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Yajima, Takeshi*; Hinuma, Yoyo*; Hori, Satoshi*; Iwasaki, Rui*; Kanno, Ryoji*; Ohara, Takashi; Nakao, Akiko*; Munakata, Koji*; Hiroi, Zenji*
Journal of Materials Chemistry A, 9(18), p.11278 - 11284, 2021/05
Times Cited Count:23 Percentile:80.28(Chemistry, Physical)Fujii, Kotaro*; Yashima, Masatomo*; Hibino, Keisuke*; Shiraiwa, Masahiro*; Fukuda, Koichiro*; Nakayama, Susumu*; Ishizawa, Nobuo*; Hanashima, Takayasu*; Ohara, Takashi
Journal of Materials Chemistry A, 6(23), p.10835 - 10846, 2018/06
Times Cited Count:29 Percentile:68.41(Chemistry, Physical)Hamada, Takashi; Hasegawa, Shin; Fukasawa, Hideyuki*; Sawada, Shinichi; Koshikawa, Hiroshi; Miyashita, Atsumi; Maekawa, Yasunari
Journal of Materials Chemistry A, 3(42), p.20983 - 20991, 2015/11
Times Cited Count:36 Percentile:70.80(Chemistry, Physical)no abstracts in English
Taminato, So*; Hirayama, Masaaki*; Suzuki, Kota*; Kim, K.-S.*; Zheng, Y.*; Tamura, Kazuhisa; Mizuki, Junichiro; Kanno, Ryoji*
Journal of Materials Chemistry A, 2(34), p.17875 - 17882, 2014/11
Times Cited Count:22 Percentile:55.59(Chemistry, Physical)The surface structure of a lithium-rich layered material and its relation to intercalation properties were investigated by synchrotron X-ray surface structural analyses using LiRuO epitaxial-film model electrodes with different lattice planes of (010) and (001). Electrochemical charge-discharge measurements confirmed reversible lithium intercalation activity through both planes, corresponding to three-dimensional lithium diffusion within the LiRuO. The (001) plane exhibited higher discharge capacities compared to the (010) plane under high rate operation (over 5 C). Direct observations of surface structural changes by surface X-ray diffraction (XRD) and surface X-ray absorption near edge structure (XANES) established that an irreversible phase change occurs at the (010) surface during the first (de)intercalation process, whereas reversible structural changes take place at the (001) surface.
Matsumoto, Yoshihiro; Entani, Shiro; Koide, Akihiro*; Otomo, Manabu; Avramov, P.; Naramoto, Hiroshi*; Amemiya, Kenta*; Fujikawa, Takashi*; Sakai, Seiji
Journal of Materials Chemistry C, 1(35), p.5533 - 5537, 2013/09
Times Cited Count:32 Percentile:76.07(Materials Science, Multidisciplinary)Fukidome, Hirokazu*; Takahashi, Ryota*; Abe, Shunsuke*; Imaizumi, Kei*; Handa, Hiroyuki*; Kang, H. C.*; Karasawa, Hiromi*; Suemitsu, Tetsuya*; Otsuji, Taiichi*; Enta, Yoshiharu*; et al.
Journal of Materials Chemistry, 21(43), p.17242 - 17248, 2011/11
Times Cited Count:28 Percentile:62.37(Chemistry, Physical)Enomoto, Kazuyuki*; Takahashi, Shuichi*; Iwase, Takanori*; Yamashita, Takashi*; Maekawa, Yasunari
Journal of Materials Chemistry, 21(25), p.9343 - 9349, 2011/07
Times Cited Count:38 Percentile:71.44(Chemistry, Physical)The degradation manner of graft-type polymer electrolyte membranes consisting of hydrophilic poly(styrenesulfonic acid) (PSSA) graft polymers (grafts) and thermally and mechanically stable hydrophobic polymer substrates was examined in hot water. Severe weight loss was observed in PSSA-grafted cPTFE and ETFE films but not in a PSSA-grafted PEEK film. The decomposed extracts in water were characterized as PSSA during the whole course of degradation, clearly showing that the PSSA grafts detached from the fluorinated substrates without decomposition or scission of graft polymer chains. This is quite a new degradation manner for graft-type polymer electrolyte membranes; namely, hydrophilic PSSA grafts detach from hydrophobic polymer substrates due to swelling-induced stress at the interfacial boundary in the grafted films.
Brazhkin, V. V.*; Akola, J.*; Katayama, Yoshinori; Kohara, Shinji*; Kondrin, M. V.*; Lyapin, A. G.*; Lyapin, S. G.*; Tricot, G.*; Yagafarov, O.
