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揭示用于先进钠离子电池的废弃木材衍生硬碳的闭孔形成过程。

Revealing the closed pore formation of waste wood-derived hard carbon for advanced sodium-ion battery.

作者信息

Tang Zheng, Zhang Rui, Wang Haiyan, Zhou Siyu, Pan Zhiyi, Huang Yuancheng, Sun Dan, Tang Yougen, Ji Xiaobo, Amine Khalil, Shao Minhua

机构信息

Hunan Provincial Key Laboratory of Chemical Power Sources, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, P.R. China.

Department of Chemical and Biological Engineering, Energy Institute, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, P.R. China.

出版信息

Nat Commun. 2023 Sep 27;14(1):6024. doi: 10.1038/s41467-023-39637-5.

Abstract

Although the closed pore structure plays a key role in contributing low-voltage plateau capacity of hard carbon anode for sodium-ion batteries, the formation mechanism of closed pores is still under debate. Here, we employ waste wood-derived hard carbon as a template to systematically establish the formation mechanisms of closed pores and their effect on sodium storage performance. We find that the high crystallinity cellulose in nature wood decomposes to long-range carbon layers as the wall of closed pore, and the amorphous component can hinder the graphitization of carbon layer and induce the crispation of long-range carbon layers. The optimized sample demonstrates a high reversible capacity of 430 mAh g at 20 mA g (plateau capacity of 293 mAh g for the second cycle), as well as good rate and stable cycling performances (85.4% after 400 cycles at 500 mA g). Deep insights into the closed pore formation will greatly forward the rational design of hard carbon anode with high capacity.

摘要

尽管闭孔结构在钠离子电池硬碳负极的低压平台容量贡献中起着关键作用,但闭孔的形成机制仍存在争议。在此,我们采用废弃木材衍生的硬碳作为模板,系统地建立闭孔的形成机制及其对储钠性能的影响。我们发现,天然木材中的高结晶度纤维素分解形成作为闭孔壁的长程碳层,而非晶成分会阻碍碳层的石墨化并诱导长程碳层的卷曲。优化后的样品在20 mA g下表现出430 mAh g的高可逆容量(第二个循环的平台容量为293 mAh g),以及良好的倍率性能和稳定的循环性能(在500 mA g下400次循环后为85.4%)。对闭孔形成的深入了解将极大地推动高容量硬碳负极的合理设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f569/10533848/62d6d2254273/41467_2023_39637_Fig1_HTML.jpg

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