P. Kaatz, P. Prêtre, U. Meier, U. Stalder, C. Bosshard, P. Günter
{"title":"非线性光学侧链聚酰亚胺聚合物的弛豫过程","authors":"P. Kaatz, P. Prêtre, U. Meier, U. Stalder, C. Bosshard, P. Günter","doi":"10.1201/9781003078197-10","DOIUrl":null,"url":null,"abstract":"Optical, nonlinear optical and electro-optic properties of modified side-chain polyimide polymers as shown in Fig. 1 have been determined. Relaxation processes in these nonlinear optical (NLO) polymers are of considerable interest for obtaining a better understanding of the long-term stability of potential devices fabricated from these materials. The relaxation mechanisms of the side-chain chromophores have been investigated above and below the glass transition by second-harmonic decay, dielectric relaxation and differential scanning calorimetry measurements. We find that the time-temperature relaxation behavior of the NLO chromophores in a variety of polymer systems can be understood in terms of current phenomenological descriptions of the glass transition with the aid of a scaling relation.","PeriodicalId":248672,"journal":{"name":"Poled Polymers and their Applications to SHG and EO Devices","volume":"15 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Relaxation Processes in Nonlinear Optical Side-Chain Polyimide Polymers\",\"authors\":\"P. Kaatz, P. Prêtre, U. Meier, U. Stalder, C. Bosshard, P. Günter\",\"doi\":\"10.1201/9781003078197-10\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Optical, nonlinear optical and electro-optic properties of modified side-chain polyimide polymers as shown in Fig. 1 have been determined. Relaxation processes in these nonlinear optical (NLO) polymers are of considerable interest for obtaining a better understanding of the long-term stability of potential devices fabricated from these materials. The relaxation mechanisms of the side-chain chromophores have been investigated above and below the glass transition by second-harmonic decay, dielectric relaxation and differential scanning calorimetry measurements. We find that the time-temperature relaxation behavior of the NLO chromophores in a variety of polymer systems can be understood in terms of current phenomenological descriptions of the glass transition with the aid of a scaling relation.\",\"PeriodicalId\":248672,\"journal\":{\"name\":\"Poled Polymers and their Applications to SHG and EO Devices\",\"volume\":\"15 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poled Polymers and their Applications to SHG and EO Devices\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1201/9781003078197-10\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poled Polymers and their Applications to SHG and EO Devices","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1201/9781003078197-10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Relaxation Processes in Nonlinear Optical Side-Chain Polyimide Polymers
Optical, nonlinear optical and electro-optic properties of modified side-chain polyimide polymers as shown in Fig. 1 have been determined. Relaxation processes in these nonlinear optical (NLO) polymers are of considerable interest for obtaining a better understanding of the long-term stability of potential devices fabricated from these materials. The relaxation mechanisms of the side-chain chromophores have been investigated above and below the glass transition by second-harmonic decay, dielectric relaxation and differential scanning calorimetry measurements. We find that the time-temperature relaxation behavior of the NLO chromophores in a variety of polymer systems can be understood in terms of current phenomenological descriptions of the glass transition with the aid of a scaling relation.