Curriculum Vitaes

Rikukawa Masahiro

  (陸川 政弘)

Profile Information

Affiliation
Professor, Faculty of Science and Technology, Department of Materials and Life Sciences, Sophia University
Degree
工学士(上智大学)
工学修士(上智大学)
博士(工学)(上智大学)

Contact information
m-rikukasophia.ac.jp
Researcher number
10245798
J-GLOBAL ID
200901007918312440
researchmap Member ID
1000073369

1982-1985 Research of ion-conducting polymers
1985-1988 Research of electromagnetic shield
1988-1989 Research of optical recording disk
1989-1992 Research of ultra thin polymer film
1992-2008 Research of fuctional polymer and their opt-electrical properties

(Education)
I mainly teach Basic Organic Chemistry III, Polymer Chemistry IIIC, and Graduate Courses.
(Research)
My research fields are 1) polymer electrolyte fuel cells based on proton conducting polymers, 2) artificial bones based on biodegradable polymers, and 3) super-hierarchical structure and their characterizations based on electroconductive polymers.

(Subject of research)
Research of polymer electrolyte fuel cell
Research of conducting polymers
Study on Polymer thin Films
Study on Polymer Electrolyte
Systhesis and Electrical Properties of Phthalocyanines

(Proposed theme of joint or funded research)
Development of polymer electrolytes for fuel cell
Research of artificial bone
Synthesis of regioregular conducting polymers


Research History

 2

Papers

 309
  • Yoshifumi Hirotsu, Morgan L. Thomas, Yuko Takeoka, Masahiro Rikukawa, Masahiro Yoshizawa-Fujita
    SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS, 26(1), Dec 31, 2025  
    In recent years, the development of next-generation secondary batteries employing resource-abundant metals such as Na has garnered significant attention. However, the high reactivity of Na raises safety concerns, necessitating the development of safer devices. To address this, ionic liquids (ILs) and organic ionic plastic crystals (OIPCs) have emerged as promising novel electrolytes. Despite their potential, studies investigating the influence of cation structures on various properties remain scarce, particularly in composites where Na salts are introduced into OIPCs. This study focuses on the effects of cation species and Na-salt concentration in OIPCs, specifically in N,N-diethylpyrrolidinium bis(fluorosulfonyl)amide ([C2epyr][FSA]) and N-ethyl-N-isopropylpyrrolidinium bis(fluorosulfonyl)amide ([Ci3epyr][FSA]), with the addition of sodium bis(fluorosulfonyl)amide (NaFSA). The phase transition behavior, dissociation state of Na salts, and electrochemical properties exhibited significant differences based on the cationic structure of the OIPCs. The combination of each OIPC with Na salt resulted in liquid mixtures, and the ionic conductivity increased significantly as the Na salt concentration increased. High ionic conductivities were achieved with [C2epyr][FSA]/NaFSA (20 mol%) and [Ci3epyr][FSA]/NaFSA (10 mol%), showing values of 2.7 x 10-3 and 2.2 x 10-3 S cm-1 at 25 degrees C, respectively. Linear sweep voltammetry results indicated superior oxidative stability in the [Ci3epyr][FSA] system. Solvation numbers of Na+, influenced by differences in cationic side-chain structures, were determined to be 2.7 for the [C2epyr]+ system and 2.9 for the [Ci3epyr]+ system. The results suggest that controlling solvation numbers is a critical factor in the molecular design of high-performance ionic conductors.
  • Noriyuki Suzuki, Kanata Okajima, Daijiro Takayama, Bjarne L. Silkenath, Zheng Yang, Yuko Takeoka, Masahiro Rikukawa
    Current Organocatalysis, 12, Jan 8, 2025  
    Background: Developing environmentally benign processes, such as organic reactionsconducted in water, is desired from the view of sustainable technology. Concerning the palladiumcatalyzedborylation reactions of aryl halides in water, only a few examples have been reported. Objective: This study aimed to develop efficient methods for palladium-catalyzed borylation reactionsof aryl halides in water, not only increasing product yields but also extracting products withless organic solvents. Methods: We adopted polymer surfactants, such as diblock copolymers that consist of poly(Nisopropoylacrylamide)and a hydrophilic segment, and a poly(ethylene glycol)-based polymer thatconsists of poly(ethylene glycol) chain and 4-chloromethylbenzyl moiety. Results: Reactions using these polymers gave the borylation products in significantly higher yieldsthan that in pure water. The efficiency of the extraction process for the products from the reactionmixtures was evaluated, indicating that the polymer micelles enabled separation processes with lessorganic solvent. Conclusion: Applying polymer surfactants increased the product yields in Pd-catalyzed borylationof aryl halides, and it enabled the extraction of the products from the aqueous reaction mixture moreefficiently.
  • Noriyuki Suzuki, Nozomu Ebara, Rikito Arai, Chirika Takahashi, Tsai-Yu Hung, Yuko Takeoka, Masahiro Rikukawa, Yukie Yokota, Fu-Yu Tsai
    Catalysis Science & Technology, 15(3) 696-707, 2025  
    Pd complexes covalently tethered on thermoresponsive polymer catalysed coupling reactions in water.
  • Yoshifumi Hirotsu, Ryotaro Sekiguchi, Yuko Takeoka, Masahiro Rikukawa, Masahiro Yoshizawa-Fujita
    Bulletin of the Chemical Society of Japan, 97(10), Oct, 2024  
    Despite being safe for use in secondary Mg batteries, solid electrolytes exhibit lower ionic conductivities than those of traditional liquid electrolytes. Organic ionic plastic crystals-soft crystals with excellent thermal and electrochemical stabilities and ionic conductivities-are promising solid electrolytes. Herein, we investigated the effects of various anion species and Mg salt concentrations on the properties of pyrrolidinium-based organic ionic plastic crystals (N,N-diethylpyrrolidinium bis(fluorosulfonyl)amide [[C2epyr][FSA]] and N,N-diethylpyrrolidinium bis(trifluoromethylsulfonyl)amide [[C2epyr][TFSA]]) upon Mg(TFSA)2 addition. The Mg-ion transference number (tMg2+) was measured using the Vincent-Bruce method; ionic conductivity via impedance measurements; and phase transition via differential scanning calorimetry. The phase transition behavior, dissociation state of the Mg salt, and electrochemical properties varied with the organic ionic plastic crystal anionic structure. The FSA system became liquid when the Mg salt concentration exceeded 15 mol%. The ionic conductivity of the pyrrolidinium-based organic ionic plastic crystals increased substantially with the Mg salt concentration. In the solid state, [C2epyr][FSA]/Mg(TFSA)2 (5 mol%) (FT5) showed the highest ionic conductivity (2.9 × 10−4 S cm−1 at 25 °C). The tMg2+ of FT5 at 60 °C was 0.29. Mg exhibited redox behavior in FT5 but not in [C2epyr][TFSA]/Mg(TFSA)2 (5 mol%). The FSA− structure is suitable for Mg electrochemistry and will aid in developing high-performance secondary Mg batteries.
  • Takuto Ootahara, Kan Hatakeyama-Sato, Morgan L. Thomas, Yuko Takeoka, Masahiro Rikukawa, Masahiro Yoshizawa-Fujita
    ACS Applied Electronic Materials, Jul 29, 2024  

Misc.

 52

Books and Other Publications

 13

Presentations

 64

Research Projects

 29

Industrial Property Rights

 13

Social Activities

 2

Other

 5