光致变色
光致发光
材料科学
光化学
拉曼光谱
电子顺磁共振
螺吡喃
离子
纳米技术
光电子学
固态
齿合度
分子
可见光谱
作者
Tiantian Gong,Shuo Wang,Yanan Chen,Lijuan Chen,Junwei Zhao
标识
DOI:10.1021/acsami.5c19350
摘要
High Resolution Image Download MS PowerPoint Slide Developing photoresponsive materials exhibiting both photochromic and photoluminescent switching properties presents a significant scientific challenge. Herein, a tetrahydroxyhexanedioic acid-ornamented phosphite-and-bismuth-bridging multi-Eu III encapsulated phospho(III)tungstate [H 2 N(CH 3 ) 2 ] 8 Na 6 [Eu 4 W 6 Bi 2 O 12 (HP III O 3 ) 2 (H 2 THHA) 2 (H 2 O) 10 ][HP III W 9 O 33 ] 4 · 50H 2 O ( 1, H 6 THHA = tetrahydroxyhexanedioic acid) was obtained, whose polyanion encompasses four trivacant Keggin-type [B-α-HP III W 9 O 33 ] 8– units and a complex heterometallic {[Eu 4 W 6 Bi 2 O 12 (HP III O 3 ) 2 (H 2 THHA) 2 (H 2 O) 10 ]} 14+ cluster, wherein [HP III O 3 ] 2– anions and Bi 3+ ions serve as bridging linkers, while the long-chain multidentate H 2 THHA 4– ligands coordinate with W and Bi atoms. Intriguingly, 1 exhibits remarkable photochromic behavior upon UV irradiation, rapidly changing from colorless to blue within 180 s and reverting to its original colorless state within 5 h in the absence of irradiation, suggesting its potential as a fast-responsive photochromic material. Moreover, the photoluminescence of 1 can be reversibly modulated through photochromic activation, indicating its applicability as a molecular switch. Importantly, the reversible color change can be cycled at least ten times without significant degradation. Spectroscopic analyses including IR, XRD, XPS, EPR and Raman confirm that the photochromic behavior arises from the structural reduction of W VI centers to W V species. Furthermore, the 1 -based photochromic film was fabricated and applied for erasable ink-free printing. This work highlights the effectiveness of integrating multicomponent systems in the design of polyoxometalates and broadens the scope of research on the photochromic properties of these materials.
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