Melinda Mohl

Low-temperature large-scale synthesis and electrical testing of ultralong copper nanowires.

Copper nanowires (NWs) with uniform diameters and lengths ranging from several hundreds of nanometers to several micrometers have been prepared with high yield by a simple hydrothermal procedure. The X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS) analysis data indicate that the copper nanowires are free of any contamination, while the electron diffraction (ED) analysis has revealed the nanowires to be single crystals. The nanowire growth mechanism has also been discussed. Hexadecylamine is the surface stabilizing agent in our method, while glucose facilitates formation of single-crystalline seeds on which the copper nanowires grow. The electrical properties of the as-synthesized copper NWs have also been investigated.

Self-assembled large scale metal alloy grid patterns as flexible transparent conductive layers

The development of scalable synthesis techniques for optically transparent, electrically conductive coatings is in great demand due to the constantly increasing market price and limited resources of indium for indium tin oxide (ITO) materials currently applied in most of the optoelectronic devices. This work pioneers the scalable synthesis of transparent conductive films (TCFs) by exploiting the coffee-ring effect deposition coupled with reactive inkjet printing and subsequent chemical copper plating. Here we report two different promising alternatives to replace ITO, palladium-copper (PdCu) grid patterns and silver-copper (AgCu) fish scale like structures printed on flexible poly(ethylene terephthalate) (PET) substrates, achieving sheet resistance values as low as 8.1 and 4.9 Ω/sq, with corresponding optical transmittance of 79% and 65% at 500 nm, respectively. Both films show excellent adhesion and also preserve their structural integrity and good contact with the substrate for severe bending showing less than 4% decrease of conductivity even after 105 cycles. Transparent conductive films for capacitive touch screens and pixels of microscopic resistive electrodes are demonstrated.

Photocatalytic reduction of CO2 with H2O over modified TiO2 nanofibers： Understanding the reduction pathway

Nanosized metal (Pt or Pd)-decorated TiO2 nanofibers (NFs) were synthesized by a wet impregnation method. CdSe quantum dots (QDs) were then anchored onto the metal-decorated TiO2 NFs. The photocatalytic performance of these catalysts was tested for activation and reduction of CO2 under UV-B light. Gas chromatographic analysis indicated the formation of methanol, formic acid, and methyl formate as the primary products. In the absence of CdSe QDs, Pd-decorated TiO2 NFs were found to exhibit enhanced performance compared to Pt-decorated TiO2 NFs for methanol production. However, in the presence of CdSe, Pt-decorated TiO2 NFs exhibited higher selectivity for methanol, typically producing ∼90 ppmg−1·h−1 methanol. The CO2 photoreduction mechanism is proposed to take place via a hydrogenation pathway from first principles calculations, which complement the experimental observations.

Layered titanate nanostructures: perspectives for industrial exploitation

Anisotropic titanate nanostructures can be synthesized by an environmentally benign, cost efficient and scalable process, the alkaline hydrothermal recrystallization of TiO2 with yields approaching 100%. Their chemistry offers more variety than that of TiO2 nanoparticles and promising preliminary results were already achieved on them in the fields of adsorption, catalysis and energy storage. In this review we first discuss the structure, synthesis and functionalization options of titanate nanotubes and nanowires, then the issues related to their industrial scale production, and finally present selected examples of their currently available applications.

Industrially benign super-compressible piezoresistive carbon foams with predefined wetting properties: from environmental to electrical applications

In the present work electrically conductive, flexible, lightweight carbon sponge materials derived from open-pore structure melamine foams are studied and explored. Hydrophobic and hydrophilic surface properties - depending on the chosen treatment conditions - allow the separation and storage of liquid chemical compounds. Activation of the carbonaceous structures substantially increases the specific surface area from ~4 m2g−1 to ~345 m2g−1, while retaining the original three-dimensional, open-pore structure suitable for hosting, for example, Ni catalyst nanoparticles. In turn the structure is rendered suitable for hydrogenating acetone to 2-propanol and methyl isobutyl ketone as well for growing hierarchical carbon nanotube structures used as electric double-layer capacitor electrodes with specific capacitance of ~40 F/g. Mechanical stress-strain analysis indicates the materials are super-compressible (>70% volume reduction) and viscoelastic with excellent damping behavior (loss of 0.69 ± 0.07), while piezoresistive measurements show very high gauge factors (from ~20 to 50) over a large range of deformations. The cost-effective, robust and scalable synthesis - in conjunction with their fascinating multifunctional utility - makes the demonstrated carbon foams remarkable competitors with other three-dimensional carbon materials typically based on pyrolyzed biopolymers or on covalently bonded graphene and carbon nanotube frameworks.

