Strategic examination of the classical catalysis of formic acid decomposition for intermittent hydrogen production, storage and supply: A review

甲酸 催化作用 制氢 分解 纳米材料基催化剂 氢气储存 无机化学 化学 化学工程 有机化学 工程类
作者
Samuel Eshorame Sanni,Peter Adeniyi Alaba,Emeka Emmanuel Okoro,Moses Emetere,Babalola Aisosa Oni,Oluranti Agboola,A. O. Ndubuisi
出处
期刊:Sustainable Energy Technologies and Assessments [Elsevier BV]
卷期号:45: 101078-101078 被引量:5
标识
DOI:10.1016/j.seta.2021.101078
摘要

Practically, an ideal catalyst for Formic acid-decomposition is one that best suits the reaction and significantly lowers its activation energy and improves the reaction rate under favourable conditions. Several catalysts for Formic Acid (FA)-decomposition reactions were examined. Based on the volcano curve and the potential of copper to give high hydrogen yields, emphasis was placed on a Cu-catalysed reaction as potential system for sustainable hydrogen production. Some recent advances in hydrogen production from formic acid were discussed and an effective system for FA-decomposition for hydrogen production was proposed. Since helium can be stored in weather balloons and weighs almost the same as hydrogen, a hydrogen buffer made from polyester fabric and coated with polyurethane or a hydrogen cylinder/tube was proposed for storing hydrogen for use as transport-fuel. Also, due to the nature of the mechanisms/pathways describing FA-conversion reactions at the sites or surfaces of the copper-nanocatalysts, it is evident that the Cu(2 1 1) coordination site possesses the highest activation energy relative to those of Cu(1 0 0) and Cu(1 1 1), hence, the reason for the noticeable high or low hydrogen yields. Thus, the potential of Cu giving high hydrogen yields from FA spans from the reactions of FA at the Cu(1 1 1) and Cu(1 0 0) sites.

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
1秒前
xdwu完成签到,获得积分10
2秒前
酷波er应助llr采纳,获得10
2秒前
圆红完成签到 ,获得积分10
2秒前
4秒前
jianjiao完成签到,获得积分10
5秒前
李健应助pete采纳,获得10
9秒前
xx发布了新的文献求助10
9秒前
此身越重洋完成签到,获得积分10
9秒前
11秒前
12秒前
happyboy2008完成签到,获得积分10
13秒前
大反应釜完成签到,获得积分10
14秒前
蓝景轩辕完成签到 ,获得积分0
14秒前
15秒前
酷炫老头发布了新的文献求助10
15秒前
科研通AI6.3应助贰拾-2采纳,获得10
17秒前
yy发布了新的文献求助30
18秒前
颖宝老公完成签到,获得积分10
19秒前
molihuakai应助Df采纳,获得10
19秒前
大知闲闲发布了新的文献求助10
20秒前
小蘑菇应助淡定的乐安采纳,获得10
20秒前
SciGPT应助YBY采纳,获得10
21秒前
22秒前
22秒前
CQZXY发布了新的文献求助10
24秒前
25秒前
NexusExplorer应助朴素代芙采纳,获得10
26秒前
26秒前
隐形的若之完成签到,获得积分10
27秒前
情怀应助淡定雪采纳,获得10
27秒前
科研通AI6.2应助酷炫老头采纳,获得10
27秒前
28秒前
28秒前
29秒前
无限妙芙发布了新的文献求助10
30秒前
领导范儿应助英勇的母鸡采纳,获得10
31秒前
31秒前
彭于晏应助Jerry采纳,获得10
32秒前
32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
The Organometallic Chemistry of the Transition Metals 800
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6437775
求助须知:如何正确求助?哪些是违规求助? 8252112
关于积分的说明 17558639
捐赠科研通 5496210
什么是DOI,文献DOI怎么找? 2898680
邀请新用户注册赠送积分活动 1875376
关于科研通互助平台的介绍 1716355