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

机译:Langmuir-Blodgett和铸膜中聚苯乙烯基链的光氧化

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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.
机译:聚(对 - 亚苯基亚乙烯基)(PPV)衍生物为它们在聚合物发光二极管(PLED)中的应用是众所周知的。这些衍生物是高度敏感的光致氧化,虽然,这主要是由于在聚合物主链乙烯基双键的断裂。在这项工作中,我们表明,朗缪尔 - 布洛杰特(LB)膜比一个PPV衍生物(OC /子1 / OC /子6 / -ppv)的流延膜退化较轻。两种膜具有相似的厚度(/ SPL SIM / 50纳米),以允许更现实的比较。光降解实验通过从卤素灯(50W,12V),放置在离样品的固定距离用白光照射的膜进行。衰减是由UV-Vis和红外光谱监测。结果表明,流延膜在约完全降解300分钟后,在LB花更长的时间,约1000分钟,对于流延膜即3倍的值。降解过程发生在至少两个阶段,其速率的计算假设反应遵循一级动力学。为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 /分钟/ SUP -1 /对分别流延和LB膜。对于第二个阶段的特征时间分别为5.6 / SPL次/ 10 / SUP -2 /和5.0 / SPL次/ 10 / SUP -3 /分钟/ SUP -1 /。的差异可以归因于LB更紧凑的形态比在流延膜。具有紧凑的形态氧在LB膜中的扩散受到阻碍,这将导致在降解过程中的延迟。

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