Functionalized gold nanoflowers on carbon screen-printed electrodes: an electrochemical platform for biosensing hemagglutinin protein of influenza A H1N1 virus

• Carlos Enrique Torres-Méndez,
• Sharmilee Nandi,
• Klara Martinovic,
• Patrizia Kühne,
• Yifan Liu,
• Sam Taylor,
• Maria Lysandrou,
• Maria Ines Berrojo Romeyro Mascarenhas,
• Viktoria Langwallner,
• Javier Enrique Sebastián Alonso,
• Ivana Jovanovic,
• Maike Lüftner,
• Georgia-Vasiliki Gkountana,
• David Bern,
• Abdul-Raouf Atif,
• Ehsan Manouchehri Doulabi,
• Gemma Mestres and
• Masood Kamali-Moghaddam

Beilstein J. Nanotechnol. 2025, 16, 540–550, doi:10.3762/bjnano.16.42

• Carlos Enrique Torres-Mendez Sharmilee Nandi Klara Martinovic Patrizia Kuhne Yifan Liu Sam Taylor Maria Lysandrou Maria Ines Berrojo Romeyro Mascarenhas Viktoria Langwallner Javier Enrique Sebastian Alonso Ivana Jovanovic Maike Luftner Georgia-Vasiliki Gkountana David Bern Abdul-Raouf Atif Ehsan

Spatial variations of conductivity of self-assembled monolayers of dodecanethiol on Au/mica and Au/Si substrates

• Julian Skolaut,
• Jędrzej Tepper,
• Federica Galli,
• Wulf Wulfhekel and
• Jan M. van Ruitenbeek

Beilstein J. Nanotechnol. 2023, 14, 1169–1177, doi:10.3762/bjnano.14.97

• contacting of molecular layers between a metal surface and a locally probing electrode. In early studies using this approach, the layers were contacted by a mercury droplet at the end of an electrode, which was then placed on top of the SAM [5][6][7]. Applying a voltage and, therefore, a current to the

• substrate and the mercury electrode yields the conductivity of the SAM, averaged over the contact area of the mercury droplet. In such studies, one of the crucial problems was mercury filling out defects in the SAMs, which leads to short circuits and unreliable currents running through the microcontact

• of current characteristics strongly depends on the substrate chosen to deposit the SAM onto. For this study, we employ alkane thiols, which are allowed to form a SAM on different types of Au substrates. We have chosen dodecanethiol (DDT) molecules and study them on commercially available Au

N-Heterocyclic carbene-based gold etchants

• Robert B. Chevalier,
• Justin Pantano,
• Matthew K. Kiesewetter and
• Jason R. Dwyer

Beilstein J. Nanotechnol. 2023, 14, 865–871, doi:10.3762/bjnano.14.71

• but also the potential for deliberate etching, with the outcome determined by choice of chemically synthesized organic species and solvent. Keywords: gold etchant; microfabrication; N-heterocyclic carbenes; self-assembled monolayer (SAM); thin films; Introduction Self-assembled monolayers (SAMs) are

• a fixture of materials science. Thiols continue to dominate as the most prevalent choice of SAM constituents on gold [1][2][3][4][5][6][7][8][9][10][11]. They benefit from a long history of widespread use and general ease of adoption. Unfortunately, the gold–sulfur bond can limit the range of

• clearly undesirable that an effort to form a stable monolayer could result in removal of underlying material, but similarly undesirable effects have been reported in the gold–thiol SAM literature. For example, gold–sulfur interactions can lead to a weaker bonding of gold surface atoms to the bulk. This

Silver-based SERS substrates fabricated using a 3D printed microfluidic device

• Phommachith Sonexai,
• Minh Van Nguyen,
• Bui The Huy and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2023, 14, 793–803, doi:10.3762/bjnano.14.65

