<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T11:46:58Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/450539" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/450539</identifier><datestamp>2024-12-20T20:46:01Z</datestamp><setSpec>com_2072_300912</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_301309</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Performance of Metal-Catalyzed Hydrodebromination of Dibromomethane Analyzed by Descriptors Derived from Statistical Learning</dc:title>
   <dc:creator>Saadun, A. J.</dc:creator>
   <dc:creator>Pablo-García, S.</dc:creator>
   <dc:creator>Paunović, V.</dc:creator>
   <dc:creator>Li, Q.</dc:creator>
   <dc:creator>Sabadell-Rendón, A.</dc:creator>
   <dc:creator>Kleemann, K.</dc:creator>
   <dc:creator>Krumeich, F.</dc:creator>
   <dc:creator>López, N.</dc:creator>
   <dc:creator>Pérez-Ramírez, J.</dc:creator>
   <dcterms:abstract>The catalyzed semihydrogenation of dibromomethane (CH2Br2) to methyl bromide (CH3Br) is a key step in the bromine-mediated upgradation of methane. This study presents a cutting-edge strategy combining density functional theory (DFT), catalytic tests complemented with the extensive characterization of a wide range of metal catalysts (Fe, Co, Ni, Cu, Ru, Rh, Ag, Ir, and Pt), and statistical tools for a computer-assisted investigation of this reaction. The steady-state catalytic tests identified four classes of materials comprising (i) poorly active (&lt;8%) Fe/SiO2, Co/SiO2, Cu/SiO2, and Ag/SiO2; (ii) Rh/SiO2 and Ni/SiO2, which exhibit intermediate CH3Br selectivity (&lt;60%); (iii) Ir/SiO2 and Pt/SiO2, which display great propensity to CH4 (>50%); and (iv) Ru/SiO2, which exhibits the highest selectivity to CH3Br (up to 96%). In-depth characterization of representative catalysts in fresh and used forms was done by X-ray diffraction, inductively coupled plasma optical emission spectroscopy, N2 sorption, temperature-programmed reduction, Raman spectroscopy, electron microscopy, and X-ray photoelectron spectroscopy. The dimensionality reduction performed on the 272 DFT intermediate adsorption energies using principal component analysis identified two descriptors that, when employed together with the experimental data in a random forest regressor, enabled the understanding of activity and selectivity trends by connecting them to the energy intervals of the descriptors. In addition, a representative analytic model was found using the Bayesian inference. These findings illustrate the exciting opportunities presented by integrated experimental/computational screening and set the fundamental basis for the accelerated discovery of superior hydrodebromination catalysts and beyond.</dcterms:abstract>
   <dcterms:dateAccepted>2021-08-23T11:31:59Z</dcterms:dateAccepted>
   <dcterms:dateAccepted>2024-04-23T10:30:47Z</dcterms:dateAccepted>
   <dcterms:available>2021-08-23T11:31:59Z</dcterms:available>
   <dcterms:available>2024-04-23T10:30:47Z</dcterms:available>
   <dcterms:created>2021-08-23T11:31:59Z</dcterms:created>
   <dcterms:created>2024-04-23T10:30:47Z</dcterms:created>
   <dcterms:issued>2020-04-10</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/2072/450539</dc:identifier>
   <dc:identifier>https://doi.org/10.1021/acscatal.0c00679</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>ETH-43 181</dc:relation>
   <dc:relation>RTI2018-101394-B100</dc:relation>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:rights>L'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons:http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:source>RECERCAT (Dipòsit de la Recerca de Catalunya)</dc:source>
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