材料科学
氢气储存
钠
金属
氢
分子
电化学
密度泛函理论
储能
组合化学
化学工程
有机化学
冶金
电极
化学
物理化学
计算化学
工程类
功率(物理)
物理
量子力学
作者
Lichang Ji,Yun Zhao,Xingguo Qi,Yong Li,Zhihong Wei,Gaoyi Han,Zongping Shao
标识
DOI:10.1002/adfm.202408242
摘要
Abstract The cost‐effective synthesis of high‐performance hard carbons (HCs) is a key step of sodium‐ion batteries toward practical applications. Considering the rich resource of low‐value aromatic hydrocarbons (e.g., pitch), there is tremendous interesting in its conversion into value‐added HCs. Unfortunately, it still lacks an efficient way for the synthesis, in addition to the time‐consuming oxygen contamination of the carbon framework. Herein, a universal strategy is reported that enables the efficient synthesis of HCs from pitch by modulating hydrogen transfer using metal chlorides. CuCl 2 is selected as the model modulator and the effect of different metal chlorides (FeCl 3 , AlCl 3 , ZnCl 2 , and MgCl 2 ) are further explored. Based on material characterizations and density functional theory calculation employing 1‐methylnaphthalene as the model molecule, it shows that the hydrogen capture and chlorination reactions mediated by CuCl 2 and FeCl 3 are thermodynamically favored, which promote the crosslinking of pitch to form HCs. After optimization, the derived HC exhibits superior performance of reversible capacity of 304.8 mAh g −1 and a high initial Columbic efficiency of 88.4%. These discoveries provide new insights into the synthesis of HCs from aromatic hydrocarbons, facilitating their utilization in electrochemical energy storage.
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