碳化
材料科学
阳极
碳纤维
化学工程
无定形碳
微型多孔材料
热解
钠离子电池
电化学
无定形固体
法拉第效率
纳米技术
电极
复合材料
化学
有机化学
扫描电子显微镜
物理化学
工程类
复合数
作者
Stevanus Alvin,Dohyeon Yoon,Christian Chandra,Ratna Frida Susanti,Wonyoung Chang,Changkook Ryu,Jaehoon Kim
标识
DOI:10.1016/j.jpowsour.2019.05.013
摘要
Hard carbon is a promising anode material for sodium ion batteries (NIBs). In this study, a two-step carbonization approach is developed to enhance the electrochemical performance of lignocellulose biomass-derived hard carbon. The first step comprises slow low-temperature pyrolysis of fir wood that produces an amorphous carbon in which hexagonal planes are embedded in the amorphous carbon region to some extent. The second step comprises high-temperature carbonization at 1300 °C, which yields a hard carbon with a high degree of graphitization, an increased layer-plane length, and a low micropore volume. Two-step carbonized hard carbon delivers a large reversible capacity of 276 mAh g−1 at 50 mA g−1 after 100 cycles and high rate capacities of 108 mAh g−1 at 1.0 A g−1 and 76.3 mAh g−1 at 2.5 A g−1. The low-voltage plateau capacity below 0.1 V is 194 mAh g−1. The results of these experiments indicate that the exceptional electrochemical performance of two-step carbonized hard carbon arises from the effective suppression of micropore formation and a good balance between the degree of graphitization and number of defect sites. High-voltage adsorption of Na+ ions in micropores inhibits Na+-ion diffusion into the graphitic region of micropore-enriched hard carbon.
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