Hollow-structured CoP nanotubes wrapped by N-doped carbon layer with interfacial charges polarization for efficiently boosting oxygen reduction/evolution reactions

极化(电化学) 氧气 Boosting(机器学习) 化学工程 材料科学 碳纳米管 纳米技术 图层(电子) 氧还原 化学 兴奋剂 电化学 氧还原反应 光电子学 有机化学 物理化学 电极 工程类 机器学习 计算机科学
作者
Bin Liu,Rongyue Wang,Yuan Yao,Jingling Ma,Yubo Sun,Jiafeng Wan,Ying Zhang,Siqi Wang,Jinlong Zou
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:431: 133238-133238 被引量:12
标识
DOI:10.1016/j.cej.2021.133238
摘要

• 1D hollow CoP nanotubes wrapped by NCL are used as efficient catalysts for ORR/OER. • The well-formed 1D hollow structure can exposure more active sites for mass transfer. • CoP/CoOOH heterostructure on CoP-HNTs surface as the main active-species for OER. • Charge redistribution at the CoP/NCL interface promotes both ORR and OER processes. • Graphene layer protects CoP-HNTs@NCL from aggregation and corrosion during ORR/OER. Structure engineering for electrocatalysts via interfacial charge redistribution plays a vital role in governing the electrocatalytic activity for both oxygen reduction and evolution reactions (ORR/OER). Herein, a hierarchical nanostructure consisting of one-dimension (1D) hollow CoP nanotubes wrapped by nitrogen-doped carbon layer (CoP-HNTs@NCL) is designed through a simple hydrothermal-phosphorization-annealing strategy. Morphology of CoP-HNTs@NCL-0.4 (mass ratio of GO to CoP is 0.4) shows that the exterior surface of hollow CoP-HNTs is firmly coated by NCL with a layer thickness of 5-8 nm. ΔE (E j10 (1.58 V, OER)-E 1/2 (0.91 V, ORR)) of CoP-HNTs@NCL-0.4 is as low as 0.67 V for ORR/OER, which outperforms commercial Pt/C and RuO 2 and ranks the top of nonprecious-metal catalysts. Excellent activity and stability of CoP-HNTs@NCL-0.4 for ORR/OER benefit from synergistic effects between CoP and NCL, enhanced mass transfer via 1D hollow structure, and abundant active sites exposed on the interior/exterior surfaces of nanotube wall. Density functional theory calculations confirm that strong coupling interactions lead to interfacial charge polarization to remarkably promote the ORR/OER activities. This study highlights the functions of 1D hollow structure and interface effects in oxygen electrocatalysis, and opens a new avenue for interface construction by synergistically integrating favorable thermodynamics with efficient kinetics through modification of electronic structure.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
明理如凡完成签到,获得积分10
刚刚
科研通AI6应助Double采纳,获得10
1秒前
pokexuejiao完成签到,获得积分10
1秒前
李雅欣发布了新的文献求助10
1秒前
完美世界应助分隔符采纳,获得10
1秒前
Fernweh完成签到,获得积分20
2秒前
shouying发布了新的文献求助10
2秒前
夜染完成签到,获得积分10
3秒前
量子星尘发布了新的文献求助10
3秒前
huangxiaomei111完成签到,获得积分10
3秒前
3秒前
小落完成签到,获得积分10
4秒前
我是弱智先帮我完成签到,获得积分10
4秒前
李爱国应助叶祥采纳,获得10
4秒前
gyh完成签到,获得积分20
4秒前
王澄橙发布了新的文献求助50
4秒前
邓娅琴发布了新的文献求助10
5秒前
6秒前
彭于晏应助ftyun采纳,获得10
7秒前
Moro完成签到,获得积分10
7秒前
9秒前
大野完成签到,获得积分10
9秒前
繁星背后完成签到 ,获得积分10
9秒前
wei完成签到,获得积分10
9秒前
CipherSage应助憨憨采纳,获得10
10秒前
CipherSage应助gyh采纳,获得10
10秒前
11秒前
科研通AI6应助gkw采纳,获得10
12秒前
锐意发布了新的文献求助10
12秒前
丁森杰发布了新的文献求助10
12秒前
13秒前
14秒前
14秒前
科研通AI6应助靓丽的如天采纳,获得10
15秒前
无极微光应助zss采纳,获得20
15秒前
15秒前
大模型应助饲养员采纳,获得10
15秒前
16秒前
16秒前
dyr完成签到,获得积分10
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
The Social Work Ethics Casebook: Cases and Commentary (revised 2nd ed.).. Frederic G. Reamer 1070
The Complete Pro-Guide to the All-New Affinity Studio: The A-to-Z Master Manual: Master Vector, Pixel, & Layout Design: Advanced Techniques for Photo, Designer, and Publisher in the Unified Suite 1000
按地区划分的1,091个公共养老金档案列表 801
The International Law of the Sea (fourth edition) 800
Machine Learning for Polymer Informatics 500
A Guide to Genetic Counseling, 3rd Edition 500
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 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5409878
求助须知:如何正确求助?哪些是违规求助? 4527416
关于积分的说明 14110521
捐赠科研通 4441833
什么是DOI,文献DOI怎么找? 2437651
邀请新用户注册赠送积分活动 1429598
关于科研通互助平台的介绍 1407728