<?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>2026-04-14T03:19:49Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/359793" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/359793</identifier><datestamp>2024-12-20T23:17:18Z</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>Enhancing electrostatic interactions to activate polar molecules: ammonia borane methanolysis on a Cu/CoĲOH)2 nanohybrid</dc:title>
   <dc:creator>Chen, Qian-Qian</dc:creator>
   <dc:creator>Li, Qiang</dc:creator>
   <dc:creator>Hou, Chun-Chao</dc:creator>
   <dc:creator>Wang, Chuan-Jun</dc:creator>
   <dc:creator>Peng, Cheng-Yun</dc:creator>
   <dc:creator>López, Núria</dc:creator>
   <dc:creator>Chen, Yong</dc:creator>
   <dcterms:abstract>Optimization of metal–support interactions (MSIs) is at the core of heterogeneous catalyst design. For polar
reactants, electrostatic interactions resulting from MSIs can facilitate their activation. In this work, a feasible
in situ method has been employed to control the electrostatic properties at the interface of a noblemetal-
free Cu/CoĲOH)2 nanohybrid catalyst. On the Cu/CoĲOH)2 interface, the positively charged copper
enhances the polar molecule adsorption. By varying the metal/support ratio, a highly efficient catalytic activity
for the methanolysis of ammonia borane (AB) with an initial turnover frequency (TOF) of 61.63 mol(H2)
mol(catalyst)
−1 min−1 and long-term stability at ambient temperature were observed. Theoretical analysis unravels
the role of charge transfer in promoting the reactions and the metal/support ratio in manipulating
the catalytic activity via tuning electrostatic interactions.</dcterms:abstract>
   <dcterms:dateAccepted>2020-04-28T02:45:07Z</dcterms:dateAccepted>
   <dcterms:dateAccepted>2024-04-23T10:48:27Z</dcterms:dateAccepted>
   <dcterms:available>2020-04-28T02:45:07Z</dcterms:available>
   <dcterms:available>2024-04-23T10:48:27Z</dcterms:available>
   <dcterms:created>2020-04-28T02:45:07Z</dcterms:created>
   <dcterms:created>2024-04-23T10:48:27Z</dcterms:created>
   <dcterms:issued>2019-04-29</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/2072/359793</dc:identifier>
   <dc:identifier>https://doi.org/10.1039/C9CY00584F</dc:identifier>
   <dc:language>eng</dc:language>
   <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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