IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Russell J. Clarke, Isaac J. Nice, Jason C. Hicks
{"title":"Plasma-Catalyst Dynamics: Nonthermal Activation of Strong Metal–Support Interactions","authors":"Russell J. Clarke, Isaac J. Nice, Jason C. Hicks","doi":"10.1021/jacs.4c12388","DOIUrl":null,"url":null,"abstract":"Nonthermal plasma-surface interactions enable transformative advancements in green chemistry, healthcare, materials processing, pollution abatement, and the ever-growing area of plasma catalysis. In the context of plasma catalysis, the fate of the active sites during plasma treatment has remained enigmatic, and observation of low-temperature plasma-catalyst events has been challenging. The induction of strong metal–support interactions (SMSI) through high-temperature hydrogen treatment is a well-documented and established, yet limited, method to impact selectivity and stability of noble metal catalysts on reducible supports. Thermally driven SMSI occurs through reduction and subsequent migration of the support to the surface of exposed metal sites, thus affecting the catalyst both electronically and geometrically and serving as an ideal system to evaluate dynamic plasma-catalyst interactions. In this study, a dielectric barrier discharge of hydrogen was used to successfully induce a plasma-SMSI state (P-SMSI) in niobia-supported platinum particles at bulk-gas temperatures as low as −30 °C, which enhances the selectivity for propane dehydrogenation and offers conclusive evidence of plasma-catalyst interactions. Time-resolved spectroscopic evidence of this phenomenon was obtained in situ using a cryogenically cooled plasma IR transmission cell, which provided evidence of diffusion-controlled surface migration. Collectively, P-SMSI constitutes a promising, low-impact technology for synthesizing SMSI-enhanced catalysts with controllable active sites, and knowledge of the nonthermal plasma-catalyst dynamics is critical in designing materials for specific applications or selecting conditions of operation.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"201 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c12388","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

非热等离子体与表面的相互作用使绿色化学、医疗保健、材料加工、污染治理以及不断发展的等离子体催化领域实现了变革性的进步。在等离子体催化方面,等离子体处理过程中活性位点的命运一直是个谜,对低温等离子体-催化剂事件的观察也极具挑战性。通过高温氢处理诱导强金属-载体相互作用(SMSI)是一种有据可查的成熟方法,但对可还原载体上贵金属催化剂的选择性和稳定性影响有限。热驱动的 SMSI 是通过还原以及随后支撑物迁移到暴露金属位点表面而发生的,因此会对催化剂的电子和几何结构产生影响,是评估等离子体与催化剂动态相互作用的理想系统。在这项研究中,利用氢的介质阻挡放电成功地在散气温度低至 -30 °C 的条件下诱导了铌铁铂支撑铂颗粒的等离子体-SMSI 状态(P-SMSI),从而提高了丙烷脱氢的选择性,并提供了等离子体-催化剂相互作用的确凿证据。利用低温冷却等离子体红外透射池,在原位获得了这一现象的时间分辨光谱证据,提供了扩散控制表面迁移的证据。总而言之,P-SMSI 是合成具有可控活性位点的 SMSI 增强催化剂的一种前景广阔、影响较小的技术,而非热等离子体-催化剂动力学知识对于为特定应用设计材料或选择操作条件至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Plasma-Catalyst Dynamics: Nonthermal Activation of Strong Metal–Support Interactions

Plasma-Catalyst Dynamics: Nonthermal Activation of Strong Metal–Support Interactions
Nonthermal plasma-surface interactions enable transformative advancements in green chemistry, healthcare, materials processing, pollution abatement, and the ever-growing area of plasma catalysis. In the context of plasma catalysis, the fate of the active sites during plasma treatment has remained enigmatic, and observation of low-temperature plasma-catalyst events has been challenging. The induction of strong metal–support interactions (SMSI) through high-temperature hydrogen treatment is a well-documented and established, yet limited, method to impact selectivity and stability of noble metal catalysts on reducible supports. Thermally driven SMSI occurs through reduction and subsequent migration of the support to the surface of exposed metal sites, thus affecting the catalyst both electronically and geometrically and serving as an ideal system to evaluate dynamic plasma-catalyst interactions. In this study, a dielectric barrier discharge of hydrogen was used to successfully induce a plasma-SMSI state (P-SMSI) in niobia-supported platinum particles at bulk-gas temperatures as low as −30 °C, which enhances the selectivity for propane dehydrogenation and offers conclusive evidence of plasma-catalyst interactions. Time-resolved spectroscopic evidence of this phenomenon was obtained in situ using a cryogenically cooled plasma IR transmission cell, which provided evidence of diffusion-controlled surface migration. Collectively, P-SMSI constitutes a promising, low-impact technology for synthesizing SMSI-enhanced catalysts with controllable active sites, and knowledge of the nonthermal plasma-catalyst dynamics is critical in designing materials for specific applications or selecting conditions of operation.
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
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
×
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