TY - JOUR
T1 - Preparation of periodic mesoporous organosilica with large mesopores using silica colloidal crystals as templates
AU - Muramoto, Naho
AU - Sugiyama, Tomoaki
AU - Matsuno, Takamichi
AU - Wada, Hiroaki
AU - Kuroda, Kazuyuki
AU - Shimojima, Atsushi
N1 - Funding Information:
The authors are grateful to Dr T. Shibue (Materials Characterization Central Lab., Waseda Univ.), Mr T. Hirohashi and Ms A. Komatsu (Waseda Univ.) for solid-state NMR measurements, Mr R. Kajiya and Ms M. Hayase (Waseda Univ.) for liquid-state NMR measurements, Mr M. Naoe for N2 adsorption–desorption analysis, Mr H. Otsuji (Kagami Memorial Research Institute for Materials Science and Technology, Waseda Univ.), Mr K. Hirota, Ms Y. Saito, Ms M. Sasaki and Ms Y. Yamada (Waseda Univ.) for SEM observation, Mr Y. Shimasaki and Mr T. Nakaya (Waseda Univ.) for TEM observation, Dr C. Urata (AIST), Dr N. Sato, Ms H. Fukui, Ms L. Cheng, Mr T. Hayashi, Mr G Koinuma, Mr A. Sakamoto, Ms S. Nagae, Mr T. Watanabe and Mr T. Hikino (Waseda Univ.) for fruitful discussion. This work was supported in part by Grant-in-Aid for Scientific Research (A) (Grant Number JP19H00833) and (B) (Grant Number JP20H02826). T. M. acknowledges the support from the Grant-in-Aid for JSPS Fellows (Grant Number JP19J13784).
Publisher Copyright:
© 2020 The Royal Society of Chemistry.
PY - 2020/11/7
Y1 - 2020/11/7
N2 - Organosiloxane-based mesoporous materials with periodically ordered pores (periodic mesoporous organosilica, PMO) have many applications due to their various organic functions, high surface areas, and large pore volumes. Conventional methods using surfactant templates (soft templates) are limited in terms of the diversity of organosilane precursors and precise control over the pore size in a relatively large mesopore region (10-50 nm). This paper demonstrates the preparation of PMOs with precisely controlled pore sizes (>10 nm in diameter) and various organosiloxane frameworks, using colloidal crystals of monodisperse silica nanospheres as a template. An inverse opal structure with interconnected spherical mesopores was obtained through polycondensation of hydrolyzed organoalkoxysilanes [(EtO)3Si-R-Si(OEt)3, R = C2H4, CHCH, and C6H4; PhSi(OEt)3], within the voids of silica colloidal crystals, followed by the preferential dissolution of silica under well-controlled basic conditions. The pore size varied depending on the size of the silica nanospheres. The versatility of this method will allow for the wide tuning of the physical and chemical properties of organosiloxane-based mesoporous materials.
AB - Organosiloxane-based mesoporous materials with periodically ordered pores (periodic mesoporous organosilica, PMO) have many applications due to their various organic functions, high surface areas, and large pore volumes. Conventional methods using surfactant templates (soft templates) are limited in terms of the diversity of organosilane precursors and precise control over the pore size in a relatively large mesopore region (10-50 nm). This paper demonstrates the preparation of PMOs with precisely controlled pore sizes (>10 nm in diameter) and various organosiloxane frameworks, using colloidal crystals of monodisperse silica nanospheres as a template. An inverse opal structure with interconnected spherical mesopores was obtained through polycondensation of hydrolyzed organoalkoxysilanes [(EtO)3Si-R-Si(OEt)3, R = C2H4, CHCH, and C6H4; PhSi(OEt)3], within the voids of silica colloidal crystals, followed by the preferential dissolution of silica under well-controlled basic conditions. The pore size varied depending on the size of the silica nanospheres. The versatility of this method will allow for the wide tuning of the physical and chemical properties of organosiloxane-based mesoporous materials.
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U2 - 10.1039/d0nr03837g
DO - 10.1039/d0nr03837g
M3 - Article
C2 - 32724951
AN - SCOPUS:85094983830
SN - 2040-3364
VL - 12
SP - 21155
EP - 21164
JO - Nanoscale
JF - Nanoscale
IS - 41
ER -