<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gao X</submitter><funding>Engineering and Physical Sciences Research Council</funding><pagination>e202300608</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10946563</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(16)</volume><pubmed_abstract>The electrochemical effect of isotope (EEI) of water is introduced in the Zn-ion batteries (ZIBs) electrolyte to deal with the challenge of severe side reactions and massive gas production. Due to the low diffusion and strong coordination of ions in D&lt;sub>2&lt;/sub> O, the possibility of side reactions is decreased, resulting in a broader electrochemically stable potential window, less pH change, and less zinc hydroxide sulfate (ZHS) generation during cycling. Moreover, we demonstrate that D&lt;sub>2&lt;/sub> O eliminates the different ZHS phases generated by the change of bound water during cycling because of the consistently low local ion and molecule concentration, resulting in a stable interface between the electrode and electrolyte. The full cells with D&lt;sub>2&lt;/sub> O-based electrolyte demonst</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>When It's Heavier: Interfacial and Solvation Chemistry of Isotopes in Aqueous Electrolytes for Zn-ion Batteries.</pubmed_title><pmcid>PMC10946563</pmcid><funding_grant_id>EP/V027433/1</funding_grant_id><funding_grant_id>EP/V027433/3</funding_grant_id><funding_grant_id>EP/V027433/2</funding_grant_id><funding_grant_id>EP/V027433/1; EP/V027433/2</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zong W</pubmed_authors><pubmed_authors>He G</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>He H</pubmed_authors><pubmed_authors>Du Z</pubmed_authors><pubmed_authors>Dai Y</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Parkin IP</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Zhao S</pubmed_authors><pubmed_authors>Dong H</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Carmalt CJ</pubmed_authors><pubmed_authors>Guo F</pubmed_authors><pubmed_authors>Zhao F</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Chen R</pubmed_authors></additional><is_claimable>false</is_claimable><name>When It's Heavier: Interfacial and Solvation Chemistry of Isotopes in Aqueous Electrolytes for Zn-ion Batteries.</name><description>The electrochemical effect of isotope (EEI) of water is introduced in the Zn-ion batteries (ZIBs) electrolyte to deal with the challenge of severe side reactions and massive gas production. Due to the low diffusion and strong coordination of ions in D&lt;sub>2&lt;/sub> O, the possibility of side reactions is decreased, resulting in a broader electrochemically stable potential window, less pH change, and less zinc hydroxide sulfate (ZHS) generation during cycling. Moreover, we demonstrate that D&lt;sub>2&lt;/sub> O eliminates the different ZHS phases generated by the change of bound water during cycling because of the consistently low local ion and molecule concentration, resulting in a stable interface between the electrode and electrolyte. The full cells with D&lt;sub>2&lt;/sub> O-based electrolyte demonst</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-20T02:50:06.167Z</modification><creation>2025-02-19T03:09:24.803Z</creation></dates><accession>S-EPMC10946563</accession><cross_references><pubmed>36809576</pubmed><doi>10.1002/anie.202300608</doi></cross_references></HashMap>