1,720,977 research outputs found
Correcting the Hydrogen Diffusion Limitation in Rotating Disk Electrode Measurements of Hydrogen Evolution Reaction Kinetics
No full textPulsiher's PDFRotating disk electrode (RDE) method is widely employed in studies on the hydrogen oxidation/evolution reaction (HOR/HER) owing to its well-defined mass transport behaviors. While it is accepted that the measured HOR current is controlled by both the electrode kinetics and the diffusion of H2, HER is typically assumed to be free of diffusion limitation. Here we demonstrate that HER could also be diffusion limited when the electrode kinetics is fast, as evidenced by the rotation speed dependent HER current on Pt in acid (pH = 1) and the overlap of the HER polarization curve with the concentration overpotential curve. The HER diffusion limitation originates from the insufficient mass transport of produced H2 from the electrode surface to the bulk electrolyte and the highly reversible nature of HOR/HER. Kinetic analyses based on HER polarization curves on Pt in acid without correcting for the diffusion limitation could lead to inaccurate Tafel slopes and mechanistic interpretations, and significantly underestimated HER activities. A general data analysis protocol based on the reversible Koutecky-Levich equation is developed to obtain accurate kinetic information of HOR/HER even when electrode kinetics is facile. This new method is compared with other existing methods on Pt disk electrodes at different pHs and thin-film electrodes with different Pt loadings.University of Delaware. Center for Catalytic Science & Technology
Universal dependence of hydrogen oxidation and evolution reaction activity of platinum-group metals on pH and hydrogen binding energy
No full textPublisher's PDFUnderstanding how pH affects the activity of hydrogen oxidation reaction (HOR) and hydrogen evolution reaction
(HER) is key to developing active, stable, and affordable HOR/HER catalysts for hydroxide exchange membrane fuel
cells and electrolyzers. A common linear correlation between hydrogen binding energy (HBE) and pH is observed
for four supported platinum-group metal catalysts (Pt/C, Ir/C, Pd/C, and Rh/C) over a broad pH range (0 to 13),
suggesting that the pH dependence of HBE is metal-independent. A universal correlation between exchange current
density and HBE is also observed on the four metals, indicating that they may share the same elementary steps
and rate-determining steps and that the HBE is the dominant descriptor for HOR/HER activities. The onset potential
of CO stripping on the four metals decreases with pH, indicating a stronger OH adsorption, which provides evidence
against the promoting effect of adsorbed OH on HOR/HER.University of Delaware. Department of Chemical & Biomolecular Engineering.University of Delaware. Center for Catalytic Science & Technology
Poisoning of Ru/C by Homogeneous Brønsted Acids in Hydrodeoxygenation of 2,5-Dimethylfuran via Catalytic Transfer Hydrogenation
No full textAuthor's final draft after peer reviewIt has been proposed that the combination of metal and acid sites is critical for effective ring opening of biomass-derived furans to linear molecules, a reaction that holds promise for the production of renewable polymer precursors and alkanes. In this work, we use 2,5-dimethylfuran (DMF) as a model compound to investigate hydrogenolysis and hydrogenation pathways using a combination of H2SO4 and Ru-mediated catalytic transfer hydrogenation in 2-propanol. Acid-catalyzed hydrolytic ring opening of DMF to 2,5-hexanedione (HDN) occurs readily at 80 °C with a selectivity of 89% in 2-propanol. Over Ru/C, HDN is fully converted after only 2 h at 80 °C, forming a mixture of both ring-closed products (~68% total yield), i.e., 2,5-dimethyltetrahydrofuran (DMTHF) and 2,5-dimethyl-2,3-dihydrofuran (DMDHF), as well as ring opened products (~28% total yield), i.e., 2,5-hexanediol (2,5-HDL) and 2-hexanol (HOL). Rather than observing sequential hydrolysis/hydrogenation reactions, we observe severe suppression of metal chemistry when having both Ru/C and H2SO4 in the reaction system. While minor leaching of Ru occurs in the presence of mineral acids, X-ray photoelectron spectroscopy coupled with CO chemisorption studies suggest that the primary cause of the lack of Ru-mediated chemistry is poisoning by strongly adsorbed sulfate species. This hypothesis is supported by the observation of Ru-catalyzed chemistry when replacing H2SO4 with Nafion, a solid Brønsted acid, as sulfonic acid groups tethered to the polymer backbone cannot adsorb on the metal sites.University of Delaware. Department of Chemical & Biomolecular Engineering
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Insights into ring opening of biomass-derived furanics over Ru/C
No full textAuthor's final draft after peer reviewSelective ring opening of cellulose-derived furanic molecules is a promising pathway for the production of industrially relevant linear oxygenates, such as 1,6-hexanediol. 2,5-dimethylfuran (DMF) is employed as a model compound in combined experimental and computational investigations to provide insights into metal-catalyzed ring opening. Ring opening to 2-hexanol and 2-hexanone and ring saturation to 2,5-dimethyltetrahydrofuran (DMTHF) are identified as two main parallel pathways. Density functional theory calculations and microkinetic modeling indicate DMF adsorbs on Ru in an open-ring configuration, which is potentially a common surface intermediate leading to both ring opening and ring saturation products. While the activation barriers for the two pathways are comparable, formation of DMTHF is more thermodynamically favorable. In addition, steric interactions with co-adsorbed 2-propoxyl, derived from the solvent, and the oxophilic nature of Ru play key roles in determining the product distribution: the former favors less bulky, i.e., ring-closed, intermediates, and the latter retards O-H bond formation. Finally, we show that hydrodeoxygenation of oxygenated furanics, such as 5-methylfurfural and (5-methyl-2-furyl)methanol, on Ru preferentially occurs at oxygen-containing side groups to form DMF, followed by either ring opening or ring saturation.University of Delaware. Catalysis Center for Energy Innovation
Variations on the Author
Full text link“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Full text linkWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Dispelling the Myths Behind First-author Citation Counts
Full text linkWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
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