Q-bands) in a range of 500-700 nm, and triangular silver nanoprisms (AgPRs), which are developed by us to exhibit precisely tuned LSP resonance wavelengths. Absorption enhancement over the whole Q-band range is induced by the combined use of three kinds of AgPRs of different aspect ratios. Furthermore, the quantitative evaluation of absorption enhancement based on the LSP-based fluorescence enhancement phenomenon has demonstrated that efficient absorption enhancement can be effected at multiple wavelengths.

Plasmonic Silver Nanoprism-Induced Emissive Mode Control between Fluorescence and Phosphorescence of a Phosphorescent Palladium Porphyrin Derivative.

We have succeeded in significantly enhancing fluorescence from intrinsically phosphorescent palladium octaethylporphyrin (Pd-porphyrin) that has an intersystem crossing efficiency of ∼1 by using silver nanoprisms (AgPRs). This was achieved by controlling the wavelength of the localized surface plasmon (LSP) resonance of AgPRs and the distance between the Pd-porphyrin molecules and the AgPR surfaces. In addition to enhancing phosphorescence by spectrally overlapping the phosphorescence band with the LSP resonance band, tuning the LSP wavelength to approximately 520 nm led to the appearance of a new emission band around the wavelength corresponding to the fluorescent radiation. The appearance of fluorescence suggests that the nonradiative energy transfer from the singlet excited state of Pd-porphyrin to the LSP of AgPRs overcame the ultrafast intramolecular intersystem crossing to the triplet excited state, manifesting the spectral properties of the singlet excited state of Pd-porphyrin. The fluorescence nature of this radiation was strongly supported by lifetime measurements of the hybrids of Pd-porphyrin and AgPRs. Furthermore, the dependence of the emissive intensities on the distance between the Pd-porphyrin molecules and the AgPR surfaces showed interesting opposite trends. The fluorescence intensity was increased as the distance between the molecules and the AgPRs was decreased from 10.5 to 1 nm, while the phosphorescence intensity was decreased, which indicates that the LSP-induced fluorescence radiation process from Pd-porphyrin near the AgPRs outweighed the quenching by the AgPRs, even though the phosphorescence significantly suffered quenching.

A dinuclear ruthenium(II) complex that functions as a label-free colorimetric sensor for DNA.

A dinuclear ruthenium(II) complex groove binds to DNA and this interaction results in distinctive color changes that are dependent on both DNA sequence and structure.