Fabrication of molecular nanotemplates in self-assembled monolayers by extreme-ultraviolet-induced chemical lithography

Extreme-UV interference lithography (EUV-IL) is applied to create chemical nanopatterns in self-assembled monolayers (SAMs) of 4'-nitro-1,1'-biphenyl-4-thiol (NBPT) on gold. X-ray photoelectron spectroscopy shows that EUV irradiation induces both the conversion of the terminal nitro groups of NBPT into amino groups and the lateral crosslinking of the underlying aromatic cores. Large-area ( approximately 2 mm(2)) nitro/amino chemical patterns with periods ranging from 2000 nm to 60 nm can be generated. Regions of pristine NBPT on the exposed samples are exchanged with protein-resistant thiol SAMs of polyethyleneglycol, resulting in the formation of molecular nanotemplates, which can serve as the basis of complex biomimetic surfaces.     

Magnetic Imaging of Cyanide‐Bridged Co‐ordination Nanoparticles Grafted on FIB‐Patterned Si Substrates

Prussian blue CsNiCr nanoparticles are used to decorate selected portions of a Si substrate. For successful grafting to take place, the Si surface needs first to be chemically functionalized. Low‐dose focused ion beam patterning on uniformly functionalized surfaces selects those portions that will not participate in the grafting process. Step‐by‐step control is assured by atomic force and high‐resolution scanning electron microscopy, revealing a submonolayer distribution of the grafted nanoparticles. By novel scanning Hall‐probe microscopy, an in‐depth investigation of the magnetic response of the nanoparticles to varying temperature and applied magnetic field is provided. The magnetic images acquired suggest that low‐temperature canted ferromagnetism is found in the grafted nanoparticles, similar to what is observed in the equivalent bulk material.     

Noble metal nanoparticles deposited on self-assembled monolayers by pulsed laser deposition show coulomb blockade at room temperature

Nanometer-sized noble-metal clusters are fabricated on top of alkylthiolate self-assembled monolayers (SAMs) on annealed gold by pulsed laser deposition at elevated pressures. The size distribution of the clusters depends on the metal and on the pressure during the deposition. Scanning tunneling microscopy (STM) and conductive probe atomic force microscopy (CP-AFM) showed that the metal clusters are insulated from the substrate on top of the SAM. Coulomb blockades could be measured at room temperature by STM for palladium clusters on decanethiol SAMs.     

Mechanically stacked 1-nm-thick carbon nanosheets: ultrathin layered materials with tunable optical, chemical, and electrical properties

Carbon nanosheets are mechanically stable, free-standing two-dimensional materials with a thickness of ≈1 nm and well defined physical and chemical properties. They are made by radiation-induced cross-linking of aromatic self-assembled monolayers. Herein, a route is presented to the scalable fabrication of multilayer nanosheets with tunable electrical, optical, and chemical properties on insulating substrates. Stacks of up to five nanosheets with sizes of ≈1 cm(2) on oxidized silicon are studied. Their optical characteristics are investigated by visual inspection, optical microscopy, UV-vis reflection spectroscopy, and model calculations. Their chemical composition is studied by X-ray photoelectron spectroscopy. The multilayer samples are then annealed in an ultrahigh vacuum at various temperatures up to 1100 K. A subsequent investigation by Raman, X-ray photoelectron, and UV-vis reflection spectroscopy, as well as by electrical four-point probe measurements, demonstrates that the layered nanosheets transform into nanocrystalline graphene. This structural and chemical transformation is accompanied by changes in the optical properties and electrical conductivity and opens up a new path for the fabrication of ultrathin functional conductive coatings.     

Carbon Nanosheets: Mechanically Stacked 1‐nm‐Thick Carbon Nanosheets: Ultrathin Layered Materials with Tunable Optical,Chemical, and Electrical Properties (Small 7/2011)

Carbon nanosheets are mechanically stable, free‐standing two‐dimensional materials with a thickness of ≈1 nm and well defined physical and chemical properties. They are made by radiation‐induced cross‐linking of aromatic self‐assembled monolayers. Herein, a route is presented to the scalable fabrication of multilayer nanosheets with tunable electrical, optical, and chemical properties on insulating substrates. Stacks of up to five nanosheets with sizes of ≈1 cm² on oxidized silicon are studied. Their optical characteristics are investigated by visual inspection, optical microscopy, UV–vis reflection spectroscopy, and model calculations. Their chemical composition is studied by X‐ray photoelectron spectroscopy. The multilayer samples are then annealed in an ultrahigh vacuum at various temperatures up to 1100 K. A subsequent investigation by Raman, X‐ray photoelectron, and UV–vis reflection spectroscopy, as well as by electrical four‐point probe measurements, demonstrates that the layered nanosheets transform into nanocrystalline graphene. This structural and chemical transformation is accompanied by changes in the optical properties and electrical conductivity and opens up a new path for the fabrication of ultrathin functional conductive coatings.     

Magnetic Nanoplatelet‐Based Spin Memory Device Operating at Ambient Temperatures

There is an increasing demand for realizing a simple Si based universal memory device working at ambient temperatures. In principle, nonvolatile magnetic memory can operate at low power consumption and high frequencies. However, in order to compete with existing memory technology, size reduction and simplification of the used material systems are essential. In this work, the chiral‐induced spin selectivity effect is used along with 30–50 nm ferromagnetic nanoplatelets in order to realize a simple magnetic memory device. The vertical memory is Si compatible, easy to fabricate, and in principle can be scaled down to a single nanoparticle size. Results show clear dual magnetization behavior with threefold enhancement between the one and zero states. The magnetization of the device is accompanied with large avalanche like noise that is ascribed to the redistribution of current densities due to spin accumulation inducing coupling effects between the different nanoplatelets.     

Single Nanoparticle Magnetic Spin Memristor

There is an increasing demand for the development of a simple Si‐based universal memory device at the nanoscale that operates at high frequencies. Spin‐electronics (spintronics) can, in principle, increase the efficiency of devices and allow them to operate at high frequencies. A primary challenge for reducing the dimensions of spintronic devices is the requirement for high spin currents. To overcome this problem, a new approach is presented that uses helical chiral molecules exhibiting spin‐selective electron transport, which is called the chiral‐induced spin selectivity (CISS) effect. Using the CISS effect, the active memory device is miniaturized for the first time from the micrometer scale to 30 nm in size, and this device presents memristor‐like nonlinear logic operation at low voltages under ambient conditions and room temperature. A single nanoparticle, along with Au contacts and chiral molecules, is sufficient to function as a memory device. A single ferromagnetic nanoplatelet is used as a fixed hard magnet combined with Au contacts in which the gold contacts act as soft magnets due to the adsorbed chiral molecules.     

Microcontact Printing: Limitations and Achievements

Microcontact printing (µCP) offers a simple and low‐cost surface patterning methodology with high versatility and sub‐micrometer accuracy. The process has undergone a spectacular evolution since its invention, improving its capability to form sub‐100 nm SAM patterns of various polar and apolar materials and biomolecules over macroscopic areas. Diverse development lines of µCP are discussed in this work detailing various printing strategies. New printing schemes with improved stamp materials render µCP a reproducible surface‐patterning technique with an increased pattern resolution. New stamp materials and PDMS surface‐treatment methods allow the use of polar molecules as inks. Flat elastomeric surfaces and low‐diffusive inks push the feature sizes to the nanometer range. Chemical and supramolecular interactions between the ink and the substrate increase the applicability of the µCP process.