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A metal-free covalent triazine framework (CTF) was synthesized from 2,4,6-tricyano-1,3,5-triazine (TCT) through open-system and liquid-phase synthesis using trifluoromethanesulfonic acid as both a ...

Oxygen-containing carbon materials have been studied extensively because of their excellent dispersibility, absorptivity, separability, and supportability of catalysts. However, structural control by existing top-down methods is almost impossible. Our group has demonstrated that phloroglucinol (PG, 1,3,5-trihydroxybenzene) can be a promising raw material to synthesize structurally controlled oxygen-containing carbon materials. In this study, in addition to PG, hexahydroxybenzene (HHB), which has more oxygen and high symmetry, was used as the raw material, and a Lewis acid catalyst, tris (pentafluorophenyl) borane (TPB), was used to enhance the structural control rate and the removability of catalysts from the carbonized samples. The solubility of heat-treated HHB was lower than that of heat-treated PG, but the oxygen content of heat-treated HHB was higher than that of heat-treated PG even at 673 K. By adding TPB to PG, dibenzofuran-like structures formed, and the structural control rate increased up to 93.6%. Besides, the content of fluorine in the catalyst was reduced to 0%, indicating that TPB can be a promising recyclable catalyst to promote the structural control rate of carbonized PG.

Antimicrobial surfactants contained in mouthrinse have excellent efficacy but are not retained on the tooth surface (are rinsed away) due to their low water resistance and thus do not exhibit sustained antibacterial activity. We have developed a new coating method using graphene oxide (GO) that retains the surfactant on the tooth surface even after rinsing with water, thus providing a sustained antibacterial effect. Ultra-thin films of GO and antimicrobial agent were prepared by (1) applying GO to the substrate surface, drying, and thoroughly rinsing with water to remove excess GO to form an ultrathin film (almost a monolayer, transparent) on the substrate surface, then (2) applying antimicrobial cationic surface active agents (CSAAs) on the GO film to form a composite coating film (GO/CSAA). GO/CSAA formation was verified by scanning electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, and ζ-potential and contact angle measurements. GO/CSAA was effective at inhibiting the growth of oral pathogens even after up to 7 days of storage in water, and antibacterial activity was recovered by reapplication of the CSAA. Antibacterial GO/CSAA films were also formed on a tooth substrate. The results suggest that GO/CSAA coatings are effective in preventing oral infections.

Oxygen-containing carbon materials such as graphene oxide have been extensively studied because of their high dispersibility. However, the oxygen-containing functional groups in most carbon materials are not controlled. Uncontrollability of the synthesis is also one of factors that prevent industrialization. Carbon materials derived from phloroglucinol (PG), which show high solubility/dispersibility and controllability of functional groups, have been developed recently by our group. The high performance of carbonized PG originates from the thermally stable backbone structure of the benzene ring with hydroxy groups of PG. However, the degree of carbonization was low. In this study, five heteropoly acids (HPAs), which are thermally stable homogeneous strong acid catalysts, were used to promote carbonization of PG without losing the controllability of functional groups and the dispersibility. HPAs promoted etherification of hydroxy groups followed by C=C coupling reactions (furan cyclization) at 523 K. Furthermore, it was confirmed that particularly furan structures, which contribute to solubility/dispersibility in solvents, and thermal stability in air, could be maintained at 673 K as suggested by spectroscopies and thermogravimetric-differential thermal analysis. Among five HPAs, phosphotungstic acid worked as the excellent catalyst to promote carbonization of PG containing furan structures, exhibiting high solubility/dispersibility and high thermal stability in air.

Pentagons in carbon materials have attracted attentions because of the potential high chemical reactivity, band gap control, and electrochemical activity. However, it is challenging to prepare a carbon film with high pentagon density because of the curvature and the high reactivity caused by the presence of pentagons, and it is also challenging to estimate the percentage of pentagons in carbon materials because of the limitation of current analytical techniques. In this work, the percentage of pentagons in carbon materials was experimentally estimated for the first time using experimental and calculated C1s X-ray photoelectron spectroscopy and elemental analysis. Carbon films with 7% of pentagons (40% of pentagons compared to the raw material) with electrical resistivity of 1.1 × 104 Ω meter were prepared by heat treatment of corannulene at 873 K. On the other hand, fluoranthene and fullerene remained as non-film solid and powder without forming films at 873 K. Experimental and calculated Raman and IR spectra revealed the peaks of different types of pentagons. Decrement of pentagons in corannulene and fluoranthene heated at high temperatures can be explained mainly by the scission of C=C bond in pentagons, as suggested by the results of reactive molecular dynamics simulation (ReaxFF).

