材料科学
酰亚胺
阳极
离子
化学工程
钠
纳米技术
高分子化学
化学
有机化学
冶金
电极
物理化学
工程类
作者
Ying Wang,Hongguan Li,Boyin Zhai,Xinglong Li,Ping Niu,Jérémy Odent,Shulan Wang,Li Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-01-16
卷期号:18 (4): 3456-3467
被引量:56
标识
DOI:10.1021/acsnano.3c10779
摘要
Carbon nitrides with layered structures and scalable syntheses have emerged as potential anode choices for the commercialization of sodium-ion batteries. However, the low crystallinity of materials synthesized through traditional thermal condensation leads to insufficient conductivity and poor cycling stability, which significantly hamper their practical applications. Herein, a facile salt-covering method was proposed for the synthesis of highly ordered crystalline C 3 N 4 -based all-carbon nanocomposites. The sealing environment created by this strategy leads to the formation of poly(heptazine imide) (PHI), the crystalline phase of C 3 N 4, with extended π-conjugation and a fully condensed nanosheet structure. Meanwhile, theoretical calculations reveal the high crystallinity of C 3 N 4 significantly reduces the energy barrier for electron transition and enables the generation of efficient charge transfer channels at the heterogeneous interface between carbon and C 3 N 4 . Accordingly, such nanocomposites present ultrastable cycling performances over 5000 cycles, with a high reversible capacity of 245.1 mAh g –1 at 2 A g –1 delivered. More importantly, they also exhibit an outstanding low-temperature capacity of 196.6 mAh g –1 at −20 °C. This work offers opportunities for the energy storage use of C 3 N 4 and provides some clues for developing long-life and high-capacity anodes operated under extreme conditions.
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