封面专题:可见光敏化二氧化碳甲烷化的松弛热可用途径(《欧洲化学杂志》63/2024)

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemistry - A European Journal Pub Date : 2024-11-13 DOI:10.1002/chem.202486302
Yangyang Du, Dongge Ma, Jiazhen Li, Qiang Huang, Qin He, Jianfei Ji, Hongwei Ji, Wanhong Ma, Jincai Zhao
{"title":"封面专题:可见光敏化二氧化碳甲烷化的松弛热可用途径(《欧洲化学杂志》63/2024)","authors":"Yangyang Du,&nbsp;Dongge Ma,&nbsp;Jiazhen Li,&nbsp;Qiang Huang,&nbsp;Qin He,&nbsp;Jianfei Ji,&nbsp;Hongwei Ji,&nbsp;Wanhong Ma,&nbsp;Jincai Zhao","doi":"10.1002/chem.202486302","DOIUrl":null,"url":null,"abstract":"<p><b>The Cover Feature</b> shows artificial photosynthesis to convert H<sub>2</sub>O vapour/CO<sub>2</sub> into the value-added chemical CH<sub>4</sub>. Intermediate temperature-sensitive Ti−H species are generated by the photosensitized PDI dye component of the Pt/N−TiO<sub>2</sub>/PDI composite catalyst; this enables incident light energy that has relaxed into waste heat to locally heat a highly nucleophilic hydride for CO<sub>2</sub> addition to a COOH* intermediate. (Until now it had been thought that photocatalysis and temperature were almost negatively dependent.) Shown top left is the photoexcitation process by which electrons are transferred to the TiO<sub>2</sub> surface to generate Ti−H species; this converts 53 % of the relaxed incident light into a thermal effect to be re-used. Shown top right is the acceleration of the reaction rate through increasing the initial energy of the rate-limiting step as the catalyst surface temperature increases and it becomes easier to cross the activation barrier. More information can be found in the Research Article by D. Ma, H. Ji, W. Ma, and co-workers (DOI: 10.1002/chem.202402102).\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":144,"journal":{"name":"Chemistry - A European Journal","volume":"30 63","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/chem.202486302","citationCount":"0","resultStr":"{\"title\":\"Cover Feature: Visible Light-Sensitized CO2 Methanation along a Relaxed Heat Available Route (Chem. Eur. J. 63/2024)\",\"authors\":\"Yangyang Du,&nbsp;Dongge Ma,&nbsp;Jiazhen Li,&nbsp;Qiang Huang,&nbsp;Qin He,&nbsp;Jianfei Ji,&nbsp;Hongwei Ji,&nbsp;Wanhong Ma,&nbsp;Jincai Zhao\",\"doi\":\"10.1002/chem.202486302\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>The Cover Feature</b> shows artificial photosynthesis to convert H<sub>2</sub>O vapour/CO<sub>2</sub> into the value-added chemical CH<sub>4</sub>. Intermediate temperature-sensitive Ti−H species are generated by the photosensitized PDI dye component of the Pt/N−TiO<sub>2</sub>/PDI composite catalyst; this enables incident light energy that has relaxed into waste heat to locally heat a highly nucleophilic hydride for CO<sub>2</sub> addition to a COOH* intermediate. (Until now it had been thought that photocatalysis and temperature were almost negatively dependent.) Shown top left is the photoexcitation process by which electrons are transferred to the TiO<sub>2</sub> surface to generate Ti−H species; this converts 53 % of the relaxed incident light into a thermal effect to be re-used. Shown top right is the acceleration of the reaction rate through increasing the initial energy of the rate-limiting step as the catalyst surface temperature increases and it becomes easier to cross the activation barrier. More information can be found in the Research Article by D. Ma, H. Ji, W. Ma, and co-workers (DOI: 10.1002/chem.202402102).\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":144,\"journal\":{\"name\":\"Chemistry - A European Journal\",\"volume\":\"30 63\",\"pages\":\"\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/chem.202486302\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - A European Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/chem.202486302\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - A European Journal","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/chem.202486302","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

