Highly Crystalline Poly(heptazine imide)-Based Carbonaceous Anodes for Ultralong Lifespan and Low-Temperature Sodium-Ion Batteries

材料科学 酰亚胺 阳极 离子 化学工程 纳米技术 高分子化学 化学 有机化学 冶金 电极 物理化学 工程类
作者
Ying Wang,Hongguan Li,Boyin Zhai,Xinglong Li,Ping Niu,Jérémy Odent,Shulan Wang,Li Li
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (4): 3456-3467 被引量:41
标识
DOI:10.1021/acsnano.3c10779
摘要

Carbon nitrides with layered structures and scalable syntheses have emerged as potential anode choices for the commercialization of sodium-ion batteries. However, the low crystallinity of materials synthesized through traditional thermal condensation leads to insufficient conductivity and poor cycling stability, which significantly hamper their practical applications. Herein, a facile salt-covering method was proposed for the synthesis of highly ordered crystalline C3N4-based all-carbon nanocomposites. The sealing environment created by this strategy leads to the formation of poly(heptazine imide) (PHI), the crystalline phase of C3N4, with extended π-conjugation and a fully condensed nanosheet structure. Meanwhile, theoretical calculations reveal the high crystallinity of C3N4 significantly reduces the energy barrier for electron transition and enables the generation of efficient charge transfer channels at the heterogeneous interface between carbon and C3N4. Accordingly, such nanocomposites present ultrastable cycling performances over 5000 cycles, with a high reversible capacity of 245.1 mAh g-1 at 2 A g-1 delivered. More importantly, they also exhibit an outstanding low-temperature capacity of 196.6 mAh g-1 at -20 °C. This work offers opportunities for the energy storage use of C3N4 and provides some clues for developing long-life and high-capacity anodes operated under extreme conditions.
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
共享精神应助家伟采纳,获得10
1秒前
diony010发布了新的文献求助10
1秒前
萝卜完成签到,获得积分10
3秒前
4秒前
4秒前
星星轨迹发布了新的文献求助10
4秒前
4秒前
4秒前
Ideal应助kento采纳,获得50
5秒前
5秒前
6秒前
6秒前
桃七七完成签到 ,获得积分10
7秒前
7秒前
7秒前
7秒前
7秒前
忧郁芹菜发布了新的文献求助10
8秒前
bkagyin应助panda采纳,获得10
8秒前
顾矜应助和谐的亦旋采纳,获得10
8秒前
9秒前
小蘑菇应助A羽采纳,获得10
9秒前
liuyue完成签到,获得积分20
9秒前
10秒前
11秒前
小航完成签到,获得积分10
12秒前
tt发布了新的文献求助50
12秒前
家伟发布了新的文献求助10
12秒前
菜菜应助迷路的曼梅采纳,获得10
13秒前
jiangmiao发布了新的文献求助10
13秒前
科研白发布了新的文献求助10
14秒前
liuyue发布了新的文献求助10
14秒前
JamesPei应助zhang005on采纳,获得10
15秒前
深情安青应助云烟成雨采纳,获得10
17秒前
17秒前
yyy完成签到,获得积分10
17秒前
17秒前
17秒前
yoyo完成签到,获得积分10
18秒前
18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 2000
Psychology and Work Today 1000
Research for Social Workers 1000
Mastering New Drug Applications: A Step-by-Step Guide (Mastering the FDA Approval Process Book 1) 800
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
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 5905555
求助须知:如何正确求助?哪些是违规求助? 6780086
关于积分的说明 15762967
捐赠科研通 5029432
什么是DOI,文献DOI怎么找? 2708043
邀请新用户注册赠送积分活动 1656940
关于科研通互助平台的介绍 1602006