<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(9)</volume><submitter>Li X</submitter><pubmed_abstract>Using the density functional theory (DFT) method, we investigated the adsorption of NO on the undoped and Ce-doped LaCoO3 (011) surface. According to our calculations, the best adsorption site is not changed after Ce doping. When the NO molecule is adsorbed on the perfect LaO-terminated LaCoO3 (011) surface, the most stable adsorption site is hollow-top, which corresponds to the hollow-NO configuration in our study. After the substitution of La with Ce, the adsorption energy of hollow-NO configuration is increased. For the perfect CoO2-terminated LaCoO3 (011) surface, it is found that Co-NO configuration is the preferential adsorption structure. Its adsorption energy can also be enhanced after Ce doping. When NO molecule is adsorbed on the undoped and Ce-doped LaO-terminated LaCoO3 (011) surface with hollow-NO configuration, it serves as the acceptor and electrons transfer from the surface to it in the adsorption process. On the contrary, for the Co-NO configuration of undoped and Ce-doped CoO2-terminated LaCoO3 (011) surface, NO molecule becomes the donor and loses electrons to the surface.</pubmed_abstract><journal>Materials (Basel, Switzerland)</journal><pagination>E1379</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6540239</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>DFT Analysis of NO Adsorption on the Undoped and Ce-Doped LaCoO3 (011) Surface.</pubmed_title><pmcid>PMC6540239</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Gao H</pubmed_authors></additional><is_claimable>false</is_claimable><name>DFT Analysis of NO Adsorption on the Undoped and Ce-Doped LaCoO3 (011) Surface.</name><description>Using the density functional theory (DFT) method, we investigated the adsorption of NO on the undoped and Ce-doped LaCoO3 (011) surface. According to our calculations, the best adsorption site is not changed after Ce doping. When the NO molecule is adsorbed on the perfect LaO-terminated LaCoO3 (011) surface, the most stable adsorption site is hollow-top, which corresponds to the hollow-NO configuration in our study. After the substitution of La with Ce, the adsorption energy of hollow-NO configuration is increased. For the perfect CoO2-terminated LaCoO3 (011) surface, it is found that Co-NO configuration is the preferential adsorption structure. Its adsorption energy can also be enhanced after Ce doping. When NO molecule is adsorbed on the undoped and Ce-doped LaO-terminated LaCoO3 (011) surface with hollow-NO configuration, it serves as the acceptor and electrons transfer from the surface to it in the adsorption process. On the contrary, for the Co-NO configuration of undoped and Ce-doped CoO2-terminated LaCoO3 (011) surface, NO molecule becomes the donor and loses electrons to the surface.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2025-04-04T09:36:16.162Z</modification><creation>2019-07-24T07:06:24Z</creation></dates><accession>S-EPMC6540239</accession><cross_references><pubmed>31035353</pubmed><doi>10.3390/ma12091379</doi></cross_references></HashMap>