Details of a Researcher - ASAI Makoto

　

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Updated on 2024/04/17

ASAI Makoto

写真a

Affiliation: Research Centers and Institutes, Keio University Global Research Institute （Mita）

Position: Project Professor (Non-tenured)

Related Websites

http://www.columbia.edu/cu/kumargroup/

External Links

Message from the Faculty Member 【 Display / hide 】

I received B.S, and Ph.D. in Applied Physics and Physico-Informatics at Keio University in 2005 and 2009 working with Prof. Yasuhiro Koike on the development of novel polymer optical fibers with the highest bandwidth in the world. I was selected as a Research Fellow of the Japan Society for the Promotion of Science for 2009-2011. After working with Prof. Mitsuhiro Shibayama in University of Tokyo on the gelation mechanism of Tetra-PEG gel in simulation and experiment, I joined the Kumar group as a postdoctoral research scientist in Spring 2013. My current project is self-assembly of polymer grafted nanoparticles. From May 2017 I joined Keio University as Project Assistant Professor with joint appointment as research scientist at Columbia University.

Career 【 Display / hide 】

2019.10

-

Present

Arclev, Inc., Co-Founder / CEO
2013.05

-

Present

Columbia University in the City of New York, Chemical Engineering, Research Scientist
2017.05

-

2019.03

Keio University, Faculty of Science and Technology, Project Assistant Professor
2011.04

-

2013.03

The University of Tokyo, Institute of The Solid State Physics, Research Scientist
2009.04

-

2011.03

Keio University, Faculty of Science and Technology, Research Fellow of the Japan Society for the Promotion of Science

Academic Background 【 Display / hide 】

2001.04

-

2005.03

Keio University, Faculty of Science and Technology, Applied Physics and Physico-Informatics

University, Graduated, Other
2005.04

-

2006.09

Keio University, School of Integrated Design Engineering

Graduate School, Completed, Master's course
2006.09

-

2009.03

Keio University, School of Integrated Design Engineering

Graduate School, Completed, Doctoral course

Academic Degrees 【 Display / hide 】

B.S (Engineering), Keio University, Coursework, 2005.03
M.S (Engineering), Keio University, Coursework, 2006.09
Ph.D (Engineering), Keio University, Coursework, 2009.03

Research Areas 【 Display / hide 】

Natural Science / Biophysics, chemical physics and soft matter physics

Research Keywords 【 Display / hide 】

Soft Matter, Self-Assembly, Nanoparticles, Active Matter, Gels, Polymers, Glass Transition

Papers 【 Display / hide 】

Cluster growth from a dilute system in a percolation process

Fujinaga I., Yasuda T., Asai M., Chung U.i., Katashima T., Sakai T.

Polymer Journal （Polymer Journal) 52 （ 3 ） 289 - 297 2020.03

ISSN 00323896

　View Summary

© 2019, The Society of Polymer Science, Japan. Abstract: The gelation process has been explained in the framework of percolation models. Although the percolation models accurately predict the gelation behaviors above the overlap concentration of prepolymers (c*0), they do not predict the gelation behaviors below c*0. We measured the osmotic pressure during the gelation of a series of model polymer gels, namely, tetra-polyethylene glycol (PEG) gels. The osmotic pressure decreased during the gelation reaction and was constant after the sol–gel transition. These results suggest that the clusters grow and fill the system at the sol–gel transition point. As a result, the gels behaved as semidilute systems regardless of the initial polymer concentration. This representation of the sol–gel transition at the overlap condition of the critical clusters corresponds well to the aggregation process predictrion. These results will help better understanding of general percolation problems in the dilute regime.
- Access to Document (DOI)
Accurate Estimation of the Polymer Coverage of Hairy Nanoparticles

ASAI MakotoZHAO DanKUMAR K Sanat

Soft Matter （The Royal Society of Chemisry) 14 （ 38 ） 7906 - 7915 2018.08

Research paper (scientific journal), Joint Work, Accepted, ISSN 1744683X

　View Summary

© The Royal Society of Chemistry. Understanding and predicting the mechanisms underpinning the self-assembly of polymer-grafted nanoparticles (PGNPs) are important for controlling the engineering applications of these novel materials. The self-assembly of these materials is driven by their surfactancy, i.e., by the fact that the (inorganic) nanoparticles energetically dislike the (organic) polymer tethers. In previous work we developed a model in which a grafted polymer chain was treated as a rigid equivalent sphere (ES) which was impenetrable to the NPs, but completely penetrable to other ESs. This description, along with a geometric analogy with patchy particles, allowed us to facilely explain the self-assembly of PGNPs. However, since we model an ES as being completely penetrable to other ESs but impenetrable to the NPs the physical correspondence between a “real” grafted polymer and an ES is not clear. The application of the ES model to experiments and to computer simulations has therefore seen limited success, and only qualitative agreement has been obtained. In this paper, we develop a more realistic description, termed the modified ES (mES) model, based on the work of Daoud and Cotton on curved polymer brushes, which takes the impenetrability of the individual chain monomers into account. While this approach increases the complexity of our formalism, we find that the resulting mES model quantitatively captures computer simulation results on the structure of the PGNPs and also quantitatively explains their self-assembly over a broad range of conditions.
- Access to Document (DOI)
Surface Fluctuations Dominate the Slow Glassy Dynamics of Polymer-Grafted Colloid Assemblies

