Molecular Catalysis in “Green” Hydrogen Production

F. Zaccaria, Gabriel Menendez Rodriguez, L. Rocchigiani, A. Macchioni
{"title":"Molecular Catalysis in “Green” Hydrogen Production","authors":"F. Zaccaria, Gabriel Menendez Rodriguez, L. Rocchigiani, A. Macchioni","doi":"10.3389/fctls.2022.892183","DOIUrl":null,"url":null,"abstract":"Molecular hydrogen (H2) is considered an ideal energy vector and a clean fuel, due to its zero-carbon combustion. Nevertheless, despite hydrogen is the most and one of the most abundant elements in the universe and in earth crust, respectively, it is always combined with other elements in our planet and never appears in its elemental state. This means that H2 must be produced through, almost always, endergonic processes, whose sustainability depend not only on the starting material but also on the source of energy necessary for these processes to occur. Colors have been assigned to identify the level of sustainability of H2 production with the green one indicating H2 produced from water using a renewable source of energy, preferably sunlight. Redox water splitting (WS) into H2 (hydrogen evolution reaction, HER) and O2 (oxygen evolution reaction, OER) is, nevertheless, an extremely difficult process not only from the thermodynamic but also from the kinetic point of view. Relevant kinetic barriers are present in both sides of the redox process, especially in OER. For this reason, performing WS in an efficient manner requires the development of active and robust catalysts capable of offering alternative reaction pathways to WS, lowering down the unfavorable kinetic barriers and thus maximizing the energy conversion efficiency. Inspiration for developing efficient catalysts for HER and OER has traditionally derived from Nature, who, over the course of many billions of years, according to the evolutionary theory, has assembled two molecular catalytic pools, namely oxygen evolving complex and ferredoxin/ferredoxin NADP+ reductase, which offer viable kinetic pathways to both OER and reduction of NADP+ (the “biological form” of H2). In reality, after several attempts of mimicking natural catalysts, the efforts of the researchers have been addressed to different molecular systems, which exhibit best performances, unfortunately often based on noble-metal atoms, especially for OER. In this contribution we review the journey of the development of molecular catalysts for both HER and the OER, highlighting selected systems, which have brought us to the current level of knowledge.","PeriodicalId":73071,"journal":{"name":"Frontiers in catalysis","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fctls.2022.892183","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Molecular hydrogen (H2) is considered an ideal energy vector and a clean fuel, due to its zero-carbon combustion. Nevertheless, despite hydrogen is the most and one of the most abundant elements in the universe and in earth crust, respectively, it is always combined with other elements in our planet and never appears in its elemental state. This means that H2 must be produced through, almost always, endergonic processes, whose sustainability depend not only on the starting material but also on the source of energy necessary for these processes to occur. Colors have been assigned to identify the level of sustainability of H2 production with the green one indicating H2 produced from water using a renewable source of energy, preferably sunlight. Redox water splitting (WS) into H2 (hydrogen evolution reaction, HER) and O2 (oxygen evolution reaction, OER) is, nevertheless, an extremely difficult process not only from the thermodynamic but also from the kinetic point of view. Relevant kinetic barriers are present in both sides of the redox process, especially in OER. For this reason, performing WS in an efficient manner requires the development of active and robust catalysts capable of offering alternative reaction pathways to WS, lowering down the unfavorable kinetic barriers and thus maximizing the energy conversion efficiency. Inspiration for developing efficient catalysts for HER and OER has traditionally derived from Nature, who, over the course of many billions of years, according to the evolutionary theory, has assembled two molecular catalytic pools, namely oxygen evolving complex and ferredoxin/ferredoxin NADP+ reductase, which offer viable kinetic pathways to both OER and reduction of NADP+ (the “biological form” of H2). In reality, after several attempts of mimicking natural catalysts, the efforts of the researchers have been addressed to different molecular systems, which exhibit best performances, unfortunately often based on noble-metal atoms, especially for OER. In this contribution we review the journey of the development of molecular catalysts for both HER and the OER, highlighting selected systems, which have brought us to the current level of knowledge.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
“绿色”制氢中的分子催化
分子氢(H2)由于其零碳燃烧,被认为是一种理想的能量载体和清洁燃料。然而,尽管氢是宇宙中含量最多的元素,也是地壳中含量最多的元素之一,但它总是与地球上的其他元素结合在一起,从不以单质状态出现。这意味着氢气几乎总是通过自耗过程产生,其可持续性不仅取决于起始材料,还取决于这些过程发生所需的能量来源。颜色表示H2生产的可持续性水平,绿色表示利用可再生能源(最好是阳光)从水中生产H2。然而,无论从热力学角度还是从动力学角度来看,氧化还原水裂解成H2(析氢反应,HER)和O2(析氧反应,OER)都是一个极其困难的过程。相关的动力学障碍存在于氧化还原过程的两侧,特别是在OER中。因此,高效地处理WS需要开发活性强的催化剂,为WS提供可选择的反应途径,降低不利的动力学障碍,从而最大限度地提高能量转换效率。开发高效HER和OER催化剂的灵感传统上来自大自然,根据进化理论,大自然在数十亿年的过程中组装了两个分子催化池,即氧进化复合物和铁氧化还蛋白/铁氧化还蛋白NADP+还原酶,它们为OER和NADP+还原(H2的“生物形式”)提供了可行的动力学途径。实际上,经过几次模仿天然催化剂的尝试,研究人员的努力已经针对不同的分子系统,这些系统表现出最好的性能,不幸的是,它们通常基于贵金属原子,特别是对于OER。在这篇文章中,我们回顾了HER和OER分子催化剂的发展历程,重点介绍了一些使我们达到当前知识水平的系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Combined anodic and cathodic peroxide production in an undivided carbonate/bicarbonate electrolyte with 144% combined current efficiency Novel concepts for the biocatalytic synthesis of second-generation biodiesel Parallel paired electrolysis of green oxidizing agents by the combination of a gas diffusion cathode and boron-doped diamond anode Parallel paired electrolysis of green oxidizing agents by the combination of a gas diffusion cathode and boron-doped diamond anode Biocatalytic route scouting and enzyme screening toward the synthesis of α-benzyl L-glutamate
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1