等离子体子
光催化
纳米尺度
时间分辨率
超短脉冲
纳米技术
材料科学
电子
显微镜
催化作用
等离子纳米粒子
化学物理
化学
光电子学
物理
光学
激光器
量子力学
生物化学
作者
Claire C. Carlin,Alan Dai,Alexander Al-Zubeidi,Emma M. Simmerman,Hyuncheol Oh,Niklas Gross,Stephen Lee,Stephan Link,Christy F. Landes,Felipe H. da Jornada,Jennifer A. Dionne
出处
期刊:Chemical physics reviews
[American Institute of Physics]
日期:2023-12-01
卷期号:4 (4)
被引量:9
摘要
Plasmonic photocatalysis uses the light-induced resonant oscillation of free electrons in a metal nanoparticle to concentrate optical energy for driving chemical reactions. By altering the joint electronic structure of the catalyst and reactants, plasmonic catalysis enables reaction pathways with improved selectivity, activity, and catalyst stability. However, designing an optimal catalyst still requires a fundamental understanding of the underlying plasmonic mechanisms at the spatial scales of single particles, at the temporal scales of electron transfer, and in conditions analogous to those under which real reactions will operate. Thus, in this review, we provide an overview of several of the available and developing nanoscale and ultrafast experimental approaches, emphasizing those that can be performed in situ. Specifically, we discuss high spatial resolution optical, tip-based, and electron microscopy techniques; high temporal resolution optical and x-ray techniques; and emerging ultrafast optical, x-ray, tip-based, and electron microscopy techniques that simultaneously achieve high spatial and temporal resolution. Ab initio and classical continuum theoretical models play an essential role in guiding and interpreting experimental exploration, and thus, these are also reviewed and several notable theoretical insights are discussed.
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