Reconfigurable Logic-in-Memory Constructed Using an Organic Antiambipolar Transistor.

We demonstrate an electrically reconfigurable two-input logic-in-memory (LIM) using a dual-gate-type organic antiambipolar transistor (DG-OAAT). The attractive feature of this device is that a phthalocyanine-cored star-shaped polystyrene is used as a nano-floating gate, which enables the electrical switching of individual logic circuits and stores the circuit information by the nonvolatile memory effect. First, the DG-OAAT exhibited Λ-shaped transfer curves with hysteresis by sweeping the bottom-gate voltage. Programming and erasing operations enabled the reversible shift of the Λ-shaped transfer curves. Furthermore, the top-gate voltage effectively tuned the peak voltages of the transfer curves. Consequently, the combination of dual-gate and memory effects achieved electrically reconfigurable two-input LIM operations. Individual logic circuits (e.g., OR/NAND, XOR/NOR, and AND/XOR) were reconfigured by the corresponding programming and erasing operations without any variations in the input signals. Our device concept has the potential to fulfill an epoch-making organic integration circuit with a simple device configuration.

Growth and characterization of melem hydrate crystals with a hydrogen-bonded heptazine framework.

In carbon nitride (CN) compounds, hydrogen bonds play a major role in cohesion, in addition to dispersion forces. The crystal structures of CN compounds produced via thermal polymerization are complex, but they possess unique and attractive features. Melem is a well-known building unit of CN compounds such as melon and g-C3N4, which have recently attracted attention as photocatalysts. Melem hydrate (Mh) forms hexagonal prismatic crystals that are sufficiently porous to accommodate small molecules. In this study, we grew and characterized single crystals of Mh and investigated their optical properties and hygroscopicity. By precisely adjusting the hydration conditions, we succeeded in growing a well-formed hexagonal prismatic single crystal of Mh (Mhr) with a length measuring several tens of micrometers. Furthermore, we discovered a parallelogram-shaped Mh single crystal (Mhp), which possessed a different crystal structure and optical properties from those of Mh and melem crystals. Although the crystal structure of Mh was greatly disrupted by dehydration, it exhibited hygroscopicity and could absorb moisture even in air, restoring the crystal structure of Mh. In addition, Mh demonstrated a high photoluminescence quantum yield and long lifetime delayed fluorescence, similar to melem crystal. The high quantum yield of Mh can be attributed to the effect of the strong anchoring of the melem molecule by several hydrogen bonds in the Mh crystal, since the strongly anchored molecule is less likely to undergo radiation-free deactivation due to the small displacement of atomic positions in the excited state after light absorption. The findings obtained in this study shed light not only on the application of CN compounds as photocatalysts, but also on a wider range of applications based on their optoelectronic functions.

Mechanism of high photoluminescence quantum yield of melem.

To produce high-efficiency organic light-emitting diodes, materials that exhibit thermally activated delayed fluorescence (TADF) are attracting attention as alternatives to phosphorescent materials containing heavy metallic elements. Melem, a small molecule with a heptazine backbone composed only of nitrogen, carbon, and hydrogen, is known to emit light in the near-ultraviolet region and exhibit high photoluminescence (PL) quantum yield and delayed fluorescence. However, the mechanism underlying the high PL quantum yield remains unclear. This study aimed to elucidate the mechanism of the high PL quantum yield of melem by examining its optical properties in detail. When the amount of dissolved oxygen in the melem solution was increased by bubbling oxygen through it, the PL quantum yield and emission lifetime decreased significantly, indicating that the triplet state was involved in the light-emission mechanism. Furthermore, the temperature dependence of the PL intensity of melem was investigated; the PL intensity decreased with decreasing temperature, indicating that it increases thermally. The experimental results show that melem is a TADF material that produces an extremely high PL quantum yield by upconversion from the triplet to the singlet excited state.

Electronic structure of n-cycloparaphenylenes directly observed by photoemission spectroscopy.

