Contrasted dynamcis in the carrier relaxation in wide band gap oxides (Conference Presentation)

S. Guizard
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Abstract

Understanding the dynamics of excited carriers in wide band gap materials is a requirement to describe a broad range of physical mechanisms such as scintillator response, radiation induced damage of crystals, or laser-induced breakdown in optical materials and coatings. The difficulty arises from the competition between all the different relaxation channels: electron-phonon collisions, impact ionization, exciton and transient or permanent defects formation. Ultrashort laser pulses are ideal tool to investigate transparent materials since they allow to induce a large excitation density, and provide a temporal resolution high enough to track in real time the carrier relaxation. Two results concerning material which are extremely important for numerous application, namely silica (SiO2) and sapphire (Al2O3), and using different techniques, will be presented. First, in Al2O3, we have measured in a broad temporal range – from 30fs to 8 ns - the absorption induced by photo-excited carriers using time revolved absorption spectroscopy. By changing the intensity of the pump pulse, and thus the initial excitation density, we could measure the induced absorption on more than two orders of magnitude and demonstrate that the carrier relaxation dynamics exhibit a complex decay, and strongly depends on the initial density of excited carriers. We have developed a two steps model based on rate equations and taking into account the laser damping, which allows to fully reproduce the decay and the amplitude of the measured absorption. We demonstrate that in sapphire the electrons are mobile and can recombine with any hole. With this experiment and our modelling we can explain for instance the complex decay of luminescence observed when sapphire is irradiated with heavy ions or VUV photons. In SiO2, an important problem related to optical breakdown is the impact ionization which can lead to avalanche: electron excited by an intense laser can gain high kinetic energy in the conduction band and collide with valence electron (impact ionization) thus multiplying the excited carrier density. By using a sequence of double pump pulse we could control independently the two key parameters: plasma density and temperature. Under appropriate conditions, using time resolved interferometry as a probe, we could directly observe for the first time an electronic avalanche induced by a laser pulse. Again a complete modeling, using multiple rate equation and taking into account the laser propagation,; allow to completely describe the experimental results.
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宽频带隙氧化物中载流子弛豫的动力学对比(会议报告)
了解宽带隙材料中受激载流子的动力学是描述各种物理机制的必要条件,如闪烁体响应、晶体辐射诱导损伤或光学材料和涂层中的激光诱导击穿。困难来自于所有不同弛豫通道之间的竞争:电子-声子碰撞、冲击电离、激子和瞬态或永久缺陷的形成。超短激光脉冲是研究透明材料的理想工具,因为它们可以诱导大的激发密度,并提供足够高的时间分辨率来实时跟踪载流子弛豫。两个关于材料的结果是非常重要的许多应用,即二氧化硅(SiO2)和蓝宝石(Al2O3),并使用不同的技术,将提出。首先,在Al2O3中,我们使用时间旋转吸收光谱法在宽时间范围内(从30fs到8ns)测量了光激发载流子诱导的吸收。通过改变泵浦脉冲的强度,从而改变初始激发密度,我们可以测量两个数量级以上的诱导吸收,并证明载流子弛豫动力学表现出复杂的衰减,并且强烈依赖于被激发载流子的初始密度。我们开发了一个基于速率方程的两步模型,并考虑了激光阻尼,它可以完全再现衰减和测量吸收的幅度。我们证明了蓝宝石中的电子是可移动的,可以与任何空穴重新组合。通过这个实验和我们的模型,我们可以解释当蓝宝石被重离子或紫外光子照射时所观察到的复杂的发光衰减。在SiO2中,与光学击穿相关的一个重要问题是可能导致雪崩的冲击电离:被强激光激发的电子在导带中获得高动能并与价电子碰撞(冲击电离),从而使被激发的载流子密度倍增。利用双泵脉冲序列可以独立控制等离子体密度和温度这两个关键参数。在适当的条件下,利用时间分辨干涉法作为探针,首次可以直接观测到激光脉冲引起的电子雪崩。再次建立了完整的模型,采用多速率方程并考虑了激光的传播;允许完整地描述实验结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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