Grazing Incidence X-ray Scattering to Probe the Self-Assembly of Phthalocyanine Nanorods on a Liquid Surface

2006 ◽  
Vol 110 (39) ◽  
pp. 19375-19379 ◽  
Author(s):  
Seán M. O'Flaherty ◽  
Lutz Wiegart ◽  
Bernd Struth
Materia Japan ◽  
1997 ◽  
Vol 36 (5) ◽  
pp. 505-507
Author(s):  
Shigeo Sato ◽  
Masatoshi Saito ◽  
Eiichiro Matsubara ◽  
Yoshio Waseda ◽  
Kazuhiko Omote

2015 ◽  
Vol 71 (a1) ◽  
pp. s391-s391
Author(s):  
Matej Jergel ◽  
Karol Vegso ◽  
Peter Šiffalovič ◽  
Eva Majková ◽  
Adeline Buffet ◽  
...  

2014 ◽  
Vol 47 (20) ◽  
pp. 7221-7229 ◽  
Author(s):  
Mireille Maret ◽  
Raluca Tiron ◽  
Xavier Chevalier ◽  
Patrice Gergaud ◽  
Ahmed Gharbi ◽  
...  

2016 ◽  
Vol 23 (2) ◽  
pp. 519-531 ◽  
Author(s):  
Masafumi Fukuto ◽  
Lin Yang ◽  
Dmytro Nykypanchuk ◽  
Ivan Kuzmenko

The need for functional materials calls for increasing complexity in self-assembly systems. As a result, the ability to probe both local structure and heterogeneities, such as phase-coexistence and domain morphologies, has become increasingly important to controlling self-assembly processes, including those at liquid surfaces. The traditional X-ray scattering methods for liquid surfaces, such as specular reflectivity and grazing-incidence diffraction, are not well suited to spatially resolving lateral heterogeneities due to large illuminated footprint. A possible alternative approach is to use scanning transmission X-ray scattering to simultaneously probe local intermolecular structures and heterogeneous domain morphologies on liquid surfaces. To test the feasibility of this approach, transmission small- and wide-angle X-ray scattering (TSAXS/TWAXS) studies of Langmuir films formed on water meniscus against a vertically immersed hydrophilic Si substrate were recently carried out. First-order diffraction rings were observed in TSAXS patterns from a monolayer of hexagonally packed gold nanoparticles and in TWAXS patterns from a monolayer of fluorinated fatty acids, both as a Langmuir monolayer on water meniscus and as a Langmuir–Blodgett monolayer on the substrate. The patterns taken at multiple spots have been analyzed to extract the shape of the meniscus surface and the ordered-monolayer coverage as a function of spot position. These results, together with continual improvement in the brightness and spot size of X-ray beams available at synchrotron facilities, support the possibility of using scanning-probe TSAXS/TWAXS to characterize heterogeneous structures at liquid surfaces.


2020 ◽  
Vol 27 (5) ◽  
pp. 1278-1288 ◽  
Author(s):  
Marta Fernández-Regúlez ◽  
Eduardo Solano ◽  
Laura Evangelio ◽  
Steven Gottlieb ◽  
Christian Pinto-Gómez ◽  
...  

An accurate knowledge of the parameters governing the kinetics of block copolymer self-assembly is crucial to model the time- and temperature-dependent evolution of pattern formation during annealing as well as to predict the most efficient conditions for the formation of defect-free patterns. Here, the self-assembly kinetics of a lamellar PS-b-PMMA block copolymer under both isothermal and non-isothermal annealing conditions are investigated by combining grazing-incidence small-angle X-ray scattering (GISAXS) experiments with a novel modelling methodology that accounts for the annealing history of the block copolymer film before it reaches the isothermal regime. Such a model allows conventional studies in isothermal annealing conditions to be extended to the more realistic case of non-isothermal annealing and prediction of the accuracy in the determination of the relevant parameters, namely the correlation length and the growth exponent, which define the kinetics of the self-assembly.


2012 ◽  
Vol 161 (23-24) ◽  
pp. 2739-2742 ◽  
Author(s):  
Cosmin Laslau ◽  
Bridget Ingham ◽  
Zoran D. Zujovic ◽  
Pavla Čapková ◽  
Jaroslav Stejskal ◽  
...  

Author(s):  
Theyencheri Narayanan ◽  
Axel Rüter ◽  
Ulf Olsson

This brief report presents an X-ray scattering investigation of self-assembled nanotubes formed by a short peptide. X-ray scattering methods enable multiscale structural elucidation of these nanotubes in solution under the same conditions involved in the self-assembly process. In particular, the dimensions of nanotubes and the crystalline organization within their walls can be determined quantitatively. This is illustrated in the case of amyloid-β(16-22) peptide nanotubes.


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