Ionomer-Free Nickel-Iron bimetallic electrodes for efficient anion exchange membrane water electrolysis

双金属片 阳极 材料科学 催化作用 电极 化学工程 电解 阴极 膜电极组件 离聚物 Nafion公司 无机化学 电化学 冶金 化学 复合材料 电解质 金属 物理化学 有机化学 共聚物 工程类 聚合物
作者
E. López-Fernández,C. Gómez-Sacedón,Jorge Gil‐Rostra,J.P. Espinós,Agustín R. González‐Elipe,F. Yubero,A. de Lucas-Consuegra
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:433: 133774-133774 被引量:45
标识
DOI:10.1016/j.cej.2021.133774
摘要

A bottleneck for the deployment of the Anion Exchange Membrane Water Electrolysis (AEMWE) is the manufacturing of efficient and long lasting anodes and cathodes for the cells. Highly performant bimetallic Ni/Fe catalyst films with various atomic ratios have been prepared by magnetron sputtering in an oblique angle configuration (MS-OAD) and used as anodes for AEMWE. Electrocatalytic experiments in a small three-electrode cell and a thorough analysis of the electrode properties with various physico-chemical characterization techniques have been used to select the nanostructured anode catalyst which, depicting an optimized Ni/Fe ratio, presents the maximum activity for the oxygen evolution reaction. These anode layers are then scale-up for their integration in an AEMWE cell where the influence of assembly conditions and the effect of adding an ionomer to the anodes have been studied. The obtained results have demonstrated the outstanding properties of the fabricated bimetallic films in terms of activity, stability, and operation under ionomer-free conditions. Current density values around 400 and 600 mA cm−2 at 40 °C and 60 °C (2.0 V), respectively, much higher than those obtained with pure Ni, were obtained with an optimized membrane electrode assembly. The high yield obtained with these electrodes gains further relevance when considering that the current yield per unit mass of the anodic active phase catalyst (i.e., 1086 mA mg−1 at 2.0 V and 40 °C) is the highest among equivalent values reported in literature. The possibilities and prospects of the use of bimetallic catalyst films prepared by MS-OAD for AEMWE are discussed.

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
张江川完成签到,获得积分10
2秒前
小宝完成签到 ,获得积分10
4秒前
liao_duoduo完成签到 ,获得积分10
4秒前
执念完成签到,获得积分10
6秒前
笑点低的凉面完成签到,获得积分10
7秒前
奇奇怪怪的大鱼完成签到,获得积分10
7秒前
阳光的伊发布了新的文献求助10
11秒前
Chikit完成签到,获得积分10
11秒前
panda完成签到,获得积分0
11秒前
kyokyoro完成签到,获得积分10
12秒前
出厂价完成签到,获得积分10
13秒前
Johan完成签到 ,获得积分10
13秒前
Yi完成签到,获得积分10
19秒前
空集完成签到 ,获得积分10
19秒前
luo完成签到 ,获得积分10
19秒前
轻舞完成签到,获得积分10
21秒前
23秒前
cl完成签到,获得积分10
24秒前
LMY1470完成签到,获得积分10
25秒前
所所应助对落日许愿采纳,获得30
28秒前
如约而至完成签到,获得积分10
28秒前
xiaoze完成签到 ,获得积分10
28秒前
奋斗的妙海完成签到 ,获得积分0
29秒前
调皮的烤鸡完成签到,获得积分10
30秒前
30秒前
顺利的初曼完成签到,获得积分10
30秒前
Eric完成签到,获得积分10
31秒前
dgqyushen完成签到,获得积分10
32秒前
HanaTerbush完成签到,获得积分10
34秒前
35秒前
36秒前
Mira完成签到,获得积分10
38秒前
GinaLundhild06完成签到,获得积分10
39秒前
Kevin发布了新的文献求助30
39秒前
CipherSage应助少看多做采纳,获得10
39秒前
苗儿完成签到,获得积分10
42秒前
踏实麦片完成签到,获得积分10
43秒前
43秒前
Monologue完成签到,获得积分10
46秒前
yunsui完成签到,获得积分10
47秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
The recovery-stress questionnaires : user manual 800
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 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7257699
求助须知:如何正确求助?哪些是违规求助? 8879600
关于积分的说明 18757547
捐赠科研通 6938076
什么是DOI,文献DOI怎么找? 3201148
关于科研通互助平台的介绍 2375264
邀请新用户注册赠送积分活动 2176963