Ln3+-Induced Diblock Copolymeric Aggregates for Fully Flexible Tunable White-Light Materials.
Xinzhi WangJianguo TangGuanghui WangWei WangJunjie RenWei DingXinbo ZhangYao WangWenfei ShenLinjun HuangLaurence A BelfiorePublished in: Nanomaterials (Basel, Switzerland) (2019)
In this research contribution, nano-aggregates have been fabricated by introducing lanthanide (Ln3+) ions into solutions of amphiphilic diblock copolymers of polystyrene-b-poly (acrylic acid) (PS-b-PAA). The coordination of acrylic acid segments to lanthanide cations induces diblock copolymer (BCPs) self-assembly in order to design stable white luminescent hybrid nanoparticles with fine uniform particle size. The introduction of Ln3+ ions (Eu3+ and Tb3+) bestows the micelles, precisely white light, upon excitation of 342 nm. Lanthanide coordination cross-linking of poly (acrylic acid) segments, or blocks, endows the micelles higher thermal stability than that of BCPs micelles without cross-linking. As the most important key point of this work, the regular and stable nano-particles with high emission quality can make fully flexible electroluminescent devices with self-formation or uncoordinated into polymer hosts. Instead of inorganic luminescent nanoparticles with hard cores, this method can potentially apply for fully flexible white-light emitting diodes (FFWLEDs).
Keyphrases
- energy transfer
- quantum dots
- metal organic framework
- drug delivery
- drug release
- cancer therapy
- single molecule
- sensitive detection
- solid state
- photodynamic therapy
- hyaluronic acid
- mycobacterium tuberculosis
- water soluble
- air pollution
- high glucose
- quality improvement
- light emitting
- drug induced
- oxidative stress
- aqueous solution