Hierarchical CuCo2O4/NiCo2O4 on self-standing Ni foam for high-performance water electrolysis

分解水 析氧 电催化剂 过电位 碱性水电解 电解 电解水 贵金属 材料科学 阳极 化学工程 制氢 双功能 无机化学 催化作用 化学 电化学 金属 电极 冶金 工程类 光催化 电解质 物理化学 生物化学
作者
V. Saranya,G. Anandha Babu,M. Navaneethan,J. Archana
出处
期刊:Journal of Alloys and Compounds [Elsevier]
卷期号:988: 173894-173894 被引量:11
标识
DOI:10.1016/j.jallcom.2024.173894
摘要

The development of overall alkaline water electrolysis process has most promising and attractive route to hydrogen production as future renewable energy resources. Nevertheless, the rational design and development of efficient noble metal - free electrodes with robust stability are great challenges to achieve efficient overall water splitting performance. Herein, we report a novel hierarchical CuCo2O4/NiCo2O4 heterostructures grown on Ni foam via facile two-step hydrothermal method and calcination processes for overall water splitting activity. The prepared heterostructures electrode demonstrates the superior electrocatalytic activity with excellent durability for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline electrolyte condition. The as-prepared CuCo2O4/NiCo2O4/NF electrodes exhibits the electrocatalytic activity with exceptionally lower overpotential of less than 250 mV at 10 mA/cm2 (OER) and 72 mV at 10 mA/cm2 (HER). Remarkably, the alkaline electrolyzer has deliver an excellent overall water splitting with fine cell voltage 1.58 V (at 10 mA/cm2) with stability test at 10 mA/cm2 for 20 hours while, electrolyzer setup has constructed using self-standing heterostructures electrodes as both anode and cathode. The improved electrocatalytic performances of heterostructures electrode could be attributed to the significant interface between active hierarchical CuCo2O4/NiCo2O4/NF heterostructures which provide enhanced catalytic active sites on catalyst surface. Thus, the proposed hierarchical heterostructures electrocatalyst opens a new pathway to design the noble metal-free efficient bifunctional electrocatalyst for water splitting electrolysis under alkaline condition.
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
fshell发布了新的文献求助10
1秒前
1秒前
1秒前
1秒前
1秒前
星辰大海应助花花草草采纳,获得10
1秒前
蓝月半完成签到,获得积分10
2秒前
自信的初蓝完成签到,获得积分10
2秒前
眯眯眼的逍遥完成签到,获得积分10
3秒前
zhouyupeng发布了新的文献求助30
3秒前
小胖子发布了新的文献求助10
4秒前
科研通AI2S应助VK2801采纳,获得10
4秒前
ve发布了新的文献求助10
5秒前
5秒前
WZ完成签到 ,获得积分10
5秒前
天天快乐应助lshcraft采纳,获得10
5秒前
充电宝应助lx采纳,获得10
6秒前
6秒前
大个应助杨YY采纳,获得10
6秒前
supercan发布了新的文献求助10
6秒前
6秒前
6秒前
TX发布了新的文献求助10
6秒前
7秒前
7秒前
科目三应助WBTT采纳,获得10
7秒前
7秒前
8秒前
8秒前
Byu完成签到,获得积分10
9秒前
研友_VZG7GZ应助阔达的起眸采纳,获得10
9秒前
香蕉觅云应助wang采纳,获得10
9秒前
笨蛋大爆炸完成签到,获得积分10
9秒前
可爱的函函应助shwang采纳,获得10
10秒前
undo发布了新的文献求助10
10秒前
10秒前
梨子发布了新的文献求助10
11秒前
11秒前
11秒前
党文英完成签到,获得积分10
11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
Standard: In-Space Storable Fluid Transfer for Prepared Spacecraft (AIAA S-157-2024) 1000
What is the Future of Psychotherapy in a Digital Age? 700
Signals, Systems, and Signal Processing 510
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 5953704
求助须知:如何正确求助?哪些是违规求助? 7158948
关于积分的说明 15931723
捐赠科研通 5088392
什么是DOI,文献DOI怎么找? 2734818
邀请新用户注册赠送积分活动 1695666
关于科研通互助平台的介绍 1617007