Resol and urea derived N-doped porous carbon for Na-ion storage

被引:9
作者
Sun, Shijiao [1 ]
Zhang, Chang [1 ]
Yao, Jian [1 ]
Wang, Huanlei [2 ]
Zhao, Xiangyu [1 ,3 ]
Shen, Xiaodong [1 ]
机构
[1] Nanjing Tech Univ, Coll Mat Sci & Engn, 30 Puzhu South Rd, Nanjing 211816, Peoples R China
[2] Ocean Univ China, Sch Mat Sci & Engn, 238 Songling Rd, Qingdao 266100, Peoples R China
[3] Nanjing Tech Univ, Jiangsu Collaborat Innovat Ctr Adv Inorgan Funct, 30 Puzhu South Rd, Nanjing 211816, Peoples R China
基金
中国国家自然科学基金;
关键词
Na ion batteries; Negative electrode; N-doped porous carbon; Ether electrolytes; PERFORMANCE ANODE MATERIAL; SODIUM; BATTERIES; GRAPHENE; LIFE; NANOPARTICLES; REDUCTION;
D O I
10.1016/j.matchemphys.2020.123535
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We demonstrate a facile tetraconstituent (Phloroglucinol, glyoxal, urea and triblock copolymer Pluronic F127) co-assembly approach to prepare N-doped porous carbon. The N-doped porous carbon has a layer spacing as large as 0.393 nm, a disordered structure and a specific surface area as high as 502 m(2) g(-1), which may boost its battery property. When assembled into Na ion batteries, the N-doped porous carbon delivered a stable capacity up to 229 mA h g(-1) at 100 mA g(-1) after 200 cycles, higher than that (123 mA h g(-1)) of the undoped porous carbon. Furthermore, the initial Coulombic efficiency of the N-doped porous carbon was increased from 21% to 91% by employing ether electrolyte instead of common ester electrolyte, which is because almost neglected solid electrolyte interface film after the first cycle was formed on the electrode. Accordingly, a high capacity over 300 mA h g(-1) was obtained for the first 20 cycles at the same current density.
引用
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页数:10
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