• developed system. The substrate was prepared from Ag NPs by decorating the surface of porous silicon with Ag NPs using self-assembled monolayers (SAMs). The SAM method offers precise control, versatility, simplicity, stability, and compatibility, making it a valuable technique for surface modification in

• submerged in concentrated HNO3, rinsed with deionized water, and then dried at room temperature to produce the PS substrates. Fabrication of the SERS substrate The deposition of Ag particles on the substrates is based on the SAM method. Colloidal Ag NPs solutions were generated at the methanol/air interface

• with an increase in the concentration of reactants. Structural characterization of the SERS substrate In Supporting Information File 1, Figure S10a shows the SEM image of the SAM of Ag NPs on the surface of methanol, while Figure S10b displays the image of the PS substrate after covering with the Ag

Gap-directed chemical lift-off lithographic nanoarchitectonics for arbitrary sub-micrometer patterning

• Chang-Ming Wang,
• Hong-Sheng Chan,
• Chia-Li Liao,
• Che-Wei Chang and
• Wei-Ssu Liao

Beilstein J. Nanotechnol. 2023, 14, 34–44, doi:10.3762/bjnano.14.4

• alkanethiol self-assembled monolayer (SAM) on Au to generate surface patterns that are orders of magnitude smaller than structures on the original elastomer stamp. The smallest achieved feature dimension is 5 nm using a micrometer-scale structured stamp in a chemical lift-off lithography (CLL) process

• ][18][19]. Instead of transferring ink molecules from a stamp reservoir, this technique selectively removes alkanethiol molecules from a self-assembled monolayer (SAM) covered flat Au surface. An oxygen-plasma-activated polydimethylsiloxane (PDMS) stamp bearing patterns originating from a silicon

• master mold is placed in contact with the SAM, which initiates a covalent bonding between stamp surface siloxyl groups and alkanethiol hydroxy tails. Removal of the stamp from the SAM-covered surface lifts off alkanethiol molecules at the contact region, and thus circumventing the lateral diffusion issue

Rapid and sensitive detection of box turtles using an electrochemical DNA biosensor based on a gold/graphene nanocomposite

• Abu Hashem,
• M. A. Motalib Hossain,
• Ab Rahman Marlinda,
• Mohammad Al Mamun,
• Khanom Simarani and
• Mohd Rafie Johan

Beilstein J. Nanotechnol. 2022, 13, 1458–1472, doi:10.3762/bjnano.13.120

• hydrochloride (EDC) were used to covalently link DNA and oligonucleotides to a carboxylate-terminated alkanethiol self-assembled monolayer (SAM) performed on a gold electrode (AuE) [70]. The Lisdat group described a label-free impedimetric sensor for the detection of hybridisation events which is based on short

Detection and imaging of Hg(II) in vivo using glutathione-functionalized gold nanoparticles

• Gufeng Li,
• Shaoqing Li,
• Rui Wang,
• Min Yang,
• Lizhu Zhang,
• Yanli Zhang,
• Wenrong Yang and
• Hongbin Wang

Beilstein J. Nanotechnol. 2022, 13, 549–559, doi:10.3762/bjnano.13.46

• GNPs were synthesized by a previously reported protocol [38], then the surface of GNPs was modified with GSH to form SAM-modified GNPs. Subsequently, the carbonyl group of Rh6G2 was conjugated with the amino groups of GSH-modified GNPs via Schiff base reaction in methanol solution [39][40]. It is worth

Investigation of electron-induced cross-linking of self-assembled monolayers by scanning tunneling microscopy

• Patrick Stohmann,
• Sascha Koch,
• Yang Yang,
• Christopher David Kaiser,
• Julian Ehrens,
• Jürgen Schnack,
• Niklas Biere,
• Dario Anselmetti,
• Armin Gölzhäuser and
• Xianghui Zhang

