Bartlomiej Kowalczyk

Photoconductance and inverse photoconductance in films of functionalized metal nanoparticles

In traditional photoconductors, the impinging light generates mobile charge carriers in the valence and/or conduction bands, causing the material’s conductivity to increase. Such positive photoconductance is observed in both bulk and nanostructured photoconductors. Here we describe a class of nanoparticle-based materials whose conductivity can either increase or decrease on irradiation with visible light of wavelengths close to the particles’ surface plasmon resonance. The remarkable feature of these plasmonic materials is that the sign of the conductivity change and the nature of the electron transport between the nanoparticles depend on the molecules comprising the self-assembled monolayers (SAMs) stabilizing the nanoparticles. For SAMs made of electrically neutral (polar and non-polar) molecules, conductivity increases on irradiation. If, however, the SAMs contain electrically charged (either negatively or positively) groups, conductivity decreases. The optical and electrical characteristics of these previously undescribed inverse photoconductors can be engineered flexibly by adjusting the material properties of the nanoparticles and of the coating SAMs. In particular, in films comprising mixtures of different nanoparticles or nanoparticles coated with mixed SAMs, the overall photoconductance is a weighted average of the changes induced by the individual components. These and other observations can be rationalized in terms of light-induced creation of mobile charge carriers whose transport through the charged SAMs is inhibited by carrier trapping in transient polaron-like states. The nanoparticle-based photoconductors we describe could have uses in chemical sensors and/or in conjunction with flexible substrates.

How and Why Nanoparticle’s Curvature Regulates the Apparent pKa of the Coating Ligands

Dissociation of ionizable ligands immobilized on nanopaticles (NPs) depends on and can be regulated by the curvature of these particles as well as the size and the concentration of counterions. The apparent acid dissociation constant (pK(a)) of the NP-immobilized ligands lies between that of free ligands and ligands self-assembled on a flat surface. This phenomenon is explicitly rationalized by a theoretical model that accounts fully for the molecular details (size, shape, conformation, and charge distribution) of both the NPs and the counterions.

Colloidal assembly directed by virtual magnetic moulds

Interest in assemblies of colloidal particles has long been motivated by their applications in photonics, electronics, sensors and microlenses. Existing assembly schemes can position colloids of one type relatively flexibly into a range of desired structures, but it remains challenging to produce multicomponent lattices, clusters with precisely controlled symmetries and three-dimensional assemblies. A few schemes can efficiently produce complex colloidal structures, but they require system-specific procedures. Here we show that magnetic field microgradients established in a paramagnetic fluid can serve as ‘virtual moulds’ to act as templates for the assembly of large numbers (∼108) of both non-magnetic and magnetic colloidal particles with micrometre precision and typical yields of 80 to 90 per cent. We illustrate the versatility of this approach by producing single-component and multicomponent colloidal arrays, complex three-dimensional structures and a variety of colloidal molecules from polymeric particles, silica particles and live bacteria and by showing that all of these structures can be made permanent. In addition, although our magnetic moulds currently resemble optical traps in that they are limited to the manipulation of micrometre-sized objects, they are massively parallel and can manipulate non-magnetic and magnetic objects simultaneously in two and three dimensions.

Self-Assembly of Nanotriangle Superlattices Facilitated by Repulsive Electrostatic Interactions†

Crystallization of triangular gold nanoprisms into close-packed mono- and multilayers is facilitated by electrostatic repulsions. The ordering of the nanotriangles causes an order-of-magnitude increase in surface-enhanced Raman spectroscopy (SERS) enhancement relative to that of disordered assemblies.

Nanoparticle oscillations and fronts

Chemical oscillations can be coupled to the dynamic self-assembly of nanoparticles. Periodic pH changes translate into protonation and deprotonation of the ligands that stabilize the nanoparticles, thus altering repulsive and attractive interparticle forces. In a continuous stirred-tank reactor, rhythmic aggregation and dispersion is observed; in spatially distributed media, propagation of particle aggregation fronts is seen.

