Masashi Kunitake

Prof. Dr. Masashi Kunitake

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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 September 2012 in Langmuir
Verified
Journal Article
Closed access
RTRyota Tanoue
Ryota Tanoue
RHRintaro Higuchi
Rintaro Higuchi
KIKiryu Ikebe
Kiryu Ikebe
SUShinobu Uemura
Shinobu Uemura
NKNobuo Kimizuka
Nobuo Kimizuka
MKMasashi Kunitake
Masashi Kunitake

16 January 2015 in Analytical Chemistry
Verified
Journal Article
Closed access
Eisuke KurayaEisuke Kuraya
Eisuke Kuraya
SNShota Nagatomo
Shota Nagatomo
KSKouhei Sakata
Kouhei Sakata
DKDai Kato
Dai Kato
ONOsamu Niwa
Osamu Niwa
MKMasashi Kunitake
Masashi Kunitake

10 September 2018 in Scientific Reports
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Journal Article
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SWSatoshi Watanabe
Satoshi Watanabe
HEHiroshi Era
Hiroshi Era
MKMasashi Kunitake
Masashi Kunitake
Two-wavelength infrared responsive soft actuators composed of rare-earth-oxide particles composited in a thermoresponsive hydrogel have been constructed. Because Nd2O3 and Yb2O3 particles possess independent narrow infrared adsorption at 808 and 980 nm, respectively, the vicinity of the particles in the gel can be individually heated by irradiation at each adsorption wavelength, inducing a local volume phase transition. The wavelength-selective volume phase transition can be controlled based on the combination of the particles incorporated in the gels and the wavelength of the irradiation laser at the optimized water temperature. Only the alternatively correct combinations successfully induced selective local clouding at the irradiation spots in the gel sheets. The original transparency of the gel was immediately recovered by turning off the light. Furthermore, rod-shaped block gels with Nd2O3 and Yb2O3 particles separately arranged on the left and right sides at the bottom of the rods were prepared to demonstrate wavelength-selective bending motion. The correct light combination caused reversible bending motion of only the side of the rod gel with the corresponding adsorbed particles.

14 March 2023 in Journal of Colloid and Interface Science
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Journal Article
Closed access
KNKodai Nakao
Kodai Nakao
KNKoji Noda
Koji Noda
HHHinako Hashimoto
Hinako Hashimoto
MNMayuki Nakagawa
Mayuki Nakagawa
TNTaisei Nishimi
Taisei Nishimi
MKMasashi Kunitake
Masashi Kunitake

1 April 2014 in Current Opinion in Colloid & Interface Science
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Journal Article
Closed access
MKMasashi Kunitake
Masashi Kunitake
RHRintaro Higuchi
Rintaro Higuchi
RTRyota Tanoue
Ryota Tanoue
SUShinobu Uemura
Shinobu Uemura

6 January 2023 in ACS Omega
Verified
Journal Article
Open access
SWSatoshi Watanabe
Satoshi Watanabe
THTaiki Hayashida
Taiki Hayashida
MIMasaru Iwai
Masaru Iwai
YIYusuke Inomata
Yusuke Inomata
MKMasashi Kunitake
Masashi Kunitake
Tetsuya  Kida Tetsuya Kida
Tetsuya Kida
We demonstrate the fabrication of millimeter-sized single crystals of 0D-Cs4PbBr6 grown in a supersaturated solution consisting of organic solvents without HBr (aq). One of the precursors, CsBr, was dissolved in ethylene glycol (EG) mixed with dimethyl sulfoxide, which is a good solvent for the other precursor, PbBr2. At a solvent ratio of 20 vol % EG, the solubility of cesium bromide decreased and the title compound, Cs4PbBr6, was selectively formed, whereas, with an EG ratio of 80 vol %, 3D-CsPbBr3 was formed. A phase diagram (solubility curve) of Cs4PbBr6 in the mixed solvent containing 20 vol % EG was obtained by visually observing dissolution and crystal precipitation while changing the temperature. Because the solubility was proportional to the temperature, the solubility curve demonstrated an upper critical solution phenomenon. The solubility near the boiling point of the solution (150 °C) was approximately 0.14 M. A single crystal of Cs4PbBr6 was formed by growing a seed crystal in a supersaturated solution on the low-temperature side of the solubility curve. X-ray analysis established the crystal structure; a fluorescence emission at 520 nm with a full width at half maximum of 20 nm confirms the composition of the single crystal to be Cs4PbBr6.