Wang Jianjiao, Zhang Qian, Han Pengyu, Luo Jiakun, Peng Kui-Qing
Key Laboratory of Multiscale Spin Physics, Ministry of Education, Beijing Key Laboratory of Energy Conversion and Storage Materials, School of Physics and Astronomy, Beijing Normal University, Beijing 100875, China.
Materials (Basel). 2025 Aug 27;18(17):4018. doi: 10.3390/ma18174018.
Heteroatom doping is an effective strategy for improving the sodium storage performance of hard carbon. However, the use of sulfur and fluorine codoped carbon materials as anodes for sodium-ion batteries has not been reported. Here, an S-infused/S, F-codoped PVDF-derived carbon SFC5 was prepared by one-step carbonization of PVDF and synchronously used as an anode for a sodium-ion battery. The prepared SFC5 containing 10.11 at% S and 9.54 at% F is a short-range ordered amorphous carbon with a microporous structure. Owing to the structural advantages of S, F codoping, and the high specific capacity of S, SFC5 exhibited an outstanding sodium storage performance of 365 mAh g after 200 cycles at 50 mA g and 212 mAh g after 500 cycles at 400 mA g. Moreover, theoretical calculations based on density functional theory (DFT) verify that S and F codoping can considerably reduce the Na adsorption energy and increase the electronic conductivity of SFC5. The current study presents a viable and facile approach to prepare high-performance, low-cost anode materials for SIBs, supported by empirical evidence and theoretical computations.
杂原子掺杂是提高硬碳储钠性能的有效策略。然而,硫和氟共掺杂碳材料作为钠离子电池负极的应用尚未见报道。在此,通过聚偏氟乙烯(PVDF)的一步碳化制备了一种硫注入/硫、氟共掺杂的PVDF衍生碳SFC5,并将其同步用作钠离子电池的负极。制备的SFC5含有10.11原子%的硫和9.54原子%的氟,是一种具有微孔结构的短程有序无定形碳。由于硫、氟共掺杂的结构优势以及硫的高比容量,SFC5在50 mA g下循环200次后表现出365 mAh g的优异储钠性能,在400 mA g下循环500次后表现出212 mAh g的性能。此外,基于密度泛函理论(DFT)的理论计算证实,硫和氟共掺杂可显著降低SFC5的钠吸附能并提高其电子导电性。当前研究通过实验证据和理论计算,提出了一种可行且简便的方法来制备用于钠离子电池的高性能、低成本负极材料。