The marriage of porous cages and metal clusters for advanced catalysis

IF 6 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jun-Yu Li, Xiao-Dong Yang, Fu-Xue Chen and Jian-Ke Sun
{"title":"The marriage of porous cages and metal clusters for advanced catalysis","authors":"Jun-Yu Li, Xiao-Dong Yang, Fu-Xue Chen and Jian-Ke Sun","doi":"10.1039/D3QM00492A","DOIUrl":null,"url":null,"abstract":"<p >Metal clusters (MCs), a special species of ultrafine metal nanoparticles with dimensions below 2 nm, serve as highly active catalysts for a broad spectrum of chemical reactions, but usually suffer from serious aggregation due to their high surface energy. A balance between the activity and stability of MCs is greatly challenging in designing efficient catalysts. Cage-bearing materials such as organic molecular cages and metal–organic cages, as another promising category of porous materials, are attracting significant research attention. Thanks to their intrinsic cavity, such materials can serve as ideal confined templates for the size-controlled synthesis of MCs without blocking their active sites. Moreover, benefiting from the easy-to-modify architecture, the cage polyhedrons can be further functionalized to obtain advanced composite catalysts in combination with the hosted MCs. As such, the multiple active sites are spatially organized and compartmentalized by the cage skeleton, which therefore avoids undesired mutual quenching. With the synergy of multi-catalytic centers, the integrated cage-bearing nanocomposite catalysts have advanced as another burgeoning candidate to perform accurate and efficient multistep cascade reactions by mimicking cell metabolism and biological synthesis. In this review, we will introduce the most recent adopted confined synthetic methodologies for MCs enabled by cage materials on the one hand, and their applications in advanced catalysis on the other hand.</p>","PeriodicalId":86,"journal":{"name":"Materials Chemistry Frontiers","volume":" 21","pages":" 5355-5376"},"PeriodicalIF":6.0000,"publicationDate":"2023-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Chemistry Frontiers","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2023/qm/d3qm00492a","RegionNum":2,"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

Metal clusters (MCs), a special species of ultrafine metal nanoparticles with dimensions below 2 nm, serve as highly active catalysts for a broad spectrum of chemical reactions, but usually suffer from serious aggregation due to their high surface energy. A balance between the activity and stability of MCs is greatly challenging in designing efficient catalysts. Cage-bearing materials such as organic molecular cages and metal–organic cages, as another promising category of porous materials, are attracting significant research attention. Thanks to their intrinsic cavity, such materials can serve as ideal confined templates for the size-controlled synthesis of MCs without blocking their active sites. Moreover, benefiting from the easy-to-modify architecture, the cage polyhedrons can be further functionalized to obtain advanced composite catalysts in combination with the hosted MCs. As such, the multiple active sites are spatially organized and compartmentalized by the cage skeleton, which therefore avoids undesired mutual quenching. With the synergy of multi-catalytic centers, the integrated cage-bearing nanocomposite catalysts have advanced as another burgeoning candidate to perform accurate and efficient multistep cascade reactions by mimicking cell metabolism and biological synthesis. In this review, we will introduce the most recent adopted confined synthetic methodologies for MCs enabled by cage materials on the one hand, and their applications in advanced catalysis on the other hand.

Abstract Image

用于高级催化的多孔笼和金属团簇的结合
金属团簇(MC)是一种尺寸低于2nm的超细金属纳米颗粒的特殊物种,在广泛的化学反应中起着高活性催化剂的作用,但由于其高表面能,通常会发生严重的聚集。MCs的活性和稳定性之间的平衡在设计高效催化剂方面具有很大的挑战性。含笼材料,如有机分子笼和金属-有机笼,作为另一类有前途的多孔材料,正吸引着大量的研究关注。由于其固有的空腔,这种材料可以作为MC尺寸控制合成的理想限制模板,而不会阻断其活性位点。此外,得益于易于修饰的结构,笼状多面体可以进一步功能化,以获得与宿主MC相结合的先进复合催化剂。因此,多个活性位点由笼骨架在空间上组织和划分,从而避免了不期望的相互猝灭。随着多催化中心的协同作用,集成笼状纳米复合催化剂已成为另一种新兴的候选者,可以通过模拟细胞代谢和生物合成来进行准确有效的多步级联反应。在这篇综述中,我们将一方面介绍笼状材料实现的MCs的最新受限合成方法,另一方面介绍它们在高级催化中的应用。
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 求助全文
来源期刊
Materials Chemistry Frontiers
Materials Chemistry Frontiers Materials Science-Materials Chemistry
CiteScore
12.00
自引率
2.90%
发文量
313
期刊介绍: Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome. This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.
×
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