Transient laser heating induced hierarchical porous structures from block copolymer–directed self-assembly

Science ◽  
2015 ◽  
Vol 349 (6243) ◽  
pp. 54-58 ◽  
Author(s):  
Kwan Wee Tan ◽  
Byungki Jung ◽  
Jörg G. Werner ◽  
Elizabeth R. Rhoades ◽  
Michael O. Thompson ◽  
...  

Development of rapid processes combining hierarchical self-assembly with mesoscopic shape control has remained a challenge. This is particularly true for high-surface-area porous materials essential for applications including separation and detection, catalysis, and energy conversion and storage. We introduce a simple and rapid laser writing method compatible with semiconductor processing technology to control three-dimensionally continuous hierarchically porous polymer network structures and shapes. Combining self-assembly of mixtures of block copolymers and resols with spatially localized transient laser heating enables pore size and pore size distribution control in all-organic and highly conducting inorganic carbon films with variable thickness. The method provides all-laser-controlled pathways to complex high-surface-area structures, including fabrication of microfluidic devices with high-surface-area channels and complex porous crystalline semiconductor nanostructures.

2005 ◽  
Vol 11 (5) ◽  
pp. 1658-1664 ◽  
Author(s):  
Wen-Cui Li ◽  
An-Hui Lu ◽  
Wolfgang Schmidt ◽  
Ferdi Schüth

2014 ◽  
Vol 49 (1) ◽  
pp. 1-8
Author(s):  
US Akhtar ◽  
MK Hossain ◽  
MS Miran ◽  
MYA Mollah

Porous silica materials were synthesized from tetraethyl orthosilicate (TEOS) using Pluronic P123 (non-ionic triblock copolymer, EO20PO70O20) as template under acidic conditions which was then used to prepare polyaniline (PAni) and porous silica composites (PAnisilica) at a fixed molar ratio. These materials were characterized by nitrogen adsorption-desorption isotherm measured by Barrett-Joyner- Halenda (BJH) method and pore size distribution from desorption branch and surface area measured by the Brunauer-Emmett-Teller (BET) method, scanning electron microscopy (SEM), transmission electron microscopy (TEM), TEM-energy dispersive X-ray (EDX) and Fourier transform infrared (FT-IR) spectroscopy. The composite maintains its structure even after the polymerization and the polymer is dispersed on the inorganic matrix. The rod-like porous silica was about 1?m to 1.5 ?m long and on an average the diameter was in the range of 300- 500 nm. The SEM and TEM images show well ordered 2d hexagonal pore, high specific surface area (850 m2g-1) and uniform pore size of ca. 6.5 nm in diameter. After incorporation of PAni inside the silica pore, framework of porous silica did not collapse and the surface area of the composite was as high as 434 m2g-1 which was 5.5 time higher than our previous report of 78.3 m2g-1. Due to shrinkage of the framework during the incorporation of aniline inside the silica, the pore diameter slightly increase to 7.5 nm but still showing Type IV isotherm and typical hysteresis loop H1 implying a uniform cylindrical pore geometry. DOI: http://dx.doi.org/10.3329/bjsir.v49i1.18847 Bangladesh J. Sci. Ind. Res. 49(1), 1-8, 2014


2017 ◽  
Vol 41 (22) ◽  
pp. 13611-13618 ◽  
Author(s):  
Longfeng Hu ◽  
Li Ma ◽  
Qizhen Zhu ◽  
Lanyong Yu ◽  
Qi Wu ◽  
...  

Nitrogen-rich, high surface area, hierarchical porous carbons were simply prepared by the pyrolysis of a nitrogen-containing organic salt, and exhibit excellent rate capability in supercapacitors.


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