Scientific publications

The break-up of a nanowire with an organic ligand shell into discrete droplets is analysed in terms of the Rayleigh-Plateau instability. Explicit account is taken of the effect of the organic ligand shell upon the energetics and kinetics of surface diffusion in the wire. Both an initial perturbation analysis and a full numerical analysis of the evolution in wire morphology are conducted, and the governing non-dimensional groups are identified. The perturbation analysis is remarkably accurate in obtaining the main features of the instability, including the pinch-off time and the resulting diameter of the droplets. It is conjectured that the surface energy of the wire and surrounding organic shell depends upon both the mean and deviatoric invariants of the curvature tensor. Such a behaviour allows for the possibility of a stable nanowire such that the Rayleigh-Plateau instability is not energetically favourable. A stability map illustrates this. Maps are also constructed for the final droplet size and pinch-off time as a function of two non-dimensional groups that characterise the energetics and kinetics of diffusion in the presence of the organic shell. These maps can guide future experimental activity on the stabilisation of nanowires by organic ligand shells.

We studied the concentration-dependent agglomeration of apolar nanoparticles in different solvents. Octanethiol-stabilized gold nanoparticles (AuNPs) in evaporating liquid droplets were observed in situ using small-angle X-ray scattering. Concurrent analysis of liquid volume and particle agglomeration provided time-dependent absolute concentrations of free and agglomerated particles. All dispersions underwent an initial stage where the particle concentration increased but no agglomerates formed. Subsequently, agglomeration started at concentrations that varied by several orders of magnitude for different solvents. While agglomerates grew, the concentration of the dispersed particles remained at a constant “colloidal solubility” in most solvents. We consistently found that the colloidal stability of AuNPs decreased as cyclohexane > heptane > nonane > decane > toluene and suggest that details of the molecular interactions between solvent and ligand shell set this order.

Surfaces with surface-bound ligand molecules generally attract each other when immersed in poor solvents but repel each other in good solvents. While this common wisdom holds, for example, for oleylamine-ligated ultrathin nanowires in the poor solvent ethanol, the same nanowires were recently observed experimentally to bundle even when immersed in the good solvent n-hexane. To elucidate the respective binding mechanisms, we simulate both systems using molecular dynamics. In the case of ethanol, the solvent is completely depleted at the interface between two ligand shells so that their binding occurs, as expected, via direct interactions between ligands. In the case of n-hexane, ligands attached to different nanowires do not touch. The binding occurs because solvent molecules penetrating the shells preferentially orient their backbone normal to the wire, whereby they lose entropy. This entropy does not have to be summoned a second time when the molecules penetrate another nanowire. For the mechanism to be effective, the ligand density appears to best be intermediate, that is, small enough to allow solvent molecules to penetrate, but not so small that ligands do not possess a clear preferred orientation at the interface to the solvent. At the same time, solvent molecules may be neither too large nor too small for similar reasons. Experiments complementing the simulations confirm the predicted trends.

We introduce a new method for the characterization of particles extracted from steels. Microalloyed steels were dissolved to extract niobium and titanium carbonitride particles, which are of critical importance for the mechanical properties of the steel. The size distribution and chemical composition of the particles were analyzed by single-particle inductively coupled plasma mass spectrometry and compared to results from electron microscopy. Mass spectrometry rapidly provided data on a large number of particles (>2000 in 1 min) and indicated two particle populations that differed in size and composition: smaller particles contained only niobium, whereas larger particles contained both niobium and titanium. Electron microscopy of a much smaller number of particles confirmed the results and indicated that the larger particles had complex, overgrown structures. The combination of single-particle mass spectrometry and electron microscopy enables a better understanding of the precipitation processes that form the particles during steel production at different stages of the thermomechanical-rolling process. A better understanding of the processes helps to improve the rolling process in order to exploit the alloying elements optimally.

The chemical extraction of niobium and titanium carbonitride precipitates from microalloyed steels was studied. Steel samples and chemically synthesized reference nanoparticles were subjected to commonly used extraction protocols, and conditions were systematically varied. High acid concentrations led to particle etching with losses above 10%; long extraction times and small etchant volumes led to the formation of dense SiOx networks that engulfed the extracted particles. The addition of surfactants was found to reduce agglomeration and limit etching. We developed an optimized extraction protocol that can extract and retain particles with diameters below 10 nm with reduced etching and negligible network formation. The resulting particle dispersions are suitable both for efficient electron microscopy of large particle numbers in a single run and colloidal analysis of large numbers of particles in dispersion.

