<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sun H</submitter><funding>Project of Hetao Shenzhen-Hong Kong Science and Technology Innovation Cooperation Zone</funding><funding>Research Grants Council of Hong Kong</funding><funding>Korea Research Council for Industrial Science and Technology</funding><funding>National Natural Science Foundation of China</funding><funding>National Research Foundation of Korea</funding><pagination>e2204800</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9731696</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(34)</volume><pubmed_abstract>Urea oxidation reaction (UOR) with a low equilibrium potential offers a promising route to replace the oxygen evolution reaction for energy-saving hydrogen generation. However, the overpotential of the UOR is still high due to the complicated 6e&lt;sup>-&lt;/sup> transfer process and adsorption/desorption of intermediate products. Herein, utilizing a cation exchange strategy, Ni-doped CuO nanoarrays grown on 3D Cu foam are synthesized. Notably, Ni-CuO NAs/CF requires a low potential of 1.366 V versus a reversible hydrogen electrode to drive a current density of 100 mA cm&lt;sup>-2&lt;/sup> , outperforming various benchmark electrocatalysts and maintaining robust stability in alkaline media. Theoretical and experimental studies reveal that Ni as the driving force center can effectively enhance the urea</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Ni-Doped CuO Nanoarrays Activate Urea Adsorption and Stabilizes Reaction Intermediates to Achieve High-Performance Urea Oxidation Catalysts.</pubmed_title><pmcid>PMC9731696</pmcid><funding_grant_id>KS2222‐10</funding_grant_id><funding_grant_id>2022M3H4A1A01008918</funding_grant_id><funding_grant_id>22109169</funding_grant_id><funding_grant_id>HZQB-KCZYB-2020083</funding_grant_id><funding_grant_id>KS2222-10</funding_grant_id><funding_grant_id>16201820</funding_grant_id><funding_grant_id>16206019</funding_grant_id><pubmed_authors>Jung W</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Kim H</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Ciucci F</pubmed_authors><pubmed_authors>Chen CT</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Lin HJ</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Fei L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ni-Doped CuO Nanoarrays Activate Urea Adsorption and Stabilizes Reaction Intermediates to Achieve High-Performance Urea Oxidation Catalysts.</name><description>Urea oxidation reaction (UOR) with a low equilibrium potential offers a promising route to replace the oxygen evolution reaction for energy-saving hydrogen generation. However, the overpotential of the UOR is still high due to the complicated 6e&lt;sup>-&lt;/sup> transfer process and adsorption/desorption of intermediate products. Herein, utilizing a cation exchange strategy, Ni-doped CuO nanoarrays grown on 3D Cu foam are synthesized. Notably, Ni-CuO NAs/CF requires a low potential of 1.366 V versus a reversible hydrogen electrode to drive a current density of 100 mA cm&lt;sup>-2&lt;/sup> , outperforming various benchmark electrocatalysts and maintaining robust stability in alkaline media. Theoretical and experimental studies reveal that Ni as the driving force center can effectively enhance the urea</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T22:14:58.672Z</modification><creation>2025-04-04T22:14:58.672Z</creation></dates><accession>S-EPMC9731696</accession><cross_references><pubmed>36266984</pubmed><doi>10.1002/advs.202204800</doi></cross_references></HashMap>