Industrially viable formate production with 50% lower CO2 emissions

IF 32.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Fanxu Meng, Zihan Shen, Xinlong Lin, Pengfei Song, Tianze Wu, Shibo Xi, Chao Wu, Zhenhui Ma, Daniel Mandler, Zhichuan J. Xu
{"title":"Industrially viable formate production with 50% lower CO2 emissions","authors":"Fanxu Meng, Zihan Shen, Xinlong Lin, Pengfei Song, Tianze Wu, Shibo Xi, Chao Wu, Zhenhui Ma, Daniel Mandler, Zhichuan J. Xu","doi":"10.1039/d5ee00452g","DOIUrl":null,"url":null,"abstract":"The conventional production of formic acid is energy-intensive, requiring methanol and carbon monoxide reactions followed by hydrolysis under high temperature and pressure. Methanol electrochemical refinery (e-refinery) offers a sustainable alternative but faces challenges like high overpotential and competing oxygen evolution reaction (OER). This study presents Pt-nanoparticle-decorated Ni(OH)<small><sub>2</sub></small> as a breakthrough catalyst, achieving a significantly lower onset potential of 0.5 V vs reversible hydrogen electrode (RHE) for methanol-to-formate conversion compared to previous reports (&gt;1.35 V vs RHE), while simultaneously generating hydrogen at the cathode. The platinum valence state is identified as an effective descriptor for formate Faradaic efficiency, validated through experimental studies and density functional theory. Pt<small><sub>1.05</sub></small>@Ni(OH)<small><sub>2</sub></small>, featuring the highest platinum valence states among the catalysts studied, exhibits an exceptional formate Faradaic efficiency of 78.8% and a high formate production rate of 1.3 mmol h<small><sup>−1</sup></small> mg<small><sub>cat</sub></small><small><sup>−1</sup></small> at 0.8 V versus RHE. This approach reduces overpotential, eliminates OER, and cuts carbon dioxide emissions by over 50% compared to traditional methods. Moreover, economic analysis shows profitability from the fourth year at 50 mA cm<small><sup>−2</sup></small>, supporting easier industrial adoption and low carbon dioxide emissions. These advancements offer a sustainable, energy-efficient, and economically viable method for formate production, advancing the commercialization of methanol e-refinery technology.","PeriodicalId":72,"journal":{"name":"Energy & Environmental Science","volume":"16 1","pages":""},"PeriodicalIF":32.4000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Environmental Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d5ee00452g","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The conventional production of formic acid is energy-intensive, requiring methanol and carbon monoxide reactions followed by hydrolysis under high temperature and pressure. Methanol electrochemical refinery (e-refinery) offers a sustainable alternative but faces challenges like high overpotential and competing oxygen evolution reaction (OER). This study presents Pt-nanoparticle-decorated Ni(OH)2 as a breakthrough catalyst, achieving a significantly lower onset potential of 0.5 V vs reversible hydrogen electrode (RHE) for methanol-to-formate conversion compared to previous reports (>1.35 V vs RHE), while simultaneously generating hydrogen at the cathode. The platinum valence state is identified as an effective descriptor for formate Faradaic efficiency, validated through experimental studies and density functional theory. Pt1.05@Ni(OH)2, featuring the highest platinum valence states among the catalysts studied, exhibits an exceptional formate Faradaic efficiency of 78.8% and a high formate production rate of 1.3 mmol h−1 mgcat−1 at 0.8 V versus RHE. This approach reduces overpotential, eliminates OER, and cuts carbon dioxide emissions by over 50% compared to traditional methods. Moreover, economic analysis shows profitability from the fourth year at 50 mA cm−2, supporting easier industrial adoption and low carbon dioxide emissions. These advancements offer a sustainable, energy-efficient, and economically viable method for formate production, advancing the commercialization of methanol e-refinery technology.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Energy & Environmental Science
Energy & Environmental Science 化学-工程:化工
CiteScore
50.50
自引率
2.20%
发文量
349
审稿时长
2.2 months
期刊介绍: Energy & Environmental Science, a peer-reviewed scientific journal, publishes original research and review articles covering interdisciplinary topics in the (bio)chemical and (bio)physical sciences, as well as chemical engineering disciplines. Published monthly by the Royal Society of Chemistry (RSC), a not-for-profit publisher, Energy & Environmental Science is recognized as a leading journal. It boasts an impressive impact factor of 8.500 as of 2009, ranking 8th among 140 journals in the category "Chemistry, Multidisciplinary," second among 71 journals in "Energy & Fuels," second among 128 journals in "Engineering, Chemical," and first among 181 scientific journals in "Environmental Sciences." Energy & Environmental Science publishes various types of articles, including Research Papers (original scientific work), Review Articles, Perspectives, and Minireviews (feature review-type articles of broad interest), Communications (original scientific work of an urgent nature), Opinions (personal, often speculative viewpoints or hypotheses on current topics), and Analysis Articles (in-depth examination of energy-related issues).
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信