A series of n-cycloparaphenylenes ([n]CPP, n = 8, 9, and 12) were studied by ultraviolet photoemission, inverse photoemission, ultraviolet-visible absorption, and X-ray photoemission spectroscopy to detect their unique electronic structures. [n]CPP has a cyclic structure in which both ends of n-poly(p-phenylene)s (nP) are connected. The molecular size dependence of the HOMO-LUMO gap of [n]CPP was investigated by direct observation and was found to increase as the molecular size increased. This trend is opposite to that of typical π-conjugated systems. Highly strained molecular structures, especially of small [n]CPPs, significantly impact their electronic structure. Insights into the electronic structure of [n]CPP obtained here will aid the design of electronic functionality of non-planar π-conjugation systems.

Effect of physisorption of inert organic molecules on Au(111) surface electronic states.

The modification of the Au(111) Shockley surface state (SS) by an n-alkane molecule (n-tetratetracontane) monolayer was observed by angle-resolved ultraviolet photoemission spectroscopy. Although there is little chance of chemical interaction in this ideal physisorption system, the volume of the Fermi surface of the SS was significantly reduced accompanied by the formation of large interface electric dipoles. Moreover, Rashba splitting of the SS by spin-orbit interactions was slightly increased upon n-tetratetracontane adsorption, which arose from the decrease in the symmetry of the wave function around the Au nuclei at the surface. The detailed information about the simple physisorption system presented in this paper provides basic knowledge for understanding the electronic structure at the interface between other organic molecules and metal substrates.

Synthesis and Characterization of Octacyano-Fe-Phthalocyanine.

Octacyano-metal-phthalocyanine MPc(CN)8 is a promising n-type stable organic semiconductor material with eight cyano groups, including a strong electron-withdrawing group at its molecular terminals. However, a thorough investigation of MPc(CN)8 has not yet been conducted. Therefore, we synthesized FePc(CN)8 and investigated its crystal structure, chemical and electronic states, electrical properties, photocatalytic activity, and magnetic properties. In this paper, we discuss the various properties of MPc(CN)8 in comparison with those of FePc. X-ray diffraction measurements indicated that the crystal structure of FePc(CN)8 was strongly influenced by the cyano groups and differed from the α- and ß-forms of FePc. The space group P4/mcc structure of FePc(CN)8 was similar to that of the x-form of LiPc. The ultraviolet-visible (UV-vis) absorption spectrum of FePc(CN)8 was observed at wavelengths longer than that of FePc. Density functional theory-based molecular orbital calculations indicated that the energy gap of FePc(CN)8 is smaller than that of FePc, which can lead to the observation of the Q-band in the UV-vis absorption spectrum of FePc(CN)8 at longer wavelengths than that of FePc. Because FePc(CN)8 has a wider optical absorption band in the visible region than FePc, its photocatalytic activity is approximately four times higher than that of FePc. The conductivity of FePc(CN)8 was also higher than that of FePc, which is due to the larger overlap of π-electron clouds of the molecules in the crystal structure of FePc(CN)8. Magnetic measurements revealed that FePc(CN)8 exists in an antiferromagnetic ground state. The magnetic properties of FePc(CN)8 are specific to its crystal structure, with direct exchange interactions between Fe2+ ions and π-electron-mediated interactions. In particular, the Pauli paramagnetic behavior at high temperatures and the antiferromagnetic behavior at low temperatures (Weiss temperature θ = -4.3 ± 0.1 K) are characteristic of the π-d system.

Electrically Reconfigurable Organic Logic Gates: A Promising Perspective on a Dual-Gate Antiambipolar Transistor.

