Ensembled Ptδ+ species on Beta zeolites for efficient preferential oxidation of CO in H2

IF 11.5 Q1 CHEMISTRY, PHYSICAL
Jia Shen, Qian Xiang, Lichuan Song, Yake Lou, Jiajie Ye, Xiao Yang, Yanglong Guo, Wangcheng Zhan, Li Wang, Xiao-Ming Cao, Xuan Tang, Sheng Dai, Yun Guo
{"title":"Ensembled Ptδ+ species on Beta zeolites for efficient preferential oxidation of CO in H2","authors":"Jia Shen, Qian Xiang, Lichuan Song, Yake Lou, Jiajie Ye, Xiao Yang, Yanglong Guo, Wangcheng Zhan, Li Wang, Xiao-Ming Cao, Xuan Tang, Sheng Dai, Yun Guo","doi":"10.1016/j.checat.2025.101302","DOIUrl":null,"url":null,"abstract":"The preferential oxidation of CO in H<sub>2</sub>-rich environments (CO-PROX) is one of the most promising strategies for purifying H<sub>2</sub>. However, developing catalysts with low noble metal loadings that can effectively operate within a wide temperature range remains a significant challenge. Here, we synthesized ensembled Pt<sup>δ+</sup> species on Beta zeolite (0.36 wt % Pt) through a reduction treatment. This catalyst achieved 100% CO conversion in CO-PROX across the temperature range of 25°C–220°C. The outstanding performance of this catalyst originates from the temperature-dependent dual mechanisms. Specifically, the ensembled Pt<sup>δ+</sup> species weaken the adsorption strength of CO and enhance activation in O<sub>2</sub> at elevated temperatures. Moreover, these Pt<sup>δ+</sup> species play a crucial role in facilitating the adsorption and dissociation of H<sub>2</sub> at lower temperatures, enabling it to react with O<sub>2</sub> and form –OH species. These –OH species readily react with CO, overcoming the challenges associated with O<sub>2</sub> activation.","PeriodicalId":53121,"journal":{"name":"Chem Catalysis","volume":"54 1","pages":""},"PeriodicalIF":11.5000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.checat.2025.101302","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The preferential oxidation of CO in H2-rich environments (CO-PROX) is one of the most promising strategies for purifying H2. However, developing catalysts with low noble metal loadings that can effectively operate within a wide temperature range remains a significant challenge. Here, we synthesized ensembled Ptδ+ species on Beta zeolite (0.36 wt % Pt) through a reduction treatment. This catalyst achieved 100% CO conversion in CO-PROX across the temperature range of 25°C–220°C. The outstanding performance of this catalyst originates from the temperature-dependent dual mechanisms. Specifically, the ensembled Ptδ+ species weaken the adsorption strength of CO and enhance activation in O2 at elevated temperatures. Moreover, these Ptδ+ species play a crucial role in facilitating the adsorption and dissociation of H2 at lower temperatures, enabling it to react with O2 and form –OH species. These –OH species readily react with CO, overcoming the challenges associated with O2 activation.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
10.50
自引率
6.40%
发文量
0
期刊介绍: Chem Catalysis is a monthly journal that publishes innovative research on fundamental and applied catalysis, providing a platform for researchers across chemistry, chemical engineering, and related fields. It serves as a premier resource for scientists and engineers in academia and industry, covering heterogeneous, homogeneous, and biocatalysis. Emphasizing transformative methods and technologies, the journal aims to advance understanding, introduce novel catalysts, and connect fundamental insights to real-world applications for societal benefit.
×
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