Stability carbon support

Recently, rhodium and ruthenium-based carbon-supported sulfide electrocatalysts were synthesized by different established methods and evaluated as ODP cathodic catalysts in a chlorine-saturated hydrochloric acid environment with respect to both economic and industrial considerations [46]. In particular, patented E-TEK methods as well as a non-aqueous method were used to produce binary RhjcSy and Ru Sy in addition, some of the more popular Mo, Co, Rh, and Redoped RuxSy catalysts for acid electrolyte fuel cell ORR applications were also prepared. The roles of both crystallinity and morphology of the electrocatalysts were investigated. Their activity for ORR was compared to state-of-the-art Pt/C and Rh/C systems. The Rh Sy/C, CojcRuyS /C, and Ru Sy/C materials synthesized by the E-TEK methods exhibited appreciable stability and activity for ORR under these conditions. The Ru-based materials showed good depolarizing behavior. Considering that ruthenium is about seven times less expensive than rhodium, these Ru-based electrocatalysts may prove to be a viable low-cost alternative to Rh Sy systems for the ODC HCl electrolysis industry. 

Palladium on a purified activated carbon support has been selected as a very suitable catalyst for the reaction. We have reported that the performance of this catalyst looks very promising and that a CFC hydrogenolysis plant based on this catalyst is both technically and economically feasible [3-5]. This paper deals with the stability of the selected catalyst, the long term influence of the hydrogen to CCI2F2 feed ratio on the catalyst performance and the influence of the possible recycle components methane and CHCIF2 on the performance of the catalyst. 

The most spectacular results, in terms of comparison between CFPs- and carbon-supported metal catalysts, were likely provided by Toshima and co-workers [33,34]. As illustrated in Section 3.3.3, they were able to produce platinum and rhodium catalysts by the covalent immobilization of pre-formed, stabilized metal nanoclusters into an amine functionalized acrylamide gel (Scheme 5). To this purpose, the metal nanopartides were stabilized by a linear co-polymer of MMA and VPYR. The reaction between its ester functions and the amine groups of the gel produced the covalent link between the support and the... 

These routes rely on the direct transformation of soluble molecular species into supported metal (or mixed metal) particles. One method that has recently become popular is the "polyol" method. This takes a solution of metal salts, the carbon support, and a polyalcohol such as ethylene glycol. On heating, the polyol acts as both stabilizer and reductant, forming reduced metal particles on the carbon. It has been used successfully to prepare Ft and PtRu catalysts. ... 

More recently the transformation of carbon-supported Pt colloids of approximately 1 nm diameter into Pt alloys has been reported, which seems to yield an even better catalyst, since the alloy particles—although coarser than the initial Pt particles—show improved catalytic activity and stability. It is not unlikely that from these alloys by in-situ oxidation transition-metal platinum bronzes like NLPt304 are formed, being the catalysts proper. 

The inherent problem of limited thermal and chemical stability of metal anchoring sites on carbon limits not only the activation temperature but also the application conditions [185]. In oxidizing environments carbon supports are much less stable than the macroscopic bum-off temperature (sec Figs 28 and 17). In order to... 

Antolini, E., Formation, microstructural characteristics and stability of carbon supported platinum catalysts for low temperature fuel cells, J. Mater. Sci., 38, 2995, 2003. 

Ball, S.C. et ah. The effect of dynamic and steady state voltage excursions on the stability of carbon supported Pt and PtCo catalysts, ECS Trans., 3, 595, 2006. 

Bezerra et al extensively reviewed heat treatment and stability effects of various Pt/C, Pt-M/C, and C-supported Pt-free alloy catalysts, taking into account particle sizes and stiuctural parameters. Appropriate heat treatment of Pt/C catalysts improves ORR activity by stabilizing the carbon support against corrosion, which in turn increases the cathode life time. Depositing mixed-metal Pt monolayers on carbon-supported metal nanoparticles or Pt monolayers on noble/non-noble core-shell nanoparticles leads to enhanced electrode performance. RRDE experiments on the catalytic activity of Pt-M (M = Au, Pd, Rh, Ir, Re or Os) monolayers on carbon-supported Pd nanoparticles showed that an 80 20 PtiM ratio for the nuxed monolayers performs better than commonly nsed Pt/C catalysts. ... 

---