Electrically reconfigurable organic logic circuits are promising candidates for realizing new computation architectures, such as artificial intelligence and neuromorphic devices. In this study, multiple logic gate operations are attained based on a dual-gate organic antiambipolar transistor (DG-OAAT). The transistor exhibits a Λ-shaped transfer curve, namely, a negative differential transconductance at room temperature. It is important to note that the peak voltage of the drain current is precisely tuned by three input signals: bottom-gate, top-gate, and drain voltages. This distinctive feature enables multiple logic gate operations with "only a single DG-OAAT," which are not obtainable in conventional transistors. Five logic gate operations, which correspond to AND, OR, NAND, NOR, and XOR, are demonstrated by adjusting the bottom-gate and top-gate voltages. Moreover, varying the drain voltage makes it possible to reversibly switch two logic gates, e.g., NAND/NOR and OR/XOR. In addition, the DG-OAATs show a high degree of stability and reliability. The logic gate operations are observed even months later. The hysteresis in the transfer curves is also negligible. Thus, the device concept is promising for realizing multifunctional logic circuits with a simple transistor configuration. Hence, these findings are expected to surpass the current limitations in complementary metal-oxide-semiconductor devices.

Mechanism of charge accumulation of poly(heptazine imide) gel.

Photo-stimuli response in materials is a fascinating feature with many potential applications. A photoresponsive gel of poly(heptazine imide), PHI, termed PHIG, exhibits photochromism, photoconductivity, and photo-induced charge accumulation, and is generated using ionic liquids and PHI. Although there are several examples of ionic liquid gels that exhibit photochromism and photoconductivity, this is the first report of an ionic liquid gel that exhibits both these properties as well as charge accumulation. We conducted experimental and theoretical investigations to understand the mechanism of the photostimulus response of PHIG, especially charge accumulation. The proposed model explains both the mechanism of charge accumulation and dark photocatalysis by PHI and provides new concepts in the field of photofunctional materials.

Interface Structures and Electronic States of Epitaxial Tetraazanaphthacene on Single-Crystal Pentacene.

The structural and electronic properties of interfaces composed of donor and acceptor molecules play important roles in the development of organic opto-electronic devices. Epitaxial growth of organic semiconductor molecules offers a possibility to control the interfacial structures and to explore precise properties at the intermolecular contacts. 5,6,11,12-tetraazanaphthacene (TANC) is an acceptor molecule with a molecular structure similar to that of pentacene, a representative donor material, and thus, good compatibility with pentacene is expected. In this study, the physicochemical properties of the molecular interface between TANC and pentacene single crystal (PnSC) substrates were analyzed by atomic force microscopy, grazing-incidence X-ray diffraction (GIXD), and photoelectron spectroscopy. GIXD revealed that TANC molecules assemble into epitaxial overlayers of the (010) oriented crystallites by aligning an axis where the side edges of the molecules face each other along the [1¯10] direction of the PnSC. No apparent interface dipole was found, and the energy level offset between the highest occupied molecular orbitals of TANC and the PnSC was determined to be 1.75 eV, which led to a charge transfer gap width of 0.7 eV at the interface.

Alkyl-chain dividing layer at an alcohol/ionic liquid buried interface studied by sum-frequency generation vibrational spectroscopy.

We demonstrate for the first time the formation of a non-polar alkyl-chain dividing layer between a room-temperature ionic liquid (RTIL) and an n-alcohol. This newly described non-polar interfacial layer, which should be more hydrophobic than both RTIL and alcohol phases, might find applications in liquid/liquid reaction systems, or serve as a soft nano-functional space.

Effect of annealing on the electronic structure of poly(3-hexylthiophene) thin film.

The electronic structure and film structure of poly(3-hexylthiophene) (P3HT) have been studied by X-ray diffraction (XRD) measurements, ultraviolet-visible (UV-vis) absorption spectroscopy, near-edge X-ray absorption fine structure (NEXAFS) measurements, ultraviolet photoemission spectroscopy (UPS) and inverse photoemission spectroscopy (IPES). As reported in previous works, XRD results show that the crystallinity of the film with regioregular P3HT is significantly improved by annealing at 170 degrees C. The effects of annealing on the electronic structure strongly depend on the substrate and the degree of regioregularity of the P3HT polymer backbone. Even in the case of the regiorandom sample, annealing considerably changes the vacuum level energy, which is the result of changes in the conformation of the hexyl groups at the free surface of the film. The pi- and pi*-band onsets uniformly shift downward by the annealing resulting in an increased hole-injection barrier at the electrode interface. The effects of annealing on the electronic structure of regioregular samples are more complex and depend on multiple factors. It is necessary to take into account variations in the pi- and pi*-band widths and the polarization energy to determine the effects of annealing. The former is associated with the conformation of the backbones of the polymer chains, and the latter is associated with the packing density of the conjugated polymer planes. The combination of these variations determines the effects of annealing on the electronic structure of the regioregular film. This is a possible reason for the strong dependence of the effects of annealing on the surface roughness of the substrate, since substrate roughness has a considerable effect on the morphology and crystallinity of regioregular P3HT films.