Photocatalytic activity of nitrogen-doped TiO2-based nanowires: a photo-assisted Kelvin probe force microscopy study

In this study, a set of nitrogen-doped TiO2-based nanomaterials demonstrating photocatalytic activity was developed by combining the efforts of lattice doping and metal nanoparticle decoration and tested for photo-degradation of methylene blue dye by applying solar simulator irradiation. The surface potential shifts of these TiO2-based photocatalytic nanomaterials measured by Kelvin probe force microscope have been used to study the degree of electron generation of the photocatalysts after irradiation and were well correlated with the photocatalytic activity. The nitrogen-doped TiO2 nanowires decorated with Pt nanoparticles can induce obvious electron accumulation and result in a large shift of surface potential. The analysis shows a clear correlation between the surface potential shift and the photodegradation activity. Furthermore, a thorough comparative photocatalytic activity study combined with X-ray photoelectron spectroscopy analysis of the materials—doped with nitrogen under various conditions—reveals that the photocatalytic efficiency of the catalysts is maintained even if the lattice doping is leached e.g., by thermal treatments after doping.Graphical AbstractBy monitoring the surface potential shifts of various TiO2-based photocatalysts by photo-assisted Kelvin probe force microscopy, we obtain a useful tool for developing novel materials with high photocatalytic activity.

INCREASING CHEMICAL SELECTIVITY OF CARBON NANOTUBE-BASED SENSORS BY FLUCTUATION-ENHANCED SENSING

Nowadays gas detection in the ppm and sub-ppm domain is essential in terms of environmental protection as well as reducing sanitary risks. However, detecting systems to perform these measurements (e.g., gas chromatographs) are expensive and take up too much space, thus their use is not likely to become wide-spread. Small, cheap and easily mountable sensors, such as resistive sensors are more applicable for this purpose. But the main disadvantage of these sensors is the lack of chemical selectivity. Yet, a novel method called fluctuation-enhanced sensing (FES), which considers the sensor noise as the source of chemical information, can be used to improve selectivity. Since carbon nanotube (CNT)-based sensors are regarded as promising devices for FES measurements, we investigated whether stationary fluctuations in output signal (dc-resistance) of a CNT sensor could be used to increase chemical selectivity. In this work we prove that FES is applicable to increase selectivity of CNT sensors: air polluting gases (N2O, NH3 and H2S) and their mixtures can be distinguished. Furthermore, we also show that different concentrations of the same analyte can be differentiated and chemical selectivity can be extended into the sub-ppm region.

A novel WS2 nanowire-nanoflake hybrid material synthesized from WO3 nanowires in sulfur vapor

In this work, WS2 nanowire-nanoflake hybrids are synthesized by the sulfurization of hydrothermally grown WO3 nanowires. The influence of temperature on the formation of products is optimized to grow WS2 nanowires covered with nanoflakes. Current-voltage and resistance-temperature measurements carried out on random networks of the nanostructures show nonlinear characteristics and negative temperature coefficient of resistance indicating that the hybrids are of semiconducting nature. Bottom gated field effect transistor structures based on random networks of the hybrids show only minor modulation of the channel conductance upon applied gate voltage, which indicates poor electrical transport between the nanowires in the random films. On the other hand, the photo response of channel current holds promise for cost-efficient solution process fabrication of photodetector devices working in the visible spectral range.

Electrocatalytic Properties of Carbon Nanotubes Decorated with Copper and Bimetallic CuPd Nanoparticles

Copper particles were deposited on the surface of palladium decorated buckypapers by the means of chemical plating, in which the palladium nanoparticles act as catalyst for initiating the reduction of complexed Cu2+ ions in the presence of formaldehyde. By adjusting the plating time, it is possible to tune the size of the highly crystalline copper particles and at the same time control the coverage of the metal on the surface of carbon nanotubes. In a subsequent step, the copper particles were partially exchanged with palladium to obtain bimetallic CuPd nanoparticles on the nanotubes by applying galvanic replacement reactions in aqueous solution of Pd2+ ions. Sufficiently high electrical conductivity of both Cu and CuPd/buckypaper composites makes them suitable to be used as electrocatalytic electrodes. The electrochemical properties of the different electrode materials were also evaluated by the model reaction of methanol electrooxidation. The degradation mechanism of copper and CuPd bimetallic catalysts were systematically studied by employing surface characterization techniques on the composite films after electrocatalytic testing in alkaline solution in the presence and absence of methanol. Chronoamperometric test of the catalysts/buckypaper composites had revealed that palladium plays a protecting role in CuPd bimetallic structure during methanol electrooxidation.

On the Interaction of Metal Nanoparticles with Supports

Abstract Metal nanoparticles supported on surfaces often undergo sintering even at moderate temperatures. The degree of sintering is typically influenced by the surface chemistry indicating that besides the commonly believed Ostwald ripening also other processes associated with metal surface diffusion are responsible for the nanoparticle size growth. In addition to the deterioration in metal dispersion, carbon supports can show chemical instability leading to their partial degradation in the proximity of the nanoparticles both in reducing and oxidizing environments at elevated temperatures. This work reports a study of Pd, Pt and Ni nanoparticles anchored on carbon (activated carbon, graphite and carbon nanotubes) as well as titania (nanoparticles and microparticles) surfaces frequently applied as catalyst materials in heterogeneous catalysis and photocatalysis, and evaluate the potential events causing metal sintering and degradation of the supports using transmission electron microscopy analysis.