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  • 1
    In: SusMat, Wiley, Vol. 2, No. 5 ( 2022-10), p. 630-645
    Abstract: FeNC catalysts are promising substitutes of platinum‐type catalysts for the oxygen reduction reaction (ORR). While previous research disclosed that high pyrolysis temperatures are required to achieve good stability, it was identified that a trade‐off needs to be made regarding the active site density. The central question is, if a good stability can also be reached at milder pyrolysis conditions but longer duration retaining more active sites, while enabling the defect‐rich carbon to heal during a long residence time? To address this, a variation of pyrolysis temperatures and durations is used in FeNC fabrication. Carbon morphology and iron species are characterized by Raman spectroscopy and Mössbauer spectroscopy, respectively. Fuel cell (FC) activity and stability data are acquired. The results are compared to ORR activity and selectivity data from rotating ring disc electrode experiments and resulting durability in accelerated stress tests mimicking the load cycle and start‐up and shut‐down cycle conditions. It is discussed how pyrolysis temperature and duration affect FC activity and stability. But, more important, the results connect the pyrolysis conditions to the required accelerated stress test protocol combination to enable a prediction of the catalyst stability in fuel cells.
    Type of Medium: Online Resource
    ISSN: 2692-4552 , 2692-4552
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
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  • 2
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-02, No. 35 ( 2019-09-01), p. 1603-1603
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 35 ( 2019-09-01), p. 1603-1603
    Abstract: Fuel cells are regarded as environmentally friendly energy converters. This, in combination with national and global intentions of energy transition from fossil based resources to renewable ones, makes fuel cells a possible key technology regarding the future energy economy. Because of their advanced state of development, proton exchange membrane fuel cells (PEMFCs) are considered to be the most promising type of fuel cells in terms of commercial use in automotive propulsion. Nevertheless, the high requirements of precious platinum metal for the cathodic oxygen reduction reaction (ORR) is one major reason that still prevents a wide-spread use of this technology to this day. A promising alternative to platinum based catalysts are the so-called non-precious metal based materials. To this day, these catalysts already achieve high current density during PEMFC operation but still need major improvements regarding their durability. In this work, the preparation and characteristics of nanotube based non-precious metal catalysts for the ORR are presented. For the commonly applied platinum based ORR catalysts the positive impact on durability and activity of using carbon nanotubes (CNTs) as carbon support has already widely been proven [1-3]. Here, three different catalyst preparations are presented. First, utilization of commercially available CNTs together with Fe-phenathroline leads to catalyst where FeN x C y moieties are present in-between the CNTs. Secondly, a preceding surface modification step of the commercially available CNTs leads to a material with the active sides directly attached onto the CNTs surface. The third preparation route gives a material where the FeN x C y moieties are directly incorporated into the nanotubes wall. TEM pictures are presented in order to show the structural morphology of the resulting catalysts and the nature of the iron nitrogen active sides is studied via Mößbauer spectroscopy. ORR activity and durability of the resulting nanotube based materials in acidic electrolyte is investigated. PEMFC performance tests clearly show that the connection between active side and nanotube play a crucial role for the activity of the catalyst. Hence, a significantly enhanced performance is found for the catalyst with the active sides incorporated into the nanotube walls. References: [1] X. Wang, W. Li et al., Journal of Power Sources 158 (2006) 154-159. [2] F. Hasché, M. Oezaslan et al., Phys Chem Chem Phys 12 (2010) 15251-15258. [3] T. Maiyalagan, B. Viswanathan et al., Electrochem. Comm. 7 (2005) 905-912.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-01, No. 51 ( 2020-05-01), p. 2795-2795
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 51 ( 2020-05-01), p. 2795-2795
