Photo-oxidation of polyphenylenevinylene chains in Langmuir-Blodgett and cast films

Marystela Ferreira, C. A. Olivati, D. Balogh, Roberto M. Faria, Osvaldo N. Oliveira
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Abstract

Poly(p-phenylene vinylene) (PPV) derivatives are well known for their applications in polymer light emitting diodes (PLEDs). These derivatives are highly susceptible to photooxidation though, which is mainly caused by the scission of the vinyl double bond on the polymer backbone. In this work, we show that Langmuir-Blodgett (LB) films are less degraded than cast films of a PPV derivative (OC/sub 1/OC/sub 6/-PPV). Both films had similar thickness (/spl sim/50 nm) to allow for a more realistic comparison. Photodegradation experiments were carried out by illuminating the films with white light from a halogen lamp (50W, 12V), placed at a fixed distance from the sample. The decay was monitored by UV-Vis and FTIR spectroscopies. The results showed that cast films are completely degraded in ca. 300 min, while LB took longer times, ca. 1000 min, i.e. 3 times the values for the cast films. The degradation process occurs in at least two stages, the rates of which were calculated assuming that the reaction follows a first order kinetics. The characteristic times for the first stage were 3.6/spl times/10/sup -2/and 1.3/spl times/10/sup -3/ min/sup -1/ for cast and LB films, respectively. For the second stage the characteristic times were 5.6/spl times/10/sup -2/ and 5.0/spl times/10/sup -3/min/sup -1/ . The differences can be attributed to the more compact morphology in the LB than in the cast films. With a compact morphology the diffusion of oxygen in the LB film is hampered and this causes a delay in the degradation process.
Langmuir-Blodgett和铸膜中聚苯乙烯链的光氧化
聚苯乙烯(PPV)衍生物以其在聚合物发光二极管(led)中的应用而闻名。然而,这些衍生物极易发生光氧化,这主要是由聚合物主链上的乙烯基双键断裂引起的。在这项工作中,我们证明了Langmuir-Blodgett (LB)薄膜比PPV衍生物(OC/sub 1/OC/sub 6/-PPV)的铸造膜的降解程度更低。两种薄膜具有相似的厚度(/spl sim/50 nm),以便进行更真实的比较。光降解实验是用50W, 12V的卤素灯在距离样品一定距离处用白光照射膜。用紫外可见光谱和红外光谱对其衰变进行了监测。结果表明,铸膜在约300 min内完全降解,而LB需要更长的时间,约1000 min,即铸膜值的3倍。降解过程发生在至少两个阶段,其速率被计算假设反应遵循一级动力学。铸型膜和LB膜第一阶段的特征时间分别为3.6/spl次/10/sup -2/和1.3/spl次/10/sup -3/ min/sup -1/。在第二阶段,特征时间为5.6/spl次/10/sup -2/和5.0/spl次/10/sup -3/min/sup -1/。这种差异可归因于LB中比铸态膜中更致密的形态。由于致密的形态,氧在LB膜中的扩散受到阻碍,这导致降解过程的延迟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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