An Ir/Ni(OH)2 Heterostructured Electrocatalyst for the Oxygen Evolution Reaction: Breaking the Scaling Relation, Stabilizing Iridium(V), and Beyond

析氧 电催化剂 材料科学 异质结 催化作用 分解水 纳米颗粒 化学工程 亚稳态 化学物理 纳米技术 物理化学 电化学 化学 光催化 有机化学 光电子学 生物化学 工程类 电极
作者
Guoqiang Zhao,Peng Li,Ningyan Cheng,Shi Xue Dou,Wenping Sun
出处
期刊:Advanced Materials [Wiley]
卷期号:32 (24): e2000872-e2000872 被引量:276
标识
DOI:10.1002/adma.202000872
摘要

Developing efficient electrocatalysts for the oxygen evolution reaction (OER) is highly challenging for hydrogen production from water splitting, due to the high energy barrier for OO bond formation and the restriction of the scaling relation between the multiple reaction intermediates. In order to simultaneously address these concerns, an Ir/Ni(OH)2 heterostructure with abundant heterointerfaces is deliberately designed as an efficient electrocatalyst system, with Ir nanoparticles (NPs) homogeneously confined on the Ni(OH)2 nanosheets. The strong electronic interaction and chemical bonding across the interface between the Ir and Ni(OH)2 can effectively stabilize the metastable electrophilic Ir(V) species, which is vital to boost the formation of OO bonds. Meanwhile, the adsorption of the multiple intermediates is synergistically optimized at the heterointerface, which breaks the restrictive scaling relation and substantially accelerates the OER kinetics. In addition, the severe agglomeration of Ir species is greatly mitigated by the confinement effect, ensuring the structural integrity of the catalyst and the constant exposure of active sites. Owing to its well-defined multifunctional interfaces, the Ir/Ni(OH)2 heterostructure exhibits exceptional OER activity and durability in alkaline media. The present results highlight the significance of heterostructure interface engineering toward the rational design and development of advanced electrocatalysts for the OER and beyond.
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
guoguo发布了新的文献求助10
刚刚
1秒前
脑洞疼应助HuanChen采纳,获得200
1秒前
1秒前
1秒前
1秒前
1秒前
1秒前
forever完成签到,获得积分10
2秒前
2秒前
2秒前
LIULIAN发布了新的文献求助10
2秒前
suniverse完成签到,获得积分10
2秒前
六六发布了新的文献求助10
2秒前
科研通AI6.4应助LL采纳,获得10
3秒前
领导范儿应助M.采纳,获得10
4秒前
领导范儿应助酷酷冰菱采纳,获得10
4秒前
清脆冬日完成签到 ,获得积分10
4秒前
真6完成签到,获得积分10
4秒前
帅气的如豹发布了新的文献求助300
4秒前
4秒前
4秒前
liuyue发布了新的文献求助10
4秒前
5秒前
5秒前
yetong发布了新的文献求助10
5秒前
5秒前
孙捕完成签到,获得积分10
6秒前
6秒前
6秒前
充电宝应助郭果儿采纳,获得10
6秒前
无花果应助lyh采纳,获得10
6秒前
小录发布了新的文献求助30
7秒前
七慕凉发布了新的文献求助10
7秒前
7秒前
7秒前
8秒前
chyvayne完成签到,获得积分10
8秒前
量子星尘发布了新的文献求助10
8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
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
Lloyd's Register of Shipping's Approach to the Control of Incidents of Brittle Fracture in Ship Structures 1000
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 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6147295
求助须知:如何正确求助?哪些是违规求助? 7973845
关于积分的说明 16565509
捐赠科研通 5258046
什么是DOI,文献DOI怎么找? 2807574
邀请新用户注册赠送积分活动 1787947
关于科研通互助平台的介绍 1656618