    Abstract: Pyrolysed transition metal porphyrins (MeN x C) were originally developed as alternative catalysts for the electrochemical reduction of oxygen (ORR). The catalytic centers were identified as base transition metal ions, integrated into graphene layers of a carbon matrix via nitrogen atoms. The carbon serves as a conductive support and influences the entire catalytic process with its variable electronic and chemical properties. Thus, this class of materials can be classified as hybrid-material between inorganic and molecular catalysts. Meanwhile it is known that this type of catalysts are also active towards the CO 2 RR. Our presentation will show results of electrochemical studies on pyrolysed transition metal porphyrins (MeN x C) as catalysts for the CO2RR under variation of the metal ions (Me: Fe, Co, Ni, Sn, Zn, Cu , Mn). Their activities are determined in gas diffusion electrode (GDE) configuration using CO 2 , CO or Ar gas feeds. The product composition of the gas phase at the outlet of the cell is analyzed simultaneously by mass spectroscopy. Soluble products are analysed via ion-chromatography. It is shown that the product composition of CO2RR, as well as the respective onset potentials, partial current densities, formation rates, and Faraday efficiencies vary strongly with the type of metal ions investigated in the catalytic center. Fe-, Co- and Ni-based catalysts form predominantly CO and suppress the competing hydrogen evolution reaction. CO-formation rates of 4 mmol/(hcm 2 )at -2V NHE and 200 mA/cm 2 (Faraday efficiency close to 100%) were achieved on not yet optimized GDEs. The formation of significant amounts of hydrocarbons from CO 2 was observed only on the Cu- based material. The analysis of the potential dependence during product formation under different gases fed to the GDE allows initial conclusions about the underlying mechanisms of the CO2RR. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 4
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-02, No. 62 ( 2020-11-23), p. 3156-3156
    Abstract: In recent years, the search for platinum group metal-free oxygen reduction reaction (ORR) catalysts as an inexpensive and sustainable replacement for state-of-the-art Pt-based materials has inspired a lot of work in the field of single-atom Fe-based catalysts (often referred to as Fe/N/C). While promising initial ORR-activities were achieved with different synthesis approaches, [1,2] tackling the lack of durability [3] will require a strategic optimization of the employed preparation routes. A comprehensive fundamental understanding of the catalysts active sites’ electronic structure and local configuration under operating conditions lies at the heart of this process and remains a subject of vivid debate. Several studies employing both ex and in situ Mössbauer and X-ray absorption spectroscopies (XAS) [4–7] have brought insights regarding these questions, but a full unambiguous conclusion has not been reached and the community is seeking for novel approaches to unravel such structure-activity and structure-stability relations. With this motivation, we have used in situ XAS to study two catalysts prepared with distinctively different synthesis approaches and widely free of detectable inorganic side phases, [5,8] and that therefore constitute ideal model systems to draw conclusions applicable to this catalyst family. We focused our attention on the spectral 1s → 3d pre-edge feature of the X-ray absorption near edge structure (XANES) spectrum that is sensitive to any changes in the local site symmetry, orbital occupancy, and spin state of the absorbing atom, [9,10] but that to the best of our knowledge has so far not been looked into in the field. In order to achieve adequate energy resolution to discern the relevant features, the spectra were acquired with a Si(311) monochromator at the SuperXAS beamline of the Swiss Light Source employing our group’s spectroelectrochemical flow cell. [11] As illustrated in Fig. 1a, pseudo-Voigt component fits allow tracking the spectral changes as a function of the applied polarization conditions, as qualitatively indicated with green arrows. When using bulk-sensitive techniques like XAS, one must bear in mind that while the catalytic process and expected site changes of interest take place only on the surface sites in contact with the electrolyte, the observed signal also contains the spectral contributions of those sites that remain unaffected by the potential. This is particularly relevant when studying such single-atom Fe-based catalysts, since it is expected that a relatively large (and hard to quantify) fraction of their sites are buried in the catalysts’ bulk. Herein we overcome this intrinsic challenge by performing modulation excitation (ME) experiments using the applied potential as a stimulus (illustrated in Fig. 1b). The technique allows to greatly enhance the signal of the species that changes with said stimulus, [12] and