Liu Sunhao, Wang Xiaoming, Dou Yixuan, Wang Qian, Kim Jiyoon, Slebodnick Carla, Yan Yanfa, Quan Lina
Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24061, United States.
Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo, Ohio 43606, United States.
J Am Chem Soc. 2024 May 1;146(17):11835-11844. doi: 10.1021/jacs.4c00619. Epub 2024 Apr 3.
Circularly polarized light emission is a crucial application in imaging, sensing, and photonics. However, utilizing low-energy photons to excite materials, as opposed to high-energy light excitation, can facilitate deep-tissue imaging and sensing applications. The challenge lies in finding materials capable of directly generating circularly polarized nonlinear optical effects. In this study, we introduce a chiral hybrid lead halide (CHLH) material system, R/S-DPEDPbBr·HO (DPED = 1,2-diphenylethylenediammonium), which can directly produce circularly polarized second harmonic generation (CP-SHG) through linearly polarized infrared light excitation, exhibiting a polarization efficiency as high as 37% at room temperature. To understand the spin relaxation mechanisms behind the high polarization efficiency, we utilized two models, so-called D'yakonov-Perel' (DP) and Bir-Aronov-Pikus (BAP) mechanisms. The unique zigzag inorganic frameworks within the hybrid structure are believed to reduce the dielectric confinement and exciton binding energy, thus enhancing spin polarization, especially in regions with a high excitation pump fluence based on the DP mechanism. In the case of low excitation pump fluence, the BAP mechanism dominates, as evidenced by the observed decrease in the polarization ratio from CP-SHG measurement. Using density functional theory analysis, we elucidate how the distinctive 8-coordination environment of lead bromide building blocks effectively suppresses spin-orbit coupling at the conduction band minimum. This suppression significantly diminishes spin-splitting, thereby slowing the spin relaxation rate.
圆偏振光发射在成像、传感和光子学中是一项关键应用。然而,与高能光激发相反,利用低能光子来激发材料有助于深部组织成像和传感应用。挑战在于找到能够直接产生圆偏振非线性光学效应的材料。在本研究中,我们引入了一种手性混合卤化铅(CHLH)材料体系,R/S-DPEDPbBr·HO(DPED = 1,2-二苯基乙二铵),它可以通过线偏振红外光激发直接产生圆偏振二次谐波产生(CP-SHG),在室温下表现出高达37%的偏振效率。为了理解高偏振效率背后的自旋弛豫机制,我们使用了两种模型,即所谓的D'yakonov-Perel'(DP)和Bir-Aronov-Pikus(BAP)机制。据信,混合结构中独特的之字形无机框架会降低介电限制和激子结合能,从而增强自旋极化,特别是在基于DP机制的高激发泵浦通量区域。在低激发泵浦通量的情况下,BAP机制占主导,这由CP-SHG测量中观察到的偏振比下降所证明。通过密度泛函理论分析,我们阐明了溴化铅结构单元独特的8配位环境如何有效地抑制导带最小值处的自旋轨道耦合。这种抑制显著减少了自旋分裂,从而减慢了自旋弛豫速率。