Ning Guoqing, Ma Xinlong, Zhu Xiao, Cao Yanming, Sun Yuzhen, Qi Chuanlei, Fan Zhuangjun, Li Yongfeng, Zhang Xin, Lan Xingying, Gao Jinsen
State Key Laboratory of Heavy Oil Processing, China University of Petroleum , Beijing 102249, China.
ACS Appl Mater Interfaces. 2014 Sep 24;6(18):15950-8. doi: 10.1021/am503716k. Epub 2014 Sep 11.
Here, we report a new approach to synthesizing S-doped porous carbons and achieving both a high capacity and a high Coulombic efficiency in the first cycle for carbon nanostructures as anodes for Li ion batteries. S-doped porous carbons (S-PCs) were synthesized by carbonization of pitch using magnesium sulfate whiskers as both templates and S source, and a S doping up to 10.1 atom % (corresponding to 22.5 wt %) was obtained via a S doping reaction. Removal of functional groups or highly active C atoms during the S doping has led to formation of much thinner solid-electrolyte interface layer and hence significantly enhanced the Coulombic efficiency in the first cycle from 39.6% (for the undoped porous carbon) to 81.0%. The Li storage capacity of the S-PCs is up to 1781 mA h g(-1) at the current density of 50 mA g(-1), more than doubling that of the undoped porous carbon. Due to the enhanced conductivity, the hierarchically porous structure and the excellent stability, the S-PC anodes exhibit excellent rate capability and reliable cycling stability. Our results indicate that S doping can efficiently promote the Li storage capacity and reduce the irreversible Li combination for carbon nanostructures.
在此,我们报道了一种合成硫掺杂多孔碳的新方法,并在作为锂离子电池阳极的碳纳米结构的首个循环中实现了高容量和高库仑效率。通过以硫酸镁晶须作为模板和硫源对沥青进行碳化来合成硫掺杂多孔碳(S-PCs),通过硫掺杂反应获得了高达10.1原子%(相当于22.5重量%)的硫掺杂量。硫掺杂过程中官能团或高活性碳原子的去除导致形成了更薄的固体电解质界面层,从而使首个循环中的库仑效率从39.6%(对于未掺杂的多孔碳)显著提高到81.0%。在50 mA g(-1)的电流密度下,S-PCs的锂存储容量高达1781 mA h g(-1),是未掺杂多孔碳的两倍多。由于导电性增强、分级多孔结构和出色的稳定性,S-PC阳极表现出优异的倍率性能和可靠的循环稳定性。我们的结果表明,硫掺杂可以有效提高碳纳米结构的锂存储容量并减少不可逆的锂结合。