Liu Qingdi, Han Fei, Zhou Jiafu, Li Yan, Chen Long, Zhang Fuquan, Zhou Dianwu, Ye Chong, Yang Jianxiao, Wu Xiao, Liu Jinshui
Hunan Province Key Laboratory for Advanced Carbon Materials and Applied Technology, College of Materials Science and Engineering, Hunan University, Changsha 410082, China.
State Key Laboratory of Advanced Design and Manufacturing for Vehicle Body, Hunan University, Changsha 410082, China.
ACS Appl Mater Interfaces. 2020 May 6;12(18):20838-20848. doi: 10.1021/acsami.0c00679. Epub 2020 Apr 26.
Soft carbon is attracting tremendous attention as a promising anode material for potassium-ion batteries (PIBs) because of its graphitizable structure and adjustable interlayer distance. Herein, nitrogen/sulfur dual-doped porous soft carbon nanosheets (NSC) have been prepared with coal tar pitch as carbon precursors in an appropriate molten salt medium. The molten salt medium and N/S dual-doping are responsible for the formation of nanosheet-like morphology, abundant microporous channels with a high surface area of 436 m g, expanded interlamellar spacing of 0.378 nm, and enormous defect-induced active sites. These structural features are crucial for boosting potassium-ion storage performance, endowing the NSC to deliver a high potassiation storage capacity of 359 mAh g at 100 mA g and 115 mAh g at 5.0 A g, and retaining 92.4% capacity retention at 1.0 A g after 1000 cycles. More importantly, the pre-intercalation of K atom from the molten salts helps improve the initial Coulombic efficiency to 50%, which outperforms those of the recently reported carbon anode materials with large surface areas. The density functional theory calculations further illuminate that the N/S dual-doping can facilitate the adsorption of K-ion in carbon materials and decrease the ion diffusion energy barrier during the solid-state charge migration.
软碳因其可石墨化结构和可调节的层间距,作为一种有前景的钾离子电池(PIB)负极材料而备受关注。在此,以煤焦油沥青为碳前驱体,在合适的熔盐介质中制备了氮/硫双掺杂多孔软碳纳米片(NSC)。熔盐介质和氮/硫双掺杂导致了纳米片状形态的形成、具有436 m²/g高比表面积的丰富微孔通道、0.378 nm的层间距扩大以及大量缺陷诱导的活性位点。这些结构特征对于提高钾离子存储性能至关重要,使NSC在100 mA/g时具有359 mAh/g的高钾化存储容量,在5.0 A/g时具有115 mAh/g的容量,并在1.0 A/g下循环1000次后保持92.4%的容量保持率。更重要的是,来自熔盐的钾原子预嵌入有助于将初始库仑效率提高到50%,这优于最近报道的具有大表面积的碳负极材料。密度泛函理论计算进一步表明,氮/硫双掺杂可以促进钾离子在碳材料中的吸附,并降低固态电荷迁移过程中的离子扩散能垒。