Beilstein J. Nanotechnol. 2022, 13, 462–471, doi:10.3762/bjnano.13.39

• β-phase and the βdistorted-phase are shown in Figure 2e (bottom panel). Initial stage of cross-linking and observation of dark spots Investigating the initial stages of cross-linking allows for the visualization of the effects of electron impact at the local molecular level. The pristine TPT SAM

• spot region in the initial cross-linking stage is limited to a maximum of 43 molecules. Reduction of the structural order and observation of subnanometer voids TPT SAMs prepared from a DMF-based solution were irradiated with 50 eV electrons at 2.5, 10, 15, or 25 mC/cm2. The SAM irradiated with 2.5 mC

• cross-linking of the TPT SAM observed by STM is schematically illustrated as follows (Figure 5a–c). At low doses, cross-linked domains appear as dark spots in the STM images. At the medium dose, the cross-linking causes variation in the local density and the structural order of the monolayer. Again, the

Exploring the fabrication and transfer mechanism of metallic nanostructures on carbon nanomembranes via focused electron beam induced processing

• Christian Preischl,
• Linh Hoang Le,
• Elif Bilgilisoy,
• Armin Gölzhäuser and
• Hubertus Marbach

Beilstein J. Nanotechnol. 2021, 12, 319–329, doi:10.3762/bjnano.12.26

• high purity. Remarkably, the EBISA process exhibits a strong time dependence, which is analyzed in detail for different electron doses. This time dependence is a new phenomenon, which, to the best of our knowledge, was not reported before. The electron-induced cross-linking of the SAM caused by the

• cleavage of C–H bonds and the subsequent formation of new C–C bonds between neighboring molecules also seems to play a crucial role in the EBISA process. Previous studies showed that iron nanostructures fabricated on top of a cross-linked SAM on Au/mica can be transferred to solid substrates and grids

• without any changes, aside from oxidation. Here we demonstrate that iron as well as cobalt oxide structures on top of a cross-linked SAM on Ag/mica do change more significantly. The Fe(NO3)3 solution used for etching of the Ag layer also dissolves the cobalt oxide structures and causes dissolution and

Fusion of purple membranes triggered by immobilization on carbon nanomembranes

• René Riedel,
• Natalie Frese,
• Fang Yang,
• Martin Wortmann,
• Raphael Dalpke,
• Daniel Rhinow,
• Norbert Hampp and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2021, 12, 93–101, doi:10.3762/bjnano.12.8

• electron irradiation-induced cross-linking of a self-assembled monolayer (SAM) of 4′-nitro-1,1′-biphenyl-4-thiol (NBPT) and second, purple membrane (PM) containing genetically modified bacteriorhodopsin (BR) carrying a C-terminal His-tag. The NBPT-CNM was further modified to carry nitrilotriacetic acid

• reflection absorption spectroscopy (IRRAS). Experimental Preparation of SAMs and CNMs NBPT was purchased from Taros Chemicals (Dortmund, Germany). Thermally evaporated Au films (300 nm) on mica supports (Georg Albert physical vapor deposition coatings) were used as substrates for the SAM preparation

• -thiol in dried and degassed N,N-dimethylformamide (DMF, anhydrous, 99.8%, Sigma-Aldrich) under nitrogen atmosphere in a sealed flask for 72 h, followed by subsequent rinsing with DMF (BioSyn, ≥99.9%, Honeywell) and absolute ethanol. Cross-linking of the SAMs was conducted by exposing the SAM to 100 eV

Cu₂O nanoparticles for the degradation of methyl parathion

• Juan Rizo,
• David Díaz,
• Benito Reyes-Trejo and
• M. Josefina Arellano-Jiménez

Beilstein J. Nanotechnol. 2020, 11, 1546–1555, doi:10.3762/bjnano.11.137

• width of 45°, acquisition time of 0.813 s, FT size of 65 K and digital resolution of 0.5 Hz per point. The number of scans varied from 512 to 4,096 per spectrum. X-ray photoelectron spectroscopy (XPS) were measured in a ESCA/SAM Perkin-Elmer model 560, using an Al Kα source with a 400 μm spot diameter

