VSe(2-x) O (x) @Pd Sensor for Operando Self-Monitoring of Palladium-Catalyzed Reactions

用于钯催化反应原位自监测的VSe(2-x)O(x)@Pd传感器

阅读:1

Abstract

Operando monitoring of catalytic reaction kinetics plays a key role in investigating the reaction pathways and revealing the reaction mechanisms. Surface-enhanced Raman scattering (SERS) has been demonstrated as an innovative tool in tracking molecular dynamics in heterogeneous reactions. However, the SERS performance of most catalytic metals is inadequate. In this work, we propose hybridized VSe(2-x) O (x) @Pd sensors to track the molecular dynamics in Pd-catalyzed reactions. Benefiting from metal-support interactions (MSI), the VSe(2-x) O (x) @Pd realizes strong charge transfer and enriched density of states near the Fermi level, thereby strongly intensifying the photoinduced charge transfer (PICT) to the adsorbed molecules and consequently enhancing the SERS signals. The excellent SERS performance of the VSe(2-x) O (x) @Pd offers the possibility for self-monitoring the Pd-catalyzed reaction. Taking the Suzuki-Miyaura coupling reaction as an example, operando investigations of Pd-catalyzed reactions were demonstrated on the VSe(2-x) O (x) @Pd, and the contributions from PICT resonance were illustrated by wavelength-dependent studies. Our work demonstrates the feasibility of improved SERS performance of catalytic metals by modulating the MSI and offers a valid means to investigate the mechanisms of Pd-catalyzed reactions based on VSe(2-x) O (x) @Pd sensors.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。