High‐performance electrodes for Li‐ion cell: Heteroatom‐doped porous carbon/ CoS structure and investigation of their structural and electrochemical properties

阳极 循环伏安法 材料科学 傅里叶变换红外光谱 无定形固体 电化学 碳纤维 化学工程 介电谱 电极 复合数 分析化学(期刊) 化学 结晶学 复合材料 有机化学 物理化学 工程类
作者
Nesrin Buğday,Emine Altin,S. Altın,Sedat Yaşar
出处
期刊:International Journal of Energy Research [Wiley]
卷期号:46 (13): 18379-18393 被引量:10
标识
DOI:10.1002/er.8452
摘要

As an essential class of anode materials, the synthesis and characterization of CoS@ZIF-12-C composite anode materials are reported. The two-step synthesis of CoS nanoparticles embedded in N-doped porous carbon by using a metal-organic framework (MOF) as the template. After structural characterization of CoS@ZIF-12-C composite materials, the main phase was found as CoS with symmetry of P63mmc. Benefiting from the CoS embedded in porous carbon structure, the half Li-ion battery cell tests of CoS@ZIF-12-C composite materials were performed by a 2-electrode method using CR2032 cells, and the capacities of the cells were measured for 200 cycles using 300 mAg−1 and 500 cycles using 1000 mAg−1. The first discharge capacities of the cells for 1000 mAg−1 were found as 458, 1178, and 815 mAhg−1 for CoS@ZIF-12-C-T, T = 700, 800, and 900°C, respectively. An unexpected capacity increase was observed for the CoS@ZIF-12-C-700 and CoS@ZIF-12-C-900 half cells during the cycling. Ex-situ x-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and cyclic voltammetry (CV) analysis were performed after cycling of the cells for explanations of the capacity increase. Ex-situ XRD analysis of these cells showed phase transitions from crystalline to amorphous type structure, and ex-situ FTIR proves the preservation of the CoS phase during the cycling. A redox reaction mechanism was suggested to explain the cells' battery performance by ex-situ XRD analysis.
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