Ultrasensitive detection of cadmium ions using a microcantilever-based piezoresistive sensor for groundwater

• Dinesh Rotake,
• Anand Darji and
• Nitin Kale

Beilstein J. Nanotechnol. 2020, 11, 1242–1253, doi:10.3762/bjnano.11.108

• the WHO limit of 3 μg/L. Keywords: BioMEMS; heavy metal ions (HMIs); limit of detection (LOD); microcantilevers; microfluidics; micro-electromechanical systems (MEMS); piezoresistive sensors; SAM (self-assembled monolayers); World Health Organization (WHO); Introduction Water is fundamentally

• . Results of the SAM detecting cadmium ions The proposed microfluidic platform provides real-time monitoring of Cd(II) in groundwater. We performed the experiment using the coating of cysteamine thiol with cross-linked ᴅʟ-glyceraldehyde (Cys-DL-GC). We have already discussed that the methods based on Au/Ag

• solution of cysteamine ([Cys] = 10 mM/10 mL) was prepared. The piezoresistive devices were gently dipped into a petri-dish containing cysteamine thiol for at least 12–24 hours. Longer times yield a better packing density of the SAM. In addition, a 2% (0.2 g/10 mL) solution of ᴅʟ-glyceraldehyde (DL-GC) in

A few-layer graphene/chlorin e6 hybrid nanomaterial and its application in photodynamic therapy against Candida albicans

• Selene Acosta,
• Carlos Moreno-Aguilar,
• Dania Hernández-Sánchez,
• Beatriz Morales-Cruzado,
• Erick Sarmiento-Gomez,
• Carla Bittencourt,
• Luis Octavio Sánchez-Vargas and
• Mildred Quintana

Beilstein J. Nanotechnol. 2020, 11, 1054–1061, doi:10.3762/bjnano.11.90

• . Funding This project was supported by CONACYT through the project A1-S-8817. SAM and CAM thank the scholarship awards 486938 and 297697, respectively. Thanks are given to the Marcos Moshinsky Foundation for financial support. CB and SA thank the Belgian Fund for Scientific Research under the FRFC contract

Stochastic excitation for high-resolution atomic force acoustic microscopy imaging: a system theory approach

• Edgar Cruz Valeriano,
• José Juan Gervacio Arciniega,
• Christian Iván Enriquez Flores,
• Susana Meraz Dávila,
• Joel Moreno Palmerin,
• Martín Adelaido Hernández Landaverde,
• Yuri Lizbeth Chipatecua Godoy,
• Aime Margarita Gutiérrez Peralta,
• Rafael Ramírez Bon and
• José Martín Yañez Limón

Beilstein J. Nanotechnol. 2020, 11, 703–716, doi:10.3762/bjnano.11.58

• . NPXY100) and a signal access module (SAM) used for signal input/output to the AFM. The apparatus was supported on a floating air table and equipped with an acoustical isolation chamber, which minimize the external thermal and vibrational disturbances, respectively. Data acquisition and FFT processing were

Comparison of fresh and aged lithium iron phosphate cathodes using a tailored electrochemical strain microscopy technique

• Matthias Simolka,
• Hanno Kaess and
• Kaspar Andreas Friedrich

Beilstein J. Nanotechnol. 2020, 11, 583–596, doi:10.3762/bjnano.11.46

• analysis was conducted with a Bruker Icon instrument inside a glovebox (MBraun, O2 and H2O < 2 ppm), equipped with a Zurich Instruments lock-in amplifier (HF2LI), a signal access module (SAM V) and PeakForce quantitative nanomechanical properties (QNM) module. In addition to the ESM signal, the topography

Mobility of charge carriers in self-assembled monolayers

• Zhihua Fu,
• Tatjana Ladnorg,
• Hartmut Gliemann,
• Alexander Welle,
• Asif Bashir,
• Michael Rohwerder,
• Qiang Zhang,
• Björn Schüpbach,
• Andreas Terfort and
• Christof Wöll

