Please use this identifier to cite or link to this item: https://doi.org/10.1039/c9ta01606f
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dc.titlePromoting defective-Li2O2 formation via Na doping for Li-O-2 batteries with low charge overpotentials
dc.contributor.authorZhiyang Lyu
dc.contributor.authorWang Tao
dc.contributor.authorRui Guo
dc.contributor.authorYin Zhou
dc.contributor.authorJunchao Chen
dc.contributor.authorXiao Wang
dc.contributor.authorMing Lin
dc.contributor.authorXinXin Tian
dc.contributor.authorMin Lai
dc.contributor.authorLuming Peng
dc.contributor.authorLi Wang
dc.contributor.authorZhangquan Peng
dc.contributor.authorWei Chen
dc.date.accessioned2020-06-04T03:49:22Z
dc.date.available2020-06-04T03:49:22Z
dc.date.issued2019-05-07
dc.identifier.citationZhiyang Lyu, Wang Tao, Rui Guo, Yin Zhou, Junchao Chen, Xiao Wang, Ming Lin, XinXin Tian, Min Lai, Luming Peng, Li Wang, Zhangquan Peng, Wei Chen (2019-05-07). Promoting defective-Li2O2 formation via Na doping for Li-O-2 batteries with low charge overpotentials. JOURNAL OF MATERIALS CHEMISTRY A 7 (17) : 10389-10396. ScholarBank@NUS Repository. https://doi.org/10.1039/c9ta01606f
dc.identifier.issn2050-7488
dc.identifier.issn2050-7496
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/169207
dc.description.abstract© The Royal Society of Chemistry. Li-O2 batteries represent a promising candidate for next-generation energy storage systems because of their high specific energy density. However, one key limitation is their low energy efficiency, which is caused by the high charge overpotential owing to the sluggish oxidation kinetics of the insulating Li2O2 product. Here, we report an approach to reduce charge overpotentials by forming Na-doped defective Li2O2 in a Na+-added electrolyte, which is verified by systematic experimental characterization. Theoretical simulations reveal that the Na-doped Li2O2 with lithium vacancies exhibits new conducting states right above the valence band edge, thereby enhancing electron transport properties. The cell with the defective-Li2O2 product achieves a charge overpotential of ∼0.4 V, much lower than that of the cell with Li2O2 (∼1.1 V). This study offers an effective approach to promote Li2O2 decomposition by forming defective Li2O2.
dc.language.isoen
dc.publisherROYAL SOC CHEMISTRY
dc.sourceElements
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectTechnology
dc.subjectChemistry, Physical
dc.subjectEnergy & Fuels
dc.subjectMaterials Science, Multidisciplinary
dc.subjectChemistry
dc.subjectMaterials Science
dc.subjectLITHIUM-OXYGEN BATTERY
dc.subjectLI-AIR BATTERIES
dc.subjectLI2O2 FORMATION
dc.subjectDISCHARGE PRODUCTS
dc.subjectPOTASSIUM-IONS
dc.subjectSODIUM
dc.subjectTRANSPORT
dc.subjectREDUCTION
dc.subjectCATALYST
dc.subjectNANOPARTICLES
dc.typeArticle
dc.date.updated2020-05-29T08:36:46Z
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1039/c9ta01606f
dc.description.sourcetitleJOURNAL OF MATERIALS CHEMISTRY A
dc.description.volume7
dc.description.issue17
dc.description.page10389-10396
dc.published.statePublished
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