ASAI MakotoCACCIUTO AngeloKumar K Sanat

ACS Central Science （American Chemical Society) 4 （ 9 ） 1179 - 1184 2018.08

Research paper (scientific journal), Joint Work, Accepted, ISSN 23747943

　View Summary

© 2018 American Chemical Society. Colloids grafted with a corona layer of polymers show glassy behavior that covers a wide range of fragilities, with this behavior being tunable through variations in grafting density and grafting chain length. We find that the corona roughness, which is maximized for long chain lengths and sparse grafting, is directly correlated to the concentration-dependence of the system relaxation time (fragility). Relatively rougher colloids result in stronger liquids because their rotational motions become orientationally correlated across the whole system even at low particle loadings leading to an essentially Arrhenius-like concentration-dependence of the relaxation times near the glass transition. The smoother colloids do not show as much orientational correlation except at higher densities leading to fragile behavior. We therefore propose that these materials are an ideal model to study the physical properties of the glass transition.
- Access to Document (DOI)
Impact of the Distributions of Core Size and Grafting Density on the Self-Assembly of Polymer Grafted Nanoparticles

Bachhar, Nirmalya; Jiao, Yang; Asai, Makoto; Akcora, Pinar; Bandyopadhyaya, Rajdip; Kumar, Sanat

Macromolecules （American Chemical Society) 50 （ 19 ） 7730 - 7738 2017.09

Research paper (scientific journal), Joint Work, Accepted
- Access to Document (DOI)
Polymer-Grafted Nanoparticle Membranes with Controllable Free-Volume

Connor Bilchak, Eileen Buenning, Makoto Asai, Kai Zhang, Christopher Durning, Sanat Kumar, Yucheng Huang, Brian Benicewicz, David Gidley, Shiwang Cheng, Alexei Sokolov, Matteo Minelli, Ferruccio DoghieriASAI Makoto

Macromolecules （American Chemical Society) 50 （ 18 ） 7111 - 7120 2017.09

Research paper (scientific journal), Joint Work, Accepted
- Access to Document (DOI)

Research Projects of Competitive Funds, etc. 【 Display / hide 】

Entropy-Driven Self-Assembly of Soft Materials

2020.04

-

2025.03

MEXT,JSPS, Grant-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (C), Principal investigator

Awards 【 Display / hide 】

International Young Scientist Fellowship

2018.04, Chinese Academy of Science, Institute of Physics

Type of Award： International academic award (Japan or overseas), Country： China
International Young Scientist Fellowship

2018.04, Chinese Academy of Science, Institute of Physics

Type of Award： International academic award (Japan or overseas), Country： China
the Marie Sklodowska-Curie Actions Seal of Excellence

Makoto Asai, David Wales, 2018.03, European Commission, Entropy Driven Self-Assembly of Soft Materials

Type of Award： International academic award (Japan or overseas)
the Marie Sklodowska-Curie Actions Seal of Excellence

Makoto Asai, David Wales, 2018.03, Entropy Driven Self-Assembly of Soft Materials
the Marie Sklodowska-Curie Actions Seal of Excellence

Makoto Asai, Daan Frenkel, 2017.04, European Commission, Predicting polymorphism in self-assembling soft materials

Type of Award： International academic award (Japan or overseas)

Courses Taught 【 Display / hide 】

NEW SOCIAL SYSTEM AND TECHNOLOGIES OF SOCIETY5.0

2024
MUFG ENDOWED COURSE : REBUILDING OF "TRUST" TOWARDS SUSTAINABLE SOCIETY: "2040" AND BEYOND 2

2024
MUFG ENDOWED COURSE : REBUILDING OF "TRUST" TOWARDS SUSTAINABLE SOCIETY: "2040" AND BEYOND 1

2024
INTERNSHIP D(GLOBAL ENVIRONMENTAL SYSTEM LEADERS PROGRAM)

2024
INTERNSHIP C(GLOBAL ENVIRONMENTAL SYSTEM LEADERS PROGRAM)

2024

Courses Previously Taught 【 Display / hide 】

環境情報システム構築法

Keio University

2018.04

-

2019.03
,
Spring Semester, Lecture, Lecturer outside of Keio, 20people
Environmental Information System Architecture

Keio University

2017.04

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2018.03
,
Spring Semester, Lecture, Lecturer outside of Keio, 1h, 20people

Social Activities 【 Display / hide 】

Reviewer of Japan Society for the Promotion of Science Postdoctoral Fellowship for Researchers in US and EU

2016.06

-

Present

Memberships in Academic Societies 【 Display / hide 】

American Physical Society,

2013

-

Present