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An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
It is a great honor to receive this prize from the International Schumpeter Society. It is especially an honor to receive it in Vienna, the European capital where Schumpeter received the education that was central to his intellectual development. I have had a few occasions over the years to enjoy the hospitality of the Austrian National Bank and the University of Vienna. It is always a pleasure to be back in this exceptional city.
Traditional approaches to identify ion-transport pathways often presume equal probability of occupying all hopping sites and focus entirely on finding the lowest migration barrier channels between them. Although this strategy has been applied successfully to solid-state Li battery materials, which historically have mostly been ordered frameworks, in the emerging class of disordered electrode materials some Li-sites can be significantly more stable than others due to a varied distribution of transition metal (TM) environments. Using kinetic Monte Carlo simulations, we show that in such cation-disordered compounds only a fraction of the Li-sites connected by the so-called low-barrier ``0-TM" channels actually participate in Li-diffusion. The Li-diffusion behavior through these sites, which are determined primarily by the voltage applied during Li-extraction, can be captured using an effective migration barrier larger than that of the 0-TM barrier itself. The suppressed percolation due to cation disorder can decrease the ionic diffusion coefficient at room temperature by over 2 orders of magnitude.
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRaman study of the preparation of silica-supported titania from titanium tetrachloride and hydrogen chlorideMark G. Reichmann and Alexis T. BellCite this: Langmuir 1987, 3, 1, 111–116Publication Date (Print):January 1, 1987Publication History Published online1 May 2002Published inissue 1 January 1987https://pubs.acs.org/doi/10.1021/la00073a020https://doi.org/10.1021/la00073a020research-articleACS PublicationsRequest reuse permissionsArticle Views207Altmetric-Citations40LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Abstract Es wurden Potential‐pH‐Diagramme für das System Al‐H2O bei Temperaturen zwischen 25 und 300°C durch Integration von Funktionen der Freien Energie unter Verwendung des Korrespondenzprinzips von Criss und Cobble erhalten.