Publications by authors named "Magnus Hummelgard"

Triboelectric nanogenerators (TENGs) represent a promising technology for energy harvesting and self-powered sensing with a wide range of applications. Despite their potential, challenges such as the need for cost-effective, large-area electrodes and engineering sustainable triboelectric materials remain, especially given the impending restrictions on single-use engineering plastics in Europe. To address these challenges, engineering nano-graphite-coated paper is presented as a sustainable and high-performance alternative for triboelectric layers.

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Considerable research has been devoted to the development of cathode materials for Al-ion batteries, but challenges remain regarding the behavior of aluminum anodes. Inert oxide (AlO) film on Al surfaces presents a barrier to electrochemical activity. The structure of the oxide film needs to be weakened to facilitate ion transfer during electrochemical activity.

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Material development is essential when studying triboelectric nanogenerators (TENGs). This importance is because the performance of TENGs is highly dependent on the properties of the utilized triboelectric materials. To obtain more specific properties, composites have been developed that combine the features of their components.

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The cycling performance of supercapacitors sometimes becomes limited when electrode materials slough off during frequent charge-discharge cycles, due to weak bonding between the active material and the current collector. In this work, a flexible graphite foil substrate was successfully used as the current collector for supercapacitor electrodes. Graphite foil substrates were treated in different ways with different acid concentrations and temperatures before being coated with an active material (NiMoO4/nanographite).

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Silicon anodes are considered as promising electrode materials for next-generation high capacity lithium-ion batteries (LIBs). However, the capacity fading due to the large volume changes (∼300%) of silicon particles during the charge-discharge cycles is still a bottleneck. The volume changes of silicon lead to a fracture of the silicon particles, resulting in recurrent formation of a solid electrolyte interface (SEI) layer, leading to poor capacity retention and short cycle life.

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Triboelectric nanogenerators (TENGs) have attracted increasing attention because of their excellent energy conversion efficiency, the diverse choice of materials, and their broad applications in energy harvesting devices and self-powered sensors. New materials have been explored, including green materials, but their performances have not yet reached the level of that for fluoropolymers. Here, a high-performance, fully green TENG (FG-TENG) using cellulose-based tribolayers is reported.

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To increase the energy storage density of lithium-ion batteries, silicon anodes have been explored due to their high capacity. One of the main challenges for silicon anodes are large volume variations during the lithiation processes. Recently, several high-performance schemes have been demonstrated with increased life cycles utilizing nanomaterials such as nanoparticles, nanowires, and thin films.

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Metal-semiconductor junctions and interfaces have been studied for many years due to their importance in applications such as semiconductor electronics and solar cells. However, semiconductor-metal networks are less studied because there is a lack of effective methods to fabricate such structures. Here, we report a novel Au-ZnO-based metal-semiconductor (M-S) network in which ZnO nanowires were grown horizontally on gold particles and extended to reach the neighboring particles, forming an (M-S) network.

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Industrially scalable methods for the production of graphene and other nanographites are needed to achieve cost-efficient commercial products. At present, there are several available routes for the production of these materials but few allow large-scale manufacturing and environmentally friendly low-cost solvents are rarely used. We have previously demonstrated a scalable and low-cost industrial route to produce nanographites by tube-shearing in water suspensions.

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Antibacterial agents based on nanoparticles (NPs) have many important applications, e.g., for the textile industry, surface disinfection, wound dressing, water treatment, and food preservation.

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MoS has been studied intensively during recent years as a semiconducting material in several fields, including optoelectronics, for applications such as solar cells and phototransistors. The photoresponse mechanisms of MoS have been discussed but are not fully understood, especially the phenomenon in which the photocurrent slowly increases. Here, we report on a study of the photoresponse flash-light-processed MoS films of different thicknesses and areas.

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Electrically conductive films are key components in most printed and flexible electronics applications. For the solution processing of conductive films, inks containing silver nanoparticles (AgNPs) remain important because of their relatively easy processing and generally low resistivity after a sintering procedure. Because the commonly used, moderate sintering temperatures of 150-300 °C are still too high for most low-cost flexible substrates, expanding the knowledge of surface-ink interactions that affect the sintering temperature is desirable.

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The number of applications based on graphene, few-layer graphene, and nanographite is rapidly increasing. A large-scale process for production of these materials is critically needed to achieve cost-effective commercial products. Here, we present a novel process to mechanically exfoliate industrial quantities of nanographite from graphite in an aqueous environment with low energy consumption and at controlled shear conditions.

