scholarly journals Bottom-electrode induced defects in self-assembled monolayer (SAM)-based tunnel junctions affect only the SAM resistance, not the contact resistance or SAM capacitance

RSC Advances ◽  
2018 ◽  
Vol 8 (36) ◽  
pp. 19939-19949 ◽  
Author(s):  
C. S. Suchand Sangeeth ◽  
Li Jiang ◽  
Christian A. Nijhuis

In large area molecular junctions, defects are always present and can be caused by impurities and/or defects in the electrode materials and/or SAMs, but how they affect the electrical characteristics of junctions has rarely been studied.

2020 ◽  
Vol 20 (8) ◽  
pp. 4648-4651
Author(s):  
Wang-Taek Hwang ◽  
Yeonsik Jang ◽  
Minwoo Song ◽  
Takhee Lee

In this study, we demonstrated the molecular ensemble junctions fabricated by the inverted selfassembled monolayer (iSAM) method in which the molecular layer was deposited on the top electrode surface. The alkyl thiolate molecules were used to benchmark this method and we found that the electrical characteristics of these molecular junctions were comparable to the results reported previously by performing statistical analysis. We expect this iSAM method to enable the molecular junctions with bottom electrode of various materials.


2010 ◽  
Vol 97 (17) ◽  
pp. 173302 ◽  
Author(s):  
A. J. Kronemeijer ◽  
E. H. Huisman ◽  
H. B. Akkerman ◽  
A. M. Goossens ◽  
I. Katsouras ◽  
...  

2011 ◽  
Vol 1335 ◽  
Author(s):  
Qiong Wu ◽  
Juanyuan Hao ◽  
Shoulei Shi ◽  
Weifeng Wang ◽  
Nan Lu

ABSTRACTWe report a low-cost and high-throughput method to fabricate large-area light emitting pattern via thermal evaporation of organic molecules on the patterned self-assembled monolayer of homogenous 3-aminopropyltrimethoxysilane. This method is based on the selective deposition of the organic light emitting molecules on the template of self-assembled monolayer (SAM), which is patterned with nanoimprinting lithography. The selectivity can be controlled by adjusting the design of the pattern, the storage duration and the substrate temperature. The deposition selectivity of the molecules may be caused by the different binding energy of the molecules with the SAM and the substrate surface.


2020 ◽  
Vol 12 (3) ◽  
pp. 333-336
Author(s):  
Jungmoon Lim ◽  
Gahyun Ahn ◽  
Inho Jeong ◽  
Hyunwook Song

We report on the temperature-dependent transport behaviors of large-area molecular junctions fabricated with poly-(3,4-ethylene-dioxythiophene) stabilized with polystyrene sulphonic acid (PEDOT:PSS) interlayer electrodes and the archetypal benzenethiol molecules. In this study, we investigated two different benzenethiol molecules: 4-methylbenzenethiol (MBT) and 1,4-benzenedithiol (BDT), which have the identical backbone structure but different top end-groups. The charge transport through the molecular junctions was dominated by distinct interfacial contact properties between the PEDOT:PSS electrodes and the component molecules. We also observed that the electrical characteristics of the MBT junctions are influenced by the PEDOT grain size, particularly depending on the annealing temperature.


2007 ◽  
Vol 104 (27) ◽  
pp. 11161-11166 ◽  
Author(s):  
H. B. Akkerman ◽  
R. C. G. Naber ◽  
B. Jongbloed ◽  
P. A. van Hal ◽  
P. W. M. Blom ◽  
...  

2008 ◽  
Vol 18 (45) ◽  
pp. 5459 ◽  
Author(s):  
Fernanda Camacho-Alanis ◽  
Lingling Wu ◽  
Giovanni Zangari ◽  
Nathan Swami

2014 ◽  
Vol 5 ◽  
pp. 258-267 ◽  
Author(s):  
Cai Shen ◽  
Manfred Buck

The intercalation of Cu at the interface of a self-assembled monolayer (SAM) and a Au(111)/mica substrate by underpotential deposition (UPD) is studied as a means of high resolution patterning. A SAM of 2-(4'-methylbiphenyl-4-yl)ethanethiol (BP2) prepared in a structural phase that renders the Au substrate completely passive against Cu-UPD, is patterned by modification with the tip of a scanning tunneling microscope. The tip-induced defects act as nucleation sites for Cu-UPD. The lateral diffusion of the metal at the SAM–substrate interface and, thus, the pattern dimensions are controlled by the deposition time. Patterning down to the sub-20 nm range is demonstrated. The difference in strength between the S–Au and S–Cu bond is harnessed to develop the latent Cu-UPD image into a patterned binary SAM. Demonstrated by the exchange of BP2 by adamantanethiol (AdSH) this is accomplished by a sequence of reductive desorption of BP2 in Cu free areas followed by adsorption of AdSH. The appearance of Au adatom islands upon the thiol exchange suggests that the interfacial structures of BP2 and AdSH SAMs are different.


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