Preparation and Electrochemical Performance of a Graphene Cathode Catalyst Decorated With Pt by Prolysis

For fuel cells, to produce high-quality and low-platinum catalyst is a pressing technical problem. In this study, graphene cathode catalysts with controllable platinum content were decorated by pyrolyzing chloroplatinic acid under various process parameters to obtain a high catalytic activity and durability. The results show that platinum particles generated by pyrolyzing chloroplatinic acid are uniformly loaded on graphene without agglomeration. The average particle size of platinum particles is about 2.12 nm. The oxygen reduction reaction catalytic activity of catalyst samples first increases, then decreases with increasing platinum loading in cyclic voltammetry and LSV. Compared with the commercial Pt/C (20 wt% Pt) catalyst, the initial potential and the current density retention rate of the catalyst decorated with 8% platinum are 55 mV and 23.7% higher, respectively. From i-t curves, it was found that the stability of the catalyst prepared in this paper was improved compared with the commercial Pt/C catalyst. The catalysts prepared in the present research exhibits superior catalytic activity and stability.

pH-responsive Pt-based nanoradiosensitizer for enhanced radiotherapy via oxidative stress amplification

Tumor radioresistance is a major issue in radiotherapy. To address it, a pH-responsive nanoradiosensitizer was synthesized employing a simple method. Initially, chloroplatinic acid was reduced by human serum albumin (HSA)...

Influence of Boron, Tungsten and Molybdenum Modifiers on Zirconia Based Pt Catalyst for Glycerol Valorization

The influence of boron, tungsten and molybdenum modifiers on zirconia-based Pt catalyst was studied for glycerol valorization. Zirconia modified supports were prepared by impregnation of ZrO2 with either boric, silicontungstic or phosphomolybdic acids to obtain supports with enhanced Brönsted acidic properties. The modified supports were subsequently impregnated with chloroplatinic acid to obtain Pt-based catalysts. Pt incorporation resulted in the increase in Lewis acidity of the solids, being more significant for the Pt//W/ZrO2 catalyst. Reduced Pt catalysts were tested for the liquid-phase glycerol hydrogenolysis, observing a synergistic effect between catalyst acid sites and metal function that proved to be crucial in glycerol hydrogenolysis. The Pt//W/ZrO2 catalyst was the most active catalyst in this reaction, being the only leading to 1,3-PDO (45% sel., 160 °C) while Pt//Mo/ZrO2 is the best option for 1,2-PDO (49% sel., 180 °C). Reusability studies carried out for Pt//W/ZrO2 showed that catalytic activity dropped after the first use, remaining constant for the second and subsequent ones. Selectivity to reaction products also changes during reuses. Therefore, the selectivity to 1,2 PDO increases in the first reuse in detriment to the selectivity to n-propanol whereas the selectivity to 1,3-PDO remains constant along the uses. This behavior could be associated to the lixiviation of W species and/or catalyst fouling during reaction runs.

Comparative Study of Different Electrochemical Techniques for the Preparation of Supported Pt-Ru Catalysts

Bimetallic Pt-Ru particles supported on glassy carbon rods were synthesized by simultaneous electrochemical deposition. Pt-Ru alloy particles were deposited from a dilute aqueous acid solution of chloroplatinic acid and ruthenium trichloride by different electrochemical techniques: (i) coulostatic deposition at constant potential; (ii) double potentiostatic steps; and (iii) multiple cycles of potentiostatic pulses. It was found that particle size distribution, and the morphology and composition of the deposits strongly depend on the deposition method. Scanning electron microscopy images showed the presence of agglomerates with diameters in the submicrometre scale composed of nano-sized particles. The catalysts prepared by multiple cycles of potentiostatic pulses exhibited better activity for methanol oxidation and enhanced tolerance to CO poisoning compared with those prepared by the other techniques. This behaviour could be associated with the structure containing a high number of defects of the particles and a higher ruthenium content in the solid solution.