Unlocking the positive effect of non-polar ZnO facets in ZrZnOx catalysts for CO2 hydrogenation

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-03-28 DOI:10.1016/j.mcat.2025.115059
Xiaohong Guo, Liqiang Deng, Xiaoyue Wang, Yongjie Zhao, Zhifan Cao, Pengwei Li, Congming Li
{"title":"Unlocking the positive effect of non-polar ZnO facets in ZrZnOx catalysts for CO2 hydrogenation","authors":"Xiaohong Guo,&nbsp;Liqiang Deng,&nbsp;Xiaoyue Wang,&nbsp;Yongjie Zhao,&nbsp;Zhifan Cao,&nbsp;Pengwei Li,&nbsp;Congming Li","doi":"10.1016/j.mcat.2025.115059","DOIUrl":null,"url":null,"abstract":"<div><div>A pivotal aspect in advancing ZrZnO<sub>x</sub> catalysts for CO<sub>2</sub> hydrogenation lies in the modulation of Zr-O-Zn active sites, with ZnO facets emerging as potential modulators of site activity. Whereas the beneficial influence of non-polar ZnO facets on ZrZnO<sub>x</sub> catalysts has been scarcely documented. Our investigation reveals that ZrZnO<sub>x</sub> catalysts exposed non-polar ZnO facets (ZrZnO-n) exhibit superior methanol selectivity (74 %) compared to those with randomly exposed ZnO facets (ZrZnO-r, 35 %). Characterization results demonstrate that it is ascribed to the formation of highly active Zr-O-Zn<sup>(2−δ)+</sup> sites on ZrZnO-n, which facilitate H<sub>2</sub> adsorption and dissociation. In situ spectroscopic studies and DFT calculations further substantiate this finding, demonstrating enhanced intermediates formation and more efficient hydrogenation processes. This research underscores the significance of ZnO facet engineering in the purposeful creation of efficient ZrZnO<sub>x</sub> catalysts for CO<sub>2</sub> hydrogenation.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"579 ","pages":"Article 115059"},"PeriodicalIF":4.9000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823125002457","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A pivotal aspect in advancing ZrZnOx catalysts for CO2 hydrogenation lies in the modulation of Zr-O-Zn active sites, with ZnO facets emerging as potential modulators of site activity. Whereas the beneficial influence of non-polar ZnO facets on ZrZnOx catalysts has been scarcely documented. Our investigation reveals that ZrZnOx catalysts exposed non-polar ZnO facets (ZrZnO-n) exhibit superior methanol selectivity (74 %) compared to those with randomly exposed ZnO facets (ZrZnO-r, 35 %). Characterization results demonstrate that it is ascribed to the formation of highly active Zr-O-Zn(2−δ)+ sites on ZrZnO-n, which facilitate H2 adsorption and dissociation. In situ spectroscopic studies and DFT calculations further substantiate this finding, demonstrating enhanced intermediates formation and more efficient hydrogenation processes. This research underscores the significance of ZnO facet engineering in the purposeful creation of efficient ZrZnOx catalysts for CO2 hydrogenation.

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
揭示非极性ZnO面在ZrZnOx催化剂中对CO2加氢的积极作用
推进ZrZnOx催化剂用于CO2加氢的一个关键方面在于Zr-O-Zn活性位点的调节,ZnO方面成为潜在的位点活性调节剂。而非极性ZnO晶面对ZrZnOx催化剂的有益影响几乎没有文献记载。我们的研究表明,与随机暴露ZnO面(ZrZnO-r, 35%)相比,暴露在非极性ZnO面(ZrZnO-n)下的ZrZnOx催化剂表现出更高的甲醇选择性(74%)。表征结果表明,这是由于ZrZnO-n上形成了高活性的Zr-O-Zn(2−δ)+位点,有利于H2的吸附和解离。原位光谱研究和DFT计算进一步证实了这一发现,证明了中间产物的形成和更有效的氢化过程。这项研究强调了ZnO小面工程在有目的地创造高效的ZrZnOx CO2加氢催化剂中的重要性。
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
文献相关原料
公司名称
产品信息
阿拉丁
hexadecyltrimethylammonium bromide
来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
期刊最新文献
Biochemical characterization, crystal structure, and catalytic mechanism of a PET-hydrolase double mutant Chemoenzymatic synthesis of mirabegron using an engineered styrene monooxygenase Hydrogen Rich Syngas Production from Methane using Partial Oxidation over Sm-promoted Tungsten-zirconia Supported Ni Catalysts Graphical abstract TOC
×
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