The role of nickel cobalt sulphide MOFs hybrids in electrochemical hydrogen generation: A critical review

催化作用 电解水 电解 电化学 塔菲尔方程 析氧 制氢 材料科学 分解水 电解法 过电位 化学工程 电催化剂 无机化学 电化学能量转换 化学 冶金 电解质 电极 有机化学 物理化学 光催化 工程类
作者
Ayesha Rehman,Arslan Khan,Erum Pervaiz
出处
期刊:Materials Chemistry and Physics [Elsevier]
卷期号:315: 129027-129027 被引量:6
标识
DOI:10.1016/j.matchemphys.2024.129027
摘要

Hydrogen has become an increasingly important source of energy due to the growing global population and energy demands. To meet these needs, electrolysis of water offers a substitute process for generating hydrogen from renewable sources. During this process, water was split with a catalyst into hydrogen and oxygen. Electrolysis of water could follow either acidic or a basic mechanism. The benchmark electro catalyst for electrolysis was Pt/C, which had 1.23 V is a low potential. However, the catalyst used in this process was expensive and composed of noble and precious metals. Therefore, a profoundly productive, non-precious, and stable electro catalyst was required for the hydrogen evolution process. Nickel (Ni) and cobalt (Co) when two metals combined showed the improved electrochemical characteristics. Promising improvements in electro catalytic efficiency are revealed while examining the synergistic effects of sulphide hybridization with NiCo for the Hydrogen Evolution Reaction (HER). In order to create NiCoS hybrids, researchers used metal-organic frameworks (MOFs), which shows a sizable surface area and are stable. Nickel cobalt sulfide (NiCoS) has thereby become a very reliable, economical, and effective electro-catalyst for the hydrogen evolution process, particularly in low pH settings. In this review, we discussed various NiCoS MOFs for electrochemical reactions, highlighting their different over potentials and Tafel slopes, it displayed how well the hydrogen evolution process had performed.
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
wanli445发布了新的文献求助10
刚刚
SYLH应助敏感草丛采纳,获得10
刚刚
1秒前
送外卖了完成签到,获得积分10
1秒前
2秒前
123456789hyb发布了新的文献求助10
2秒前
ye发布了新的文献求助10
2秒前
wadaxiwa应助晓晓采纳,获得10
3秒前
3秒前
5秒前
zhao发布了新的文献求助10
5秒前
所所应助干净的新梅采纳,获得10
5秒前
zqxu发布了新的文献求助30
5秒前
5秒前
创不可贴发布了新的文献求助10
6秒前
6秒前
加鲁鲁发布了新的文献求助10
6秒前
6秒前
6秒前
英俊的铭应助lio采纳,获得10
7秒前
fanjinhua完成签到,获得积分20
7秒前
施耐德完成签到,获得积分10
7秒前
直率的乐萱完成签到 ,获得积分10
7秒前
7秒前
7秒前
7秒前
赘婿应助haosu采纳,获得10
7秒前
7秒前
8秒前
8秒前
苏木发布了新的文献求助10
9秒前
yiryir发布了新的文献求助10
10秒前
10秒前
领导范儿应助Sodagreen2023采纳,获得10
10秒前
xuxu完成签到,获得积分10
11秒前
11秒前
11秒前
11秒前
12秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Mechanistic Modeling of Gas-Liquid Two-Phase Flow in Pipes 2500
Comprehensive Computational Chemistry 1000
Kelsen’s Legacy: Legal Normativity, International Law and Democracy 1000
Conference Record, IAS Annual Meeting 1977 610
Interest Rate Modeling. Volume 3: Products and Risk Management 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 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 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3552796
求助须知:如何正确求助?哪些是违规求助? 3128883
关于积分的说明 9379843
捐赠科研通 2828004
什么是DOI,文献DOI怎么找? 1554841
邀请新用户注册赠送积分活动 725605
科研通“疑难数据库(出版商)”最低求助积分说明 715056