Facilitating excited-state plasmonics and photochemical reaction dynamics

被引:3
作者
Warren, Natalie L. [1 ]
Yunusa, Umar [1 ]
Singhal, Arnav B. [1 ]
Sprague-Klein, Emily A. [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
来源
CHEMICAL PHYSICS REVIEWS | 2024年 / 5卷 / 01期
关键词
ENHANCED RAMAN-SCATTERING; OPTICAL-PROPERTIES; METAL NANOPARTICLES; ELECTRON-TRANSFER; GOLD NANORODS; SURFACE; ULTRAFAST; SILVER; SPECTROSCOPY; ABSORPTION;
D O I
10.1063/5.0167266
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Continuously advancing technologies is crucial to tackling modern challenges such as efficient energy transfer, directing catalytic behavior, and better understanding of microscopic phenomena. At the heart of many of these problems is nanoscale chemistry. In previous decades, the scientific community has made significant progress in nanoscale structures and technologies, especially relating to their interactions with light. Plasmonic nanostructures have been extensively studied over the past decades because of their fascinating properties and vast technological applications. They can confine light into intense local electromagnetic fields, which has been exploited in the fields of spectroscopy, energy harvesting, optoelectronics, chemical sensing, and biomedicine. Recently, however, plasmonic nanostructures have shown great potential to trigger chemical transformations of proximal molecular species via hot carrier and thermally driven processes. In this review, we discuss the basic concepts governing nanoscale light-matter interactions, the immediate phenomena induced by them, and how we can use nanoscale light-matter interactions to our advantage with surface-enhanced spectroscopy techniques and chemical reactions in confined plasmonic environments.
引用
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页数:24
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