TY - JOUR
T1 - Transformation of Mesostructured Silica Nanoparticles into Colloidal Hollow Nanoparticles in the Presence of a Bridged-Organosiloxane Shell
AU - Yamamoto, Eisuke
AU - Uchida, Saki
AU - Shimojima, Atsushi
AU - Wada, Hiroaki
AU - Kuroda, Kazuyuki
N1 - Funding Information:
*E-mail: kuroda@waseda.jp. ORCID Atsushi Shimojima: 0000-0003-2863-1587 Kazuyuki Kuroda: 0000-0002-1602-0335 Author Contributions The manuscript was written through contributions of all authors. E.Y. contributed to the design of concept and preparation of manuscript under the supervision of K.K. E.Y. and S.U. carried out the experiment. A.S., H.W., and K.K. discussed the data and revised important contents in the manuscript. Funding This work was supported in part by two grants of JSPS KAKENHI (Grant-in-Aid for Challenging Exploratory Research (No. 15K13809) and Grant-in-Aid for JSPS Fellows (No. 15J06919)). Grant-in-Aid for Strategic International Collaborative Research Program (SICORP) “France-Japan Joint Call on MOLECULAR TECHNOLOGY” from the Japan Science and Technology Agency is also acknowledged. Notes The authors declare no competing financial interest.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2018/1/23
Y1 - 2018/1/23
N2 - Hollow siloxane-based nanoparticles (HSNs) have attracted significant attention because of their unique properties and applications. Recently, it was discovered that the simple covering of silica nanoparticles with an organosiloxane shell leads to the spontaneous formation of HSNs; however, the detailed mechanism of their formation has not yet been established. In this study, colloidal 30 nm HSNs were prepared by adding organically bridged alkoxysilane to an aqueous dispersion of mesostructured silica-surfactant composite nanoparticles, and the temporal changes of the morphology and chemical state of the nanoparticles were monitored to elucidate the formation mechanism. Core silica was dissolved after the formation of the core-shell structured nanoparticles, and almost all the dissolved silicate species were incorporated in the organosiloxane shell, changing the shell thickness. Two conditions were essential for silica dissolution induced by covering with organosiloxane: (i) presence of a sufficient amount of uncondensed Si-OH groups in the organosiloxane shell, and (ii) elevated temperature and pH for the promotion of the hydrolysis of silica. These findings will enable the fabrication of various HSNs through organosiloxane-induced silica dissolution and redeposition.
AB - Hollow siloxane-based nanoparticles (HSNs) have attracted significant attention because of their unique properties and applications. Recently, it was discovered that the simple covering of silica nanoparticles with an organosiloxane shell leads to the spontaneous formation of HSNs; however, the detailed mechanism of their formation has not yet been established. In this study, colloidal 30 nm HSNs were prepared by adding organically bridged alkoxysilane to an aqueous dispersion of mesostructured silica-surfactant composite nanoparticles, and the temporal changes of the morphology and chemical state of the nanoparticles were monitored to elucidate the formation mechanism. Core silica was dissolved after the formation of the core-shell structured nanoparticles, and almost all the dissolved silicate species were incorporated in the organosiloxane shell, changing the shell thickness. Two conditions were essential for silica dissolution induced by covering with organosiloxane: (i) presence of a sufficient amount of uncondensed Si-OH groups in the organosiloxane shell, and (ii) elevated temperature and pH for the promotion of the hydrolysis of silica. These findings will enable the fabrication of various HSNs through organosiloxane-induced silica dissolution and redeposition.
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U2 - 10.1021/acs.chemmater.7b04860
DO - 10.1021/acs.chemmater.7b04860
M3 - Article
AN - SCOPUS:85041030300
SN - 0897-4756
VL - 30
SP - 540
EP - 548
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 2
ER -