Surface Morphology Treatment of Lithium Metal Anode for Dendrite Suppression

To accomplish higher mileage targets of electric vehicles (EVs), lithium/air or lithium/sulfur batteries using lithium metal as an anode have attracted much attention owing to their high energy density. However, lithium metal has a major drawback, the so-called lithium dendrite which results in inhi...

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Published inMeeting abstracts (Electrochemical Society) Vol. MA2016-02; no. 3; p. 429
Main Authors Park, Joonam, Byun, Seoungwoo, Appiah, Williams Agyei, Jeong, Jiseon, Lee, Yunju, Cho, Kuk Young, Lee, Young-Gi, Ryou, Myung-Hyun, Lee, Yong Min
Format Journal Article
LanguageEnglish
Published 01.09.2016
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Abstract To accomplish higher mileage targets of electric vehicles (EVs), lithium/air or lithium/sulfur batteries using lithium metal as an anode have attracted much attention owing to their high energy density. However, lithium metal has a major drawback, the so-called lithium dendrite which results in inhibited battery performance and instability. Hence, it is essential to generate effective technologies for suppressing lithium dendrite formation on the lithium metal surface. We have proposed dendrite-free lithium metals by using surface morphology treatment technology. This has advantages of not only simple process but also improved battery performance such as rate capability and cycle performance. This work is focused on developing a more well-designed and improved dendrite-free lithium metal anode for lithium metal secondary batteries. We adopted a mathematical model to optimise the metal surface morphology of different shapes by considering process technique of the treatment tool. To reflect the simulation results, the electrochemical performance of cells assembled with and without controlled lithium metal surface was experimentally conducted. Field-emission scanning electron microscope (FE-SEM, S-4800, Hitachi) was also used to confirm dendrite formation on lithium metal surface during charge and discharge. References 1. J. Park, J. Jeong, Y. Lee , M. Oh, M. –H. Ryou, Y. M. Lee, Adv. Mater. Interfaces , 1600140 (2016) 2. M. -H. Ryou, Y. M. Lee, Y. Lee, M. Winter and P. Bieker, Adv. Funct. Mater , 25 , 825-825 (2015) 3. A. Ferrese, P. Albertus, J. Christensen and J. Newman, Journal of The Electrochemicla Society , 159 , A1615-A1623 (2012) 4. W. A. Appiah, J. Park, L. Van Khue, Y. Lee, J. Choi, M.-H. Ryou and Y. M. Lee, Electrochimica Acta , 187 , 422 (2016) Acknowledgements This work was supported by the international Collaborative Energy Technology R&D Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP), granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea. (No. 20158510050020). Figure 1
AbstractList To accomplish higher mileage targets of electric vehicles (EVs), lithium/air or lithium/sulfur batteries using lithium metal as an anode have attracted much attention owing to their high energy density. However, lithium metal has a major drawback, the so-called lithium dendrite which results in inhibited battery performance and instability. Hence, it is essential to generate effective technologies for suppressing lithium dendrite formation on the lithium metal surface. We have proposed dendrite-free lithium metals by using surface morphology treatment technology. This has advantages of not only simple process but also improved battery performance such as rate capability and cycle performance. This work is focused on developing a more well-designed and improved dendrite-free lithium metal anode for lithium metal secondary batteries. We adopted a mathematical model to optimise the metal surface morphology of different shapes by considering process technique of the treatment tool. To reflect the simulation results, the electrochemical performance of cells assembled with and without controlled lithium metal surface was experimentally conducted. Field-emission scanning electron microscope (FE-SEM, S-4800, Hitachi) was also used to confirm dendrite formation on lithium metal surface during charge and discharge. References 1. J. Park, J. Jeong, Y. Lee , M. Oh, M. –H. Ryou, Y. M. Lee, Adv. Mater. Interfaces , 1600140 (2016) 2. M. -H. Ryou, Y. M. Lee, Y. Lee, M. Winter and P. Bieker, Adv. Funct. Mater , 25 , 825-825 (2015) 3. A. Ferrese, P. Albertus, J. Christensen and J. Newman, Journal of The Electrochemicla Society , 159 , A1615-A1623 (2012) 4. W. A. Appiah, J. Park, L. Van Khue, Y. Lee, J. Choi, M.-H. Ryou and Y. M. Lee, Electrochimica Acta , 187 , 422 (2016) Acknowledgements This work was supported by the international Collaborative Energy Technology R&D Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP), granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea. (No. 20158510050020). Figure 1
Author Lee, Yong Min
Park, Joonam
Lee, Yunju
Lee, Young-Gi
Appiah, Williams Agyei
Jeong, Jiseon
Ryou, Myung-Hyun
Byun, Seoungwoo
Cho, Kuk Young
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