From Synthesis to Mechanisms: In‐Depth Exploration of the Dual‐Atom Catalytic Mechanisms Toward Oxygen Electrocatalysis

电催化剂 材料科学 催化作用 对偶(语法数字) 氧还原反应 Atom(片上系统) 氧气 氧原子 析氧 纳米技术 化学物理 化学工程 电化学 物理化学 有机化学 电极 化学 计算机科学 艺术 文学类 分子 工程类 嵌入式系统
作者
Lei Lei,Xinghua Guo,Han Xu,Ling Fei,Xiao Guo,Degao Wang
出处
期刊:Advanced Materials [Wiley]
卷期号:36 (37): e2311434-e2311434 被引量:48
标识
DOI:10.1002/adma.202311434
摘要

Abstract Dual‐atom catalysts (DACs) hold a higher metal atom loading and provide greater flexibility in terms of the structural characteristics of their active sites in comparison to single‐atom catalysts. Consequently, DACs hold great promise for achieving improved catalytic performance. This article aims to provide a focused overview of the latest advancements in DACs, covering their synthesis and mechanisms in reversible oxygen electrocatalysis, which plays a key role in sustainable energy conversion and storage technologies. The discussion starts by highlighting the structures of DACs and the differences in diatomic coordination induced by various substrates. Subsequently, the state‐of‐the‐art fabrication strategies of DACs for oxygen electrocatalysis are discussed from several different perspectives. It particularly highlights the challenges of increasing the diatomic loading capacity. More importantly, the main focus of this overview is to investigate the correlation between the configuration and activity in DACs in order to gain a deeper understanding of their active roles in oxygen electrocatalysis. This will be achieved through density functional theory calculations and sophisticated in situ characterization technologies. The aim is to provide guidelines for optimizing and upgrading DACs in oxygen electrocatalysis. Additionally, the overview discusses the current challenges and future prospects in this rapidly evolving area of research.
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
缓慢板凳发布了新的文献求助10
1秒前
李健的小迷弟应助HsuJuly采纳,获得10
1秒前
1秒前
kingwhitewing发布了新的文献求助10
1秒前
1733应助nnnn采纳,获得20
2秒前
2秒前
2秒前
2秒前
3秒前
科目三应助司马惜儿采纳,获得10
4秒前
kklkimo发布了新的文献求助10
4秒前
mervynzcy发布了新的文献求助10
7秒前
科研通AI6.2应助ZY采纳,获得10
7秒前
orixero应助吴龙采纳,获得10
7秒前
7秒前
科研通AI6.1应助Andy采纳,获得10
7秒前
Ava应助BJTXZG采纳,获得10
7秒前
8秒前
8秒前
FashionBoy应助布医采纳,获得10
8秒前
优秀的书萱完成签到,获得积分10
8秒前
wei发布了新的文献求助10
9秒前
9秒前
9秒前
HHHH发布了新的文献求助10
9秒前
10秒前
10秒前
11秒前
云游归尘发布了新的文献求助10
11秒前
上官若男应助狂野的白枫采纳,获得10
11秒前
12秒前
12秒前
Scss发布了新的文献求助10
12秒前
junge完成签到,获得积分10
12秒前
12秒前
13秒前
Strawberry应助李子采纳,获得10
13秒前
13秒前
彩色一手发布了新的文献求助10
13秒前
CarolineOY发布了新的文献求助10
13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 3000
Les Mantodea de guyane 2500
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 2000
What is the Future of Psychotherapy in a Digital Age? 700
The Psychological Quest for Meaning 600
Zeolites: From Fundamentals to Emerging Applications 600
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 5955238
求助须知:如何正确求助?哪些是违规求助? 7165701
关于积分的说明 15937623
捐赠科研通 5090084
什么是DOI,文献DOI怎么找? 2735520
邀请新用户注册赠送积分活动 1696354
关于科研通互助平台的介绍 1617271