2009
DOI: 10.1021/ja901646j
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Formation of Silicon-Based Molecular Electronic Structures Using Flip-Chip Lamination

Abstract: We report the fabrication of molecular electronic test structures consisting of Au-molecule-Si junctions by first forming omega-functionalized self-assembled monolayers on ultrasmooth Au on a flexible substrate and subsequently bonding to Si(111) with flip-chip lamination by using nanotransfer printing (nTP). Infrared spectroscopy (IRS), spectroscopic ellipsometry (SE), water contact angle (CA), and X-ray photoelectron spectroscopy (XPS) verified the monolayers self-assembled on ultrasmooth Au were dense, rela… Show more

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Cited by 48 publications
(74 citation statements)
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References 80 publications
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“…The observation of similar molecular conformation within the junction following FCL is consistent with previous studies of COOH-terminated alkyl molecules used in FCL (14,19). Bonding of the thiol-linkage to the H-terminated silicon surface is thought to occur through a Si-S linkage.…”
Section: Infrared Spectroscopysupporting
confidence: 88%
See 1 more Smart Citation
“…The observation of similar molecular conformation within the junction following FCL is consistent with previous studies of COOH-terminated alkyl molecules used in FCL (14,19). Bonding of the thiol-linkage to the H-terminated silicon surface is thought to occur through a Si-S linkage.…”
Section: Infrared Spectroscopysupporting
confidence: 88%
“…In order to address these concerns a novel fabrication technique, flip-chip lamination (FCL), was developed to create ordered, dense organic monolayers covalently bound between gold and semiconductor electrodes (14). This procedure takes advantage of well established thiol-gold chemistry and combines it with nanotransfer printing (nTP) in order to make reliable molecular junctions.…”
Section: Introductionmentioning
confidence: 99%
“…During this transition, the molecular chain orientation retains the same d -C-H peak position, indicating the monolayer remains highly ordered. The C-O and Si-O spectral regions change with increasing pressure indicating bonding between the carboxyl groups and the H-terminated silicon surface (4). Evolution of this spectral region has been attributed to bonding of the oxygen atoms within the carboxyl group to the silicon surface through a symmetric bidentate coordination.…”
Section: Novel Fabrication Approaches: Flip-chip Laminationmentioning
confidence: 96%
“…[159] As shown in Figure 15, Coll et al formed SAMs of carboxylic acid terminated alkanethiols on Au TS on poly(ethylene terephthalate) (PET). [159] They then inverted these films and applied them to passivated silicon wafers, forming SiÀO linkages. The properties of the junctions were verified by observing reasonable values of V trans and magnitudes of I.…”
Section: Nanotransfer Printingmentioning
confidence: 99%