Journal of Materials Chemistry, 21(28), p.10442 - 10447, 2011/07
Times Cited Count:18 Percentile:48.84(Chemistry, Physical)PO compound is an archetypical glass-forming oxide with a high hygroscopicity. We found that the quenching from the POmelt under ultrahigh pressures enables obtaining densified PO glasses with a residual densification up to 12% at normal conditions. These glasses have a low hygroscopicity and can exist under air conditions for several weeks. An examination of the structure of the new form of PO glass reveals a cardinal decrease of the volume of nanovoids in the glassy matrix.
Dopieralski, P.*; Anjukandi, P.*; Rckert, M.*; Shiga, Motoyuki; Ribas-Arino, J.*; Marx, D.*
Journal of Materials Chemistry, 21(23), p.8309 - 8316, 2011/06
The role played by polyethylene-like oligomers in transducing external tensile forces to benzo-cyclobutene mechanophores is investigated computationally. It is demonstrated that the oligomerchains do indeed exert a notable influence on the force-dependence of the activation energies of bothconrotatory and disrotatory ring-opening processes of a 1,2-disubstituted benzocyclobutene. This opens the doorway to tuning the properties of mechanoresponsive materials not only bychanging the properties of the mechanophore itself, but also by tailoring the force-transducing chain molecules attached to it. Furthermore, it is found that these chains even have a profound impact on the topology of the force-transformed potential energy surface in the vicinity of conrotatory transition states. Hitherto unexpected and most striking is the phenomenon that some of these conrotatory transition states are found to drive the system to disrotatory products.
Dopieralski, P.*; Anjukandi, P.*; Rckert, M.*; Shiga, Motoyuki; Ribas-Arino, J.*; Marx, D.*
Journal of Materials Chemistry, 21(23), p.8309 - 8316, 2011/06
Times Cited Count:50 Percentile:78.58(Chemistry, Physical)The role played by polyethylene-like oligomers in transducing external tensile forces to benzocyclobutene mechanophores is investigated computationally. It is demonstrated that the oligomer chains do indeed exert a notable influence on the force dependence of the activation energies of both conrotatory and disrotatory ring-opening processes of a cis 1,2-disubstitutedbenzocyclobutene. This opens the doorway to tuning the properties of mechanoresponsive materials not only by changing the properties of the mechanophore itself, but also by tailoring the force-transducing chain molecules attached to it.
Alam, M.*; Miserque, F.*; Taguchi, Mitsumasa; Boulanger, L.*; Renault, J. P.*
Journal of Materials Chemistry, 19(24), p.4261 - 4267, 2009/06
Times Cited Count:16 Percentile:45.33(Chemistry, Physical)The production of molecular hydrogen in the radiolysis with TiO grafted silica has been carefully studied using 10 MeV electrons. In all cases, H yield increases linearly with absorbed dose. Under the irradiation it was observed that with the increasing number of titanium dioxide deposition cycle a decrease in dihydrogen production were observed. A faster decrease in dihydrogen production was observed with a very small amount of titanium dioxide deposition i.e with an average thickness of 0.1 nm as measured by XPS. The productions of H were found to be decreased almost by 50 % with a TiO thickness at around 1 nm.
Uchida, Yoshiaki*; Ikuma, Naohiko*; Tamura, Rui*; Shimono, Satoshi*; Noda, Yohei; Yamauchi, Jun*; Aoki, Yoshio*; Nohira, Hiroyuki*
Journal of Materials Chemistry, 18(25), p.2950 - 2952, 2008/07
Times Cited Count:44 Percentile:75.68(Chemistry, Physical)We found out an unusual intermolecular magnetic interaction in the liquid-crystalline (LC) state of an all-organic radical compound on surface of water (73 C); the magnetic interaction actually allows the LC droplet on water to be attracted by a weak permanent magnet, whereas the crystalline phase did not respond to the magnet.
Kozai, Naofumi; Onuki, Toshihiko; Komarneni, S.*
Journal of Materials Chemistry, 17(12), p.2993 - 2996, 2002/12
Here we report the extremely high and selective uptake of selenium oxyanions by a novel exchanger, NiZn(OH)(OCOCH)・nHO that has brucite-type hydroxide layers with OCOCH anions in the interlayers. This Ni-Zn basic salt exhibited very high selectivity for Se(IV) (Kd = 9.0x10 ml/g with an initial Se(IV) concentration of 1x10 M) in the presence of 0.1M Cl solution while the well known anionic clay, MgAl(OH)NO・nHO showed a Kd of 6.0x10 ml/g under the same conditions. The uptake of Se(IV) on the Ni-Zn basic salt was found to be irreversible when treated with solutions containing 1N Cl, 1N NO, or 1N PO, while the Se(IV) sorbed on anionic clay was easily desorbed in a 1M Cl solution. This novel exchanger also showed high Kd (2.610 ml/g at an initial Se concentration of 110 M) for Se(VI) and therefore it is expected to be useful for decontamination and removal of selenium oxyanions from contaminated water.