Synthesis and Characterization of PT-based Fuel Cell Catalysts PDF Download

Author: Hee Soo Kim
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Category :
Languages : en
Pages : 262

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Author: Sudharsan Sridhar
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Category : Carbon compounds
Languages : en
Pages : 0

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Fuel Cells convert the chemical energy of a fuel and an oxidizing agent into electricity through a pair of redox reactions. Proton Exchange Membrane (PEM) fuel cells convert (efficiency-60%) hydrogen and air to power the electric motors with zero emissions, facilitating the development of environmentally friendly and sustainable automobile technologies. One of the major obstacles for larger commercial viability of Fuel Cells for automobile applications is their cost-effectiveness. Currently, fuel cells use platinum as a catalyst material, which is prohibitively expensive for commercial automobile applications. The development of non-Platinum Group Metal (non-PGM) catalyst materials with similar electrochemical performance to that of Platinum is essential for adopting fuel cells in automobile technologies in a big way. Hence, this research focused on the synthesis and characterization of three different non-PGM catalyst materials based on graphene and graphene oxide with nitrogen and Zeolite Imidazole Frameworks (ZIF) and an additional transition metal (Fe) loading. Various characterization techniques were performed to analyze the chemical, morphological, and electrochemical properties of each of these synthesized materials. The synthesized catalyst materials are N-GR-ZIF, N-RGO-ZIF, and N-RGO-Fe-ZIF with varying nitrogen doping. N-RGO-Fe-ZIF exhibited electrochemical characteristics that are quite comparable to that of Pt-based catalysts. The details of the synthesis process and characterization of the synthesized materials are discussed in this dissertation.

Author: Christopher Odetola
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Languages : en
Pages : 0

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Catalysts in the electrodes of polymer exchange membrane fuel cells (PEMFCs) serve a critical function in reactions which can be used to generate electrical energy from chemical fuels. Pt nanoparticles are commonly dispersed on a conductive support and used as electrode materials in these devices because of their exceptional catalytic activity and electrochemical active surface area. The performance and stability of these electrodes strongly depend on the characteristics of the support. Catalysts supported on high surface area carbon black are widely used in low-temperature fuel cells. In PEMFCs, these catalyst materials can be exposed to high potential and low pH values, resulting in irreversible loss of activity that will limit the useful lifetime of the cell, ultimately leading to its failure. Pt is a noble metal which has good intrinsic stability, but carbon is not thermodynamically stable resulting in the corrosion of the catalyst support under these conditions. The design of more resilient platinum catalyst supports to carry out the successful reaction in a fuel cell's catalyst layer is required to extend the lifetime of PEMFCs degradation. In this thesis, two approaches were used to synthesize robust catalyst support materials for fuel cell applications. In the first case, carbon surfaces were functionalised to enhance their interactions with the catalyst and secondly, stable metal oxide was combined with modified carbon substrates, to maximise contacts within the composite electrocatalysts and to prevent carbon corrosion of a single phase carbon support catalyst. TiO2 NPs, were first chemically bonded to the surfaces of Vulcan carbon to help anchor the Pt catalyst nanoparticles through strong metal-support interactions. Validation of a dual phase catalyst support is an important goal of this research. Each material phase offers a unique advantage that can only be recognized by the preparation of a composite electrocatalyst. Pristine Vulcan (PV) was functionalised with glucose hydroxyl functional groups that react with the base titanium metal alkoxide in a sol-gel reaction and then calcined to form a more chemically crystalline surface. This is followed by impregnation reduction process to deposit the nanostructured Pt catalyst. Material characterization data of synthesized materials were used to correlate the effects of support structure and composition on resilient performance. Advantages from the TiO2/C supports toward performance and durability were contrasted against a set of control samples and demonstrated ex situ. The prepared composite catalysts showed substantial enhancements toward oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR) as well as improved stability of the Pt-TiO2 heterogeneous interface formed between catalyst and support. The enhanced performance and durability of these composite catalysts is improved by applying the science of materials and interfaces to the synthesis of composite supports, thus serving as an example for further progress and optimization. Irradiation of these composite catalysts with UV-visible light also showed ~ 171 % photo enhanced activity for MOR, which clearly demonstrates a synergistic effect between the photo- and electrocatalysts. The comparison between the prepared catalysts indicates that there is an appropriate ratio of carbon and TiO2 to obtain the best performance of these photoelectroactive materials. These results demonstrate that methanol oxidation is achieved by electro- and photoelectrocatalysis using a simple and affordable method. This procedure can be conveniently exploited to enhance the response of direct methanol fuel cell electrodes.

