<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He X</submitter><funding>Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology)</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>9923</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11568296</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>The membrane electrode assembly (MEA) is promising for practical applications of the electrocatalytic CO&lt;sub>2&lt;/sub> reduction reaction (CO&lt;sub>2&lt;/sub>RR) to multi-carbon (C&lt;sub>2+&lt;/sub>) compounds. Water management is crucial in the MEA electrolyser without catholyte, but few studies have clarified whether the co-feeding water in cathode can enhance C&lt;sub>2+&lt;/sub> formation. Here, we report our discovery of pivotal roles of a suitable nanocomposite electrocatalyst with abundant Cu&lt;sub>2&lt;/sub>O-Cu&lt;sup>0&lt;/sup> interfaces in accomplishing water-promoting effect on C&lt;sub>2+&lt;/sub> formation, achieving a current density of 1.0 A cm&lt;sup>-2&lt;/sup> and a 19% single-pass C&lt;sub>2+&lt;/sub> yield at 80% C&lt;sub>2+&lt;/sub> Faradaic efficiency in MEA. The operando characterizations confirm the co-existence of </pubmed_abstract><journal>Nature communications</journal><pubmed_title>Roles of copper(I) in water-promoted CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; electrolysis to multi-carbon compounds.</pubmed_title><pmcid>PMC11568296</pmcid><funding_grant_id>22121001</funding_grant_id><funding_grant_id>2022YAF1504603</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Zhu M</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Sun F</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Lin L</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Xie S</pubmed_authors><pubmed_authors>Mei B</pubmed_authors><pubmed_authors>Cheng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Roles of copper(I) in water-promoted CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; electrolysis to multi-carbon compounds.</name><description>The membrane electrode assembly (MEA) is promising for practical applications of the electrocatalytic CO&lt;sub>2&lt;/sub> reduction reaction (CO&lt;sub>2&lt;/sub>RR) to multi-carbon (C&lt;sub>2+&lt;/sub>) compounds. Water management is crucial in the MEA electrolyser without catholyte, but few studies have clarified whether the co-feeding water in cathode can enhance C&lt;sub>2+&lt;/sub> formation. Here, we report our discovery of pivotal roles of a suitable nanocomposite electrocatalyst with abundant Cu&lt;sub>2&lt;/sub>O-Cu&lt;sup>0&lt;/sup> interfaces in accomplishing water-promoting effect on C&lt;sub>2+&lt;/sub> formation, achieving a current density of 1.0 A cm&lt;sup>-2&lt;/sup> and a 19% single-pass C&lt;sub>2+&lt;/sub> yield at 80% C&lt;sub>2+&lt;/sub> Faradaic efficiency in MEA. The operando characterizations confirm the co-existence of </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2025-04-03T23:23:51.876Z</modification><creation>2025-04-03T23:23:51.876Z</creation></dates><accession>S-EPMC11568296</accession><cross_references><pubmed>39548110</pubmed><doi>10.1038/s41467-024-54282-2</doi></cross_references></HashMap>