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Efficient terahertz-wave generation and its ultrafast optical modulation in charge ordered organic ferroelectrics

机译:电荷有序有机铁电体中的高效太赫兹波产生及其超快光调制

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摘要

Efficient terahertz (THz) wave generation in strongly correlated organic compounds α-(ET)2I3 and α′-(ET)2IBr2 (ET:bis(ethylenedithio)-tetrathiafulvalene) was demonstrated. The spontaneous polarization induced by charge ordering or electronic ferroelectricity was revealed to trigger the THz-wave generation via optical rectification; the estimated 2nd-order nonlinear optical susceptibility for α-(ET)2I3 is over 70 times larger than that for prototypical THz-source ZnTe. Ultrafast (<1 ps) and sensitive (∼40%) photoresponse of the THz wave was observed for α-(ET)2I3, which is attributable to photoinduced quenching of the polarization accompanied by insulator(ferroelectric)-to-metal transition. Modulation of the THz wave was observed for α′-(ET)2IBr2 upon the poling procedure, indicating the alignment of polar domains.
机译:证明了在强相关有机化合物α-(ET)2I3和α'-(ET)2IBr2(ET:双(亚乙基二硫代)-四硫富瓦烯)中产生的太赫兹(THz)波。电荷排序或电子铁电引起的自发极化被揭示通过光整流触发太赫兹波的产生;据估计,α-(ET)2I3的二阶非线性光学磁化率比典型THz源ZnTe的二阶非线性光学磁化率大70倍以上。对于α-(ET)2I3,观察到了THz波的超快(<1 ps)和灵敏(〜40%)的光响应,这归因于极化的光诱导猝灭以及绝缘体(铁电)向金属的转变。在极化过程中观察到了α'-(ET)2IBr2的太赫兹波的调制,表明极性域的排列。

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