Fojt Jakub, Erhart Paul, Schäfer Christian
Department of Physics, Chalmers University of Technology, 412 96 Göteborg, Sweden.
Nano Lett. 2024 Sep 25;24(38):11913-11920. doi: 10.1021/acs.nanolett.4c03153. Epub 2024 Sep 12.
Plasmonic excitations decay within femtoseconds, leaving nonthermal (often referred to as "hot") charge carriers behind that can be injected into molecular structures to trigger chemical reactions that are otherwise out of reach─a process known as plasmonic catalysis. In this Letter, we demonstrate that strong coupling between resonator structures and plasmonic nanoparticles can be used to control the spectral overlap between the plasmonic excitation energy and the charge injection energy into nearby molecules. Our atomistic description couples real-time density-functional theory self-consistently to an electromagnetic resonator structure via the radiation-reaction potential. Control over the resonator provides then an additional knob for nonintrusively enhancing plasmonic catalysis, here more than 6-fold, and dynamically reacting to deterioration of the catalyst─a new facet of modern catalysis.
等离子体激元激发在飞秒内衰减,留下非热(通常称为“热”)电荷载流子,这些载流子可注入分子结构以触发否则无法实现的化学反应——这一过程称为等离子体催化。在本信函中,我们证明谐振器结构与等离子体纳米颗粒之间的强耦合可用于控制等离子体激发能量与注入附近分子的电荷注入能量之间的光谱重叠。我们的原子描述通过辐射反应势将实时密度泛函理论自洽地耦合到电磁谐振器结构。对谐振器的控制进而提供了一个额外的旋钮,用于非侵入性地增强等离子体催化,在此增强超过6倍,并对催化剂的劣化进行动态反应——这是现代催化的一个新方面。