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dc.contributor.author이승용-
dc.date.accessioned2021-05-18T06:24:52Z-
dc.date.available2021-05-18T06:24:52Z-
dc.date.issued2020-03-
dc.identifier.citationNANO ENERGY, v. 72, article no. 104721en_US
dc.identifier.issn2211-2855-
dc.identifier.issn2211-3282-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S2211285520302780?via%3Dihub-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/162277-
dc.description.abstractNa metal is an attractive anode material for rechargeable Na ion batteries, however, the dendritic growth of Na can cause serious safety issues. Along with modifications of solid-electrolyte interphase (SEI), engineering the electrode has been reported to be effective in suppressing Na dendritic growth, likely by reducing localized current density accumulation. However, fundamental understanding of Na growth at the nanoscale is still limited. Here, we report an in-situ study of Na electrodeposition in electrochemical liquid cells with the electrodes in different surface roughness, e.g., flat or sharp curvature. Real time observation using transmission electron microscopy (TEM) reveals the Na electrodeposition with remarkable details. Relatively large Na grains (in the micrometer scale) are achieved on the flat electrode surface. The local SEI thickness variations impact the growth rate, thus the morphology of individual grains. In contrast, small Na grains (in tens of nanometers) grow explosively on the electrode at the point with sharp curvature. The newly formed Na grains preferentially deposit at the base of existing grains close to the electrode. Further studies using continuum-based computational modeling suggest that the growth mode of an alkali metal (e.g. Na) is strongly influenced by the transport properties of SEI. Our direct observation of Na deposition in combination with the theoretical modeling provides insights for comprehensive understanding of electrode roughness and SEI effects on Na electrochemical deposition.en_US
dc.description.sponsorshipThis work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences (BES), Materials Sciences and Engineering Division under Contract No. DE-AC02-05-CH11231 within the in-situ TEM program (KC22ZH). The work at the Molecular Foundry and the XAS experiments at the Advanced Light Source in Lawrence Berkeley National Laboratory (LBNL) were supported by DOE BES under Contract #DE-AC02-05CH11231. Z. Zeng acknowledge support from the City University of Hong Kong (grant number 9610435) and ECS scheme (grant number 9048163) from RGC in Hong Kong. X. Zhang acknowledges the support of National Basic Research Program of China (2013CB632101) and China Scholarship Council under No.201406190080. S.-Y. Lee was supported by an LDRD project at LBNL.en_US
dc.language.isoenen_US
dc.publisherELSEVIERen_US
dc.subjectLiquid cell TEMen_US
dc.subjectElectrochemical liquid cellen_US
dc.subjectNa depositionen_US
dc.subjectSolid-electrolyte interphaseen_US
dc.subjectSodium ion batteriesen_US
dc.titleElectrode roughness dependent electrodeposition of sodium at the nanoscaleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.nanoen.2020.104721-
dc.relation.journalNANO ENERGY-
dc.contributor.googleauthorZeng, Zhiyuan-
dc.contributor.googleauthorBarai, Pallab-
dc.contributor.googleauthorLee, Seung-Yong-
dc.contributor.googleauthorYang, Juan-
dc.contributor.googleauthorZhang, Xiaowei-
dc.contributor.googleauthorZheng, Wenjing-
dc.contributor.googleauthorLiu, Yi-Sheng-
dc.contributor.googleauthorBustillo, Karen C.-
dc.contributor.googleauthorErcius, Peter-
dc.contributor.googleauthorGuo, Jinghua-
dc.relation.code2020048631-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDIVISION OF MATERIALS SCIENCE AND ENGINEERING-
dc.identifier.pidsyonglee-
dc.identifier.orcidhttp://orcid.org/0000-0002-8363-4142-
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > MATERIALS SCIENCE AND ENGINEERING(신소재공학부) > Articles
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