Looking at Electron Dynamics to Better Understand Photo-Active Materials

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Abstract

The generation of free and energetic electrons is the key to the next generation of photo-voltaic and photo-catalysts. In order to produce such electrons, the sunlight is so far the most promising sustainable source of energy. However, the conversion efficiency from light to the liberation of a functional electron depends on numerous factors and processes that are difficult to account for. One of the reasons is the difficulty of monitoring the early electron dynamics such as the charge separation event and the subsequent electronic relaxation and migration. Here, I propose the use of ultrafast transient absorption spectroscopy to watch these electronic events “live” in the femto- to nano-seconds (10-15-10-9 sec.) time scales. In this presentation, I will demonstrate this technique on iron and copper oxides thin films. In this study, we produce ultrashort laser pulses to mimic sunlight and trigger charge separations that ultimately lead to the generation of the reactive oxygen species that confer the films their antibacterial properties. With this technique, we are able to harvest information such as the charge separation efficiency, electron dynamics, excited state’s bandgap energy, and even material deformation upon photo-excitation, all of which are key to understand, control and enhance the conversion process.
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通过电子动力学来更好地理解光活性材料
自由和高能电子的产生是下一代光伏和光催化剂的关键。为了产生这样的电子,太阳光是迄今为止最有希望的可持续能源。然而,从光到释放功能电子的转换效率取决于许多难以解释的因素和过程。其中一个原因是难以监测早期的电子动力学,如电荷分离事件和随后的电子弛豫和迁移。在这里,我建议使用超快瞬态吸收光谱在飞秒到纳秒(10-15-10-9秒)的时间尺度上观察这些电子事件。在这次演讲中,我将在铁和铜氧化物薄膜上演示这种技术。在这项研究中,我们产生超短激光脉冲来模拟阳光,并触发电荷分离,最终导致活性氧的产生,从而赋予薄膜抗菌性能。利用该技术,我们可以获得电荷分离效率、电子动力学、激发态带隙能量,甚至光激发时的材料变形等信息,这些都是理解、控制和增强转换过程的关键。
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