Ni–MoO2 heterostructure encapsulated in mesoporous silica microtubes: a structured hydrogenation catalyst with enhanced activity for reduction of 4-nitrophenol

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY CrystEngComm Pub Date : 2024-11-14 DOI:10.1039/D4CE01044B
Yiran Sun, Mintong Guo, Suping Han, Jingli Xu, Xue-Bo Yin and Min Zhang
{"title":"Ni–MoO2 heterostructure encapsulated in mesoporous silica microtubes: a structured hydrogenation catalyst with enhanced activity for reduction of 4-nitrophenol","authors":"Yiran Sun, Mintong Guo, Suping Han, Jingli Xu, Xue-Bo Yin and Min Zhang","doi":"10.1039/D4CE01044B","DOIUrl":null,"url":null,"abstract":"<p >Metallic Ni catalysts often suffer from serious aggregation and poor stability during the process of catalysis. In this work, core–shell nanostructures with nanosized MoO<small><sub>2</sub></small>–Ni nanoparticles (NPs) and mesoporous SiO<small><sub>2</sub></small>(mSiO<small><sub>2</sub></small>) shells were well designed to address these issues. The Ni–MoO<small><sub>2</sub></small> hybrid cores were converted from hierarchical NiMoO<small><sub>4</sub></small> microtubes inside the SiO<small><sub>2</sub></small> shell through carbonization treatment to remove the hexadecyl trimethyl ammonium bromide (CTAB) template under the protection of a nitrogen atmosphere. The mesoporous SiO<small><sub>2</sub></small> shells in Ni–MoO<small><sub>2</sub></small>@mSiO<small><sub>2</sub></small> nanoreactors prevented the agglomeration/sintering of Ni NPs, while allowing the mass diffusion of small molecules. Owing to the high catalytic performance of Ni–MoO<small><sub>2</sub></small> cores, good protection of mesoporous silica, and the unique sandwich-like structure, the obtained Ni–MoO<small><sub>2</sub></small>@mSiO<small><sub>2</sub></small> nanoreactors showed tremendous improvement in catalytic activity and stability.</p>","PeriodicalId":70,"journal":{"name":"CrystEngComm","volume":" 48","pages":" 6813-6822"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CrystEngComm","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ce/d4ce01044b","RegionNum":3,"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

Abstract

Metallic Ni catalysts often suffer from serious aggregation and poor stability during the process of catalysis. In this work, core–shell nanostructures with nanosized MoO2–Ni nanoparticles (NPs) and mesoporous SiO2(mSiO2) shells were well designed to address these issues. The Ni–MoO2 hybrid cores were converted from hierarchical NiMoO4 microtubes inside the SiO2 shell through carbonization treatment to remove the hexadecyl trimethyl ammonium bromide (CTAB) template under the protection of a nitrogen atmosphere. The mesoporous SiO2 shells in Ni–MoO2@mSiO2 nanoreactors prevented the agglomeration/sintering of Ni NPs, while allowing the mass diffusion of small molecules. Owing to the high catalytic performance of Ni–MoO2 cores, good protection of mesoporous silica, and the unique sandwich-like structure, the obtained Ni–MoO2@mSiO2 nanoreactors showed tremendous improvement in catalytic activity and stability.

Abstract Image

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
介孔二氧化硅微管封装的Ni-MoO2异质结构:具有增强还原4-硝基苯酚活性的结构化加氢催化剂
金属镍催化剂在催化过程中往往聚集严重,稳定性差。在这项工作中,由纳米MoO2-Ni纳米粒子(NPs)和介孔SiO2(mSiO2)壳组成的核壳纳米结构被很好地设计来解决这些问题。在氮气气氛的保护下,通过炭化处理去除十六烷基三甲基溴化铵(CTAB)模板,将层次化NiMoO4微管转化为Ni-MoO2杂化芯。Ni - MoO2@mSiO2纳米反应器中的介孔SiO2壳层阻止了Ni NPs的团聚/烧结,同时允许小分子的大量扩散。由于Ni - moo2核的高催化性能,介孔二氧化硅的良好保护,以及独特的三明治状结构,所获得的Ni - MoO2@mSiO2纳米反应器在催化活性和稳定性方面有了巨大的提高。
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
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
期刊最新文献
Cooling cocrystallization of acetazolamide & p-aminobenzoic acid in continuous slug flow crystallizer Impact of halogen-bonding interactions on M–X bond activation pathways: a perspective Multicolor luminescence and anti-counterfeiting applications in Cs2KGdCl6 double perovskite Crystallization, replacement, and redox pathways governing rare earth carbonate and phosphate formation A triazolate-based MOF with amino-induced triazolate reorientation enabling pore-size regulation for CO2/CH4 separation
×
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