Constructing nitrogen-doped porous carbon immobilized Co9S8 composite as high-performance anode material for sodium-ion batteries

阳极 复合数 碳化 材料科学 碳纤维 多孔性 纳米颗粒 硫化 化学工程 纳米技术 复合材料 化学 电极 冶金 物理化学 硫黄 工程类 扫描电子显微镜
作者
Hongming Chen,Yilin Niu,Yanhong Meng,Xianzhuo Ren,Yingchun Huang,Mingshan Wang,Woon‐Ming Lau,Dan Zhou
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:923: 166373-166373 被引量:16
标识
DOI:10.1016/j.jallcom.2022.166373
摘要

Transition metal sulfides (TMSs) as anode materials deliver promising potential in achieving high-capacity sodium-ion batteries (SIBs). But the undesirable volume change for structure upon redox process always hinder the realization of satisfactory cycling stability and rate capability. Herein, a novel Co9S8/carbon composite (Co9S8 @NPC) with Co9S8 nanoparticles (NPs) immobilized into nitrogen-doped porous carbon networks was synthesized via the successive procedures of sol-gel, pyrolysis carbonization and in situ sulfidation and employed as anode material for SIBs. By virtue of the yielded porous feature, nitrogen-doping and space confinement of Co9S8 NPs in conductive carbon sheet networks, the Co9S8 @NPC is able to offer integrated merits of sufficient active sites, improved reaction dynamics and rigid structural stability for high-performance Na-storage. As a result, the assembled Co9S8 @NPC electrode possesses large initial discharge/charge capacities (752.5/325.3 mAh g−1 at 50 mA g−1), considerable rate capability (138.5 mAh g−1 at 3000 mA g−1) and high cycling stability (275.3 mAh g−1 at 50 mA g−1 after 100 cycles; 120.4 mAh g−1 at 500 mA g−1 after 3000 cycles). In order to uncover the diffusion and storage mechanism of Na+ ions in the electrode material, pseudocapacitive behavior, reaction dynamics and related theoretical simulation based on first-principles calculations are initially conducted. The facile synthesis strategy and desirable Na-storage performance might enable the Co9S8 @NPC composite great potential in advanced SIBs.
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