封面特写展示了将 H2O 蒸汽/CO2 转化为高附加值化学品 CH4 的人工光合作用。Pt/N-TiO2/PDI 复合催化剂中的光敏化 PDI 染料成分产生了对温度敏感的中间 Ti-H 物种;这使得释放为废热的入射光能在局部加热高亲核氢化物,从而将 CO2 加成 COOH* 中间体。(到目前为止,人们一直认为光催化与温度几乎呈负相关)。左上角显示的是光激发过程,电子通过该过程转移到二氧化钛表面,生成 Ti-H 物种;这将 53% 的弛豫入射光转化为热效应,以便再次利用。右上图显示的是随着催化剂表面温度的升高和活化障碍的越过,通过增加限速步骤的初始能量来加快反应速率。更多信息,请参阅 D. Ma、H. Ji、W. Ma 及合作者的研究文章(DOI: 10.1002/chem.202402102)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Cover Feature: Visible Light-Sensitized CO2 Methanation along a Relaxed Heat Available Route (Chem. Eur. J. 63/2024)

The Cover Feature shows artificial photosynthesis to convert H2O vapour/CO2 into the value-added chemical CH4. Intermediate temperature-sensitive Ti−H species are generated by the photosensitized PDI dye component of the Pt/N−TiO2/PDI composite catalyst; this enables incident light energy that has relaxed into waste heat to locally heat a highly nucleophilic hydride for CO2 addition to a COOH* intermediate. (Until now it had been thought that photocatalysis and temperature were almost negatively dependent.) Shown top left is the photoexcitation process by which electrons are transferred to the TiO2 surface to generate Ti−H species; this converts 53 % of the relaxed incident light into a thermal effect to be re-used. Shown top right is the acceleration of the reaction rate through increasing the initial energy of the rate-limiting step as the catalyst surface temperature increases and it becomes easier to cross the activation barrier. More information can be found in the Research Article by D. Ma, H. Ji, W. Ma, and co-workers (DOI: 10.1002/chem.202402102).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Chemistry - A European Journal
Chemistry - A European Journal 化学-化学综合
CiteScore
7.90
自引率
4.70%
发文量
1808
审稿时长
1.8 months
期刊介绍: Chemistry—A European Journal is a truly international journal with top quality contributions (2018 ISI Impact Factor: 5.16). It publishes a wide range of outstanding Reviews, Minireviews, Concepts, Full Papers, and Communications from all areas of chemistry and related fields. Based in Europe Chemistry—A European Journal provides an excellent platform for increasing the visibility of European chemistry as well as for featuring the best research from authors from around the world. All manuscripts are peer-reviewed, and electronic processing ensures accurate reproduction of text and data, plus short publication times. The Concepts section provides nonspecialist readers with a useful conceptual guide to unfamiliar areas and experts with new angles on familiar problems. Chemistry—A European Journal is published on behalf of ChemPubSoc Europe, a group of 16 national chemical societies from within Europe, and supported by the Asian Chemical Editorial Societies. The ChemPubSoc Europe family comprises: Angewandte Chemie, Chemistry—A European Journal, European Journal of Organic Chemistry, European Journal of Inorganic Chemistry, ChemPhysChem, ChemBioChem, ChemMedChem, ChemCatChem, ChemSusChem, ChemPlusChem, ChemElectroChem, and ChemistryOpen.
期刊最新文献
Basic-functionalized Ionic Porous Organic Polymers: Triple Roles in One for Highly Efficient and Recyclable Carboxylative Cyclization of CO2 under Mild Conditions. ​Dual-Coreactants Enhanced Electrochemiluminescence. A Multistep Oxidative Cascade Reaction from a Naphthalenediol-Based pre-Ligand to a Tetranuclear Perylenequinone-Based FeIII Complex. In-situ reduced Cu3N nanocrystals enable high-efficiency ammonia synthesis and zinc-nitrate batteries. Magnetohydrodynamic Enhancement of Biofuel Cell Performance.
×
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