Giri Sajal Kumar, Schatz George C
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, USA.
J Chem Phys. 2024 Jul 28;161(4). doi: 10.1063/5.0216887.
In this study, we investigate second- and third-harmonic generation processes in Au nanorod systems using the real-time time-dependent density functional tight binding method. Our study focuses on the computation of nonlinear signals based on the time dependent dipole response induced by linearly polarized laser pulses interacting with nanoparticles. We systematically explore the influence of various laser parameters, including pump intensity, duration, frequency, and polarization directions, on harmonic generation. We demonstrate all the results using Au nanorod dimer systems arranged in end-to-end configurations, and disrupting the spatial symmetry of regular single nanorod systems is crucial for second-harmonic generation processes. Furthermore, we study the impact of nanorod lengths, which lead to variable plasmon energies, on harmonic generation, and estimates of polarizabilities and hyper-polarizabilities are provided.
在本研究中,我们使用实时含时密度泛函紧束缚方法研究了金纳米棒系统中的二次和三次谐波产生过程。我们的研究重点是基于与纳米粒子相互作用的线偏振激光脉冲所诱导的含时偶极响应来计算非线性信号。我们系统地探讨了各种激光参数,包括泵浦强度、持续时间、频率和偏振方向,对谐波产生的影响。我们使用端对端配置的金纳米棒二聚体系统展示了所有结果,并且破坏规则单纳米棒系统的空间对称性对于二次谐波产生过程至关重要。此外,我们研究了导致等离激元能量可变的纳米棒长度对谐波产生的影响,并给出了极化率和超极化率的估计值。