Electronic structure of delocalized singlet biradical Ph2-IDPL solid film.

The film structure and electronic structure of a biradical hydrocarbon, diphenyl derivative of s-indacenodiphenalene (Ph(2)-IDPL) solid film has been investigated. A small energy gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) compared with that of typical π-conjugated small molecules was observed even for the amorphous film of Ph(2)-IDPL. This result indicates that the small HOMO-LUMO gap is an important characteristic of the singlet biradical electronic structure and well explains the previously reported ambipolar field effects of amorphous Ph(2)-IDPL film by Chikamatsu et al., Appl. Phys. Lett. 2007, 91, 043506. It was found that the gas-deposition method substantially improved the crystallinity of the film where Ph(2)-IDPL molecules form quasi one-dimensional (1D) molecular chains normal to the substrate surface. An extremely small HOMO-LUMO gap was observed in the polycrystalline Ph(2)-IDPL film, which is possibly caused by strong intermolecular coupling. The photon energy dependence of ultraviolet photoemission spectra shows that the stacked Ph(2)-IDPL molecular chain in the polycrystalline film develops an energy band structure in the direction of the surface normal of the film. The intermolecular covalency therefore evolves into the quasi 1D energy band along the molecular stacking direction.

Electronic structure of disjoint diradical 4,4'-bis(1,2,3,5-dithiadiazolyl) thin films.

The electronic structure of the thiazyl diradical, 4,4'-bis(1,2,3,5-dithiadiazolyl) (BDTDA), has been investigated by ultraviolet photoemission spectroscopy. Stacked BDTDA dimers showed an energy band dispersion of about 0.3 eV for the highest occupied molecular orbital in the direction of the surface normal of the BDTDA solid film. The pi-orbital overlap between the stacked dimers therefore evolves into a quasi one-dimensional energy band along the dimer stacking direction.

Interactive radical dimers in photoconductive organic thin films.

Fully interactive: Overlap between extended unoccupied molecular orbitals leads to the high photoconductivity of interactive radical dimers. Sandwich-type cells (see picture; ITO = indium tin oxide) comprising highly oriented thin films of a disjoint diradical, 4,4'-bis(1,2,3,5-dithiadiazolyl) (BDTDA) exhibit a photocurrent with a high on/off ratio at reverse bias voltages and photovoltaic behavior at zero bias voltage.

Anion configuration at the air/liquid interface of ionic liquid [bmim]OTf studied by sum-frequency generation spectroscopy.

The air/liquid interface of a room temperature ionic liquid, 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([bmim]OTf), is investigated using infrared-visible sum frequency generation (SFG) spectroscopy. The SFG spectra clearly show low-frequency modes [CF3-symmetric stretching (ss) mode and SO3-symmetric stretching (ss) mode] of the OTf anion, demonstrating the existence of anions polar oriented at the interface. The amplitude of the CF3-ss peak of the OTf anion has the opposite sign with respect to that of the SO3-ss peak, indicating that OTf anions at the surface have polar ordering where the nonpolar CF3 group points away from the bulk into the air, whereas the SO3 group points toward the bulk liquid. The line width of the SFG peak from the submerged SO3 group is appreciably narrower than that from IR absorption, suggesting the environment of the surface OTf anions is much more homogeneous than that of the bulk. The vibrational calculations also suggest that the anions and the cations form a more specific aggregated configuration at the surface as compared to the bulk.

Local structure at the air/liquid interface of room-temperature ionic liquids probed by infrared-visible sum frequency generation vibrational spectroscopy: 1-alkyl-3-methylimidazolium tetrafluoroborates.

