Ce-Substituted Spinel CuCo2O4 Quantum Dots with High Oxygen Vacancies and Greatly Improved Electrocatalytic Activity for Oxygen Evolution Reaction

析氧 过电位 塔菲尔方程 化学 尖晶石 催化作用 电解水 电催化剂 量子点 化学工程 电解 分解水 纳米技术 物理化学 材料科学 电化学 光催化 电极 冶金 工程类 电解质 生物化学
作者
Wenping Shi,Yuning Zhang,Lili Bo,Xiaolin Guan,Yunxia Wang,Jinhui Tong
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:60 (24): 19136-19144 被引量:61
标识
DOI:10.1021/acs.inorgchem.1c02931
摘要

Exploring effective electrocatalysts for oxygen evolution reaction (OER) is a crucial requirement of many energy storage and transformation systems, involving fuel cells, water electrolysis, and metal-air batteries. Transition-metal oxides (TMOs) have attracted much attention to OER catalysts because of their earth abundance, tunable electronic properties, and so forth. Defect engineering is a general and the most important strategy to tune the electronic structure and control size, and thus improve their intrinsic activities. Herein, OER performance on spinel CuCo2O4 was greatly enhanced through cation substitution and size reduction. Ce-substituted spinel CuCeδCo2-δOx (δ = 0.45, 0.5 and 0.55) nanoparticles in the quantum dot scale (2-8 nm) were synthesized using a simple and facile phase-transfer coprecipitation strategy. The as-prepared samples were highly dispersed and have displayed a low overpotential of 294 mV at 10 mA·cm-2 and a Tafel slope of 57.5 mV·dec-1, which outperform commercial RuO2 and the most high-performance analogous catalysts reported. The experimental and calculated results all confirm that Ce substitution with an appropriate content can produce rich oxygen vacancies, tune intermediate absorption, consequently lower the energy barrier of the determining step, and greatly enhance the OER activity of the catalysts. This work not only provides advanced OER catalysts but also opens a general avenue to understand the structure-activity relationship of pristine TMO catalysts deeply in the quantum dot scale and the rational design of more efficient OER catalysts.
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
2秒前
bkagyin应助拉布拉多多不多采纳,获得10
3秒前
4秒前
5秒前
aguiguigui完成签到,获得积分10
7秒前
Kyrie发布了新的文献求助10
8秒前
8秒前
8秒前
liweb完成签到,获得积分10
8秒前
10秒前
Akim应助cd采纳,获得10
11秒前
11秒前
11秒前
容与发布了新的文献求助10
12秒前
12秒前
Jasper应助Kyrie采纳,获得10
13秒前
13秒前
Pei发布了新的文献求助10
14秒前
czz发布了新的文献求助10
15秒前
一棵树发布了新的文献求助10
16秒前
du完成签到 ,获得积分10
17秒前
jiaxlnn完成签到,获得积分20
17秒前
zhangpeng完成签到,获得积分10
17秒前
17秒前
19秒前
斑鸠津发布了新的文献求助10
19秒前
tian完成签到,获得积分10
19秒前
慕青应助czz采纳,获得10
22秒前
一棵树完成签到,获得积分10
22秒前
24秒前
元元元完成签到,获得积分10
25秒前
华仔应助拉布拉多多不多采纳,获得10
27秒前
斑鸠津完成签到,获得积分10
27秒前
冷傲白开水完成签到 ,获得积分10
30秒前
30秒前
30秒前
31秒前
Pei完成签到,获得积分10
32秒前
元元元发布了新的文献求助20
35秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Advanced Memory Technology 500
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
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 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6864585
求助须知:如何正确求助?哪些是违规求助? 8567298
关于积分的说明 18216924
捐赠科研通 6233310
什么是DOI,文献DOI怎么找? 3048832
关于科研通互助平台的介绍 2050505
邀请新用户注册赠送积分活动 2026607