Author: Min Chen
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Category : Catalysts
Languages : en
Pages :

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"Synthesis of high performance catalysts is one of the tasks for fuel cell researchers. In this thesis work, carbon supported Pt and Pt-Co alloy catalysts were prepared by several improved methods. Thermal gravity analysis (TGA), transmission electron microscope (TEM), and X-ray diffraction (XRD) were used to characterize these catalysts. Electrochemical activities of the catalysts were measured by cyclic voltammetry (CV) and oxygen reduction reaction (ORR)"--Abstract, leaf iii.

Author:
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Category :
Languages : en
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Languages : en
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The present state-of-art Proton Exchange Membrane Fuel Cell (PEMFC) technology is based on platinum (Pt) as a catalyst for both the fuel (anode) and air (cathode) electrodes. This catalyst is highly active but susceptible to poisoning by CO, which may be present in the H2-fuel used or may be introduced during the fuel processing. Presence of trace amount of CO and H2S in the H2-fuel poisons the anode irreversibly and decreases the performance of the PEMFCs. In an effort to reduce the Pt-loading and improve the PEMFC performance, we propose to synthesize a number of Pt-based binary, ternary, and quaternary electrocatalysts using Ru, Mo, Ir, Ni, and Co as a substitute for Pt. By fine-tuning the metal loadings and compositions of candidate electrocatalysts, we plan to minimize the cost and optimize the catalyst activity and performance in PEMFC. The feasibility of the novel electrocatalysts will be demonstrated in the proposed effort with gas phase CO and H2S concentrations typical of those found in reformed fuel gas with coal/natural gas/methanol feedstocks. During this reporting period we synthesized four Pt-based electrocatalysts catalysts (Pt/Ru/Mo/Se, Pt/Ru/Mo/Ir, Pt/Ru/Mo/W, Ptr/Ru/Mo/Co) on Vulcan XG72 Carbon support by both conventional and ultra-sonication method. From current-voltage performance study, the catalytic activity was found in the increasing order of Pt/Ru/Mo/Ir> Pt/Ru/Mo/W> Pt/Ru/Mo/Co> Pt/Ru/MO/Se. Sonication method appears to provide better dispersion of catalysts on carbon support.

Author: Sonam Patel
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Category :
Languages : en
Pages :

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Platinum (Pt) and platinum alloys have attracted wide attention as catalysts to attain high performance to increase the power density and reduce the component cost of polymer electrolyte membrane fuel cells (PEMFCs). Extensive research has been conducted in the areas of new alloy development and understanding of mechanisms of electrochemical oxygen reduction reaction (ORR). The durability of PEMFCs is also a major barrier to the commercialization of these fuel cells. Recent studies have suggested that potential cycling can gradually lead to loss of active surface area due to Pt dissolution and nanoparticle grain growth [1]. In this thesis we report a one-step synthesis of highly-dispersed Pt nanoparticles and Pt- Cobalt supported on Ketjen carbon black (20% Pt/C & 20% Pt3Co/C) as electro-catalysts for PEMFCs. Pt particles with size in the range of ~ 2.6nm (Pt/C) and 3.9 nm (Pt3Co/C) were obtained through adsorption on carbon supports and subsequently thermal decomposition of platinum acetylacetonate (Pt(acac)2). A comparative characterization analysis, including X-ray diffraction (XRD), high resolution transmission electron microscope (HR-TEM), FT-iR, EDAX, cyclic voltammetry (CV), and oxygen reduction reaction (ORR) activity, was performed on the synthesized and commercial (46.5wt% TKK) catalysts. The analysis was to reveal the Pt dispersion on the carbon support, particle size and distribution, electrochemical surface area (ECA), and ORR activities of these catalysts. It was found that the synthesized Pt/C showed similar particle size to that of the TKK catalysts (2.6nm and 2.7nm, respectively), but narrower particle size distribution; while the particle size for Pt3Co/C was found to be ~3.9 nm. Accelerated durability tests (ADT) under potential cycles were also performed for Pt/C and TKK to study the electrochemical degradation of the catalysts in corrosive environments. The ADTs revealed that the two catalysts (Pt/C & TKK) were comparable with respect to degradation in ECA and ORR activities. Initial electrochemical evaluation of Pt3Co/C was conducted, but durability studies were not attempted in this thesis due to its worse ORR kinetics than those of the Pt/C catalyst. From the experimental data, it was found that particle size impacted negatively the ECA and ORR activity of the catalysts.

