Lu Wang, Hao Dang, Tianqi He, Rui Liu, Rui Wang, Fen Ran
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引用次数: 0
摘要
作为钒基硫化物的典型代表,二硫化钒因其高理论容量和独特的晶体结构而备受研究人员的关注。然而,在克服其结构塌陷的同时,实现既是活性材料又是粘合剂的双重功能化仍然具有挑战性。本研究通过二硫化钒与多巴胺之间的 V-O 键和氢键的协同作用,设计了一种多巴胺包覆的二硫化钒核壳结构,并将其进一步用作双功能电极材料。无粘合剂的多巴胺包覆二硫化钒在循环 400 次后,电流密度为 200 mA g-1 时,比容量为 682.03 mAh g-1,库仑效率为 99.78%。更重要的是,在 1000 mA g-1 的更大电流密度下,1500 次循环后的比容量为 385.44 mAh g-1。循环 3150 次后,在电流密度为 2000 mA g-1 时,比容量为 200.32 mAh g-1。电化学动力学分析表明,不含粘合剂的多巴胺涂层二硫化钒表现出快速的离子扩散动力学,离子扩散系数的数量级在 10-11 到 10-12 之间。这种材料有望成为 "快速充电 "锂离子电池的电极材料。
Dual-functional and polydopamine-coated vanadium disulfide for “fast-charging” lithium-ion batteries
As a typical representative of vanadium-based sulfides, vanadium disulfide has attracted the attention of researchers ascribed to its high theoretical capacity and unique crystal structure. However, overcoming its structural collapse while achieving dual functionalization that serves as both active material and binder remains challenging. This study designs a dopamine-coating vanadium disulfide core-shell structure through the synergistic effect of V-O bonds and hydrogen bonds between vanadium disulfide and dopamine, which is further employed as a dual-function electrode material. The polydopamine-coated vanadium disulfide without binder exhibits specific capacity of 682.03 mAh g−1, and the Coulombic efficiency of 99.78% at a current density of 200 mA g−1 after 400 cycles. More importantly, at a larger current density of 1000 mA g−1, the specific capacity is 385.44 mAh g−1 after 1500 cycles. After 3150 cycles, the specific capacity is 200.32 mAh g−1 at 2000 mA g−1. Electrochemical kinetics analysis displays that the polydopamine-coated vanadium disulfide without binder exhibits fast ion-diffusion kinetics, with the order of magnitude of ion-diffusion coefficients ranging from 10−11 to 10−12. This kind of material has the potential to be a significantly promising electrode material for “fast-charging” lithium-ion batteries.