4 years ago

In situ synthesis of coaxial CsPbX3@polymer (X=Cl, Br, I) fibers with significantly enhanced water stability

Wenna Liu, Hui Fu, Hao Liao, Zhao Liang, Yumin Ye, Jinju Zheng, Weiyou Yang
Inorganic perovskites (IP) CsPbX3 (X = Cl, Br, I) have rapidly emerged as excellent candidate materials for optoelectronic devices, due to their superior optical/electronic performances. However, poor stability related to their intrinsic ionic character greatly limits their practical applications. Here, a coaxial electrospinning strategy is reported for in situ growth of IP nanocrystals (NCs) in polymer fibers with core/shell structure, which is based on one-step electrospinning of core solutions containing IPs precursors and polymers while shell solutions containing polymers only. Contributed to the coaxial structure, the NCs in/out the surface of the core were further encapsulated by the shell layer. Compared with the traditional CsPbBr3@polymer fibers without shell layer, the obtained coaxial fibers exhibit fundamentally improved water stabilities. Their PL quantum yield (QY) retains beyond 90% of its original value after being immersed in water for 10 d and maintains over 84% after 180 d.
You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.