Conjugated Polyimidazole Nanoparticles as Biodegradable Electrode Materials for Organic Batteries

Conjugated polymers are promising active materials for batteries. Batteries not only need to have high energy density but should also combine safe handling with recyclability or biodegradability after reaching their end-of-life. Here, π-conjugated polyimidazole particles are developed, which are prepared using atom economic direct arylation adapted to a dispersion polymerization protocol. The synthesis yields polyimidazole nanoparticles of tunable size and narrow dispersity. In addition, the degree of crosslinking of the polymer particles can be controlled. It is demonstrated that the polyimidazole nanoparticles can be processed together with carbon black and biodegradable carboxymethyl cellulose binder as an active material for organic battery electrodes. Electrochemical characterization shows that a higher degree of crosslinking significantly improves the electrochemical performance and leads to clearer oxidation and reduction signals of the polymer. Polyimidazole as part of the composite electrode shows complete degradation by exposure to composting bacteria over the course of 72 h

Electrodeposition of Cu onto Au(111) from Deep Eutectic Solvents: Molar Ratio of Salt and Hydrogen Bond Donor

The electrodeposition of copper onto Au(111) from Deep Eutectic Solvents (DESs) type III has been studied by cyclic voltammetry. Investigations were carried out with mixtures of choline chloride (ChCl) and ethylene glycol (EG) or trifluoroacetamide (TFA). The eutectic compositions and temperatures were determined by differential scanning calorimetry (DSC). For the ChCl/EG DES, a eutectic ratio of 16 : 84 (ChCl:EG) was found instead of the previously reported ratio of 33 : 67. The electrodeposition of copper was studied for electrolytes with different ratios of ChCl to hydrogen bond donor (HBD) to resolve the influence of the composition on the deposition behavior. Both CuCl and CuCl$_{2}$ were used as Cu salts. Underpotential deposition (UPD) is followed by bulk deposition with the diffusion rate of Cu species being dependent on the ratio of ChCl to HBD. With CuCl$_{2}$, both Cu$^{+}$ and Cu$^{2+}$ species are reduced and deposited, whereby the two-electron reduction is more dominant with higher chloride content and presence of EG. However, the properties of the Cu electrodeposition do not result from the freezing-point depression of the DESs, but from the high concentration of ions