consequently to effectively surmount the lack of surface sensitivity described above. Furthermore, these ME experiments acquired with fluorescence-detected quick-scanning XAS [13] complemented with a multivariate curve resolution (MCR) analysis of the data provide quantitative information about the kinetics of the structural changes undergone by the sites in these Fe/N/C catalysts upon modifying the potential (Fig. 1c). In summary, this work will provide a novel perspective by exploiting the sensitivity of pre-edge XANES features and ME-experiments for the first time for the analysis of Fe/N/C-catalysts allowing insights that will broaden the greatly-needed understanding of the potential-dependent structure of the active sites. [1] E. Proietti et al., Nat. Commun. 2011 , 2:416. [2] J. Shui et al., Proc. Natl. Acad. Sci. 2015 , 112 , 10629–10634. [3] D. Banham et al., J. Power Sources 2015 , 285 , 334–348. [4] U. I. Kramm et al., Phys. Chem. Chem. Phys. 2012 , 14 , 11673–88. [5] A. Zitolo et al., Nat. Mater. 20 15 , 14 , 937–42. [6] Q. Jia et al., Nano Energy 2016 , 29 , 65–82. [7] S. Wagner et al., Angew. Chemie Int. Ed. 2019 , 58 , 10486–10492. [8] S. Wagner et al., Hyperfine Interact. 2018 , 239:10 . [9] T. E. Westre et al., J. Am. Chem. Soc. 1997 , 119 , 6297–6314. [10] M. Wilke et al., Am. Mineral. 2001 , 86 , 714–730. [11] T. Binninger et al., J. Electrochem. Soc. 2016 , 163 , H913–H920. [12] A. Urakawa et al., Chem. Eng. Sci. 2008 , 63 , 4902–4909. [13] A. H. Clark et al., J. Synchrotron Radiat. 2020 , 27 , 1–8. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 33 ( 2019-05-01), p. 1757-1757
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 33 ( 2019-05-01), p. 1757-1757
    Abstract: The application of proton exchange fuel cells (PEFCs) in the automotive sector is rising to be an alternative to petroleum fuel based transportation. Nevertheless, the obstacle of cost reduction of the PEFC remains, which is due to highly expensive Pt catalysts on the cathode side for oxygen reduction reaction (ORR).[1] A possible way to substitute Pt for ORR is the use of Fe-N-C-catalysts which have been shown to be a promising option.[2] For Fe-N-C-catalysts the required catalyst loading needs to be significantly higher than for Pt-based catalysts in order to achieve sufficient current densities. This leads to a change in catalyst layer thickness of roughly one order of magnitude where transport phenomena of gases and liquids become more important.[3] Based on this, the gap between Pt/C and Fe-N-C at high current densities is significantly higher compared to the kinetic controlled region. Therefore, further optimization is needed in order to enhance activity also under high current flow. In addition to this, it need to be understood to what extent problems in the transport properties affect the durability behavior of Fe-N-C catalysts in fuel cells. The ionomer distribution and loading of the catalyst layer has found to be crucial for proton transport towards the active sites, but also influences the hydrophilicity of the catalysts pores which enhances gas transport resistance. [1] In addition, it has been shown that the preparation of the membrane electrode assembly (MEA) for the fuel cell plays a key role. [3] The widely used hot-pressing technique might influence the catalyst layer pore size which is also an important parameter for species transport. In this work, different catalyst to ionomer ratios are evaluated in fuel cell tests for Fe-N-C catalysts. Furthermore, the preparation by hot-pressing is investigated in respect to the application of different compression pressures. The results are brought in relation to structural investigations of the MEAs and serve for the validation of a theoretical model. [1] S. Komini Babu, et al. ACS Appl. Mater. Infertaces 2016, 8, 32764-32777 (2016) [2] U.I. Kramm, et al. J. Am. Chem. Soc., 138 (2), 635–640 (2016) [3] X. Yin, et al. ECS Transactions, 77 (11) 1273-1281 (2017) [4] S. Komini Babu, et al. Journal of The Electrochemical Society, 164 (9), F1037-F1049 (2017)
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-02, No. 35 ( 2019-09-01), p. 1606-1606
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 35 ( 2019-09-01), p. 1606-1606
