Kocoj Conrad A, Xie Xinran, Jiang Hongyu, Li Shunran, Sarker Suchismita, Yang Ankun, Guo Peijun
Department of Chemical and Environmental Engineering, Yale University, New Haven, Connecticut 06520, United States.
Energy Sciences Institute, Yale University, West Haven, Connecticut 06516, United States.
ACS Nano. 2025 Aug 5;19(30):27310-27317. doi: 10.1021/acsnano.5c04946. Epub 2025 Jul 21.
Alkali metals are considered as a promising alternative to conventional noble metals for plasmonic applications, offering lower optical loss and significantly reduced material costs. The recent development of a thermo-assisted spin-coating process paired with phase-shift photolithography has enabled the creation of stable nanostructured sodium, which exhibits narrow resonances in the near-infrared (NIR) region and demonstrates free electron relaxation times comparable to noble metals. Through the control of nanostructure pitch and light incident angle, the surface plasmon polariton (SPP) resonance wavelength can be tuned throughout the visible and NIR regions, making nanostructured sodium particularly attractive for nanophotonics, surface-enhanced sensing, and photocatalytic applications. In this work, we investigate hot electron dynamics in nanostructured sodium thin films on polyurethane supports by leveraging the high sensitivity of SPPs to their metal's bulk properties. Through optical transient reflectance measurements, we probe the distinct signatures of electron-electron and electron-phonon interactions in sodium at ultrafast time scales. Our results show the unique early time response of sodium that differs from those observed in noble metals, providing key insight into sodium-based plasmonics. This comprehensive understanding of hot electron dynamics will enable more efficient design and implementation of sodium in next-generation plasmonic devices and applications where hot electron processes are critical considerations.
碱金属被认为是传统贵金属在等离子体应用方面有前景的替代物,具有更低的光学损耗和显著降低的材料成本。热辅助旋涂工艺与相移光刻技术的最新发展使得稳定的纳米结构钠得以制备,其在近红外(NIR)区域呈现出窄共振,并且展现出与贵金属相当的自由电子弛豫时间。通过控制纳米结构间距和光入射角,表面等离子体激元(SPP)共振波长可在整个可见光和近红外区域进行调谐,这使得纳米结构钠在纳米光子学、表面增强传感和光催化应用方面极具吸引力。在这项工作中,我们利用表面等离子体激元对其金属体性质的高灵敏度,研究了聚氨酯支撑体上纳米结构钠薄膜中的热电子动力学。通过光学瞬态反射率测量,我们在超快时间尺度上探测了钠中电子 - 电子和电子 - 声子相互作用的独特特征。我们的结果显示了钠独特的早期时间响应,这与在贵金属中观察到的不同,为基于钠的等离子体学提供了关键见解。对热电子动力学的这种全面理解将使钠在下一代等离子体器件和热电子过程是关键考虑因素的应用中能够更高效地设计和实现。