Masaki Takata

Molecular Aggregation State and Photovoltaic Properties of Chlorophyll-Doped Conducting Poly(3-hexylthiophene)/MCM-41 Nanocomposites

Chlorophyll (Chl) was immobilized into a 1,4-butanediol-modified MCM-41 (BMCM-41) intercalated by poly(3-hexylthiophene) (P3HT) to form BMCM-41/P3HT/Chl nanocomposites having P3HT contents of 10, 30, 60, and 90 wt % from a solution-casting method. Wide-angle X-ray diffraction and transmission electron microscopy studies indicate that the pore structure of MCM-41 was retained after surface modification and a subsequent P3HT intercalation process. Scanning electron microscopy images showed that the BMCM-41 nanoparticles dispersed into the polymer matrix of BMCM-41/P3HT/Chl, and the sample with 10 wt % P3HT content gives the most homogeneous nanoparticle dispersion. Nitrogen adsorption-desorption results confirmed that the P3HT intercalation and Chl immobilization inside the BMCM-41 mesopore were successfully carried out. The pore volume and surface area of BMCM-41 decreased significantly when the amount of P3HT was increased from 10 to 90 wt %. The UV-vis study showed a blue shift of the pi-pi* transition band of P3HT in the spectra of BMCM-41/P3HT/Chl nanocomposites. The FT-IR study indicates an increase of the thiophene ring stretching and a decrease of the C horizontal lineO stretching when P3HT and Chl were inside the mesopore. The photovoltaic property of Chl-doped P3HT was improved significantly upon the addition of BMCM-41 nanoparticles, and BMCM-41/P3HT-10/Chl exhibits the highest incident photon-to-current conversion efficiency of 7.16%.

Rewriting the phase diagram of a diamagnetic liquid crystal by a magnetic field

Magnetic fields have been considered to only interact with organic materials non-destructively, leaving their fundamental structures unaffected, even when a strong magnetic field generated from a superconducting magnet is applied. Here we report an unprecedented observation that a liquid-crystalline mesophase of a diamagnetic molecular assembly with an orthorhombic or a cubic structure is formed selectively in the absence or presence of a strong magnetic field. The constituent molecule is a triphenylene derivative carrying six imidazolium bromide-terminated alkyl side chains and exhibits a cubic, orthorhombic, or hexagonal columnar mesophase when complexed with an appropriate amount of lanthanum(III) bromide. Thermal processing of the La3+-containing liquid-crystalline assembly in the presence of a 10-tesla magnetic field resulted in a phase diagram, in which the orthorhombic phase is completely replaced with the cubic phase. The discovery of this magneto-induced phase-selection offers an insight into the interactions between magnetic fields and organic material.Magnetically induced phase behaviour in a soft matter system is of potential interest for magneto-responsive compounds. Here the authors fabricate a discotic ionic liquid crystalline hybrid material which can be switched from orthorhombic to cubic phase in the absence or presence of a strong magnetic field.

Terminal Functionalization with a Triptycene Motif that Dramatically Changes the Structural and Physical Properties of an Amorphous Polymer

A surprising terminal-group effect on the structural and physical properties of an amorphous polymer is reported. We recently demonstrated that triptycene derivatives with substituents at the 1,8,13-positions show specific self-assembly behavior, enabling the formation of a well-defined 2D + 1D structure based on nested hexagonal packing of the triptycenes. Upon terminal functionalization with a 1,8-substituted triptycene (1,8-Trip), a liquid polymer, polydimethylsiloxane (PDMS, Mn = 18-24 kDa), turned into a highly viscous solid that exhibits birefringence at 25 °C. Small-angle and wide-angle X-ray scattering measurements revealed that the resulting telechelic PDMS assembles into a 2D + 1D structure, where layers of PDMS domains, formed between 2D assemblies of the triptycene termini, stack into a 1D multilayer structure with a layer spacing of 18-20 nm. Because of this structuring, the complex viscosity of the telechelic PDMS was dramatically enhanced, providing a value 4 orders of magnitude greater than that of the original PDMS. Remarkably, the structural and physical properties of PDMS were hardly changed upon terminal functionalization with another regioisomer of triptycene (1,4-Trip), which differs only in the substitution pattern.

Superionic Conduction in Co-Vacant P2-NaxCoO2 Created by Hydrogen Reductive Elimination

Abstract The layered P2‐NaxMO2 (M: transition metal) system has been widely recognized as electronic or mixed conductor. Here, we demonstrate that Co vacancies in P2‐NaxCoO2 created by hydrogen reductive elimination lead to an ionic conductivity of 0.045u2005Su2009cm−1 at 25u2009°C. Using in situ synchrotron X‐ray powder diffraction and Raman spectroscopy, the composition of the superionic conduction phase is evaluated to be Na0.61(H3O)0.18Co0.93O2. Electromotive force measurements as well as molecular dynamics simulations indicate that the ion conducting species is proton rather than hydroxide ion. The fact that the Co‐stoichiometric compound Nax(H3O)yCoO2 does not exhibit any significant ionic conductivity proves that Co vacancies are essential for the occurrence of superionic conductivity.