4.7 Article

Phase Separated Morphology of Ferroelectric-Semiconductor Polymer Blends Probed by Synchrotron X-ray Methods

期刊

MACROMOLECULES
卷 48, 期 16, 页码 5861-5867

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.5b01354

关键词

-

资金

  1. Air Force Office of Scientific Research (AFOSR) under MURI Grant [FA9S50-12-1-0038]
  2. National Science Foundation Graduate Research Fellowship [DGE-1144085]
  3. ALS Doctoral Fellowship
  4. U.S. Department of Energy [DE-ACO2-05CH11231]
  5. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-ACO2-98CH10886]
  6. MRSEC Program of the NSF [DMR 1121053]

向作者/读者索取更多资源

Control of the domain size and morphology of ferroelectric-semiconductor polymer blend thin films is essential for producing working organic ferroelectric resistive switches that can be used for low-cost, flexible memory applications. However, improvements in characterization techniques that can selectively probe these polymers are still needed. The unique core-level absorption profiles of these polymers make synchrotron based soft X-ray techniques ideal to achieve contrast and chemical sensitivity between polymers and characterize thin film morphology. Transmission soft Xray microscopy and scattering reveal that a phase separated structure exists through the bulk for a blend of a semicrystalline semiconducting polythiophene with a functionalized side chain and a well-studied ferroelectric polymer. Surface sensitive soft X-ray spectroscopy and wide-angle X-ray scattering suggest a potential enhancement of polythiophene at the film surface, and that the surface layer is more amorphous in character. This work demonstrates the utility of soft X-rays to characterize ferroelectric-semiconductor polymer blends both in the bulk and at the film surface. Understanding differences in composition and morphology between the bulk and thin film interfaces is critical to further improve organic-based memory technology.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据