Reversible Control of Radius and Morphology of Fluorene-Azobenzene Copolymer Nanowires by Light Exposure

被引:10
作者
Cheng, Hoi Lok [1 ,2 ]
Tang, Michael T. [1 ,3 ]
Tuchinda, Wasin [1 ,2 ]
Enomoto, Kazuyuki [1 ,2 ]
Chiba, Atsuya [4 ]
Saito, Yuichi [4 ]
Kamiya, Tomihiro [4 ]
Sugimoto, Masaki [4 ]
Saeki, Akinori [1 ]
Sakurai, Tsuneaki [1 ]
Omichi, Masaaki [1 ]
Sakamaki, Daisuke [1 ]
Seki, Shu [1 ,2 ]
机构
[1] Osaka Univ, Dept Appl Chem, Grad Sch Engn, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Int Coll, Toyonaka, Osaka 5600043, Japan
[3] Univ Calif San Diego, Dept Nanoengn, Warren Coll, La Jolla, CA 92093 USA
[4] Japan Atom Energy Agcy, Takasaki Adv Radiat Res Inst, Takasaki, Gunma 3701292, Japan
来源
ADVANCED MATERIALS INTERFACES | 2015年 / 2卷 / 01期
关键词
CONJUGATED POLYMERS; FABRICATION; ENERGY; MEMORIES; MOIETIES;
D O I
10.1002/admi.201400450
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparation of photoresponsive polymer nanowires comprising photochromic azobenzene (Azo) and p-conjugated fluorene (FO) units is reported. Well-defined and uniform nanowires of the copolymer (PFOAzo) were successfully fabricated by the single particle nanofabrication technique after optimizing the FO: Azo ratio and the development conditions. Azo units in the PFOAzo nanowires underwent reversible trans-cis-trans isomerization upon exposure to ultraviolet or visible light, leading to changes in the radius (between ca. 6 and 8 nm) and morphology (straight or wavy) of the nanowires. The oligo(alkylfluorene) units in the backbone are found to profit the crosslinking efficiency upon high-energy ion beam irradiation, and more importantly, provide sufficient flexibility to allow reversible photoswitching. This demonstration of the photoluminescence, semiconducting, and mechanical properties of the PFOAzo nanowires is an important advance in the evolution of electro-mechanical nanomaterials.
引用
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页数:9
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