Author: Geng, Xi
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Category :
Languages : en
Pages : 238

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Abstract: Fuel cell, as an alternative green power source for automobiles and portable electronics, has attracted worldwide attention due to its desirable properties such as high energy density and low greenhouse gas emission. Despite great progress in the past decades, several challenges still remain as obstacles for the large-scale commercialization. Among them, the high cost of Pt-based electrode material is considered as a major barrier, while the life span or stability of electrode catalysts is another concern since the electrocatalysts can be easily poisoned during the fuel cell operation. In order to overcome these issues, nanostructured carbon materials, especially carbon nanotubes (CNTs), are studied as catalyst support. In addition, recent research also suggests that the coupling of a second metal element with Pt can effectively protect the electrocatalysts from being poisoned and thus improve their long-term durability. The objective of the present work was to demonstrate an efficient synthetic method for the preparation of CNTs supported binary PtM (M=Ru, Sn) electrocatalysts. In this project, a polymer wrapping technique along with an in-situ polyol reduction strategy was adopted to decorate well-dispersed binary PtM nanoparticles on the surface of modified-CNTs. The unique nanostructures as well as the excellent catalytic activities of the as-prepared nanohybirds were investigated through a diversity of physiochemical and electrochemical characterization techniques. This fabrication method provided a simple and convenient route to assemble Pt-based catalyst on carbon substrates, which is useful for the further development of high-performance fuel cell catalysts.

Author: Shamsuddin Ilias
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Category :
Languages : en
Pages : 10

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The present state-of-art Proton Exchange Membrane Fuel Cell (PEMFC) technology is based on platinum (Pt) as a catalyst for both the fuel (anode) and air (cathode) electrodes. This catalyst is highly active but susceptible to poisoning by CO, which may be present in the H{sub 2}-fuel used or may be introduced during the fuel processing. Presence of trace amount of CO and H{sub 2}S in the H{sub 2}-fuel poisons the anode irreversibly and decreases the performance of the PEMFCs. In an effort to reduce the Pt-loading and improve the PEMFC performance, we propose to synthesize a number of Pt-based binary, ternary, and quaternary electrocatalysts using Ru, Mo, Ir, Ni, and Co as a substitute for Pt. By fine-tuning the metal loadings and compositions of candidate electrocatalysts, we plan to minimize the cost and optimize the catalyst activity and performance in PEMFC. The feasibility of the novel electrocatalysts will be demonstrated in the proposed effort with gas phase CO and H{sub 2}S concentrations typical of those found in reformed fuel gas with coal/natural gas/methanol feedstocks. During this reporting period several tri-metallic electrocatalysts were synthesized using both ultra-sonication and conventional method. These catalysts (Pt/Ru/Mo, Pt/Ru/Ir, Pt/Ru/W, Ptr/Ru/Co, and Pt/Ru/Se on carbon) were tested in MEAs. From Galvonstatic study the catalytic activity was found in the order of: Pt/Ru/Mo/C> Pt/Ru/Ir/C> Pt/Ru/W/C> Ptr/Ru/Co/C> and Pt/Ru/Se. It appears that electrocatalysts prepared by ultra-sonication process are more active compared to the conventional technique. Work is in progress to further study these catalysts for CO-tolerance in PEMFC.

Author: Li Ren
Publisher:
ISBN:
Category : Fuel cells
Languages : en
Pages : 154

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"In the thesis work, Pt-based binary, ternary, quaternary alloy anode catalysts supported on sonochemically treated multi-walled carbon nanotubes (CNTs) were synthesized with ethylene glycol reduction of corresponding metal chloride salts. Inductively coupled plasma-mass spectroscopy (ICP-MS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM) were used for catalyst characterization. Cyclic voltammetry for methanol oxidation and CO stripping were used to evaluate the performance of the catalysts. PtRu nanoparticles supported on CNTs (PtRu/CNT) were prepared under a series of pHs. It was found that the PtRu particle size, composition, and catalytic activity were all sensitive to the deposition pHs. CO stripping results provided the peak potential and active surface area for each catalyst. The atomic ratios tended to approach the predetermined ratio 1:1 with the increase of pH, which is favored by bi-functional catalytic mechanism. PtRu catalysts prepared at higher pHs presented better electrochemical activity toward methanol oxidation. Humidified oxygen treatment of the PtRu/CNT led to improved activity of the catalysts toward methanol electro-oxidation, implying that Ru hydroxide is better than Ru as a co-catalyst. PtRu, PtOs, PtRuOs, and PtRuOsIr nanoparticles supported on CNTs with atomic ratios of Pt:Ru (tr:46), Pt:Os (80:20), Pt:Ru:Os (54:36:10), and Pt:Ru:Os:Ir (44:36:10:5) were prepared. Cyclic voltammetry for the methanol oxidation and CO stripping at the catalysts showed that PtRu/CNT and PtRuOsIr/CNT have the best performance toward methanol oxidation, PtRuOs/CNT has the lowest activity, but PtOs/CNT exhibits better catalytic activity only at potential or 0.73 V"--Abstract, leaf iii.