The air/liquid interface of 1-alkyl-3-methylimidazolium tetrafluoroborates with the general formula [C(n)mim]BF(4) (n = 4-11) was studied using infrared-visible sum frequency generation (SFG) vibrational spectroscopy. The probability of the gauche defect per CH2-CH2 bond in the alkyl chain decreases as the number of carbon atoms in the alkyl chain increases. This observation suggests that the interaction between the alkyl chains is enhanced as the alkyl chain length becomes longer. The frequencies of the C-H stretching vibrational modes observed in the SFG spectra are higher than those of the corresponding peak positions observed in the infrared spectra of the bulk liquids. This shift is consistent with a structure in which the alkyl chain protrudes from the bulk liquid into the air. A local structure, which originates from the intermolecular interaction between the ionic liquid molecules, is proposed to explain these observations.

Intraocular biodistribution of mono-L-aspartyl chlorin e6 in a primate choroidal neovascularization model.

BACKGROUND AND OBJECTIVE: To describe the biodistribution of a hydrophilic sensitizer, mono-L-aspartyl chlorin e6 (NPe6), in a primate model of choroidal neovascularization (CNV). MATERIALS AND METHODS: NPe6 (25 mg/kg) and indocyanine green (ICG, 15 mg/kg) were intravenously administered simultaneously in monkeys with laser-induced CNVs. Eyes were enucleated and examined by fluorescence microscopy immediately, 20 minutes, and 1, 4, and 24 hours after dye injection. RESULTS: Fluorescence peaked in retinal vessels immediately after dye administration; rapid washout began 1 hour postinjection. In contrast, experimental CNV demonstrated little fluorescence immediately after injection, with increased intensity at later time points. Peak dye fluorescence in CNV occurred 1 hour following dye injection. NPe6 fluorescence diminished rapidly and washed out completely by 24 hours. The dye accumulation and retention pattern of ICG dye resembled that of NPe6. CONCLUSIONS: This study demonstrated the selective accumulation of NPe6 photosensitizer and ICG dye within experimental CNV and rapid clearance from the circulation and retinochoroidal tissue.

Halide-Substituted Electronic Properties of Organometal Halide Perovskite Films: Direct and Inverse Photoemission Studies.

Solution-processed perovskite solar cells are attracting increasing interest due to their potential in next-generation hybrid photovoltaic devices. Despite the morphological control over the perovskite films, quantitative information on electronic structures and interface energetics is of paramount importance to the optimal photovoltaic performance. Here, direct and inverse photoemission spectroscopies are used to determine the electronic structures and chemical compositions of various methylammonium lead halide perovskite films (MAPbX3, X = Cl, Br, and I), revealing the strong influence of halide substitution on the electronic properties of perovskite films. Precise control over halide compositions in MAPbX3 films causes the manipulation of the electronic properties, with a qualitatively blue shift along the I → Br → Cl series and showing the increase in ionization potentials from 5.96 to 7.04 eV and the change of transport band gaps in the range from 1.70 to 3.09 eV. The resulting light absorption of MAPbX3 films can cover the entire visible region from 420 to 800 nm. The results presented here provide a quantitative guide for the analysis of perovskite-based solar cell performance and the selection of optimal carrier-extraction materials for photogenerated electrons and holes.

Characteristics of monolayer behavior and multilayer film structures of comb polymers having different kinds of fluorocarbon side-chains.

With comb polymers with different kinds of fluorocarbon side-chains, significant effects of spreading solvents on the monolayers at the air/water interface and the molecular arrangement in the deposited films could be found by the use of trifluoroacetic acid and its mixed solvents with n-hexane, depending on the atoms, fluorine or hydrogen, substituted at the end of the fluorocarbon side-chains. These facts are probably due to intralayer hydrogen bonding cooperating with the carbonyl groups of the long-chain esters. The deposited films of solid substrates were characterized by polarized near-edge X-ray absorption fine structure (NEXAFS) spectroscopy as well as in-plane X-ray diffraction and scanning electron and atomic force microscopy.