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Polyaniline induced nano-carbon with multi-doped heteroatoms for high-rate lithium ion battery anodes.

作者信息

Liu Jiaqi, Jiang Le, Wu Hanfeng, Dong Shuo, Jin Yanyang, Yuan Yongjun, Bai Wangfeng, Shi Xiaowei, Wu Shiting

机构信息

Hangzhou Dianzi University, New Energy Materials Research Center, College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018, P. R. China, Hangzhou, Zhejiang, 310018, CHINA.

College of Materials & Environmental Engineering, Hangzhou Dianzi University, New Energy Materials Research Center, College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018, P. R. China, Hangzhou, Zhejiang, 310018, CHINA.

出版信息

Nanotechnology. 2025 Aug 21. doi: 10.1088/1361-6528/adfded.

Abstract

Nanostructure design, construction of porous architecture and heteroatom doping are three feasible strategies for advanced lithium ion batteries (LIBs) based on carbon anodes. Here, a unique polyaniline (PANI) @carbon@PANI sandwiched structure has been constructed via simultaneously PANI loading on both the inner and outer surfaces of ultra-wide graphitic carbon nanotubes. The morphology and thickness of PANI coating could be regulated by polymerizing agent of aniline and surface ethanol modification, and N, O and P heteroatoms are efficiently doped in the carbon lattice as extra Lireservoirs through thermal annealing. Particularly, pyrrolic nitrogen and pyridinic nitrogen dopants could result in high-activity sites conducive to Liadsorption, and reduce the diffusion barrier of Li. Therefore, when the multi-doped nano-carbon is utilized as anodes for LIBs, PCPm-excess-600 with expanded interlayer spacing (0.425 nm) could exhibit a specific cycling capacity up to 944.44 mAh/g. And the high doping level of active pyridinic nitrogen contributes a large number of Liadsorption sites to PCPm-600 with multi-level pore structures, and the resulting surface pseudo-capacitance greatly improves its rate capability. After 5000 reversible cycles under a ultra-large rate of 2000 mA/g, its specific capacity is as high as 388.57 mAh/g with capacity retention over 80%, and finally a high-capacity and fast-charging anode material with extremely long service life is obtained, providing new thoughts for the design and synthesis of carbon anodes.

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