<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Y</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>Natural Science Foundation of Shanghai</funding><pagination>1219-1225</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9048752</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(3)</volume><pubmed_abstract>In this study, we have developed a continuous-flow electrochemical system towards the rapid and selective conversion of ammonia to N&lt;sub>2&lt;/sub>, based on a tubular substoichiometric titanium dioxide (Ti&lt;sub>4&lt;/sub>O&lt;sub>7&lt;/sub>) anode and a Pd-Cu co-modified Ni foam (Pd-Cu/NF) cathode, both of which are indispensable. Under the action of a suitable anode potential, the Ti&lt;sub>4&lt;/sub>O&lt;sub>7&lt;/sub> anode enables the conversion of Cl&lt;sup>-&lt;/sup> to chloride radicals (Cl˙), which could selectively react with ammonia to produce N&lt;sub>2&lt;/sub>. The anodic byproducts, &lt;i>e.g.&lt;/i> NO&lt;sub>3&lt;/sub> &lt;sup>-&lt;/sup>, were further reduced to N&lt;sub>2&lt;/sub> at the Pd-Cu/NF cathode. EPR and scavenger experiments confirmed the dominant role of Cl˙ in ammonia conversion. Complete transformation of 30 mg L&lt;sup>-</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Rapid and selective electrochemical transformation of ammonia to N&lt;sub>2&lt;/sub> by substoichiometric TiO&lt;sub>2&lt;/sub>-based electrochemical system.</pubmed_title><pmcid>PMC9048752</pmcid><funding_grant_id>18ZR1401000</funding_grant_id><funding_grant_id>2232019G-11</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Mei J</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Sand W</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Huang M</pubmed_authors><pubmed_authors>Shen C</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid and selective electrochemical transformation of ammonia to N&lt;sub>2&lt;/sub> by substoichiometric TiO&lt;sub>2&lt;/sub>-based electrochemical system.</name><description>In this study, we have developed a continuous-flow electrochemical system towards the rapid and selective conversion of ammonia to N&lt;sub>2&lt;/sub>, based on a tubular substoichiometric titanium dioxide (Ti&lt;sub>4&lt;/sub>O&lt;sub>7&lt;/sub>) anode and a Pd-Cu co-modified Ni foam (Pd-Cu/NF) cathode, both of which are indispensable. Under the action of a suitable anode potential, the Ti&lt;sub>4&lt;/sub>O&lt;sub>7&lt;/sub> anode enables the conversion of Cl&lt;sup>-&lt;/sup> to chloride radicals (Cl˙), which could selectively react with ammonia to produce N&lt;sub>2&lt;/sub>. The anodic byproducts, &lt;i>e.g.&lt;/i> NO&lt;sub>3&lt;/sub> &lt;sup>-&lt;/sup>, were further reduced to N&lt;sub>2&lt;/sub> at the Pd-Cu/NF cathode. EPR and scavenger experiments confirmed the dominant role of Cl˙ in ammonia conversion. Complete transformation of 30 mg L&lt;sup>-</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-19T12:58:15.068Z</modification><creation>2025-04-19T12:58:15.068Z</creation></dates><accession>S-EPMC9048752</accession><cross_references><pubmed>35494680</pubmed><doi>10.1039/c9ra07470h</doi></cross_references></HashMap>