Electrochemically synthesized H2O2 at industrial-level current densities enabled by in situ fabricated few-layer boron nanosheets.

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2024-12-30 DOI:10.1038/s41467-024-55071-7
Yuhan Wu, Yuying Zhao, Qixin Yuan, Hao Sun, Ao Wang, Kang Sun, Geoffrey I N Waterhouse, Ziyun Wang, Jingjie Wu, Jianchun Jiang, Mengmeng Fan
{"title":"Electrochemically synthesized H<sub>2</sub>O<sub>2</sub> at industrial-level current densities enabled by in situ fabricated few-layer boron nanosheets.","authors":"Yuhan Wu, Yuying Zhao, Qixin Yuan, Hao Sun, Ao Wang, Kang Sun, Geoffrey I N Waterhouse, Ziyun Wang, Jingjie Wu, Jianchun Jiang, Mengmeng Fan","doi":"10.1038/s41467-024-55071-7","DOIUrl":null,"url":null,"abstract":"<p><p>Carbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating H<sub>2</sub>O<sub>2</sub> at industrial-level current densities (>300 mA cm<sup>-2</sup>) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (B<sub>n</sub>-C) with H<sub>2</sub>O<sub>2</sub> production rates of industrial relevance in neutral or alkaline media. B<sub>n</sub>-C maintained > 95% Faradaic efficiency during a 140-hour test at 300 mA cm<sup>-2</sup> and 0.1 V vs. RHE, and delivered a mass activity of 25.1 mol g<sub>catalyst</sub><sup>-1</sup> h<sup>-1</sup> in 1.0 M Na<sub>2</sub>SO<sub>4</sub> using a flow cell. Theoretical simulations and experimental studies demonstrate that the superior catalytic performance originates from B atoms with adsorbed O atoms in the boron nanosheets. B<sub>n</sub>-C outperforms all metal-based and metal-free carbon catalysts reported to date for H<sub>2</sub>O<sub>2</sub> synthesis at industrial-level current densities.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"15 1","pages":"10843"},"PeriodicalIF":15.7000,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11685507/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-55071-7","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Carbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (H2O2) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating H2O2 at industrial-level current densities (>300 mA cm-2) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (Bn-C) with H2O2 production rates of industrial relevance in neutral or alkaline media. Bn-C maintained > 95% Faradaic efficiency during a 140-hour test at 300 mA cm-2 and 0.1 V vs. RHE, and delivered a mass activity of 25.1 mol gcatalyst-1 h-1 in 1.0 M Na2SO4 using a flow cell. Theoretical simulations and experimental studies demonstrate that the superior catalytic performance originates from B atoms with adsorbed O atoms in the boron nanosheets. Bn-C outperforms all metal-based and metal-free carbon catalysts reported to date for H2O2 synthesis at industrial-level current densities.

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
利用原位制造的几层硼纳米片,在工业级电流密度下电化学合成 H2O2。
碳纳米材料作为双电子氧还原反应合成过氧化氢(H2O2)的电催化剂具有突出的应用前景。然而,能够在工业级电流密度(>300 mA cm-2)下产生高选择性和长期稳定性的碳基电催化剂仍有待发现。在此,将几层硼纳米片原位引入多孔碳基体中,形成无金属电催化剂(Bn-C),在中性或碱性介质中具有工业相关的H2O2产率。在300 mA cm-2和0.1 V相对于RHE的条件下,Bn-C在140小时的测试中保持了95%的法拉第效率,并在1.0 M Na2SO4中提供了25.1 mol gcatalyst-1 h-1的质量活性。理论模拟和实验研究表明,优异的催化性能源于硼纳米片上吸附了O原子的B原子。Bn-C在工业级电流密度下合成H2O2的性能优于迄今为止报道的所有金属基和无金属碳催化剂。
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
文献相关原料
公司名称
产品信息
麦克林
Isopropanol (C3H8O)
麦克林
Ethanol (C2H6O)
麦克林
Sodium sulfate (Na2SO4)
麦克林
Potassium hydroxide (KOH)
麦克林
Boric acid (H3BO3)
麦克林
Citric acid (C6H8O7)
麦克林
Isopropanol
麦克林
Ethanol
麦克林
Cerium sulfate
麦克林
Sodium sulfate
麦克林
Potassium hydroxide
麦克林
Nickel (II) acetylacetonate
麦克林
Cobalt (II) acetylacetonate
麦克林
Iron (III) acetylacetonate
麦克林
Copper (II) acetylacetonate
麦克林
Boric acid
麦克林
Citric acid
阿拉丁
Commercial Boron powder
阿拉丁
Boron powder
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
期刊最新文献
Evolving epigenomics of immune cells at single-nucleus resolution in children en route to type 1 diabetes Solvation chemistry tailored via dielectric constant engineering for stable low-temperature aqueous zinc batteries Rising Air-Conditioning Use Intensifies Global Warming ERCC6L2 ensures repair fidelity for staggered-end DNA double-strand breaks A gated hydrophobic funnel within BAX binds bioactive lipids to potentiate pro-apoptotic function
×
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:604180095
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