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Many solution processing methods of exfoliation of layered materials have been studied during the last few years; most of them are based on organic solvents or rely on surfactants and other funtionalization agents. Pure water should be an ideal solvent, however, it is generally believed, based on solubility theories that stable dispersions of water could not be achieved and systematic studies are lacking. Here we describe the use of water as a solvent and the stabilization process involved therein.

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Low-cost solution-processing of highly conductive films is important for the expanding market of printed electronics. For roll-to-roll manufacturing, suitable flexible substrates and compatible postprocessing are essential. Here, custom-developed coated papers are demonstrated to facilitate the inkjet fabrication of high performance copper patterns.

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Highly sensitive graphene-based gas sensors can be made using large-area single layer graphene, but the cost of large-area pure graphene is high, making the simpler reduced graphene oxide (rGO) an attractive alternative. To use rGO for gas sensing, however, require a high active surface area and slightly different approach is needed. Here, we report on a simple method to produce kaolin-graphene oxide (GO) nanocomposites and an application of this nanocomposite as a gas sensor.

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Printed electronics is a rapidly developing field where many components can already be manufactured on flexible substrates by printing or by other high speed manufacturing methods. However, the functionality of even the most inexpensive microcontroller or other integrated circuit is, at the present time and for the foreseeable future, out of reach by means of fully printed components. Therefore, it is of interest to investigate hybrid printed electronics, where regular electrical components are mounted on flexible substrates to achieve high functionality at a low cost.

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The coating of thin films is applied in numerous fields and many methods are employed for the deposition of these films. Some coating techniques may deposit films at high speed; for example, ordinary printing paper is coated with micrometre-thick layers of clay at a speed of tens of meters per second. However, to coat nanometre thin films at high speed, vacuum techniques are typically required, which increases the complexity of the process.

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Gold nanobelts are of interest in several areas; however, there are only few methods available to produce these belts. We report here on a simple evaporation induced self-assembly (EISA) method to produce porous gold nanobelts with dimensions that scale across nanometer (thickness ∼80 nm) and micrometer (width ∼20 µm), to decimeter (length ∼0.15 m).

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By applying a voltage pulse to a scanning tunneling microscope tip the surface under the tip will be modified. We have in this paper taken a closer look at the model of electric field induced surface diffusion of adatoms including the van der Waals force as a contribution in formations of a mound on a surface. The dipole moment of an adatom is the sum of the surface induced dipole moment (which is constant) and the dipole moment due to electric field polarisation which depends on the strength and polarity of the electric field.

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Metallic nanoparticle inks are used for printed electronics, but to reach acceptable conductivity the structures need to be sintered, usually using a furnace. Recently, sintering by direct resistive heating has been demonstrated. For a microscopic understanding of this Joule heating sintering method, we studied the entire process in real time inside a transmission electron microscope equipped with a movable electrical probe.

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A single-step, premixing method was used to directly deposit gold nanoparticles on Mo(6)S(3)I(6) (MSI) molecular wire bundles. Gold nanoparticles with different sizes and densities were coated on the MSI by changing the concentration of the gold containing salt, HAuCl(4). TEM, SEM, and EDX characterization showed deposition of gold nanoparticles on the MSI nanowire surface.

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Joule heating of bundles of Mo(6)S(3)I(6) nanowires, in real time, was studied using in situ TEM probing. TEM imaging, electron diffraction, and conductivity measurements showed a complete transformation of Mo(6)S(3)I(6) into Mo via thermal decomposition. The resulting Mo nanowires had a conductivity that was 2-3 orders higher than the starting material.

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Clay-based nanocomposites have been studied for several decades, mainly focusing on clay-polymer nanocomposites. Here, we report on a simple wet chemical method to synthesize clay-APTES-Au (CAAu) nanocomposites, where 3-aminopropyltriethoxysilane (APTES) acts as the linkage. The silane terminal of APTES formed bonds with the clay surface, while the other -NH(2) terminal bonds to gold nanoparticles.

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Films that are nanostructured in two- or three-dimensions, such as porous ones, are made by several methods including templated growth and self-assembly. Here, we report on a new method that is based on evaporation-induced growth of nanoparticle gold films on a water surface. The film growth was done in a similar way to the well-known evaporation-induced colloidal crystal growth method, but in contrast, we did not directly deposit the film on a solid substrate.

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