    Abstract: Proton exchange fuel cells (PEFCs) are a promising technology for energy conversion, but are not yet commercialized due to highly expensive platinum as state-of-the-art catalyst for the cathodic oxygen reduction reaction (ORR). As low-cost materials with earth abundant metals, non-precious metal and nitrogen doped carbon catalysts (Me-N-C) have become a viable alternative for platinum. Encouraging results were especially achieved with the use of iron as the metal center.[1] Me-N-C catalysts are obtained from pyrolysis of different metal, nitrogen and carbon precursors, which results in highly amorphous structures. The latter causes difficulties for the spectroscopic characterization of the active sites. Thus the exact chemical nature of the active center and the oxygen reduction reaction (ORR) mechanism are still being debated. [2] So far, three sites were proposed as possible contributors to the ORR activity. In Mössbauer spectroscopy they give rise to the D1, D2 and D3 doublets. They are all assigned to some type of FeN 4 centers that are either integrated in graphene layers (D1: FeN 4 ) or situated between two graphene layers (D2 and D3: FeN 2+2 ). [3] While in the case of the D1 doublet, FeN 4 macrocycles seem to work well as a model system, in the case of the FeN 2+2 sites it is difficult to find suitable molecular model systems as references for the interpretation of the Mössbauer data. Furthermore, in the literature this site is often displayed as a flat structure. However, it remains unclear to what extent the graphene layers could possibly be tilted against each other. In this contribution, we will use density functional theory calculations to determine structure-property relationships of FeN 2+2 site models with different Fe coordination environments – in particular the angle between adjacent graphene layers – with respect to relative energy, preferred spin state, Mössbauer spectroscopic parameters, and likely reaction intermediates for ORR. [1] Szakacs, C.E. et al., Phys. Chem. Chem. Phys. , 2014 , 16, 13654. [2] Kramm, U.I. et al., Adv. Mater. , 2019 , 1805623. [3] Kramm, U.I. et al., Phys. Chem. Chem. Phys. , 2012 , 14, 11673–11688.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 7
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-02, No. 35 ( 2017-09-01), p. 1501-1501
    Abstract: In view of the transfer from fossil fuels to renewable energies, electrochemical reactions offer the chance of a fast and environmentally friendly production of chemicals or the transfer of chemical energy into electric energy (e.g. via fuel cells). While Me-N-C catalysts are already well-established as promising alternative to Pt/C in fuel cell applications [1], some of them might also be of interest for the electrochemical production of H 2 O 2 (hydrogenperoxide) as an intermediate product.[2, 3] So far the largest efforts in electrochemical production of hydrogen peroxide are made by using supported metal (e.g. Pd, Au-Pd, Pd-Hg) nanoparticles [4, 5] and nitrogen coordinated metal complexes [6, 7] but recently also non-precious MNC catalysts have attracted attention due to their high ORR activity.[7-9] In a previous publication we have shown that the presence of protonated nitrogen groups can enhance the ORR activity of Fe-N-C catalysts.[10] In addition theoretical calculations reveal that the largest enhancement in terms of required overpotential would be expected for the combination of MnN 4 sites with carboxylic group.[11] In this work, we try to apply this promotor concept to our MNC catalysts (M= Co, Fe, Mn) by introducing targeted carboxylic groups via plasma treatments in different gas atmospheres (O 2 , CO 2 ). Fe-N-C was selected as most promising candidate for FC application, Co-N-C as possible candidate for hydrogen peroxide formation and Mn-N-C due to previous findings on the improvement of the overpotential by carboxylic groups.[11] Rotating ring disk (RRDE) studies were performed to investigate the positive effect of plasma treatments on the activity and selectivity of the MNC catalysts. In addition, the initial and the modified MNCs were characterized using X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy to identify the plasma induced structural changes and their effect on the activity and selectivity data. References: 1. Kramm, U.I., et al., Correlations between Mass Activity and Physicochemical Properties of Fe/N/C Catalysts for the ORR in PEM Fuel Cell via 57Fe Mössbauer Spectroscopy and Other Techniques. Journal of the American Chemical Society, 2014. 136 (3): p. 978-985. 2. Bonakdarpour, A., et al., Impact of Loading in RRDE Experiments on Fe–N–C Catalysts: Two- or Four-Electron Oxygen Reduction? Electrochemical and Solid-State Letters, 2008. 11 (6): p. B105-B108. 3. Hasché, F., et al., Electrocatalytic hydrogen peroxide formation on mesoporous non-metal nitrogen-doped carbon catalyst. Journal of Energy Chemistry, 2016. 25 (2): p. 251-257. 4. Edwards, J.K., et al., Comparison of supports for the direct synthesis of hydrogen peroxide from H2 and O2 using Au–Pd catalysts. Catalysis Today, 2007. 122 (3–4): p. 397-402. 5. Verdaguer-Casadevall, A., et al., Trends in the Electrochemical Synthesis of H2O2: Enhancing Activity and Selectivity by Electrocatalytic Site Engineering. Nano Letters, 2014. 