Facile Approach To Prepare Multiple Heteroatom-Doped Carbon Material from Bagasse and Its Applications toward Lithium-Ion and Lithium–Sulfur Batteries

杂原子 阳极 法拉第效率 锂(药物) 材料科学 化学工程 碳纤维 电化学 化学 电极 有机化学 复合数 戒指(化学) 复合材料 物理化学 医学 工程类 内分泌学
作者
Dasari Bosubabu,S. Ramakumar,Guruprakash Karkera,K. Ramesha
出处
期刊:Energy & Fuels [American Chemical Society]
卷期号:35 (9): 8286-8294 被引量:39
标识
DOI:10.1021/acs.energyfuels.0c03887
摘要

The constant search for cost-effective and high-performance materials for Li-ion batteries (LIBs) has increased with time. Here, we synthesized low-cost multi-heteroatom co-doped carbon from biowaste bagasse [N, S, and O co-doped carbon (NSOC-10)]. We also investigated the influence of heteroatom doping in the carbon matrix and its effect on the electrochemical properties when used in Li-ion and Li–S batteries. Interestingly, the NSOC-10 sample shows a capacity of 574 mAh g–1 even after 1000 cycles, which is much higher than the theoretical capacity of a traditional graphite anode (372 mAh g–1), while undoped carbon degrades quickly (pristine bagasse) and displays only 26.6% capacity retention within 250 cycles. The excellent capacity retention of NSOC-10 could be attributed to a highly porous carbon matrix that tends to increase Li+ percolation, shorten the Li+ diffusion path, and boost the lithium-ion storage capability. Further, we studied the use of the heteroatom-doped NSOC-10 carbon matrix as a carbon host for the sulfur cathode in a Li–S battery. Indeed, the Li–S cell showed an initial capacity of 1200 mAh g–1 with a capacity retention of 79% by the end of 250 cycles and maintained high coulombic efficiency of >99%. This is attributed to the heteroatom (N, S, and O) doping in the activated carbon scaffold that resulted in better electrode wettability, high Li+ diffusion rate, and good electron conductivity of the carbon matrix, and this polar carbon adsorbs polar polysulfides through polar–polar interactions and maintains its capacity. Hence, the designed cost-effective co-doped NSOC-10 was identified to be a promising candidate as an anode material in LIBs and also as a potential sulfur host in Li–S batteries.
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
Tumbleweed668发布了新的文献求助10
1秒前
哈哈发布了新的文献求助10
3秒前
bosszjw发布了新的文献求助10
3秒前
3秒前
大鱼完成签到 ,获得积分10
4秒前
8秒前
zho发布了新的文献求助10
9秒前
9秒前
z1y1p1完成签到,获得积分10
10秒前
11秒前
南楼小阁主完成签到,获得积分10
11秒前
杨gj发布了新的文献求助10
13秒前
13秒前
17秒前
院子完成签到,获得积分10
18秒前
斯文败类应助杨gj采纳,获得10
18秒前
贝木泥舟关注了科研通微信公众号
21秒前
小屁孩发布了新的文献求助10
22秒前
星辰大海应助谢富杰采纳,获得30
22秒前
活力雁枫完成签到,获得积分10
23秒前
路漫漫其修远兮完成签到 ,获得积分10
24秒前
25秒前
负责的方盒完成签到,获得积分10
26秒前
yusuf完成签到,获得积分10
26秒前
Aaron发布了新的文献求助10
29秒前
bkagyin应助哈哈采纳,获得10
29秒前
bigheadear完成签到,获得积分10
29秒前
Aaron完成签到,获得积分10
34秒前
34秒前
活力听兰完成签到,获得积分10
35秒前
916应助Tumbleweed668采纳,获得10
36秒前
共享精神应助Tumbleweed668采纳,获得10
36秒前
金木木完成签到,获得积分10
37秒前
39秒前
烟花应助Birdy采纳,获得10
40秒前
40秒前
41秒前
DONNYTIO发布了新的文献求助10
43秒前
43秒前
哈哈完成签到,获得积分10
44秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Fashion Brand Visual Design Strategy Based on Value Co-creation 350
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3777801
求助须知:如何正确求助?哪些是违规求助? 3323321
关于积分的说明 10213817
捐赠科研通 3038554
什么是DOI,文献DOI怎么找? 1667549
邀请新用户注册赠送积分活动 798161
科研通“疑难数据库(出版商)”最低求助积分说明 758275