scholarly journals Enhanced Hybridization and Nanopatterning via Heated Liquid-Phase Infiltration into Self-Assembled Block Copolymer Thin Films

2019 ◽  
Vol 12 (1) ◽  
pp. 1444-1453 ◽  
Author(s):  
Ashwanth Subramanian ◽  
Nikhil Tiwale ◽  
Gregory Doerk ◽  
Kim Kisslinger ◽  
Chang-Yong Nam
ACS Nano ◽  
2014 ◽  
Vol 8 (10) ◽  
pp. 10582-10588 ◽  
Author(s):  
Kevin G. Yager ◽  
Erica Lai ◽  
Charles T. Black

2019 ◽  
Vol 1 (2) ◽  
pp. 849-857 ◽  
Author(s):  
Alberto Alvarez-Fernandez ◽  
Karim Aissou ◽  
Gilles Pécastaings ◽  
Georges Hadziioannou ◽  
Guillaume Fleury ◽  
...  

Block copolymer-templated gold nanostructured surfaces of high refractive index due to controlled plasmonic nanoparticle shape.


2015 ◽  
Vol 3 (38) ◽  
pp. 19575-19581 ◽  
Author(s):  
G. Hauffman ◽  
A. Vlad ◽  
T. Janoschka ◽  
U. S. Schubert ◽  
J.-F. Gohy

Nanostructured thin film organic radical cathodes have been prepared from poly(styrene)-block-poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) diblock copolymers.


2014 ◽  
Vol 50 (3) ◽  
pp. 362-364 ◽  
Author(s):  
Hidenori Mizuno ◽  
Tetsuya Kaneko ◽  
Isao Sakata ◽  
Koji Matsubara

2006 ◽  
Vol 532-533 ◽  
pp. 165-168
Author(s):  
Yong Zhi Cao ◽  
Shen Dong ◽  
Ying Chun Liang ◽  
Tao Sun

As a “bottom-up” approach to nanostructures for nanofabrication, self-assembled block copolymer thin films have received much attention not only thanks to the scale of the microdomains but also due to the convenient shape tunability. In order to realize applications of self-assembled block copolymer thin films in nanotechnologies, control over microdomain spatial and orientational order is paramount. In this paper, using atomic force microscopy (AFM), we studied systemically nanostructure transitions induced by post-solvent annealing in self-assembled block copolymer thin films. Furthermore, a variety of thin films with well-ordered nanostructures, which can be employed as templates for nanotechnologies, have been realized simply and at low cost.


2019 ◽  
Vol 2 (2) ◽  
pp. 487-496 ◽  
Author(s):  
Alexandros El Sachat ◽  
Jean Spièce ◽  
Charalambos Evangeli ◽  
Alexander James Robson ◽  
Martin Kreuzer ◽  
...  

2012 ◽  
Vol 512-515 ◽  
pp. 1175-1179
Author(s):  
Han Lin ◽  
Guo Qiang Tan ◽  
Hui Jun Ren

Using (NH4)2TiF6, Bi(NO3)3•5H2O and H3BO3 as raw materials, Bi4Ti3O12 thin films were synthesized with liquid phase self-assembled monolayers on the glass substrate. The different precursor solution concentrations and acid contents had the effects on the physical phase and morphology of Bi4Ti3O12 thin films. The Bi4Ti3O12 thin films were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The results indicate that the precursor solution with 10.0 mmol/L concentration was prepared by 3:4:9 molar ratio of (NH4)2TiF6: Bi(NO3)3•5H2O: H3BO3 and 6.0 ml acid content, depositing at 50°C for 20h, and heat treating at 590°C for 2h. The as-prepared thin films are well-crystal. The surface is even and dense. The formation mechanism of the Bi4Ti3O12 thin films is as follows: [TiF6-n(OH)n]2- complex ions are formed in the (NH4)2TiF6 aqueous solution. Then H3BO3 continually consumed F- ions of the solution, which made the amounts of [TiF6-n(OH)n]2- ions increase gradually. Under the induction of the electrostatic force, Bi3+ ions and [TiF6-n(OH)n]2- ions would grow naturally on the substrate surface in the form of Bi2[TiF6-n(OH)n]3 or Bi2[TiF6-nOm/2(OH)n-m]3. The samples lost the bound water after the heat treatment and finally the Bi4Ti3O12 thin films with pure phase were obtained.


2010 ◽  
Vol 2 (3) ◽  
pp. 847-853 ◽  
Author(s):  
William A. Phillip ◽  
Brandon O’Neill ◽  
Marc Rodwogin ◽  
Marc A. Hillmyer ◽  
E. L. Cussler

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