Temperature dependent charge transport across tunnel junctions of single-molecules and self-assembled monolayers: a comparative study

2016 ◽  
Vol 45 (43) ◽  
pp. 17153-17159 ◽  
Author(s):  
Alvar R. Garrigues ◽  
Li Yuan ◽  
Lejia Wang ◽  
Simranjeet Singh ◽  
Enrique del Barco ◽  
...  

In this work we present a comparative study of the temperature behavior of charge current in both single-molecule transistors and self-assembled monolayer-based tunnel junctions with ferrocene molecules.

Small ◽  
2013 ◽  
Vol 10 (3) ◽  
pp. 454-461 ◽  
Author(s):  
Galina V. Dubacheva ◽  
Mélanie Devynck ◽  
Guillaume Raffy ◽  
Lionel Hirsch ◽  
André Del Guerzo ◽  
...  

Langmuir ◽  
2008 ◽  
Vol 24 (5) ◽  
pp. 2219-2223 ◽  
Author(s):  
Yabing Qi ◽  
Imma Ratera ◽  
Jeong Y. Park ◽  
Paul D. Ashby ◽  
Su Ying Quek ◽  
...  

2018 ◽  
Vol 767 ◽  
pp. 69-76 ◽  
Author(s):  
Ingo Ross ◽  
André Temmler ◽  
Moritz Küpper ◽  
Stephan Prünte ◽  
Marco Teller ◽  
...  

Liquid lubrication guarantees high precision and surface quality of workpieces in industrial forming processes. In the case of aluminum cold extrusion, wear and cold welding due to direct contact of tool and workpiece are usually prevented by the extensive use of lubricants. Since the use of lubricants is economically and ecologically unfavorable, surface treatments of tools by, e.g. laser polishing and/or coatings are in the focus of current investigations to substitute these lubricants and establish so called “dry metal forming” processes. The material AISI D2, a ledeburitic 12% chromium steel which is known to have a significant amount of chromium carbide precipitations, is widely used in cold extrusion for forming tools. The large fraction of chromium carbide precipitations, however, hinder the formation of a dense self-assembled monolayer (SAM) that is necessary to avoid direct contact of reactive aluminum with surface oxides of the tool. Therefore, a homogeneous distribution of the chemical elements with a smaller fraction or no chromium carbides in the steel matrix, particularly in the tool surface, is aimed for. Using laser polishing, the surface layer is molten by continuous or pulsed laser radiation. Within the melt pool, the elementary distribution is homogenized as a result of thermal convection and diffusion processes, as well as a smoothed surface and a grain refinement are achieved. Consequently, the effects of the surface treatment by laser polishing on the area coverage of self-assembled monolayers are investigated. Thus, a combined surface treatment by laser polishing and functionalization with a dense self-assembled monolayer shall reduce overall adhesive wear. For this investigation, several specimens of conventional manufactured and powder metallurgical molten AISI D2 are laser polished using continuous or pulsed laser radiation or a combination of both. The resulting surfaces are investigated by microscopy and spectroscopic techniques to analyze the surface topography and the elemental distribution near to the surface. These results are compared to those of conventionally hand-polished specimens. Furthermore, the influence of the element homogenization and grain refinement on the area coverage of self-assembled monolayers is explored. First results show that laser polishing of AISI D2 is suitable to achieve a reduction of grain size and a more homogeneous distribution of chromium carbides within the surface layer.


1999 ◽  
Vol 77 (5-6) ◽  
pp. 1077-1084 ◽  
Author(s):  
R Scott Reese ◽  
Marye Anne Fox

Self-assembled monolayers of sulfur-terminated oligonucleotide duplexes were formed on flat gold surfaces, either by exposure of a self-assembled monolayer bearing one oligonucleotide strand to the complementary strand or by preformation of a oligonucleotide duplex that was then deposited on a fresh gold surface. Virtually identical spectral behavior was observed whether the duplex was produced before deposition or by in situ complementary association. With a duplex bearing an appropriate pyrene end-label, the resulting thin film was photoresponsive. Surface emission measurements show no evidence for pyrene aggregation on the modified surfaces. The polarity of the photocurrent, reflecting photoinduced electron transfer initiated by photoexcitation of pyrene, is opposite that expected from the oligonucleotide-mediated reduction of the appended pyrene excited state.Key words: oligonucleotide, self-assembled monolayer, duplex formation, photoelectrochemistry, surface emission.


2006 ◽  
Vol 6 (11) ◽  
pp. 3487-3490 ◽  
Author(s):  
Tae-Wook Kim ◽  
Gunuk Wang ◽  
Hyunwook Song ◽  
Nak-Jin Choi ◽  
Hyoyoung Lee ◽  
...  

2004 ◽  
Vol 847 ◽  
Author(s):  
Sébastien Anthérieu ◽  
Florence Brodard-Séverac ◽  
Gilles Guerrero ◽  
P. Hubert Mutin

ABSTRACTTitania particles (P25 DEGUSSA AG) were treated by a solution of 12-mercaptododecyl-phosphonic acid (MDPA) in toluene to obtain an organic-inorganic hybrid material with thiol functions at the surface. This material was characterized by chemical analysis, solid state 31P MAS NMR and FTIR spectroscopies, and XPS. Reaction of the phosphonic acid end of MDPA with the TiO2 surface led to the formation of a relatively dense and well-ordered self-assembled monolayer (SAM), with a density of about 3.9 SH functions per nm2. This material was tested for the extraction of mercury in water at pH 7, 9, and 11. Chemical analysis indicated no loss of SH functionality, even at pH 11. The best extraction results were obtained at pH 9 and 11, with a metal extraction ability between 85 and 90%.


2007 ◽  
Vol 121-123 ◽  
pp. 495-498 ◽  
Author(s):  
Jun Hyung Park ◽  
Buyng Su Park ◽  
Gu Huh ◽  
Seung Hyun Lee ◽  
Hyun Sook Lee ◽  
...  

We report on the distribution of mixed self-assembled monolayers (SAMs) composed of biotinylated and diluent alkylthiolates for streptavidin immobilization. Two thiol derivatives, 11-mercapto-1-undecanol (MUOH) and 11-mercaptoundecanoic-(8-biotinylamido-3,6-dioxaoctyl) amide (MBDA), were employed for mixed SAM. These thiols formed self-assembled monolayer without local domain, and streptavidins were immobilized onto biotinylated gold surface without nonspecific binding. In order to find the optimized condition of immobilization of streptavidin, we controlled the mixing ratio of two kind thiols by colorimetric detection assay, and the immobilization was characterized by atomic force microscopy (AFM), scanning tunneling microscopy (STM), and ellipsometer.


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