Photocatalytic Conversion of Methane to Ethane and Propane Using Cobalt-Cluster-Activated GaN Nanowires

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-01-20 DOI:10.1002/anie.202500158
Zhengwei Ye, Zhuoran Long, Bingxing Zhang, Ishtiaque Ahmed Navid, Jan Paul Menzel, Yifan Shen, Shubham Mondal, Facheng Guo, Theodore B. Norris, Victor S. Batista, Zetian Mi
{"title":"Photocatalytic Conversion of Methane to Ethane and Propane Using Cobalt-Cluster-Activated GaN Nanowires","authors":"Zhengwei Ye, Zhuoran Long, Bingxing Zhang, Ishtiaque Ahmed Navid, Jan Paul Menzel, Yifan Shen, Shubham Mondal, Facheng Guo, Theodore B. Norris, Victor S. Batista, Zetian Mi","doi":"10.1002/anie.202500158","DOIUrl":null,"url":null,"abstract":"The photocatalytic nonoxidative coupling of methane (PNOCM) offers a promising route to synthesize valuable C2+ hydrocarbons while minimizing side reactions. Oxide-based photocatalysts have been predominant in this field, but suffering from limited conversion rates, selectivity, and durability due to poor C-C coupling as well as overoxidation of CH4 by lattice oxygen. Here, we introduce an advancement in PNOCM for methane conversion into ethane and propane using GaN, one of the most produced semiconductors, together with trace amounts of metallic cobalt clusters (0.1 wt%). The photocatalytic system exhibits outstanding stability, maintaining performance over 110 hours, achieving conversion rates of approximately 192.3 mmol g-1 h-1 for ethane and ~17.9 mmol g-1 h-1 for propane, with virtually no coke byproducts detected, representing the highest activity and stability ever reported to our knowledge. This high activity is attributed to the critical methane activation and C-C coupling on Co cluster, which can be greatly accelerated via the ultrafast photogenerated charge transfer from p-GaN to Co cluster. Additionally, the GaN support further synergistically enhances methane activation by in situ generating N-H and O-H species under reaction, as well as provides a vital anti-overoxidation effect to CH4 for high selectivity and stability.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"9 1","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202500158","RegionNum":1,"RegionCategory":"化学","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 photocatalytic nonoxidative coupling of methane (PNOCM) offers a promising route to synthesize valuable C2+ hydrocarbons while minimizing side reactions. Oxide-based photocatalysts have been predominant in this field, but suffering from limited conversion rates, selectivity, and durability due to poor C-C coupling as well as overoxidation of CH4 by lattice oxygen. Here, we introduce an advancement in PNOCM for methane conversion into ethane and propane using GaN, one of the most produced semiconductors, together with trace amounts of metallic cobalt clusters (0.1 wt%). The photocatalytic system exhibits outstanding stability, maintaining performance over 110 hours, achieving conversion rates of approximately 192.3 mmol g-1 h-1 for ethane and ~17.9 mmol g-1 h-1 for propane, with virtually no coke byproducts detected, representing the highest activity and stability ever reported to our knowledge. This high activity is attributed to the critical methane activation and C-C coupling on Co cluster, which can be greatly accelerated via the ultrafast photogenerated charge transfer from p-GaN to Co cluster. Additionally, the GaN support further synergistically enhances methane activation by in situ generating N-H and O-H species under reaction, as well as provides a vital anti-overoxidation effect to CH4 for high selectivity and stability.
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
钴簇活化氮化镓纳米线光催化甲烷转化为乙烷和丙烷的研究
甲烷的光催化非氧化偶联(PNOCM)为合成有价值的C2+碳氢化合物提供了一条有前途的途径,同时减少了副反应。基于氧化物的光催化剂在该领域占据主导地位,但由于C-C偶联性差以及晶格氧对CH4的过度氧化,其转化率、选择性和耐久性有限。在这里,我们介绍了一项PNOCM技术的进展,该技术使用氮化镓(生产最多的半导体之一)以及微量的金属钴团簇(0.1 wt%)将甲烷转化为乙烷和丙烷。该光催化系统表现出优异的稳定性,在110小时内保持性能,乙烷的转化率约为192.3 mmol g-1 h-1,丙烷的转化率约为17.9 mmol g-1 h-1,几乎没有检测到焦炭副产品,代表了我们所知的最高活性和稳定性。这种高活性归因于Co簇上的临界甲烷活化和C-C耦合,这可以通过p-GaN到Co簇的超快光生电荷转移而大大加速。此外,GaN载体通过原位生成N-H和O-H,进一步协同增强了甲烷的活性,并为CH4提供了重要的抗过氧化作用,从而实现了高选择性和稳定性。
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
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
期刊最新文献
Self-optimizing Cobalt Tungsten Oxide Electrocatalysts toward Enhanced Oxygen Evolution in Alkaline Media Achieving Room-Temperature Phosphorescence in Solution Phase from Carbon Dots Confined in Nanocrystals Activating Organic Electrode for Zinc Batteries via Adjusting Solvation Structure of Zn Ions Unlocking the Power of Photothermal Agents: A Universal Platform for Smart Immune NIR-Agonists for Precise Cancer Therapy Efficient Infrared-Detecting Organic Semiconductors Featuring a Tetraheterocyclic Core with Reduced Ionization Potential
×
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