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dc.contributor.author윤종승-
dc.date.accessioned2018-04-26T02:54:54Z-
dc.date.available2018-04-26T02:54:54Z-
dc.date.issued2014-02-
dc.identifier.citationNANO LETTERS, Vol.14 No.2 [2014], 416-422en_US
dc.identifier.issn1530-6984-
dc.identifier.issn1530-6992-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/nl402747x-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/70722-
dc.description.abstractFor the first time, we report the electrochemical activity of anatase TiO2 nanorods in a Na cell. The anatase TiO2 nanorods were synthesized by a hydrothermal method, and their surfaces were coated by carbon to improve the electric conductivity through carbonization of pitch at 700 °C for 2 h in Ar flow. The resulting structure does not change before and after the carbon coating, as confirmed by X-ray diffraction (XRD). Transmission electron microscopic images confirm the presence of a carbon coating on the anatase TiO2 nanorods. In cell tests, anodes of bare and carbon-coated anatase TiO2 nanorods exhibit stable cycling performance and attain a capacity of about 172 and 193 mAh g–1 on the first charge, respectively, in the voltage range of 3–0 V. With the help of the conductive carbon layers, the carbon-coated anatase TiO2 delivers more capacity at high rates, 104 mAh g–1 at the 10 C-rate (3.3 A g–1), 82 mAh g–1 at the 30 C-rate (10 A g–1), and 53 mAh g–1 at the 100 C-rate (33 A g–1). By contrast, the anode of bare anatase TiO2 nanorods delivers only about 38 mAh g–1 at the 10 C-rate (3.3 A g–1). The excellent cyclability and high-rate capability are the result of a Na+ insertion and extraction reaction into the host structure coupled with Ti4+/3+ redox reaction, as revealed by X-ray absorption spectroscopy.en_US
dc.description.sponsorshipThis research was partly supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Education, Science and Technology (2011-0024683), the Human Resources Development program (No. 20124010203310) of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Korea government Ministry of Trade, Industry, and Energy, and a grant from the National Research Foundation of Korea and funded by the Korean government (MEST) (NRF-2009-C1AAA001-0093307). This work was also supported by the U.S. Department of Energy under Contract DE-AC0206CH11357 with the main support provided by the Vehicle Technologies Office, Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE). J.L. was supported by the Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE) Postdoctoral Research Award under the EERE. Vehicles Technology Program administered by the Oak Ridge Institute for Science and Education (ORISE) for the DOE.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USAen_US
dc.subjectNatase TiO2en_US
dc.subjectnanorodsen_US
dc.subjectcarbon coatingen_US
dc.subjectintercalationen_US
dc.subjectanodeen_US
dc.subjectsodium batteryen_US
dc.titleAnatase Titania Nanorods as an Intercalation Anode Material for Rechargeable Sodium Batteriesen_US
dc.typeArticleen_US
dc.relation.volume14-
dc.identifier.doi10.1021/nl402747x-
dc.relation.page416-422-
dc.relation.journalNANO LETTERS-
dc.contributor.googleauthorKim, Ki-Tae-
dc.contributor.googleauthorGhulam Ali-
dc.contributor.googleauthorChung, Kyung Yoon-
dc.contributor.googleauthorYoon, Chong Seung-
dc.contributor.googleauthorHitoshi Yashiro-
dc.contributor.googleauthorSun, Yang-Kook-
dc.contributor.googleauthorLu, Jun-
dc.contributor.googleauthorKhalil Amine-
dc.contributor.googleauthorMyung, Seung-Taek-
dc.relation.code2014036375-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDIVISION OF MATERIALS SCIENCE AND ENGINEERING-
dc.identifier.pidcsyoon-
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COLLEGE OF ENGINEERING[S](공과대학) > MATERIALS SCIENCE AND ENGINEERING(신소재공학부) > Articles
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