Hierarchically porous bio-inspired films prepared by combining “breath figure” templating and selectively degradable block copolymer directed self-assembly

2016 ◽  
Vol 52 (61) ◽  
pp. 9562-9565 ◽  
Author(s):  
Arthur Bertrand ◽  
Antoine Bousquet ◽  
Christine Lartigau-Dagron ◽  
Laurent Billon
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Bottom Up ◽  
Hierarchically Porous ◽  
Breath Figure

Hierarchically porous bio-inspired honeycomb films prepared by combining the breath figure bottom-up process and selectively degradable block copolymer directed self-assembly.

Block Copolymer Films Hierarchical Assembly in Confinement

2007 ◽  
Vol 364-366 ◽  
pp. 437-441
Author(s):  
Yong Zhi Cao ◽  
Shen Dong ◽  
Ying Chun Liang ◽  
Tao Sun ◽  
Yong Da Yan
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Structural Control ◽  
Computer Control ◽  
The Self ◽  
Top Down ◽  
Bottom Up ◽  
Dimensional Precision ◽  
Periodic Arrays ◽  
Copolymer Films

Ultrathin block copolymer films are promising candidates for bottom-up nanotemplates in hybrid organic-inorganic electronic, optical, and magnetic devices. Key to many future applications is the long range ordering and precise placement of the phase-separated nanoscale domains. In this paper, a combined top-down/bottom-up hierarchical approach is presented on how to fabricate massive arrays of aligned nanoscale domains by means of the self-assembly of asymmetric poly (styrene-block-ethylene/butylenes-block-styrene) (SEBS) tirblock copolymers in confinement. The periodic arrays of the poly domains were orientated via the introduction of AFM micromachining technique as a tool for locally controlling the self-assembly process of triblock copolymers by the topography of the silicon nitride substrate. Using the controlled movement of 2- dimensional precision stage and the micro pressure force between the tip and the surface by computer control system, an artificial topographic pattern on the substrate can be fabricated precisely. Coupled with solvent annealing technique to direct the assembly of block copolymer, this method provides new routes for fabricating ordered nanostructure. This graphoepitaxial methodology can be exploited in hybrid hard/soft condensed matter systems for a variety of applications. Moreover, Pairing top-down and bottom-up techniques is a promising, and perhaps necessary, bridge between the parallel self-assembly of molecules and the structural control of current technology.

CO2-Driven reversible wettability in a reactive hierarchically patterned bio-inspired honeycomb film

2019 ◽  
Vol 10 (27) ◽  
pp. 3751-3757 ◽  
Author(s):  
Pierre Marcasuzaa ◽  
Hongyao Yin ◽  
Yujun Feng ◽  
Laurent Billon
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Surface Wettability ◽  
Breath Figure

A triple structured honeycomb film is fabricated through block copolymer directed self-assembly in “Breath Figure” templating as a clickable patterned platform to enhance its reversible surface wettability between hydrophobicity and hydrophilicity upon a biological CO2 trigger.

Universal vertical standing of block copolymer microdomains enabled by a gradient block

2021 ◽  
Author(s):  
Seungwon Song ◽  
Yoon Hyung Hur ◽  
Ye Min Park ◽  
Eugene N. Cho ◽  
Hyeuk Jin Han ◽  
...  
Keyword(s):  
Thin Films ◽  
Block Copolymer ◽  
Self Assembly ◽  
Bottom Up ◽  
Vertically Aligned

Directed self-assembly of vertically aligned block copolymer (BCP) thin films have extensively been explored as one of the possible bottom-up routes for sub-10 nm patterning technology. To achieve a vertical...

When block copolymer self-assembly in hierarchically ordered honeycomb films depicts the breath figure process

Soft Matter ◽  
2016 ◽  
Vol 12 (3) ◽  
pp. 790-797 ◽  
Author(s):  
Pierre Escalé ◽  
Maud Save ◽  
Laurent Billon ◽  
Janne Ruokolainen ◽  
Laurent Rubatat
Keyword(s):  
Block Copolymer ◽  
Self Assembly ◽  
Film Formation ◽  
Detailed Observation ◽  
Breath Figure

A detailed observation of the block copolymer self-assembly, kinetically trapped during the breath figure process, and used as an imprint to elucidate the complex honeycomb film formation.

