Metal oxide- and metal-loaded mesoporous carbon for practical high-performance Li-ion battery anodes

材料科学 阳极 纳米材料 氧化物 纳米复合材料 电池(电) 法拉第效率 介孔材料 石墨 金属 纳米技术 纳米颗粒 氧化锡 电极 化学工程 复合材料 冶金 催化作用 化学 功率(物理) 物理 生物化学 工程类 物理化学 量子力学
作者
Ayman A. AbdelHamid,Adriana Mendoza‐Garcia,Su Seong Lee,Jackie Y. Ying
出处
期刊:Nano Energy [Elsevier BV]
卷期号:119: 109025-109025 被引量:25
标识
DOI:10.1016/j.nanoen.2023.109025
摘要

The rapidly expanding Li-ion battery market needs new materials that can satisfy the increasing energy storage demand. Metal oxides and some metals such as tin are viable alternatives to graphite as Li-ion battery anodes, but their low conductivity and large volume change during cycling impose severe challenges that need to be overcome. Confinement of metal oxide and metal nanomaterials within mesoporous carbon (MC) is an effective strategy in this regard, but complex synthesis and nanoparticle aggregation have hindered its application. Herein, we report a facile, scalable and generalized methodology for the room-temperature synthesis of metal oxide and metal nanoparticles within a MC host. The approach has been successfully applied to achieve uniform distribution and prevent aggregation of a large variety of metal oxide and metal nanomaterials in MC support. These nanocomposites were screened as Li-ion battery anodes, and the optimal candidates were shown to be superior to previously reported systems. Our synthesis method was scaled up using commercial MC. The nanocomposites were validated in a high-loading electrode (4 mg/cm2) with a practical voltage range (< 2 V vs. Li+/Li), impressive initial Coulombic efficiency (> 100%), and excellent stability (~ 500 mAh/g after 250 cycles at 0.2 A/g), which was 1.5–2x better than commercial graphite at the same testing conditions. The facile nature, universality and versatility of our approach make it possible to load various metal oxide and metal nanomaterials within different types of MC. These nanocomposites would be of significant interest to different fields, such as energy storage and conversion, sensing, and catalysis.
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
姜丽发布了新的文献求助10
1秒前
WYY完成签到,获得积分10
2秒前
2rrd发布了新的文献求助10
2秒前
领导范儿应助顺心的皓轩采纳,获得10
3秒前
勤劳的靖儿完成签到,获得积分10
3秒前
gaoqaing完成签到,获得积分20
3秒前
所所应助KSung采纳,获得10
3秒前
ihhh完成签到,获得积分20
3秒前
伶俐送终发布了新的文献求助10
4秒前
4秒前
科研通AI6.2应助某云采纳,获得10
4秒前
4秒前
我是老大应助LIUYU采纳,获得10
5秒前
星辰大海应助多疑的柯南采纳,获得10
6秒前
6秒前
jiangzhiyun完成签到,获得积分10
6秒前
红3完成签到,获得积分10
6秒前
7秒前
Alarack发布了新的文献求助10
8秒前
科研通AI6.4应助艾雪采纳,获得10
9秒前
9秒前
10秒前
aku30完成签到,获得积分10
10秒前
longjiafang发布了新的文献求助10
12秒前
调皮的皓轩完成签到,获得积分10
12秒前
ni_xiao完成签到 ,获得积分10
12秒前
12秒前
12秒前
fzx发布了新的文献求助10
13秒前
13秒前
发的不太好完成签到,获得积分10
14秒前
烟花应助ghost采纳,获得10
14秒前
在水一方应助lingboxian采纳,获得10
14秒前
菩桃发布了新的文献求助10
14秒前
zx发布了新的文献求助10
14秒前
15秒前
charlins完成签到,获得积分10
15秒前
15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
Inorganic Chemistry Eighth Edition 1200
Free parameter models in liquid scintillation counting 1000
Anionic polymerization of acenaphthylene: identification of impurity species formed as by-products 1000
Standards for Molecular Testing for Red Cell, Platelet, and Neutrophil Antigens, 7th edition 1000
HANDBOOK OF CHEMISTRY AND PHYSICS 106th edition 1000
ASPEN Adult Nutrition Support Core Curriculum, Fourth Edition 1000
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6310968
求助须知:如何正确求助?哪些是违规求助? 8127263
关于积分的说明 17029655
捐赠科研通 5368499
什么是DOI,文献DOI怎么找? 2850424
邀请新用户注册赠送积分活动 1828033
关于科研通互助平台的介绍 1680654