材料科学
硫黄
热解
碳纤维
阳极
杂原子
兴奋剂
化学工程
拉曼光谱
电导率
无机化学
复合数
有机化学
化学
复合材料
电极
物理化学
光电子学
戒指(化学)
冶金
工程类
物理
光学
作者
Chunlei Chi,Zheng Liu,Xiaolong Lu,Meng Yu,Chao Huangfu,Yingchun Yan,Zhipeng Qiu,Bin Qi,Guanwen Wang,Huan Pang,Tong Wei,Zhuangjun Fan
标识
DOI:10.1016/j.ensm.2022.11.008
摘要
Sulfur-doped hard carbon (SC) with high capacity has been considered as a promising anode for potassium ion batteries (PIBs). However, due to the uncontrollable pyrolysis, the sulfur doping content and conductive carbon network of SC exhibit an intrinsic trade-off, resulting in poor rate performance and cycle stability. To address this issue, we chose highly conjugated polythiophene (Pth) as precursor for the easy formation of sp2 carbon skeleton with high sulfur doping. With increasing pyrolysis temperature, the structural evolution of Pth such as successive desulfuration, dehydrogenation and cyclization is systematically verified. Based on the balanced control of pyrolysis degree, sulfur-doped hard carbon at 700 °C (SC-700) has a high sulfur content (7.59 at.%) and high conductivity (56.5 S m−1), affording a high reversible capacity (442 mAh g−1 at 0.05 A g−1), excellent rate capability (162 mAh g−1 at 10 A g−1) and exceptional cycling stability (87% retention at 1 A g−1 after 1000 cycles). Ex-situ Raman and X-ray photoelectron spectroscopies demonstrate that the balance between sulfur doping and conductivity not only improve the faraday capacitance, but also promote K+ intercalation kinetics. The strategy can provide novel enlightenment for designing heteroatom doped carbon in energy storage and conversion.
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