碳化
阳极
钠
法拉第效率
碳纤维
热解炭
材料科学
无定形固体
电化学
化学
化学工程
复合材料
有机化学
电极
热解
工程类
复合数
物理化学
扫描电子显微镜
冶金
作者
Ran Xu,Ning Sun,Huanyu Zhou,Xiaqing Chang,Razium Ali Soomro,Bin Xu
标识
DOI:10.1002/bte2.20220054
摘要
Abstract Hard carbons are widely studied as anode materials for sodium‐ion batteries (SIBs) due to their high Na‐storage capacity, long cycle life, and low cost. However, the low initial coulombic efficiency (ICE) and poor cycle performance remain bottleneck concerns that necessitate a comprehensive material engineering solution. Herein, we propose a facile strategy to synthesize amorphous carbons with pseudo‐graphitic dominated crystalline, expanded interlayer spacing, and reduced surface defects via carbonization of the cross‐linking network of phenolic resin and sucrose. An elaborate structural and electrochemical characteristics analysis has been investigated against different sucrose contents and carbonization temperatures. The representative PF‐S‐55‐1200 with the optimum cross‐linking degree as well as carbonization temperature realizes a high reversible Na‐storage capacity of 323.0 mAh g −1 with an ICE as high as 86.4%, much superior to the pristine phenolic resin pyrolytic carbon with a capacity of 267.1 mAh g −1 and an ICE of 46.3%. The hybrid hard carbons also exhibit robust structural stability with a prolonged cycle lifespan evidenced by a retained capacity of 238.3 mAh g −1 at a current density of 200 mA g −1 over 1500 cycles. The proposed route promises low‐cost and high‐performance hybrid hard carbons with optimized structural configuration for advanced SIBs.
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