Beilstein J. Nanotechnol. 2019, 10, 2449–2458, doi:10.3762/bjnano.10.235

• within OSC-based SAMs with regions of insulating SAM made from large band gap alkanethiolates. The new method is demonstrated using a phenyl-linked anthracenethiolate (PAT), 4-(anthracene-2-ylethynyl)benzyl thiolate. I–V characteristics of differently shaped PAT-islands were measured using the AFM tip as

• vertical charge transport through individual molecules of aromatic SAMs by using conductive atomic force microscope (c-AFM) [12][13][14][15] and scanning tunneling microscope (STM) techniques [16][17]. Using these methods, current–voltage (I–V-) curves on the SAM-forming organothiolates has been determined

• before the SAM preparation. The formation of the PAT monolayers was carried out by immersing the substrates into 0.1 mM absolute ethanolic solution (≥99.8%, AnalaR NORMAPUR® ACS, Reag. Ph. Eur. zur Analyse) of PAT for 24 h at RT and, optionally, at an elevated temperature (70 °C). The samples were

Multiwalled carbon nanotube based aromatic volatile organic compound sensor: sensitivity enhancement through 1-hexadecanethiol functionalisation

• Nadra Bohli,
• Meryem Belkilani,
• Juan Casanova-Chafer,
• Eduard Llobet and
• Adnane Abdelghani

Beilstein J. Nanotechnol. 2019, 10, 2364–2373, doi:10.3762/bjnano.10.227

• 1011), operating at 100 kV. An Alpha FTIR spectrometer (Bruker, France) equipped with an ATR platinum crystal diamond module was used, in absorbance mode, to obtain the infrared spectra of the gold-decorated MWCNTs before and after the deposition of the SAM monolayer. This technique provides useful

• sensor before and after the HDT deposition. HRTEM image of MWCNTs decorated with Au nanoparticles at a magnification of (a) 300 K, (b) 600 K and (c) 400 K. Infrared spectra of Au-MWCNT and SAM/Au-MWCNT layers. Au-MWCNT sensor response for different concentrations of the injected vapours of (a) toluene

Adsorption and desorption of self-assembled L-cysteine monolayers on nanoporous gold monitored by in situ resistometry

• Elisabeth Hengge,
• Eva-Maria Steyskal,
• Rupert Bachler,
• Alexander Dennig,
• Bernd Nidetzky and
• Roland Würschum

Beilstein J. Nanotechnol. 2019, 10, 2275–2279, doi:10.3762/bjnano.10.219

• resistometry. From the desorption peak related to the (111) surface of the structure, which is associated with a resistance change of 4.8%, an initial surface coverage of 0.48 monolayers of cysteine could be estimated. Keywords: L-cysteine; in situ resistometry; nanoporous gold; self-assembled monolayer (SAM

• -/desorption of SAMs on nanoporous gold (npAu), based on our experience on in situ resistometry as a highly sensitive diagnosis tool for ad-/desorption processes [9]. The selected SAM material for this study is cysteine, due to its beneficial properties such as the short carbon backbone, the solubility in

• . Figure 1 shows the in situ resistance measurement during SAM formation, which yields a total resistance increase of approximately 18%. Both samples exhibit a similar trend, demonstrating the high reproducibility. This overall resistance change is well in line with ex situ studies on npAu in the

Hydrophilicity and carbon chain length effects on the gas sensing properties of chemoresistive, self-assembled monolayer carbon nanotube sensors

• Juan Casanova-Cháfer,
• Carla Bittencourt and
• Eduard Llobet

Beilstein J. Nanotechnol. 2019, 10, 565–577, doi:10.3762/bjnano.10.58

• ); self-assembled monolayer (SAM); thiol; Introduction Carbon nanotubes were first observed by Sumio Iijima in 1991 [1] and since then, this nanostructure has been widely used in chemoresistive gas sensors [2][3][4][5] due to the possibility to engineer its sensitivity towards chemicals present in a

