4.7 Article

Diatom-inspired self-assembly for silica thin sheets of perpendicular nanochannels

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 584, Issue -, Pages 647-659

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2020.10.114

Keywords

Silicate transport micelles; Small-angle X-ray and neutron scattering; Freeze-fracture replica transmission electron microscopy

Funding

  1. NSF [DMR-0520547]
  2. European Union's Horizon 2020 research and innovation programme under the SINE2020 project [654000]
  3. Ministry of Science and Technology of Taiwan
  4. program of user cultivation of Taiwan neutron facility (under National Synchrotron Radiation Research Center) are acknowledged. [2009-2-074-4]

Ask authors/readers for more resources

The research reveals the potential of biomimetic silica self-organization for synthesizing innovative silica-based nanomaterials, with the use of block copolymer micelles shelled with charged catanionic surfactants directing the silication process. By adjusting the ratios of surfactants, mesoporous silica nanochannel plates with perpendicular orientation were successfully synthesized, laying the groundwork for innovative materials inspired by diatom frustules.
Hypothesis: Multistage silicate self-organization into light-weight, high-strength, hierarchically patterned diatom frustules carries hints for innovative silica-based nanomaterials. With sodium silicate in a biomimetic sol-gel system templated by a tri-surfactant system of hexadecyltrimethylammonium bromide, sodium dodecylsulfate, and poly(oxyethylene-b-oxypropylene-b-oxyethylene) (P123), mesoporous silica nanochannel plates with perpendicular channel orientation are synthesized. The formation process, analogous to that of diatom frustules, is postulated to be directed by an oriented self-assembly of the block copolymer micelles shelled with charged catanionic surfactants upon silication. Experiments: The postulated formation process for the oriented silica nanochannel plates was investigated using time-resolved small-angle X-ray and neutron scattering (SAXS/SANS) and freeze fracture replication transmission electron microscopy (FFR-TEM). Findings: With fine-tuned molar ratios of the anionic, cationic, and nonionic surfactants, the catanionic combination and the nonionic copolymer form charged, prolate ternary micelles in aqueous solutions, which further develop into prototype monolayered micellar plates. The prolate shape and maximized surfactant adsorption of the complex micelles, revealed from combined SAXS/SANS analysis, are of critical importance in the subsequent micellar self-assembly upon silicate deposition. Time-resolved SAXS and FFR-TEM indicate that the silicate complex micelles coalesce laterally into the prototype micellar nanoplates, which further fuse with one another into large sheets of monolayered silicate micelles of in-plane lamellar packing. Upon silica polymerization, the in-plane lamellar packing of the micelles further transforms to 2D hexagonal packing of vertically oriented silicate channels. The unveiled structural features and their evolution not only elucidate the previously unresolved self-assembly process of through-thickness silica nanochannels but also open a new line of research mimicking free-standing frustules of diatoms. (C) 2020 The Author(s). Published by Elsevier Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available