Light-responsive color switching of self-doped TiO2-x/WO3•0.33H2O hetero-nanoparticles for highly efficient rewritable paper

被引:32
|
作者
Zhao, Jingmei [1 ,2 ]
Liu, Luntao [1 ,2 ]
Zhang, Yun [1 ,2 ]
Feng, Zhenyu [1 ,2 ]
Zhao, Feifei [1 ,2 ]
Wang, Wenshou [1 ,2 ]
机构
[1] Shandong Univ, Natl Engn Res Ctr Colloidal Mat, Jinan 250100, Peoples R China
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
light-response; color switching; self-doping; hetero-nanoparticles; rewritable paper; ELECTRON-SPIN-RESONANCE; PHOTOCATALYTIC DEGRADATION; ANATASE TIO2; SURFACE; WO3;
D O I
10.1007/s12274-020-3061-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Smart materials that reversibly change color upon light illumination are widely explored for diverse appealing applications. However, light-responsive color switching materials are mainly limited to organic molecules. The synthesis of inorganic counterparts has remained a significant challenge because of their slow light response and poor reversibility. Here, we report a seeded growth strategy for the synthesis of TiO2-x/WO3 center dot 0.33H(2)O hetero-nanoparticles (HNPs) with networked wire-like structure of similar to 10 nm in diameters that enable the highly reversible light-responsive color switching properties. For the TiO2-x/WO3 center dot 0.33H(2)O HNPs, Ti(3+)species self-doped in TiO(2-x)nanoparticles (NPs) act as efficient sacrificial electron donors (SEDs) and Ti-O-W linkages formed between TiO(2-x)and WO3 center dot 0.33H(2)O NPs ensure the nanoscale interfacial contact, endowing the HNPs enhanced photoreductive activity and efficient interfacial charge transfer upon ultraviolet (UV) illumination to achieve highly efficient color switching. The TiO2-x/WO3 center dot 0.33H(2)O HNPs exhibits rapid light response (< 15 s) and long reversible color switching cycles (> 180 times). We further demonstrate the applications of TiO2-x/WO3 center dot 0.33H(2)O HNPs in ink-free, light-printable rewritable paper that can be written on freehand or printed on through a photomask using UV light. This work opens an avenue for designing inorganic light-responsive color switching nanomaterials and their smart applications.
引用
收藏
页码:165 / 171
页数:7
相关论文
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