<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Genz NS</submitter><funding>Academy of Finland</funding><funding>Norges Forskningsråd</funding><funding>Jenny and Antti Wihuri foundation</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Research Council of Norway</funding><funding>Dutch Research Council (NWO)</funding><funding>University of Helsinki Doctoral Programme for Materials Research and Nanoscience</funding><funding>Wihuri Research Institute</funding><pagination>e202209334</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9828672</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(48)</volume><pubmed_abstract>Laboratory-based X-ray absorption spectroscopy (XAS) and especially X-ray absorption near-edge structure (XANES) offers new opportunities in catalyst characterization and presents not only an alternative, but also a complementary approach to precious beamtime at synchrotron facilities. We successfully designed a laboratory-based setup for performing operando, quasi-simultaneous XANES analysis at multiple K-edges, more specifically, operando XANES of mono-, bi-, and trimetallic CO&lt;sub>2&lt;/sub> hydrogenation catalysts containing Ni, Fe, and Cu. Detailed operando XANES studies of the multielement solid catalysts revealed metal-dependent differences in the reducibility and re-oxidation behavior and their influence on the catalytic performance in CO&lt;sub>2&lt;/sub> hydrogenation. The applicability o</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Operando Laboratory-Based Multi-Edge X-Ray Absorption Near-Edge Spectroscopy of Solid Catalysts.</pubmed_title><pmcid>PMC9828672</pmcid><funding_grant_id>00200134</funding_grant_id><funding_grant_id>197405</funding_grant_id><funding_grant_id>452243354</funding_grant_id><funding_grant_id>Gravitation Program - MCEC</funding_grant_id><funding_grant_id>295696</funding_grant_id><pubmed_authors>Genz NS</pubmed_authors><pubmed_authors>Krumeich F</pubmed_authors><pubmed_authors>Huotari S</pubmed_authors><pubmed_authors>Oord R</pubmed_authors><pubmed_authors>Pokle A</pubmed_authors><pubmed_authors>Olsbye U</pubmed_authors><pubmed_authors>Prytz O</pubmed_authors><pubmed_authors>Meirer F</pubmed_authors><pubmed_authors>Kallio AJ</pubmed_authors><pubmed_authors>Weckhuysen BM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Operando Laboratory-Based Multi-Edge X-Ray Absorption Near-Edge Spectroscopy of Solid Catalysts.</name><description>Laboratory-based X-ray absorption spectroscopy (XAS) and especially X-ray absorption near-edge structure (XANES) offers new opportunities in catalyst characterization and presents not only an alternative, but also a complementary approach to precious beamtime at synchrotron facilities. We successfully designed a laboratory-based setup for performing operando, quasi-simultaneous XANES analysis at multiple K-edges, more specifically, operando XANES of mono-, bi-, and trimetallic CO&lt;sub>2&lt;/sub> hydrogenation catalysts containing Ni, Fe, and Cu. Detailed operando XANES studies of the multielement solid catalysts revealed metal-dependent differences in the reducibility and re-oxidation behavior and their influence on the catalytic performance in CO&lt;sub>2&lt;/sub> hydrogenation. The applicability o</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-21T17:55:49.886Z</modification><creation>2025-04-05T17:04:18.315Z</creation></dates><accession>S-EPMC9828672</accession><cross_references><pubmed>36205032</pubmed><doi>10.1002/anie.202209334</doi></cross_references></HashMap>