Controlled synthesis of ACo2O4 (A = Fe, Cu, Zn, Ni) as an environmentally friendly electrocatalyst for urea electrolysis

电催化剂 析氧 电解 电化学 阳极 制氢 化学 环境友好型 无机化学 电流密度 化学工程 吉布斯自由能 分解水 煅烧 材料科学 催化作用 电极 物理化学 电解质 热力学 有机化学 工程类 物理 生物 光催化 量子力学 生态学
作者
Ping Li,Yanhong Wang,Xiaoqiang Du,Xiaoshuang Zhang
出处
期刊:Dalton Transactions [The Royal Society of Chemistry]
卷期号:52 (30): 10499-10506 被引量:76
标识
DOI:10.1039/d3dt01845h
摘要

Water electrolysis is relatively an environmentally friendly hydrogen production technology, but due to the slow transfer of four electrons in the anodic oxidation reaction, it needs a theoretical voltage of up to 1.23 V. Therefore, in this experiment, a series of transition metal oxides, ACo2O4 (A = Fe, Cu, Zn, Ni), was synthesized on Ni foam current collectors by a hydrothermal and calcination method, and the material was applied in urea electrolysis to produce hydrogen. What is noteworthy is that the CuCo2O4 electrode has a unique flower-like nanoneedle structure, and has a larger electrochemical active area, more reactive active sites, and a faster charge transfer rate. In 1.0 M KOH and 0.5 M urea solution, CuCo2O4 provides a potential of only 1.268 V at a current density of 10 mA cm-2 during the urea oxidation reaction (UOR), while in 1.0 M KOH solution, with the same current density, the oxygen evolution reaction (OER) is required to provide a potential of 1.53 V, indicating that the UOR can effectively replace the OER. Density functional theory calculations show that the CuCo2O4 material exhibits Gibbs free energy of the hydrogen closest to zero, thus promoting the electrochemistry performance of the electrode. In a cell composed of CuCo2O4//CuCo2O4, the current density of 10 mA cm-2 can be achieved by providing a potential of only 1.509 V. This work offers a novel scheme for reducing energy consumption of the OER and improving catalytic performance of the UOR.
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
敛袂完成签到,获得积分10
2秒前
2秒前
3秒前
konosuba完成签到,获得积分0
4秒前
fengqian发布了新的文献求助10
4秒前
11完成签到,获得积分10
4秒前
羊六七发布了新的文献求助10
6秒前
6秒前
SciGPT应助NattyPoe采纳,获得10
7秒前
半夜汽笛完成签到 ,获得积分10
7秒前
顾矜应助肖子瑶采纳,获得10
7秒前
frl完成签到,获得积分10
8秒前
zhyi发布了新的文献求助10
8秒前
科研通AI6.1应助丽丽采纳,获得10
9秒前
9秒前
10秒前
zZ完成签到,获得积分10
11秒前
英吉利25发布了新的文献求助10
12秒前
12秒前
13秒前
shiyi完成签到,获得积分10
13秒前
frl发布了新的文献求助10
14秒前
Dang发布了新的文献求助10
15秒前
赘婿应助默默的青烟采纳,获得30
15秒前
ding应助啦啦啦啦啦采纳,获得10
16秒前
16秒前
17秒前
17秒前
18秒前
18秒前
星辰大海应助冰冷的心采纳,获得10
19秒前
Horizon发布了新的文献求助10
19秒前
ooo发布了新的文献求助10
20秒前
21秒前
11发布了新的文献求助10
22秒前
lize5493发布了新的文献求助10
22秒前
小二郎应助时宁采纳,获得10
23秒前
23秒前
bkagyin应助羊六七采纳,获得10
24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
Relation between chemical structure and local anesthetic action: tertiary alkylamine derivatives of diphenylhydantoin 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Principles of town planning : translating concepts to applications 500
Iron‐Sulfur Clusters: Biogenesis and Biochemistry 400
Healable Polymer Systems: Fundamentals, Synthesis and Applications 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6071281
求助须知:如何正确求助?哪些是违规求助? 7902822
关于积分的说明 16339597
捐赠科研通 5211704
什么是DOI,文献DOI怎么找? 2787534
邀请新用户注册赠送积分活动 1770240
关于科研通互助平台的介绍 1648145