Conformation heterogeneity of alkylammonium surfactants self-assembled on montmorillonite: Effect of head-group structure and temperature

2020 ◽  
Vol 503 ◽  
pp. 144125 ◽  
Author(s):  
J. Madejová ◽  
Ľ. Jankovič ◽  
M. Slaný ◽  
V. Hronský
2019 ◽  
Vol 10 ◽  
pp. 565-577 ◽  
Author(s):  
Juan Casanova-Cháfer ◽  
Carla Bittencourt ◽  
Eduard Llobet

Here we describe the development of chemoresistive sensors employing oxygen-plasma-treated, Au-decorated multiwall carbon nanotubes (MWCNTs) functionalized with self-assembled monolayers (SAMs) of thiols. For the first time, the effects of the length of the carbon chain and its hydrophilicity on the gas sensing properties of SAMs formed on carbon nanotubes are studied, and additionally, the gas sensing mechanisms are discussed. Four thiols differing in the length of the carbon chain and in the hydrophobic or hydrophilic nature of the head functional group are studied. Transmission electron microscopy, Raman spectroscopy and X-ray photoelectron spectroscopy are used to analyze the resulting gas-sensitive hybrid films. Among the different nanomaterials tested, short-chain thiols having a hydrophilic head group, self-assembled onto Au-decorated carbon nanotubes were most responsive to nitrogen dioxide and ethanol vapors, even in the presence of ambient humidity. In particular, this nanomaterial was about eight times more sensitive to nitrogen dioxide than bare Au-decorated carbon nanotubes when operated at room temperature. This response enhancement is attributed to the interaction, via strong hydrogen bonding, of the polar molecules tested to the polar surface of hydrophilic thiols. The approach discussed here could be extended further by combining hydrophilic and hydrophobic thiol SAMs in Au-MWCNT sensor arrays as a helpful strategy for tuning sensor response and selectivity. This would make the detection of polar and nonpolar gas species employing low-power gas sensors easier, even under fluctuating ambient moisture conditions.


MRS Advances ◽  
2019 ◽  
Vol 4 (44-45) ◽  
pp. 2441-2451
Author(s):  
Amare Benor ◽  
Asman Tamang ◽  
Veit Wagner ◽  
Alberto Salleo ◽  
Dietmar Knipp

ABSTRACTThe patterning of gold and silver micro and nanostructures on rigid and flexible substrates is investigated by microcontact printed thiol based self-assembled monolayers. The aspect ratio of the noble metal micro and nanostructures is determined by interaction of the -SH head group of the CH3(CH2)19SH molecules and the surface of the noble metal. Silver micro and nanostructures with >10 times higher aspect ratios can be realized in comparison to commonly realized gold micro and nanostructures. The printing process is described, and the etching process is characterized in terms of etching window and etching selectivity. Potential electronic and photonic applications of the micro and nanostructures are discussed taking the boundary conditions of the printing process and the selected material system into consideration.


1999 ◽  
Vol 182 (2) ◽  
pp. 221-236 ◽  
Author(s):  
M.P. Savelli ◽  
P. Van Roekeghem ◽  
O. Douillet ◽  
G. Cavé ◽  
P. Godé ◽  
...  

1987 ◽  
Vol 897 (1) ◽  
pp. 69-82 ◽  
Author(s):  
Harold C. Jarrell ◽  
A.Joshua Wand ◽  
J.B. Giziewicz ◽  
Ian C.P. Smith
Keyword(s):  

1994 ◽  
Vol 242 (1-2) ◽  
pp. 112-117 ◽  
Author(s):  
Mathias Lösche ◽  
Christian Erdelen ◽  
Elmar Rump ◽  
Helmut Ringsdorf ◽  
Kristian Kjaer ◽  
...  

2003 ◽  
Vol 81 (11) ◽  
pp. 1228-1240 ◽  
Author(s):  
Adam J Dickie ◽  
Ashok K Kakkar ◽  
Michael A Whitehead

Geometric modelling techniques are used to map the potential energies of packing for self-assembled alkyl- and phenyl-backboned monolayers across a range of intermolecular separations. Natural packing distances of 4.2–4.4 Å produce less stable, more isotropic monolayers because of repulsive interchain contacts. Optimizations at unnatural surface densities found thin films of lower energy and higher symmetry existed at increased chain–chain separations. Head-group bonding is therefore identified as a force for controlling monolayer order. Analysis of the natural monolayer structures on a silicon dioxide surface determined the favourable head-group structures, and allowed the topochemical polymerization of p-bis(butadiynyl)benzene monolayers to be rationalized.Key words: self-assembled monolayers, molecular modelling studies, repeating symmetry units, thin-film order, topochemical polymerization.


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