Kerner Paul, Arul Rakesh, Thompson Damien, Baumberg Jeremy J, de Nijs Bart
Nanophotonics Centre, Department of Physics, Cavendish Laboratory, University of Cambridge, Cambridge CB3 0US, England, UK.
Department of Physics, Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.
Sci Adv. 2025 Jul 18;11(29):eadx3216. doi: 10.1126/sciadv.adx3216.
Observing and controlling dynamics of single atoms in ambient conditions is challenging when using conventional atomic-scale techniques due to their invasive character. Here, such control is achieved optically, by confining pulses of visible light within extreme plasmonic nanogaps, where they rapidly create ("write") an adatom on one facet surface. Such adatoms are shown to be storable in ambient conditions for at least a week in the dark and are observed ("read") using low-intensity surface-enhanced Raman spectroscopy (SERS). Writing at higher optical intensities stabilizes the atomic protrusion through light-induced local restructuring, which imposes a higher energy barrier for its return into the metal surface. Fluctuations in these "picocavity" SERS spectra show that while adatom movement is significantly slower under low light intensities, ambient thermal energy still enables them to explore the surrounding energetic landscape. Optical control over single metal atom dynamics opens promising avenues for next-generation microelectronics, atomic-scale imaging, and catalysis.
在环境条件下,使用传统的原子尺度技术来观察和控制单个原子的动力学具有挑战性,因为这些技术具有侵入性。在此,通过将可见光脉冲限制在极端的等离子体纳米间隙内,以光学方式实现了这种控制,在那里可见光脉冲会在一个小面表面上快速产生(“写入”)一个吸附原子。研究表明,这些吸附原子在黑暗的环境条件下至少可存储一周,并使用低强度表面增强拉曼光谱(SERS)进行观察(“读取”)。在较高光强度下写入可通过光诱导的局部重构使原子突起稳定,这为其返回金属表面施加了更高的能量势垒。这些“皮腔”SERS光谱中的波动表明,虽然在低光强度下吸附原子的移动明显较慢,但环境热能仍能使它们探索周围的能量景观。对单个金属原子动力学的光学控制为下一代微电子学、原子尺度成像和催化开辟了充满希望的途径。