<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ye R</submitter><funding>Natural Science Foundation of Jiangxi Province</funding><funding>Natural Science Foundation of Jiangxi Province (Jiangxi Province Natural Science Foundation)</funding><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>2159</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924954</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>CO&lt;sub>2&lt;/sub> hydrogenation to chemicals and fuels is a significant approach for achieving carbon neutrality. It is essential to rationally design the chemical structure and catalytic active sites towards the development of efficient catalysts. Here we show a Ce-CuZn catalyst with enriched Cu/Zn-O&lt;sub>V&lt;/sub>-Ce active sites fabricated through the atomic-level substitution of Cu and Zn into Ce-MOF precursor. The Ce-CuZn catalyst exhibits a high methanol selectivity of 71.1% and a space-time yield of methanol up to 400.3 g·kg&lt;sub>cat&lt;/sub>&lt;sup>-1&lt;/sup>·h&lt;sup>-1&lt;/sup> with excellent stability for 170 h at 260 °C, comparable to that of the state-of-the-art CuZnAl catalysts. Controlled experiments and DFT calculations confirm that the incorporation of Cu and Zn into CeO&lt;sub>2&lt;/sub> with abund</pubmed_abstract><journal>Nature communications</journal><pubmed_title>A Ce-CuZn catalyst with abundant Cu/Zn-O&lt;sub>V&lt;/sub>-Ce active sites for CO&lt;sub>2&lt;/sub> hydrogenation to methanol.</pubmed_title><pmcid>PMC10924954</pmcid><funding_grant_id>22005296</funding_grant_id><funding_grant_id>U23A20132</funding_grant_id><funding_grant_id>20232ACB213001;20224BAB213015</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Duyar MS</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Mao J</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Gallo A</pubmed_authors><pubmed_authors>Hong X</pubmed_authors><pubmed_authors>Ye R</pubmed_authors><pubmed_authors>Luo W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Ce-CuZn catalyst with abundant Cu/Zn-O&lt;sub>V&lt;/sub>-Ce active sites for CO&lt;sub>2&lt;/sub> hydrogenation to methanol.</name><description>CO&lt;sub>2&lt;/sub> hydrogenation to chemicals and fuels is a significant approach for achieving carbon neutrality. It is essential to rationally design the chemical structure and catalytic active sites towards the development of efficient catalysts. Here we show a Ce-CuZn catalyst with enriched Cu/Zn-O&lt;sub>V&lt;/sub>-Ce active sites fabricated through the atomic-level substitution of Cu and Zn into Ce-MOF precursor. The Ce-CuZn catalyst exhibits a high methanol selectivity of 71.1% and a space-time yield of methanol up to 400.3 g·kg&lt;sub>cat&lt;/sub>&lt;sup>-1&lt;/sup>·h&lt;sup>-1&lt;/sup> with excellent stability for 170 h at 260 °C, comparable to that of the state-of-the-art CuZnAl catalysts. Controlled experiments and DFT calculations confirm that the incorporation of Cu and Zn into CeO&lt;sub>2&lt;/sub> with abund</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T12:58:32.243Z</modification><creation>2025-04-04T12:58:32.243Z</creation></dates><accession>S-EPMC10924954</accession><cross_references><pubmed>38461315</pubmed><doi>10.1038/s41467-024-46513-3</doi></cross_references></HashMap>