Unlocking Performance: The Transformative Influence of Single Atom Catalysts on Advanced Lithium‐Sulfur Battery Design

材料科学 锂硫电池 催化作用 电池(电) 硫黄 转化式学习 锂(药物) 纳米技术 Atom(片上系统) 工程物理 化学工程 冶金 计算机科学 有机化学 工程类 功率(物理) 嵌入式系统 热力学 医学 心理学 教育学 化学 物理 内分泌学
作者
Sandip Maiti,Matthew T. Curnan,Keon‐Woo Kim,Kakali Maiti,Jin Kon Kim
出处
期刊:Advanced Energy Materials [Wiley]
卷期号:14 (38) 被引量:42
标识
DOI:10.1002/aenm.202401911
摘要

Abstract Theoretically, lithium–sulfur (Li‐S) batteries are highly promising candidates for renewable energy applications, given their scalable energy density and low cost. However, their current practical performance is limited below theoretical expectations, despite attempts to accommodate volumetric expansion and improve electrical conductivity with porous S‐anchoring supports. Battery performance is primarily rate‐limited by the sluggish redox and conversion reaction kinetics of lithium polysulfides (LiPS), which respectively transform into lithium sulfide (Li 2 S) and elemental S through charging and discharging galvanostatic cycles. Given their strong electrocatalytic performance and other pertinent benefits, recent research highlights single‐atom catalysts (SACs) as candidates for enhancing Li‐S batteries. Thus, this review summarizes contemporary advancements regarding SAC implementation in Li‐S batteries, primarily emphasizing catalyst morphology, battery performance, and mechanistic elucidation. More specifically, separators and cathodes can be engineered via SACs to better anchor LiPS and improve their reductive kinetics, thereby inhibiting the “shuttle effect” known to impact Li‐S batteries. In addition, SACs can be modulated with functional groups to synergistically improve performance, enabling higher S loadings and redistributing transferred charge. Overall, SACs conspicuously boost Li‐S battery performance, justifying further research toward their implementation 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
aajhajkahna应助文静凌瑶采纳,获得10
刚刚
huang完成签到,获得积分20
刚刚
大意的晓兰完成签到,获得积分10
刚刚
左耳东完成签到,获得积分10
1秒前
SciGPT应助ll采纳,获得10
1秒前
1秒前
我是老大应助散装洋芋采纳,获得10
2秒前
Cheery发布了新的文献求助10
2秒前
迷路的懒熊完成签到,获得积分10
2秒前
天荣关注了科研通微信公众号
2秒前
一目完成签到,获得积分10
3秒前
福多多完成签到,获得积分10
3秒前
科研通AI6.4应助wuwen采纳,获得10
3秒前
4秒前
DDL发布了新的文献求助10
4秒前
英姑应助sunqk0117采纳,获得10
4秒前
5秒前
zeke发布了新的文献求助10
5秒前
5秒前
刘刘刘完成签到 ,获得积分10
5秒前
俭朴苑博完成签到,获得积分0
6秒前
Tigher发布了新的文献求助30
7秒前
7秒前
7秒前
JamesPei应助Marina采纳,获得10
8秒前
zhiou完成签到,获得积分10
8秒前
9秒前
11秒前
11秒前
sheng发布了新的文献求助10
12秒前
Soen发布了新的文献求助10
12秒前
CipherSage应助zeke采纳,获得10
12秒前
JyangBiao发布了新的文献求助10
12秒前
12秒前
深情安青应助DDL采纳,获得10
12秒前
14秒前
14秒前
14秒前
123123完成签到,获得积分20
14秒前
深情安青应助ddddddd采纳,获得10
14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
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
Management and the Arts 310
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 7629637
求助须知:如何正确求助?哪些是违规求助? 9204013
关于积分的说明 19736623
捐赠科研通 7199062
什么是DOI,文献DOI怎么找? 3274298
关于科研通互助平台的介绍 2436431
邀请新用户注册赠送积分活动 2270449