杂原子
锡
材料科学
锂(药物)
碳纤维
X射线光电子能谱
碳化
化学工程
多孔性
兴奋剂
硫黄
复合材料
化学
有机化学
冶金
复合数
扫描电子显微镜
戒指(化学)
医学
光电子学
工程类
内分泌学
作者
Kun Liu,Hongfei Zheng,Jiaao Wang,Yuhao Zhou,Ning Zhang,Yehong Du,Jianzong Man,Graeme Henkelman,Juncai Sun
标识
DOI:10.1016/j.apsusc.2021.152319
摘要
• N, S co-doped porous carbon/Sn composites are made by self-derived template method. • The synergistic effect of N, S co-doping is demonstrated by DFT calculations. • The Sn/NSPC anode yields a high discharge capacity of 712.6 mAh/g after 200 cycles. • Sn/NSPC full cell obtains a specific capacity of 572.6 mAh/g after 100 cycles. • The lithium storage mechanism is comprehensively revealed by in-situ XRD. Although single-heteroatom doped porous carbon/tin (Sn) composites have been extensively studied, an overall understanding of the effects of dual-heteroatoms doped porous carbon on the lithium storage properties of Sn is still insufficient. Herein, we provide a green self-derived templating strategy to synthesize the nitrogen, sulfur co-doped porous carbon/Sn composites (Sn/NSPC) with synergistic effect through one-step carbonization. The key to this approach is the self-generation of Na 2 CO 3 template, and it is apt to eliminate with water directly. The resultant NSPC can prevent the agglomeration of Sn particles. The synergistic effect is confirmed by density functional theoretical (DFT) calculations, revealing that N, S co-doped improves the electronic conductivity. The lithium storage mechanism and structural stability of Sn/NSPC electrode are researched via in-situ XRD and ex-situ XPS. The obtained electrode affords a discharge capacity (200 cycles, 712.6 mAh/g at 0.1 A/g) and long-life cyclability (2000 cycles, 330.1 mAh/g at 3 A/g). Additionally, the Sn/NSPC||LiCoO 2 full cell achieves excellent discharge capacity (572.6 mAh/g at 0.1 A/g) while remaining impressive cyclability (440.6 mAh/g at 1 A/g). This green and eco-friendly approach may be extended to the preparation of other heteroatom-doped carbon/Sn composites.
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