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Direct and simultaneous observation of ultrafast electron and hole dynamics in germanium

机译:直接和同时观察锗中超快电子和孔动力学

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Understanding excited carrier dynamics in semiconductors is crucial for the development of photovoltaics and efficient photonic devices. However, overlapping spectral features in optical pump-probe spectroscopy often render assignments of separate electron and hole carrier dynamics ambiguous. Here, ultrafast electron and hole dynamics in germanium nanocrystalline thin films are directly and simultaneously observed by ultrafast transient absorption spectroscopy in the extreme ultraviolet at the germanium M4,5 edge. We decompose the spectra into contributions of electronic state blocking and photo-induced band shifts at a carrier density of 8 × 1020?cm?3. Separate electron and hole relaxation times are observed as a function of hot carrier energies. A first-order electron and hole decay of ~1?ps suggests a Shockley–Read–Hall recombination mechanism. The simultaneous observation of electrons and holes with extreme ultraviolet transient absorption spectroscopy paves the way for investigating few- to sub-femtosecond dynamics of both holes and electrons in complex semiconductor materials and across junctions.
机译:了解半导体中的励磁载体动态对于光伏和高效光子器件的开发至关重要。然而,光学泵探针光谱中的重叠光谱特征通常呈现单独的电子和孔载体动力学的分配模糊。这里,通过在锗M 4,5 边缘处的极端紫外线中的超快瞬态吸收光谱直接且同时观察在锗纳米晶薄膜中的超快电子和空穴动力学。我们将光谱分解为电子状态阻塞和光引起的带密度为8×10 20 Δcm 3 的光带偏移的贡献。作为热载体能量的函数观察单独的电子和孔弛豫时间。一阶电子和孔衰减的〜1?PS表明了震撼读音乐厅的重组机制。具有极端紫外瞬态吸收光谱的电子和孔的同时观察铺设了在复杂的半导体材料和交叉口中研究孔和电子的少数至子模秒动态的方式。

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