Alkali Cation Effect on CO2 Electroreduction to CO: A Local Colligative Property

Converting carbon dioxide (CO2) into valuable products is one of the most important processes for a sustainable society. Especially, the electrochemical CO2 reduction reaction (CO2RR) offers an effective means, but its reaction mechanism is not yet fully understood. Here, we demonstrate that cation-coupled electron transfer (CCET) is a rate-determining step in the CO2RR to carbon monoxide. The first-principles-based multiscale simulation identifies a single cation that coordinates a CO2− intermediate adsorbed on Ag electrode. The CCET is experimentally verified by a collapse of the CO2RR polarization curves upon correcting Nernstianly for a bulk cation concentration. As further confirmation, a kinetic study shows that the CO2RR obeys first-order kinetics on a local cation concentration. Finally, this work unveils that the cation effect on CO2RR originates from the local colligative property, and further highlights the importance of ion-pairing tendency for electrochemical interface design to achieve high-performance CO2 electrolysis.

Alkali Cation Effect on CO2 Electroreduction to CO: A Local Colligative Property

Converting carbon dioxide (CO2) into valuable products is one of the most important processes for a sustainable society. Especially, the electrochemical CO2 reduction reaction (CO2RR) offers an effective means, but its reaction mechanism is not yet fully understood. Here, we demonstrate that cation-coupled electron transfer (CCET) is a rate-determining step in the CO2RR to carbon monoxide. The first-principles-based multiscale simulation identifies a single cation that coordinates a CO2− intermediate adsorbed on Ag electrode. The CCET is experimentally verified by a collapse of the CO2RR polarization curves upon correcting Nernstianly for a bulk cation concentration. As further confirmation, a kinetic study shows that the CO2RR obeys first-order kinetics on a local cation concentration. Finally, this work unveils that the cation effect on CO2RR originates from the local colligative property, and further highlights the importance of ion-pairing tendency for electrochemical interface design to achieve high-performance CO2 electrolysis.

Influence of single charge salting-out agents on solvent extraction of iron (III) from chloride solutions with oxygen-containing extractants

The work is devoted to the solvent extraction of iron(III) from chloride solutions of single-charge salting-out agents with 2-octanone, 1-octanol, and their mixture at a 1:1 ratio. A comparison of the effect of the salting-out ability of single-charge cations on the extraction of iron (III) was made. It was found that at the cation concentration is less than 6 mol∙dm-3, the salting-out ability increases in the row NH4+ < K+ < Na+ < Li+ < H+.

Impact of Sintered Temperature on the Heat and Cation Transport in NaK-BASE Tube

Alkali metal thermoelectric converter (AMTEC) is a clean energy converter that can be coupled with biomass for power generation. In present research, the transport of heat and cation was investigated in NaK-BASE tubes prepared at different sintered temperatures. The heat conduction and the fractal model were employed to investigate the temperature distributions based on the microstructures of the NaK-BASE tubes sintered at different temperatures, and the transport of Na+ and K+ in NaK-BASE tube was simulated by Poisson-Nernst-Planck multi-ions transport model, and the cation concentrations and surface charge densities were obtained in the NaK-BASE tubes with different temperatures. The results showed that microstructure of the NaK-BASE was related to the sintered temperature, and the microstructure of the NaK-BASE impacted the temperature distribution, the cation concentration and the surface charge density of Na+ and K+ in the NaK-BASE tubes. At the same heat source temperature, the average temperature in the NaK-BASE prepared at high sintered temperature was higher than that prepared at low sintered temperature. In addition, the increase of the average temperature resulted in the increase of the cation concentration and the surface charge density of Na+ and K+ in the NaK-BASE, therefore, the performance of the NaK-AMTEC could be enhanced by increasing the sintered temperature and the average temperature of the NaK-BASE.

A fundamental study of the thermoelectrochemistry of ferricyanide/ferrocyanide: cation, concentration, ratio, and heterogeneous and homogeneous electrocatalysis effects in thermogalvanic cells

Thermocells can sustainably generate electricity from waste heat temperature gradients. This study investigates numerous fundamental aspects of thermocells, and how to explain and model such aspects.