Vertical graphene nanowalls coating of copper current collector for enhancing rate performance of graphite anode of Li ion battery: The merit of optimized interface architecture | |
Liu, XF; Wang, D; Zhang, BS; Luan, C; Qin, TT; Zhang, W; Shi, XY; Deng, T; Zheng, WT; Zheng, WT (reprint author), Jilin Univ, Key Lab Mobile Mat MOE, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Sch Mat Sci & Engn, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Int Ctr Future Sci, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Electron Microscopy Ctr, Changchun 130012, Jilin, Peoples R China. | |
2018-04-01 | |
发表期刊 | ELECTROCHIMICA ACTA
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ISSN | 0013-4686 |
卷号 | 268页码:234-240 |
摘要 | Carbon coating has been attracting wide interests as optimum protection technology for Li ion batteries. Recently, carbon-coating has been considered as effective modification for copper/aluminum current collector. Although rate performance and lifetime of electrodes have been widely investigated, interfacial insight remains very superficial, hampering considerable improvement of electrode performance. Here we propose mechanistic models of double interfaces: one interface locates between Cu and active materials, and the other is referred to as solid electrolyte interphase (SEI) film coating on the current collector. Then vertical graphene nanowalls coated copper (VG) was prepared to reduce interfacial resistance of SEI film derived from an amorphous carbon coating layer. As a result, it exhibited a good rate performance with similar to 190 mAh/g at 3 C, in contrast with similar to 160 mAh/g for commercial carbon-coated copper (CC) and similar to 90 mAh/g for traditional bare copper (BC). (c) 2018 Elsevier Ltd. All rights reserved.; Carbon coating has been attracting wide interests as optimum protection technology for Li ion batteries. Recently, carbon-coating has been considered as effective modification for copper/aluminum current collector. Although rate performance and lifetime of electrodes have been widely investigated, interfacial insight remains very superficial, hampering considerable improvement of electrode performance. Here we propose mechanistic models of double interfaces: one interface locates between Cu and active materials, and the other is referred to as solid electrolyte interphase (SEI) film coating on the current collector. Then vertical graphene nanowalls coated copper (VG) was prepared to reduce interfacial resistance of SEI film derived from an amorphous carbon coating layer. As a result, it exhibited a good rate performance with similar to 190 mAh/g at 3 C, in contrast with similar to 160 mAh/g for commercial carbon-coated copper (CC) and similar to 90 mAh/g for traditional bare copper (BC). (c) 2018 Elsevier Ltd. All rights reserved. |
部门归属 | [liu, xiaofei ; wang, dong ; luan, chen ; qin, tingting ; zhang, wei ; shi, xiaoyuan ; deng, ting ; zheng, weitao] jilin univ, key lab mobile mat moe, changchun 130012, jilin, peoples r china ; [liu, xiaofei ; wang, dong ; luan, chen ; qin, tingting ; zhang, wei ; shi, xiaoyuan ; deng, ting ; zheng, weitao] jilin univ, sch mat sci & engn, changchun 130012, jilin, peoples r china ; [liu, xiaofei ; wang, dong ; luan, chen ; qin, tingting ; zhang, wei ; shi, xiaoyuan ; deng, ting ; zheng, weitao] jilin univ, int ctr future sci, changchun 130012, jilin, peoples r china ; [liu, xiaofei ; wang, dong ; luan, chen ; qin, tingting ; zhang, wei ; shi, xiaoyuan ; deng, ting ; zheng, weitao] jilin univ, electron microscopy ctr, changchun 130012, jilin, peoples r china ; [zhang, bingsen] chinese acad sci, inst met res, shenyang natl lab mat sci, shenyang 110016, liaoning, peoples r china ; [zhang, wei] cic energigune, albert einstein 48, minano 01510, spain ; [zhang, wei] ikerbasque, basque fdn sci, bilbao 48013, spain ; [wang, duo] tianjin polytech univ, sch mat sci & engn, inst nanostruct mat, tianjin 300387, peoples r china ; [wang, duo] tianjin polytech univ, sch mat sci & engn, tianjin key lab fiber modificat & funct fibers, tianjin 300387, peoples r china ; [wang, duo] jilin zhongyin zhihe technol co ltd, changchun 130031, jilin, peoples r china |
关键词 | Lithium Batteries Carbon Anodes Electrode Surface Supercapacitor Intercalation Spectroscopy Stability Cells |
学科领域 | Electrochemistry |
资助者 | National Key R&D Program of China [2016YFA0200400]; Jilin Province/Jilin University co-Construction Project-Funds for New Materials [SXGJSF2017-3, Branch-2/440050316A36]; Program for JLU Science and Technology Innovative Research Team (JLUSTIRT); "Double-First Class" Discipline for Materials Science & Engineering, and Special Funding for Academic Leaders at Jilin University |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000427657600026 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.imr.ac.cn/handle/321006/79406 |
专题 | 中国科学院金属研究所 |
通讯作者 | Zhang, W; Zheng, WT (reprint author), Jilin Univ, Key Lab Mobile Mat MOE, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Sch Mat Sci & Engn, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Int Ctr Future Sci, Changchun 130012, Jilin, Peoples R China.; Zheng, WT (reprint author), Jilin Univ, Electron Microscopy Ctr, Changchun 130012, Jilin, Peoples R China. |
推荐引用方式 GB/T 7714 | Liu, XF,Wang, D,Zhang, BS,et al. Vertical graphene nanowalls coating of copper current collector for enhancing rate performance of graphite anode of Li ion battery: The merit of optimized interface architecture[J]. ELECTROCHIMICA ACTA,2018,268:234-240. |
APA | Liu, XF.,Wang, D.,Zhang, BS.,Luan, C.,Qin, TT.,...&Zheng, WT .(2018).Vertical graphene nanowalls coating of copper current collector for enhancing rate performance of graphite anode of Li ion battery: The merit of optimized interface architecture.ELECTROCHIMICA ACTA,268,234-240. |
MLA | Liu, XF,et al."Vertical graphene nanowalls coating of copper current collector for enhancing rate performance of graphite anode of Li ion battery: The merit of optimized interface architecture".ELECTROCHIMICA ACTA 268(2018):234-240. |
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