<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Y</submitter><funding>Pioneer Talent Recruitment Program ( Category B), Chinese Academy of Sciences</funding><funding>Key Research and Development Program of Jiangxi Province</funding><funding>National Natural Science Foundation of China</funding><funding>Science and Technology Agency of Henan Province</funding><funding>National Key Research and Development Program of China</funding><pagination>e2407051</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11653596</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(47)</volume><pubmed_abstract>Advancing and deploying Fenton-inactive Cd that combines excellent catalytic activity, selectivity, and stability remains a serious challenge, predominantly owing to the difficulty in regulating the intrinsic electronic states and local geometric structures of such fully occupied d&lt;sup>10&lt;/sup>s&lt;sup>2&lt;/sup> configuration. In this work, a combination of experiments and theoretical calculations reveals that the incorporation of boron (B) enables the tuning of the average oxidation state of Cd&lt;sup>0&lt;/sup> to Cd&lt;sup>δ+&lt;/sup>, facilitating electron localization and implementing a different electrocatalytic preference compared to conventional d&lt;sup>10&lt;/sup>-electron configurations. The resulting Cd(B) catalyst demonstrates high selectivity (>90% on average) in the O&lt;sub>2&lt;/sub>-to-H&lt;sub>2&lt;/sub>O</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Fenton-Inactive Cd Enables Highly Selective O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-Derived Domino Reaction.</pubmed_title><pmcid>PMC11653596</pmcid><funding_grant_id>E425C002</funding_grant_id><funding_grant_id>2020YFE0204500</funding_grant_id><funding_grant_id>21702045</funding_grant_id><funding_grant_id>222102240120</funding_grant_id><funding_grant_id>20243BBG71021</funding_grant_id><funding_grant_id>grants 21401203</funding_grant_id><pubmed_authors>Deng R</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Hao Z</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Dong Q</pubmed_authors><pubmed_authors>You H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fenton-Inactive Cd Enables Highly Selective O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-Derived Domino Reaction.</name><description>Advancing and deploying Fenton-inactive Cd that combines excellent catalytic activity, selectivity, and stability remains a serious challenge, predominantly owing to the difficulty in regulating the intrinsic electronic states and local geometric structures of such fully occupied d&lt;sup>10&lt;/sup>s&lt;sup>2&lt;/sup> configuration. In this work, a combination of experiments and theoretical calculations reveals that the incorporation of boron (B) enables the tuning of the average oxidation state of Cd&lt;sup>0&lt;/sup> to Cd&lt;sup>δ+&lt;/sup>, facilitating electron localization and implementing a different electrocatalytic preference compared to conventional d&lt;sup>10&lt;/sup>-electron configurations. The resulting Cd(B) catalyst demonstrates high selectivity (>90% on average) in the O&lt;sub>2&lt;/sub>-to-H&lt;sub>2&lt;/sub>O</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-27T00:31:47.101Z</modification><creation>2025-04-06T17:52:05.839Z</creation></dates><accession>S-EPMC11653596</accession><cross_references><pubmed>39513409</pubmed><doi>10.1002/advs.202407051</doi></cross_references></HashMap>