Wei Dong, Zhaomeng Wu, Xiaochen Xu, Su Li and Yang Ji
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引用次数: 0
摘要
锂硫电池因其高能量密度和低成本被认为是下一代电池的最佳选择之一。然而,硫及其产物电导率低、电化学过程中体积变化大、多硫化锂的“穿梭效应”等问题是其面临的三大挑战。碳材料可以缓解硫的电导率和体积变化问题。通过掺杂杂原子或负载极性化合物可以进一步抑制多硫化物的穿梭。本文采用硼氮共掺杂多孔碳前驱体制备了CoS2/多孔硼氮共掺杂碳(CoS2/BNC)。中空结构能更好地适应硫反应过程中的体积膨胀,从多个角度增强了LiPSs的化学吸附和氧化还原动力学,抑制了LiPSs的穿梭。在0.1C条件下,CoS2/BNC/S锂硫电池的初始放电容量高达1639.1 mAh g−1。在2C电流密度下循环500次后,容量仍保持在752.7 mAh g−1,每循环容量衰减仅为0.048%,库仑效率仍能保持在97.8%,表现出满意的电化学性能。
CoS2 nanoparticles anchored on N,B co-doped porous carbon for high-rate and long-life lithium–sulfur batteries
Lithium–sulfur (Li–S) batteries are regarded as one of the best choices for next-generation batteries due to their high energy density and low cost. However, there are three major challenges, namely the low electrical conductivity of sulfur and its products, the volume change during the electrochemical process, and the “shuttle effect” of lithium polysulfide. Carbon materials can alleviate the problems of electrical conductivity and volume change of sulfur. The shuttle of polysulfides can be further inhibited by doping heteroatoms or loading polar compounds. In this work, CoS2/porous boron–nitrogen co-doped carbon (CoS2/BNC) was prepared using a boron–nitrogen co-doped porous carbon precursor. The hollow structure can better adapt to the volume expansion during the sulfur reaction, and the chemisorption and redox kinetics of LiPSs are strengthened from multiple angles to inhibit the shuttle of LiPSs. The CoS2/BNC/S lithium–sulfur battery has a high initial discharge capacity of 1639.1 mAh g−1 under the condition of 0.1C. After 500 cycles at a current density of 2C, the capacity still remains at 752.7 mAh g−1, with a capacity decay of only 0.048% per cycle, and the coulombic efficiency can still be maintained at 97.8%, showing satisfactory electrochemical performance.