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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
寒冷悲发布了新的文献求助10
刚刚
细腻海蓝发布了新的文献求助10
1秒前
一坨发布了新的文献求助10
1秒前
2秒前
科研通AI6.3应助烂漫笑晴采纳,获得10
2秒前
玖月发布了新的文献求助10
3秒前
岁峰柒发布了新的文献求助10
4秒前
4秒前
4秒前
5秒前
SciGPT应助LEEGAN采纳,获得10
5秒前
6秒前
小二郎应助boyue采纳,获得10
6秒前
7秒前
7秒前
嘎嘎完成签到,获得积分10
8秒前
8秒前
8秒前
寒天帝发布了新的文献求助10
8秒前
123发布了新的文献求助10
9秒前
9秒前
儒雅新波发布了新的文献求助10
10秒前
Tutu完成签到,获得积分10
10秒前
wyby发布了新的文献求助10
10秒前
汉堡包应助茉莉雨采纳,获得10
10秒前
科研通AI6.1应助yodel采纳,获得10
10秒前
chengyue9939发布了新的文献求助20
11秒前
12秒前
燕燕于飞发布了新的文献求助30
12秒前
12秒前
14秒前
like_Y应助无忧采纳,获得10
14秒前
15秒前
细腻海蓝完成签到,获得积分10
15秒前
南孚阮桑发布了新的文献求助10
15秒前
PENGCHENGDAI完成签到,获得积分10
15秒前
Anan发布了新的文献求助10
16秒前
领导范儿应助燕燕于飞采纳,获得10
16秒前
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 3000
Les Mantodea de guyane 2500
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 2000
What is the Future of Psychotherapy in a Digital Age? 700
The Psychological Quest for Meaning 600
Zeolites: From Fundamentals to Emerging Applications 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5955015
求助须知:如何正确求助?哪些是违规求助? 7164861
关于积分的说明 15936949
捐赠科研通 5089962
什么是DOI,文献DOI怎么找? 2735472
邀请新用户注册赠送积分活动 1696310
关于科研通互助平台的介绍 1617257