Enhanced stability of symmetrical polymer electrolyte membrane fuel cell single cells based on novel hierarchical microporous-mesoporous carbon supports

Fuel cell electrodes were prepared from Pt nanocluster activated hierarchical microporous-mesoporous carbon powders. The carbon supports were synthesized from molybdenum carbide applying the high-temperature chlorination method. Six different synthesis temperatures within the range from 600 to 1000 °C were used for preparation of carbon supports. Thermogravimetric analysis, X-ray diffraction, low-temperature nitrogen sorption, and high-resolution scanning electron microscopy methods were used to characterize the structure of the electrode materials and symmetrical membrane electrode assemblies (MEAs). The MEAs prepared were used to conduct the proton exchange membrane fuel cell (PEMFC)single-cell measurements. The polarization and power density curves for single cells were calculated to evaluate the activity of the catalyst materials synthesized. The electrochemically active surface area (from 2.4 to 11.9 m² g^?1) was obtained in order to estimate the contact surface areas of platinum and Nafion® electrolyte. The values of the electrolyte resistance, polarization resistance, and cell degradation rate were calculated from electrochemical impedance spectroscopy data. The carbon materials synthesized within temperature range from 600 to 850 °C were found to be the most suitable supports for PEMFCs, having higher maximum power density values and better stability (cell potential degradation 240 μV h^?1) than commercial carbon-based (Vulcan XC72; 670 μV h^?1) single cells.     

The electrochemical activity of two binary alloy catalysts toward oxygen reduction reaction in 0.1 M KOH

The platinum group metals (Pt, Ir and Ru) and the carbide-derived carbon support with the very high specific surface area were used to synthesise the low noble metal loading Pt-C, IrPt-C and RuPt-C alloy catalysts. The alloying of the platinum group metals in the studied catalysts was proved by the several independent physical characterization methods like: the X-ray diffraction, time of flight secondary ion mass-spectrometry, X-ray photoelectron spectroscopy, scanning and transmission electron microscopy. The electrocatalytic activity toward oxygen reduction reaction of the synthesised catalysts in an alkaline solution was studied and compared with the commercially available Pt-Vulcan. The combined and detail approach using the transmission electron microscopy and inductively coupled plasma mass spectrometry for estimation of the surface area of metal particles is provided. The noticeably higher calculated mass corrected and specific kinetic current density values for Pt-C catalyst were established. For IrPt-C and RuPt-C alloy catalysts, mass corrected current density values are comparable with the commercial Pt-Vulcan. The specific kinetic current density values increase in the following sequence: RuPt-C < IrPt-C < Pt-Vulcan < Pt-C.     

Influence of chemical composition and amount of intermixed ionomer in the catalyst on the oxygen reduction reaction characteristics

Influence of chemical composition of the ionomers (polyvinyl alcohol (PVA) or Nafion®) on the oxygen reduction reaction (ORR) kinetics has been studied. The 5 wt% Nafion-Vulcan showed higher electrochemical activity toward ORR compared with that for the 5 wt% PVA-Vulcan. Four different Nafion® amounts were used to intermixing a carbide-derived carbon (CDC) or Pt-modified CDC catalysts and the highest electrochemical activity toward ORR was established for the 30 wt% Nafion-Pt/CDC catalyst. Influence of the different amounts of Nafion® ionomer in the catalyst is moderate compared to the effect of variation of the carbon support (Vulcan vs. CDC) or the ionomer (PVA vs. Nafion®). The Randles–?evcik relationship was used to estimate the effective electrochemical active surface area (S _eff) of the electrodes, depending on the chemical composition of the ionomer studied.     

The review of advances in interfacial electrochemistry in Estonia: electrochemical double layer and adsorption studies for the development of electrochemical devices

The electrochemistry nowadays has many faces and challenges. Although the focus has shifted from fundamental electrochemistry to applied electrochemistry, one needs to acknowledge that it is impossible to develop and design novel green energy transition devices without a comprehensive understanding of the electrochemical processes at the electrode and electrolyte interface that define the performance mechanisms. The review gives an overview of the systematic research in the field of electrochemistry in Estonia which reflects on the excellent collaboration between fundamental and applied electrochemistry.