Vacancy-engineered LiMn2O4 embedded in dual-heteroatom-doped carbon via metal-organic framework-mediated synthesis towards longevous lithium ion battery

杂原子 材料科学 空位缺陷 阴极 电池(电) 电化学 溶解 碳纤维 化学工程 锂(药物) 金属有机骨架 纳米技术 电解质 化学 电极 吸附 复合材料 物理化学 结晶学 有机化学 热力学 戒指(化学) 功率(物理) 内分泌学 工程类 物理 复合数 医学
作者
Xiaoming Lin,Jia Lin,Xiaomeng Lü,Xiaohong Tan,Hao Li,Wanxin Mai,Yuhong Luo,Yongbo Wu,Shuangqiang Chen,Chao Yang,Yong Wang
出处
期刊:Materials futures [IOP Publishing]
卷期号:4 (2): 025101-025101 被引量:21
标识
DOI:10.1088/2752-5724/ad9e08
摘要

Abstract Spinel LiMn 2 O 4 (LMO) is deemed to be a promising cathode material for commercial lithium-ion batteries (LIBs) in prospect of its cost-effectiveness, nontoxicity, fabulous rate capability, and high energy density. Nevertheless, the LMO is inevitably confronted with sluggish diffusion kinetics and drastic capacity degradation triggered by multiple issues, including Jahn–Teller distortion, Mn dissolution, and structural attenuation. Thereinto, a metal-organic framework (MOF) chemistry engineering for hierarchical micro-/nano-structural F, O-dual-doped carbon embedded oxygen vacancy enriched LiMn 2 O 4 cathode (O V -LMO@FOC) is proposed for longevous LIBs. Bestowed by experimental and theoretical implementations, systematic investigations of O V -LMO@FOC endow that the meticulous integration of F, O-dual-doped carbon and oxygen vacancy in LMO-based cathode reconfigures the electronic structure, boosts electronic conductivity, expedites diffusion capability, facilitates energetically preferable Li + adsorption, and suppresses Mn dissolution in the electrolyte, consequently achieving fabulous long-term cycling stability. As expected, the O V -LMO@FOC behaves with compelling electrochemical performance with prosperous reversible capacity (130.2 mAh g −1 at 0.2 C upon 200 cycles), exceptional rate capacity (93.7 mAh g −1 even at 20 C), and pronounced long-term cyclability (112.5 mAh g −1 after 1200 cycles with 77.6% capacity retention at 1 C). Even at the ultrahigh current density of 5 C, the O V -LMO@FOC bears a brilliant capacity of 96.9 mAh g −1 upon 1000 cycles with an extraordinary capacity retention of 90.7%, and maintains a discharge capacity of 70.9 mAh g −1 upon 4000 cycles. This work envisions the MOF-chemistry in surface modification and electronic modulation engineering of high-performance cathode materials towards industrialization in automotive market.
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
1秒前
上岸发布了新的文献求助10
1秒前
小小鸟发布了新的文献求助10
2秒前
aging00发布了新的文献求助10
2秒前
大苹果完成签到,获得积分10
2秒前
渡人舟应助月见清和采纳,获得10
4秒前
英俊的铭应助哲轩采纳,获得10
4秒前
5秒前
大模型应助七月不远采纳,获得10
5秒前
无花果应助慈祥的网络采纳,获得10
5秒前
7秒前
7秒前
7秒前
8秒前
麻麻薯完成签到 ,获得积分10
8秒前
隐形书文完成签到,获得积分10
9秒前
冷酷的绝悟完成签到,获得积分10
9秒前
11秒前
11秒前
66666发布了新的文献求助10
12秒前
12秒前
12秒前
13秒前
上岸发布了新的文献求助10
13秒前
李爱国应助蔡宇滔采纳,获得10
13秒前
若一发布了新的文献求助150
15秒前
Bubu完成签到,获得积分10
15秒前
Sthwrong发布了新的文献求助10
15秒前
言瓒完成签到,获得积分10
15秒前
哲轩发布了新的文献求助10
16秒前
搜集达人应助TGM_Hedwig采纳,获得10
17秒前
19秒前
19秒前
CipherSage应助sss采纳,获得10
20秒前
12完成签到,获得积分10
21秒前
21秒前
kento发布了新的文献求助10
21秒前
希望天下0贩的0应助66666采纳,获得10
22秒前
23秒前
独特微笑完成签到,获得积分20
24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
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
Comparative Elite Sport Development Systems, Structures and Public Policy 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Auslegungsgeschichte 500
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7637743
求助须知:如何正确求助?哪些是违规求助? 9211300
关于积分的说明 19758409
捐赠科研通 7204937
什么是DOI,文献DOI怎么找? 3275767
关于科研通互助平台的介绍 2437385
邀请新用户注册赠送积分活动 2272928