Bridging Interactions and Selective Nanoparticle Aggregation Mediated by Monovalent Cations

Selective aggregation and precipitation of like-charged nanoparticles (NPs) covered with carboxylate ligands can be induced by different monovalent cations. The ordering of critical concentrations required for NP precipitation is Cs(+) ≫ K(+) > Li(+) > Na(+) > Rb(+) and does not correlate with the size of hydrated cations M(+), nor can it be predicted by the Hofmeister series. On the other hand, different anions have no effect on the precipitation trends. These observations are rationalized by a theoretical model combining the elements of the DLVO theory with molecular-level calculations. The key component of the model is the cation-specific binding of various metal cations to the carboxylate ligands.

Control of Surface Charges by Radicals as a Principle of Antistatic Polymers Protecting Electronic Circuitry

Dissipating Static The accumulation of a static charge on polymers and other insulators often causes little more than a slight annoyance but it can lead to the destruction of sensitive electrical equipment. Thus, approaches are required that prevent and dissipate static electricity through improved electrical conductivity, or that ensure complete discharge before a contact with a key piece of equipment. Baytekin et al. (p. 1368) show that surface charges will colocalize with radicals on the surface of a polymer, and that the addition of free radical scavengers causes a discharge of the surface as the charges are removed. The approach was used successfully to produce coatings that protected electronic circuits from damage caused by electrostatic discharge. Removal of radicals destabilizes surface charges, providing a means for rapid dissipation of static electricity. Even minute quantities of electric charge accumulating on polymer surfaces can cause shocks, explosions, and multibillion-dollar losses to electronic circuitry. This paper demonstrates that to remove static electricity, it is not at all necessary to “target” the charges themselves. Instead, the way to discharge a polymer is to remove radicals from its surface. These radicals colocalize with and stabilize the charges; when they are scavenged, the surfaces discharge rapidly. This radical-charge interplay allows for controlling static electricity by doping common polymers with small amounts of radical-scavenging molecules, including the familiar vitamin E. The effectiveness of this approach is demonstrated by rendering common polymers dust-mitigating and also by using them as coatings that prevent the failure of electronic circuitry.

Antibacterial Nanoparticle Monolayers Prepared on Chemically Inert Surfaces by Cooperative Electrostatic Adsorption (CELA)

Cooperative electrostatic adsorption (CELA) is used to deposit monolayer coatings of silver nanoparticles on relatively chemically inert polymers, polypropylene, and Tygon. Medically relevant components (tubing, vials, syringes) coated by this method exhibit antibacterial properties over weeks to months with the coatings being stable under constant-flow conditions. Antibacterial properties of the coatings are due to a slow release of Ag(+) from the particles. The rate of this release is quantified by the dithiol-precipitation method coupled with inductively coupled plasma optical emission spectrometer (ICP-OES) analysis.

Charged nanoparticles as supramolecular surfactants for controlling the growth and stability of microcrystals

Microcrystals of desired sizes are important in a range of processes and materials, including controlled drug release, production of pharmaceutics and food, bio- and photocatalysis, thin-film solar cells and antibacterial fabrics. The growth of microcrystals can be controlled by a variety of agents, such as multivalent ions, charged small molecules, mixed cationic-anionic surfactants, polyelectrolytes and other polymers, micropatterned self-assembled monolayers, proteins and also biological organisms during biomineralization. However, the chief limitation of current approaches is that the growth-modifying agents are typically specific to the crystalizing material. Here, we show that oppositely charged nanoparticles can function as universal surfactants that control the growth and stability of microcrystals of monovalent or multivalent inorganic salts, and of charged organic molecules. We also show that the solubility of the microcrystals can be further tuned by varying the thickness of the nanoparticle surfactant layers and by reinforcing these layers with dithiol crosslinks.

Precision assembly of oppositely and like-charged nanoobjects mediated by charge-induced dipole interactions.

The range of electrostatic interactions controls precisely the mutual orientations of assembling charged nanoobjects. For nonspherically symmetric particles, polarization effects and induced dipoles can dominate charge-charge interactions. These charge-induced dipole interactions mediate orientation-specific aggregation of both oppositely and like-charged particles.