Oxygen-containing carbon materials such as graphene oxide have been studied intensively for a decade because of the high oxygen content, which is beneficial to disperse carbon materials in solutions and to support either metals or metal oxides on carbon materials. However, various oxygen-containing functional groups exist on carbon materials and controlling the structures is almost impossible. In this work, phloroglucinol (PG), which has a symmetrical structure with three hydroxyl groups relative to six aromatic carbon atoms, was found to be the best precursor among PG, cyanuric acid, trimesic acid, and melamine because of the high yield (63 wt%) at 573 K even in an open system which is essential for mass production. The materials synthesized from PG also showed the high dispersibility and/or solubility in solvents (N-methyl-2-pyrrolidone and N,N-dimethylformamide) and the low temperature to form carbon materials (573 K), which can be explained from (002) and (10) in X-ray diffraction pattern. X-ray photoelectron spectroscopy, Fourier transform infrared spectrometer, carbon-13 nuclear magnetic resonance with the aid of calculation of both spectra and carbonization mechanisms revealed that the high solubility of carbonized PG originates from the presence of ether and cyclic ether, which were formed from dehydration of hydroxy groups, and also some remained hydroxyl groups in carbonized PG. Oxygen-containing groups in carbonized PG were effective as an antioxidant. In addition, the coating of carbonized PG on silica nanoparticles imparted conductivity and lubricity to silica nanoparticles.

Acetylene black, activated carbon, and Ketjenblack were subjected to microwave heating up to 1000 °C under N2 atmosphere to rapidly convert them into graphene-like materials. Few carbon materials exhibit a favorable increase in the intensity of the G’ band with increasing temperature. Upon electric field heating of acetylene black to 1000 °C, the observed relative intensity ratios of D and G bands (or G’ and G band) were equivalent to those of reduced graphene oxide heated under identical conditions. In addition, microwave irradiation under different conditions, i.e., electric field or magnetic field heating, produced graphene of qualities different from those of the same carbon material conventionally treated at the same temperature. We propose that this difference arises from the different mesoscale temperature gradients. The conversion of inexpensive acetylene black and Ketjenblack into graphene-like materials within 2 min of microwave heating is a major achievement toward low-cost mass synthesis of graphene.

CO2 removal and sensing, especially by amine groups, are necessary to prevent global warming. However, understanding the dynamic mechanism of CO2 capture on nitrogen sites remains challenging. We f...

Edges of carbon materials have been known to work as active sites for various applications such as catalysts, adsorbent, and electrodes, but selecting precursors for carbon materials with controlled edges in the absence of metallic substrate is challenging. This work developed a method to select the superior precursors instantaneously using molecular dynamic simulation. This simulation predicted that hydrogen in precursors gasified and the hydrogen attacked the active sites in precursors upon carbonization, causing the decrement of active sites. Thus, it is essential to reduce the concentration of hydrogen in precursors and it is also necessary to introduce reactive functional groups near the active site to protect the active sites. We indeed synthesized the selected precursors such as diethynyl anthracene, diethynyl chrysene, divinyl naphthyridine, and divinyl phenanthroline and proved that edges in those precursors were maintained even after carbonization at 773 K using diffuse reflectance infrared Fourier transform and X-ray photoelectron spectroscopy with the aid of spectra simulated by density functional theory calculation. Especially, ca. 100% of edge structures of zigzag edges and armchair edges in diethynyl anthracene and diethynyl chrysene was maintained even after carbonization at 773 K.

Four different porphyrin-imide dyads bearing different central metals (zinc or rhodium) and different substituents on the porphyrin macrocycles (tert-butyl or methoxy) were synthesized for single molecular diode measurements. The molecules were designed to separate the donor component (porphyrin) from the acceptor component (imide) by bonding in a perpendicular arrangement, thus enhancing the rectification properties. UV/Vis absorption spectra and density functional theory calculations showed that the design was successful and that the molecular orbitals of the dyads were the summation of the two components, with minimal interaction between them. The effect of the central metal was found to be significant, with the lowest energy absorption for the zinc dyads being attributed to the mixed state of charge transfer from porphyrin to imide and the Q band, whereas that of the rhodium dyads indicated insignificant charge-transfer character.

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