14 (3): p. 1603-1608. 6. Mase, K., K. Ohkubo, and S. Fukuzumi, Efficient Two-Electron Reduction of Dioxygen to Hydrogen Peroxide with One-Electron Reductants with a Small Overpotential Catalyzed by a Cobalt Chlorin Complex. Journal of the American Chemical Society, 2013. 135 (7): p. 2800-2808. 7. Yamanaka, I., et al., Catalytic Synthesis of Neutral Hydrogen Peroxide at a CoN2Cx Cathode of a Polymer Electrolyte Membrane Fuel Cell (PEMFC). ChemSusChem, 2010. 3 (1): p. 59-62. 8. Yamanaka, I., et al., Electrocatalysis of heat-treated cobalt-porphyrin/carbon for hydrogen peroxide formation. Electrochimica Acta, 2013. 108 : p. 321-329. 9. Park, J., et al., Highly Selective Two-Electron Oxygen Reduction Catalyzed by Mesoporous Nitrogen-Doped Carbon. ACS Catalysis, 2014. 4 (10): p. 3749-3754. 10. Herranz, J., et al., Unveiling N-Protonation and Anion-Binding Effects on Fe/N/C Catalysts for O2 Reduction in Proton-Exchange-Membrane Fuel Cells. The Journal of Physical Chemistry C, 2011. 115 (32): p. 16087-16097. 11. Busch, M., et al., Beyond the top of the volcano? – A unified approach to electrocatalytic oxygen reduction and oxygen evolution. Nano Energy, 2016. 29 : p. 126-135.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 8
    In: Plasma Processes and Polymers, Wiley, Vol. 7, No. 6 ( 2010-06-22), p. 515-526
    Abstract: Low temperature plasma (LTP) treatment of cobalt‐tetramethoxyphenylporphyrin (CoTMPP) has been applied as a promising alternative method to the conventional heat treatment in order to attain highly active catalysts for the electroreduction of oxygen. In this contribution it is shown that CoTMPP can be completely transformed into a carbon matrix by adjusting adequate LTP parameters. The carbonisation process of CoTMPP is investigated at different operation conditions by Raman and IR spectroscopy and compared with the structural features of the heat‐treated samples. As a result it appears that the LTP occurs via a different carbonisation process, which yields in a more homogeneously defined molecular carbon structure. magnified image
    Type of Medium: Online Resource
    ISSN: 1612-8850 , 1612-8869
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2010
    detail.hit.zdb_id: 2159694-3
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  • 9
    In: ECS Transactions, The Electrochemical Society, Vol. 80, No. 8 ( 2017-08-24), p. 691-700
    Type of Medium: Online Resource
    ISSN: 1938-6737 , 1938-5862
    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 10
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 35 ( 2019-09-01), p. 1607-1607
    Abstract: Today, state of the catalysts in proton exchange fuel cells are platinum-based. Cost estimates show that basically the catalyst is one of the most expensive components in the FC stack. While platinum is very active for the hydrogen oxidation reaction, large quantities (approx. 80 % of the overall Pt content) are required on the cathode for the oxygen reduction reaction (ORR). Thus, alternative catalysts are required. Fe-N-C catalysts achieve very promising ORR activities in PEFC applications. The most active ones are prepared from zinc immidazole frameworks in combination with an iron source (and nitrogen precursor), that are then pyrolysed at temperatures of 900 °C or even higher. This makes it very likely that inorganic spectator species are formed. In order to get some more fundamental insight, in this work we focused on the characterization of a Fe-N-C model catalyst. The material was prepared from iron porphyrin supported on carbon with low iron loading at 600 °C followed by acid leaching. For this condition, previous results indicate that still the overall amount of FeN 4 centers remain intact, but transforms to slightly different local environments. Herein, we will show by the use of nuclear inelastic scattering (also known as Nuclear Resonance Vibrational Spectroscopy), low temperature Mössbauer spectroscopy and Electron Paramagentic Resonance spectroscopy that the above given conclusion was wrong: even for these mild preparation conditions large amounts of spectator species are found, that overlay in room temperature Mössbauer spectroscopy with the so-called D1 doublet, previously assigned as ORR active site by us and others. Nevertheless, still the catalyst contains about 50 % FeN 4 centers, thereof a partial fraction that is coordinated by oxygen molecules. These results underline the importance of in-depth analysis of Fe-N-C catalysts as the amount of spectator species should be decreased in best case to zero, in order to avoid side reactions.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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