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The self-activated radical doping effects on the catalyzed surface of amorphous metal oxide films

机译:自活化自由基掺杂对非晶态金属氧化物薄膜催化表面的影响

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摘要

In this study, we propose a self-activated radical doping (SRD) method on the catalyzed surface of amorphous oxide film that can improve both the electrical characteristics and the stability of amorphous oxide films through oxidizing oxygen vacancy using hydroxyl radical which is a strong oxidizer. This SRD method, which uses UV irradiation and thermal hydrogen peroxide solution treatment, effectively decreased the amount of oxygen vacancies and facilitated self-passivation and doping effect by radical reaction with photo-activated oxygen defects. As a result, the SRD-treated amorphous indium-gallium-zinc oxide (a-IGZO) thin film transistors (TFTs) showed superior electrical performances compared with non-treated a-IGZO TFTs. The mobility increased from 9.1 to 17.5 cm2/Vs, on-off ratio increased from 8.9 × 107 to 7.96 × 109, and the threshold voltage shift of negative bias-illumination stress for 3600 secs under 5700 lux of white LED and negative bias-temperature stress at 50 °C decreased from 9.6 V to 4.6 V and from 2.4 V to 0.4 V, respectively.
机译:在这项研究中,我们提出了一种在非晶氧化物膜的催化表面上进行自活化自由基掺杂(SRD)的方法,该方法可以通过使用强氧化剂羟基自由基氧化氧空位来改善非晶氧化物膜的电特性和稳定性。 。这种SRD方法采用紫外线照射和热过氧化氢溶液处理,通过与光活化氧缺陷的自由基反应有效地减少了氧空位的数量,并促进了自钝化和掺杂效果。结果,与未处理的a-IGZO TFT相比,经SRD处理的非晶铟镓锌氧化物(a-IGZO)薄膜晶体管(TFT)表现出优异的电气性能。迁移率从9.1增加到17.5 cm 2 / Vs,开关比从8.9×10 7 增加到7.96×10 9 在5700 lux的白色LED下,负偏压照明应力在3600 s内的阈值电压漂移和50°C下的负偏压温度应力分别从9.6 V降至4.6 V和从2.4 V降至0.4V。

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