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Investigation of low temperature solution-based deposition process for flexible electronics.

机译:柔性电子器件基于低温溶液的沉积工艺研究。

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The critical contribution of this dissertation is to provide a better understanding of the fundamental Chemical Bath Deposition (CBD) growth kinetic and mechanism for the well known II-VI semiconductor CdS using the newly developed continuous flow microreactor. This continuous flow microreactor provides the temporal resolution to control the homogeneous reaction of the chemical solution before it impinges on the substrate surface. This capability was used to decouple the homogeneous particle formation and deposition from the molecular level heterogeneous surface reaction to overcome the drawbacks associated with a conventional batch process. Transmission electron microscopy (TEM) analysis indicated an impinging flux without the formation of nanoparticles which could be obtained from this reactor in a short residence time. In addition, the reactor could be operated in a homogeneous particle formation regime. Size increasing CdS nanoparticles grown by homogeneous reaction were clearly observed from TEM and SEM micrographs by increasing the residence time from 1 to 280 sec using pre-heated precursor solutions. The formation of CdS nanorod and arrayed nanorod bundle structures using the CBD recipe were also observed in some areas and reported here for the first time. The growth kinetics were studied using a particle-free flux. The deposition results suggest that HS- ions formed through the thiourea hydrolysis reaction are the dominant sulfide ion source responsible for the CdS deposition rather than thioura itself that had been widely discussed in almost all of the previous literature. This finding could not be observed previously by a conventional CBD batch setup because all the reactant solutions were sequentially pulled into the reaction beaker and mixed all at once. An impinging flux without the formation of nanoparticles enables us to deposit extremely smooth and highly oriented nanocrystalline CdS semiconductor thin films at low temperature (80°C). Enhancement-mode functional thin film transistors with an effective mobility of mueff =1.46 cm2/V s, drain current on-to-off ratio of approximately 105 and turn-on voltage at 0 V were fabricated from the as-deposited films without any post annealing process. This microreactor could be adapted for the deposition of other compound semiconductor thin films such as highly transparent amorphous Indium Oxide (In2O3) thin films at low temperature (70°C) using chemical solution deposition and opens a low-cost avenue to fabricate thin film flexible electronics on polymeric substrates.
机译:本论文的关键作用是为使用新开发的连续流微反应器对众所周知的II-VI半导体CdS的基本化学浴沉积(CBD)生长动力学和机理提供更好的理解。这种连续流动的微反应器提供时间分辨率,以控制化学溶液在撞击到基材表面之前的均匀反应。该能力用于将均质颗粒的形成和沉积与分子水平的异质表面反应脱钩,从而克服了与常规分批工艺相关的缺点。透射电子显微镜(TEM)分析表明撞击的通量没有形成纳米颗粒,该纳米颗粒可以在短停留时间内从该反应器获得。另外,反应器可以在均匀的颗粒形成方案中操作。通过使用预热的前体溶液将停留时间从1秒增加到280秒,可以从TEM和SEM显微照片中清楚地观察到通过均相反应生长的尺寸增大的CdS纳米颗粒。在某些地区还观察到了使用CBD配方形成CdS纳米棒和排列的纳米棒束结构的情况,并首次在此报道。使用无颗粒通量研究了生长动力学。沉积结果表明,通过硫脲水解反应形成的HS-离子是引起CdS沉积的主要硫化物离子源,而不是几乎所有先前文献中已广泛讨论的硫脲本身。常规的CBD批处理设置以前无法观察到该发现,因为所有的反应物溶液都被依次拉入反应烧杯中并立即混合。没有形成纳米颗粒的撞击助焊剂使我们能够在低温(80°C)下沉积极其光滑和高度取向的纳米CdS半导体薄膜。由刚沉积的薄膜制造的增强型功能薄膜晶体管,其有效迁移率为mueff = 1.46 cm2 / V s,漏极电流开/关比约为105,导通电压为0 V,无任何后置退火过程。该微反应器可适用于使用化学溶液沉积技术在低温(70°C)下沉积其他化合物半导体薄膜,例如高透明非晶氧化铟(In2O3)薄膜,并开辟了低成本的途径来制造柔性薄膜聚合物基材上的电子设备。

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