Hierarchically organized honeycomb films through block copolymer directed self-assembly in “breath figure” templating and soft microwave-triggered annealing

Soft Matter ◽  
2018 ◽  
Vol 14 (23) ◽  
pp. 4874-4880 ◽  
Author(s):  
Nicolas Benoot ◽  
Pierre Marcasuzaa ◽  
Laurence Pessoni ◽  
Sirikorn Chasvised ◽  
Stéphanie Reynaud ◽  
...  
Keyword(s):  
Block Copolymer ◽  
Polymer Films ◽  
Self Assembly ◽  
Breath Figure

Hierarchical polymer films are elaborated from the combination of block copolymer nanophase segregation in “breath figure” templating and microwave-triggered annealing.

A Bottom-Up Approach to Solution-Processed, Atomically Precise Graphitic Cylinders on Surfaces

2018 ◽  
Author(s):  
Erik Leonhardt ◽  
Jeff M. Van Raden ◽  
David Miller ◽  
Lev N. Zakharov ◽  
Benjamin Aleman ◽  
...  
Keyword(s):  
Self Assembly ◽  
Carbon Nanostructures ◽  
Carbon Nanomaterials ◽  
Circle Packing ◽  
Pyrolytic Graphite ◽  
Building Blocks ◽  
Bottom Up ◽  
Casting Technique ◽  
New Class ◽  
Solution Casting Technique

Extended carbon nanostructures, such as carbon nanotubes (CNTs), exhibit remarkable properties but are difficult to synthesize uniformly. Herein, we present a new class of carbon nanomaterials constructed via the bottom-up self-assembly of cylindrical, atomically-precise small molecules. Guided by supramolecular design principles and circle packing theory, we have designed and synthesized a fluorinated nanohoop that, in the solid-state, self-assembles into nanotube-like arrays with channel diameters of precisely 1.63 nm. A mild solution-casting technique is then used to construct vertical “forests” of these arrays on a highly-ordered pyrolytic graphite (HOPG) surface through epitaxial growth. Furthermore, we show that a basic property of nanohoops, fluorescence, is readily transferred to the bulk phase, implying that the properties of these materials can be directly altered via precise functionalization of their nanohoop building blocks. The strategy presented is expected to have broader applications in the development of new graphitic nanomaterials with π-rich cavities reminiscent of CNTs.

Reactive Nanopattern in a Triple Structured Bio-Inspired Honeycomb Film as a Clickable Platform

2018 ◽  
Author(s):  
Pierre Marcasuzaa ◽  
Samuel Pearson ◽  
Karell Bosson ◽  
Laurence Pessoni ◽  
Jean-Charles Dupin ◽  
...  
Keyword(s):  
Self Assembly ◽  
Double Porosity ◽  
Surface Groups ◽  
Specific Chemical ◽  
Site Specific ◽  
Surface Functionality ◽  
Wenzel State ◽  
Breath Figure ◽  
Responsive Surfaces ◽  
Secondary Population

A hierarchically structured platform was obtained from spontaneous self-assembly of a poly(styrene)-<i>b</i>-poly(vinylbenzylchloride) (PS-<i>b</i>-PVBC) block copolymer (BCP) during breath figure (BF) templating. The BF process using a water/ethanol atmosphere gave a unique double porosity in which hexagonally arranged micron-sized pores were encircled by a secondary population of smaller, nano-sized pores. A third level of structuration was simultaneously introduced between the pores by directed BCP self-assembly to form out-of-the-plane nano-cylinders, offering very rapid bottom-up access to a film with unprecedented triple structure which could be used as a reactive platform for introducing further surface functionality. The surface nano-domains of VBC were exploited as reactive nano-patterns for site-specific chemical functionalization by firstly substituting the exposed chlorine moiety with azide, then “clicking” an alkyne by copper (I) catalyzed azide-alkyne Huisgen cycloaddition (CuAAC). Successful chemical modification was verified by NMR spectroscopy, FTIR spectroscopy, and XPS, with retention of the micro- and nanostructuration confirmed by SEM and AFM respectively. Protonation of the cyclotriazole surface groups triggered a switch in macroscopic behavior from a Cassie-Baxter state to a Wenzel state, highlighting the possibility of producing responsive surfaces with hierarchical structure.

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

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