• characteristic peak at 1440 cm−1 related to CH2 and CH3 radicals. Note that O–H elongations do not appear in the Raman spectra, probably due to the weak intensity of the O–H peak in Raman spectroscopy. Once these thiols had been attached to Au-MWCNTs via the SAM technique, it was not possible to detect many of

• that a small peak remains in thiol-Au-MWCNT samples is indicative that basically a SAM is formed, but some thiol molecules remain unattached to gold nanoparticles, despite the cleaning step implemented after the formation of the SAM. In Figure 3, a clear localized surface plasma resonance (LSPR) effect

Electro-optical interfacial effects on a graphene/π-conjugated organic semiconductor hybrid system

• Karolline A. S. Araujo,
• Luiz A. Cury,
• Matheus J. S. Matos,
• Thales F. D. Fernandes,
• Luiz G. Cançado and
• Bernardo R. A. Neves

Beilstein J. Nanotechnol. 2018, 9, 963–974, doi:10.3762/bjnano.9.90

• probe microscopy, optical spectroscopy (photoluminescence and Raman) and ab initio calculations. The graphene/RA interaction induces the formation of a well-organized π-conjugated self-assembled monolayer (SAM) at the interface. Such structural organization leads to the high optical emission efficiency

• of the RA SAM, even at room temperature. Additionally, photo-assisted electrical force microscopy, photo-assisted scanning Kelvin probe microscopy and Raman spectroscopy indicate a RA-induced graphene doping and photo-charge generation. Finally, the optical excitation of the RA monolayer generates

• of graphene-based devices, SAM surface functionalization is employed for both doping level control and work function tuning [14][15][16]. The present work brings these two fronts together by investigating a graphene/retinoic acid (RA) – a π-conjugated organic semiconductor – hybrid system and its

Tuning adhesion forces between functionalized gold colloidal nanoparticles and silicon AFM tips: role of ligands and capillary forces

• Sven Oras,
• Sergei Vlassov,
• Marta Berholts,
• Rünno Lõhmus and
• Karine Mougin

Beilstein J. Nanotechnol. 2018, 9, 660–670, doi:10.3762/bjnano.9.61

• forces between NPs and Si tips, apart from other molecular interactions such as H-bonding and capillary forces. SAM packing density and adhesion In addition to the previously discussed factors, packing density of SAM on the surface has also an important role in adhesion [41]. The self-organization and

Wafer-scale bioactive substrate patterning by chemical lift-off lithography

• Chong-You Chen,
• Chang-Ming Wang,
• Hsiang-Hua Li,
• Hong-Hseng Chan and
• Wei-Ssu Liao

Beilstein J. Nanotechnol. 2018, 9, 311–320, doi:10.3762/bjnano.9.31

• achieved and delivers applications such as protein–ligand binding study and biological species sensing [7][8][9]. The other widely adopted system, the self-assembled monolayer (SAM), provides ease of operation and high stability under ambient conditions [10][11]. These approaches utilize the self

• create distinct regions carrying dissimilar surface properties for a variety of applications [21]. With conformal contact-induced reactions, the top layer Au–Au bond breakage on an alkanethiol SAM covered Au substrate leads to the exposure of fresh Au toward the exterior environment. These vacancies can

• behavior compared to other SAM systems. Here, the lift-off process creates a diluted molecular matrix environment which is expected to be due to partial Au thiolate removal in SAMs. With the appropriate adjustment of the experimental conditions, this “diluted artificial defect-rich” matrix provides an

