论文标题

通过连贯的拉曼散射,等离子体腔中加速的分子振动衰减和抑制电子非线性

Accelerated Molecular Vibrational Decay and Suppressed Electronic Nonlinearities in Plasmonic Cavities through Coherent Raman Scattering

论文作者

Jakob, Lukas A., Deacon, William M., Arul, Rakesh, de Nijs, Bart, Mueller, Niclas S., Baumberg, Jeremy J.

论文摘要

分子振动及其动力学对于纳米级设备的电子和热传输以及分子催化至关重要。通过使用等离子体纳米antennas的三色分辨相干抗烟药拉曼光谱(TRCAR)研究了<100个分子的振动动力学。这可以从四波混合(FWM)中分离出分子信号,同时使用异常低的纳米瓦特功率,以避免通过单光子锁定检测来避免分子损伤。与等离子纳米颗粒相比,发现FWM在NM宽的等离子间隙中得到了强烈抑制。双苯基-4-硫醇分子的超快速振动衰减速率通过这些等离激体纳米腔内增强的脉冲光场激发的局部非平衡温度的瞬时升高而加速了十倍。分离振动种群衰减和脱落的贡献仔细地探索了这些紧密约束分子的振动衰减通道。这种极端的等离激元增强纳米仪为测量单分子振动耦合动力学和多样的分子验光力学现象开辟了前景。

Molecular vibrations and their dynamics are of outstanding importance for electronic and thermal transport in nanoscale devices as well as for molecular catalysis. The vibrational dynamics of <100 molecules are studied through three-colour time-resolved coherent anti-Stokes Raman spectroscopy (trCARS) using plasmonic nanoantennas. This isolates molecular signals from four-wave mixing (FWM), while using exceptionally low nanowatt powers to avoid molecular damage via single-photon lock-in detection. FWM is found to be strongly suppressed in nm-wide plasmonic gaps compared to plasmonic nanoparticles. The ultrafast vibrational decay rates of biphenyl-4-thiol molecules are accelerated ten-fold by a transient rise in local non-equilibrium temperature excited by enhanced, pulsed optical fields within these plasmonic nanocavities. Separating the contributions of vibrational population decay and dephasing carefully explores the vibrational decay channels of these tightly confined molecules. Such extreme plasmonic enhancement within nanogaps opens up prospects for measuring single-molecule vibrationally-coupled dynamics and diverse molecular optomechanics phenomena.

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