The change from organic solvents to aqueous solvents for safe and robust battery electrolytes is desirable for electrochemical energy storage. Thermodynamically, water has an electrochemical stability window of 1.23 V, and pure water freezes at 0 °C. Such properties clearly restrict the high-voltage applications and temperature adaptability of aqueous electrolytes. Herein, we report an aqueous supporting electrolyte containing imidazolium chloride, showing unprecedented large temperature and electrochemical windows. Thermal analysis over −80 to 80 °C shows such an aqueous electrolyte to be free of transition events of icing and phase changes. X-ray scattering results of these aqueous solutions in the presence of active materials reveal the pivotal role of imidazolium chloride to preserve the liquid phase at rather low temperatures. Metal phthalocyanines with electroactive organic ligand rings and multi-electron-transfer reactions at low negative potentials (−0.2 to −1.6 V vs Ag) are demonstrated in water-based anolytes for redox flow batteries for the first time over a broad temperature range.

Soft robotic systems are increasingly emerging as robust alternatives to conventional robotics. Here, we demonstrate the development of programmable soft actuators based on volume expansion/retraction accompanying liquid–vapor phase transition of a phase-change material confined within an elastomer matrix. The combination of a soft matrix (a silicone-based elastomer) and an embedded ethanol-impregnated polyacrylonitrile nanofiber (PAN NF) mat makes it possible to form a sealed compound device that can be operated by changing the actuator temperature above/below the boiling point of ethanol. The thermo-responsive actuators based on this principle demonstrate excellent bending ability at a sufficiently high temperature (>90 °C) – comparable with compressed air-based soft actuators. The actuator using the mechanism presented here is easy to manufacture and automate and is recyclable. Finally, the actuation mechanism can be incorporated into a wide variety of shapes and configurations, making it possible to obtain tunable and programmable soft robots that could have a wide variety of industrial applications. ER

The controlled positioning of spherical gold nanoparticles and gold nanorods upon self-assembly on a substrate is of great interest for the fabrication of tailored plasmonic devices. Here, an electrostatic approach with a sequential two-step assembly protocol is presented as a cost-effective and high-yield alternative to previously presented, more complex proof of concepts. Three different geometries can be separately produced in large quantities relying on electrostatic attraction and repulsion of the charge-carrying building blocks: a single gold nanoparticle at the tip, the side or on top of a gold nanorod. DLVO theory is used to explain the electrostatic assembly strategy. The process is highly efficient and assembly yields between 79% (at the tip) and 94% (for the nanoparticle at the long side of the nanorod) are achieved.

This work aims to elucidate the role of environmental humidity on the tribological behavior of steel surfaces lubricated with an ionic liquid comprised of a fluorinated phosphonium cation—tributyl-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl-phosphonium—and a dicyanamide anion (i.e. N(CN)2−). Ball-on-disk tribotests were carried out at room temperature and at various levels of relative humidity (RH). Water was found to be required to promote the formation of a tribofilm over the contact area. The reaction layer exhibited a patchy morphology, which resembles that observed formed with conventional antiwear additives such as ZnDTP. A surface-chemical analysis of the tribofilm indicated that the tribofilm is composed of fluorides, oxides, and phosphates, pointing to a stress-induced degradation of the ions and corrosion of the sliding counterparts, which is enabled by the presence of water at the sliding interface.

Gold nanorods (AuNRs) with conductive polymer shells are interesting colloidal building blocks for electronics. Hybrid particles with AuNR cores and poly(3,4-ethylenedioxythiophene) or polystyrene sulfonate (PEDOT:PSS) shells were prepared as stable aqueous dispersions. Film formation during the drying of such dispersions is known to affect the electric conductivity of the material. We observed the mechanisms of drying in thin, spray-coated films with grazing incidence small-angle X-ray scattering (GISAXS). A sparse, uniform monolayer formed because the anisotropic shape of the AuNR inhibited “coffee-ring” effects. We used generalized two-dimensional correlation (2DC) spectroscopy to analyze the GISAXS data and to decipher the microscopic structure formation of the film during drying. Four major scattering peaks were attributed to porous PEDOT, PSS, Au, and the substrate layer. Their time-dependent intensity indicated the sequence of film formation: AuNR with mobile shells arranged on the substrate first, PEDOT and then PSS dried sequentially around the gold core. We discuss the final phase-separation of PEDOT:PSS on the hybrid rods. ER