A robust AFM-based method for locally measuring the elasticity of samples

• Alexandre Bubendorf,
• Stefan Walheim,
• Thomas Schimmel and
• Ernst Meyer

Beilstein J. Nanotechnol. 2018, 9, 1–10, doi:10.3762/bjnano.9.1

• first flexural modes of the cantilever in contact were excited with the amplitudes A1 = 22 mV and A2 = 5 mV for all samples. Samples and measurement conditions Three different polymers (polystyrene (PS), polypropylene (PP) and linear low-density polyethylene (LLDPE)) and a self-assembled monolayer (SAM

• ) of 1H,1H,2H,2H-perfluorodecyltrichlorosilane (FDTS) on a silicon oxide (SiOx) substrate were investigated. The SAM was prepared with circular holes obtained by polymer blend lithography (PBL) [24]. A reference sample consisting of polytetrafluoroethylene (PTFE), commonly called Teflon, with a nominal

• , as seen in the histograms of LLDPE, PP and the SAM: LLDPE shows three different peaks centered at 362, 380 and 393 MPa, PP shows two peaks centered at 1.468 GPa and 1.565 GPa and the SAM shows two peaks centered at 472 and 478.5 MPa. Finally, the value of the storage modulus of FDTS gives an estimate

Patterning of supported gold monolayers via chemical lift-off lithography

• Liane S. Slaughter,
• Kevin M. Cheung,
• Sami Kaappa,
• Huan H. Cao,
• Qing Yang,
• Thomas D. Young,
• Andrew C. Serino,
• Sami Malola,
• Jana M. Olson,
• Stephan Link,
• Hannu Häkkinen,
• Anne M. Andrews and
• Paul S. Weiss

Beilstein J. Nanotechnol. 2017, 8, 2648–2661, doi:10.3762/bjnano.8.265

• . The layers removed during CLL have not yet been well characterized. In CLL, the height difference between the remaining SAM and the contact region (where molecules were removed) was the thicknesses of the SAM plus ≈4 Å [1]. This height difference is consistent with one or at most two layers of Au

• accelerating voltage, sample height, and vapor pressure were adjusted so that patterns could be discerned. The level of contrast in VP-SEM also depends on the nature of the alkanethiol molecules and SAM disorder (e.g., the orientation and conformation of the molecules in the SAM) [5]. The Au–mercaptoundecanol

• ). The Au–mercaptoundecanol monolayers (Figure 4A–C) were associated with heights ranging from 0.63 ± 0.01 nm to 0.93 ± 0.01 nm determined from the Chan–Vese analysis (Figure 4D–I). These apparent heights are smaller than the height of a SAM of mercaptoundecanol on a Au surface, which is 1.3–1.4 nm with

Amplified cross-linking efficiency of self-assembled monolayers through targeted dissociative electron attachment for the production of carbon nanomembranes

• Sascha Koch,
• Christopher D. Kaiser,
• Paul Penner,
• Michael Barclay,
• Lena Frommeyer,
• Daniel Emmrich,
• Patrick Stohmann,
• Tarek Abu-Husein,
• Andreas Terfort,
• D. Howard Fairbrother,
• Oddur Ingólfsson and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2017, 8, 2562–2571, doi:10.3762/bjnano.8.256

• cross-linking efficiency, self-assembled monolayers (SAM) of biphenyl-thiols (BPTs) and halogenated biphenyl-thiols (2-Cl-BPT, 2-Br-BPT and 2-I-BPT) were prepared on an Au(111) substrate from solution (see Experimental section). Subsequently, these were irradiated by electrons at an electron energy of

• the self-termination of the cross-linking, as already shown in previous work [16][36]. A straightforward method for the unambiguous verification of cross-linking consists of the transfer of a cross-linked SAM onto a TEM grid in order to demonstrate its mechanical strength and permit its imaging using

• attached to the Au(111) substrate in the native SAM. The other is related to the formation of new sulfur species, for example, disulfide, which appears with a S 2p3/2 peak at 163.5 eV and reflects the loss of thiol groups. A reduction of the 162 eV S 2p doublet and increase of the 163.5 eV, that is, a