Shinji Imaizumi
Tokyo Institute of Technology
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Publication
Featured researches published by Shinji Imaizumi.
ACS Nano | 2010
Pritesh Hiralal; Shinji Imaizumi; Husnu Emrah Unalan; Hidetoshi Matsumoto; Mie Minagawa; Markku Rouvala; Akihiko Tanioka; G.A.J. Amaratunga
Solid-state and flexible zinc carbon (or Leclanche) batteries are fabricated using a combination of functional nanostructured materials for optimum performance. Flexible carbon nanofiber mats obtained by electrospinning are used as a current collector and cathode support for the batteries. The cathode layer consists of manganese oxide particles combined with single-walled carbon nanotubes for improved conductivity. A polyethylene oxide layer containing titanium oxide nanoparticles forms the electrolyte layer, and a thin zinc foil is used as the anode. The battery is shown to retain its performance under mechanically stressed conditions. The results show that the above configuration can achieve solid-state mechanical flexibility and increased shelf life with little sacrifice in performance.
Applied Physics Letters | 2008
Husnu Emrah Unalan; Di Wei; Kenichi Suzuki; Sharvari Dalal; Pritesh Hiralal; Hidetoshi Matsumoto; Shinji Imaizumi; Mie Minagawa; Akihiko Tanioka; Andrew J. Flewitt; W. I. Milne; G.A.J. Amaratunga
Zinc oxide (ZnO) nanowires (NWs) grown on carbon fibers using a vapor transport and condensation approach are used as the cathode of a photoelectrochemical cell. The carbon fibers were obtained by electrospray deposition and take the form of a flexible carbon fabric. The ZnO NW on carbon fiber anode is combined with a “black dye” photoabsorber, an electrolyte, and a platinum (Pt) counterelectrode to complete the cell. The results show that ZnO NW and carbon fibers can be used for photoinduced charge separation/charge transport and current collection, respectively, in a photoelectrochemical cell.
ACS Applied Materials & Interfaces | 2013
Hidetoshi Matsumoto; Shinji Imaizumi; Yuichi Konosu; Minoru Ashizawa; Mie Minagawa; Akihiko Tanioka; Wei Lu; James M. Tour
The graphene nanoribbon (GNR)/carbon composite nanofiber yarns were prepared by electrospinning from poly(acrylonitrile) (PAN) containing graphene oxide nanoribbons (GONRs), and successive twisting and carbonization. The electrospinning process can exert directional shear force coupling with the external electric field to the flow of the spinning solution. During electrospinning, the well-dispersed GONRs were highly oriented along the fiber axis in an electrified thin liquid jet. The addition of GONRs at a low weight fraction significantly improved the mechanical properties of the composite nanofiber yarns. In addition, the carbonization of the matrix polymer enhanced not only the mechanical but also the electrical properties of the composites. The electrical conductivity of the carbonized composite yarns containing 0.5 wt % GONR showed the maximum value of 165 S cm(-1). It is larger than the maximum value of the reported electrospun carbon composite yarns. Interestingly, it is higher than the conductivities of both the PAN-based pristine CNF yarns (77 S cm(-1)) and the monolayer GNRs (54 S cm(-1)). These results and Raman spectroscopy supported the hypothesis that the oriented GONRs contained in the PAN nanofibers effectively functioned as not only the 1-D nanofiller but also the nanoplatelet promoter of stabilization and template agent for the carbonization.
ACS Applied Materials & Interfaces | 2011
Shinji Imaizumi; Hidetoshi Matsumoto; Yuichi Konosu; Kazuma Tsuboi; Mie Minagawa; Akihiko Tanioka; Krzysztof Koziol; Alan H. Windle
Multiwalled carbon nanotube (MWNT)/poly(vinyl butyral) (PVB) composite nanofibers were prepared by electrospinning, successive twisting and heat treatment. The MWNTs were highly oriented in an electrified thin jet during electrospinning. The heat treatment of the twisted electrospun nanofiber yarns produced the characteristics of the CNT in the composite nanofiber yarns and enhanced their electrical properties, mechanical properties, and thermal properties. The electrical conductivity of the heated yarn was significantly enhanced and showed the maximum value of 154 S cm(-1) for the yarn heated at 400 °C. It is an order of magnitude higher than other electrospun CNT composite materials. These results demonstrated that the novel top-down process based on electrospinning, twisting, and heat treatment provide a promising option for simple and large-scale manufacture of CNT assemblies.
Applied Physics Express | 2011
Yan Yu; Hiroshi Wada; Junichi Inoue; Shinji Imaizumi; Yuichi Kounosu; Kazuma Tsuboi; Hidetoshi Matsumoto; Minoru Ashizawa; Takehiko Mori; Mie Minagawa; Akihiko Tanioka
An unzipped graphene oxide nanoribbon is patterned by surface selective deposition or inkjet printing, and its successive reduction to a graphene nanoribbon by vacuum annealing leads to highly conducting transparent graphene nanoribbon films. Such graphene nanoribbon films are used as source and drain electrodes in bottom-contact organic transistors based on pentacene and sexithiophene as well as C60.
RSC Advances | 2012
Shinji Imaizumi; Hidetoshi Matsumoto; Minoru Ashizawa; Mie Minagawa; Akihiko Tanioka
In the present paper, we report a novel ion-exchange carbon nanomaterial, surface sulfonated carbon nanofiber (S-CNF) fabrics, with a high surface area and high ion-exchange and adsorption capacities. S-CNF fabrics bearing SO3H groups were prepared by electrospinning, successive carbonization and sulfonation. We observed a nanosize effect, in which the surface area, and ion-exchange and adsorption capacities significantly increase with a decrease in the fiber diameter. The prepared fabrics with a diameter of 80 nm had the maximum values for the total pore surface area of 32.2 m2 g−1, the ion-exchange capacity of 2.94 mmol g−1, and an adsorption capacity of 943.1 mg g−1 for methylene blue (MB). The MB adsorption capacity is two times higher than that of commercial activated carbons. These results highlight the fact that the surface functionalized CNF fabrics with ionic groups are promising materials for high-capacity ion-exchangers.
Polymer Journal | 2009
Shinji Imaizumi; Hidetoshi Matsumoto; Kenichi Suzuki; Mie Minagawa; Masaru Kimura; Akihiko Tanioka
Archive | 2014
望 瀧口; Nozomi Takiguchi; 伸治 今泉; Shinji Imaizumi; 正則 岩崎; Masanori Iwasaki
Technical Textiles/Technische Textilien | 2015
英俊 松本; Hidetoshi Matsumoto; 伸治 今泉; Shinji Imaizumi; 祥平 増田; Shohei Masuda; 裕一 鴻巣; Yuichi Konosu; 実 芦沢; Minoru Ashizawa; 明彦 谷岡; Akihiko Tanioka
Archive | 2015
Nozomi Takiguchi; Shinji Imaizumi; Masanori Iwasaki