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Space Charge in Thermally Poled Fused Silica

机译:热稳定的熔化二氧化硅中的空间电荷

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Various groups continue to make progress improving in-line and all-fiber electro-optic switches and wavelength converters based on thermal poling of fused silica. However, there is still much to be understood of the thermal poling processes that lead to the establishment of the second-order nonlinearity (Χ~(2)) that makes these devices possible. The predictable control of the the Χ~(2) distribution is a difficult endeavor. The location, strength, and profile of the Χ~(2) distribution based on poling conditions has not yet been fully described, although several groups have contributed to our basic understanding using Maker fringes, etching techniques, laser-induced pulse probes, and other measurement techniques. We performed several Secondary Ion Mass Spectrometry (SIMS) analyses to complement earlier etching and electrical current/second harmonic generation (SHG) measurements in an attempt to understand the dynamic behavior of the Χ~(2) distribution. These measurements revealed an alkali depleted space charge region whose depth into the glass evolves logarithmically with poling time. Our data demonstrate that Na~+, Li~+, and K~+ are mobilized by thermal poling in type II fused silica (flame fused natural quartz, 1-10 ppm alkali impurity levels). We also suspect H~+ or H_3O~+ plays a role, due to the abundance of H and H_2O in glass surfaces and air. We observed that the poling environment plays an important role in the charge profile and depth of the space charge region. Impurities from the electrodes, handling, the atmosphere, as well as impurities already adsorbed onto the glass surface, act as reservoirs for an ion exchange process in which alkali ions are pulled into the space charge region. We have observed that the presence of impurities near the glass surface can reduce overall mobility and slow formation of the space charge region. Pruneri et al. have also noted that the poling atmosphere makes a difference in the Χ~(2) distribution, observing that given similar poling times, the Χ~(2) distribution extends further into the glass for vacuum-poled samples than for samples poled in air.
机译:各种组继续基于熔化二氧化硅的热抛光改善在线和全纤维电光开关和波长转换器的进展。然而,仍有许多值得理解的热杆过程,导致建立二阶非线性(χ〜(2)),使得这些装置成为可能。可预测的χ〜(2)分布的控制是难以努力的努力。尚未完全描述基于极化条件的χ〜(2)分布的位置,强度和概况,尽管有几个组使用Maker Fringes,蚀刻技术,激光诱导的脉冲探针等我们的基本理解促进了我们的基本理解。测量技术。我们进行了几个二次离子质谱(SIMS)分析以补充更早的蚀刻和电流/第二谐波产生(SHG)测量,以了解χ〜(2)分布的动态行为。这些测量揭示了一种碱耗尽的空间电荷区域,其深度进入玻璃上的对数地发出,极化时间。我们的数据表明Na〜+,Li +和K〜+通过II型熔融二氧化硅(火焰融合天然石英,1-10ppm碱杂质水平)的热抛光动员。我们也怀疑H〜+或H_3O〜+起作用,由于玻璃表面和空气中的H和H_2O丰富。我们观察到,极化环境在空间电荷区域的充电轮廓和深度中起重要作用。来自电极,处理,气氛以及已经吸附在玻璃表面上的杂质的杂质,作为用于离子交换过程的储存器,其中碱金属离子被拉入空间电荷区域。我们已经观察到,玻璃表面附近的杂质的存在可以降低空间电荷区域的整体迁移率和缓慢形成。 pruneri等。还注意到极化气氛在χ〜(2)分布中具有差异,观察给定相似的抛光时间,χ〜(2)分布进一步延伸到玻璃中,用于真空抛光样品,而不是在空气中抛光的样品。

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