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Exploiting Mixed Valence Charge Transfer for Electrochromic and Electrofluorochromic Use.
Anthony Raj, Mohan Raj; Yao, Chengzhang; Frémont, Mathieu; Skene, W G.
Afiliación
  • Anthony Raj MR; Laboratoire de caractérisation photophysique des matériaux conjugués, Département de Chimie, Université de Montréal, CP 6128, succ. Centre-ville, Montréal, Québec, H3C 3J7, Canada.
  • Yao C; Laboratoire de caractérisation photophysique des matériaux conjugués, Département de Chimie, Université de Montréal, CP 6128, succ. Centre-ville, Montréal, Québec, H3C 3J7, Canada.
  • Frémont M; Laboratoire de caractérisation photophysique des matériaux conjugués, Département de Chimie, Université de Montréal, CP 6128, succ. Centre-ville, Montréal, Québec, H3C 3J7, Canada.
  • Skene WG; Laboratoire de caractérisation photophysique des matériaux conjugués, Département de Chimie, Université de Montréal, CP 6128, succ. Centre-ville, Montréal, Québec, H3C 3J7, Canada.
Chemistry ; 30(42): e202401417, 2024 Jul 25.
Article en En | MEDLINE | ID: mdl-38970532
ABSTRACT
An asymmetric mixed valence fluorophore with two different electron rich termini was investigated as a dual-role active material for electrochromism and electrofluorochromism. The fluorescence quantum yield (Φfl) and emission wavelength of the fluorophore were dependent on solvent polarity. The quantum yield of the material in an electrolyte gel, on a glass substrate and in a device was 40 %, 20 % and 13 % respectively. The fluorophore further underwent two near-simultaneous electrochemical oxidations. The first oxidation resulted in a 1000 nm red shift in the absorption to broadly absorb in the NIR, corresponding to the intervalence charge transfer (IVCT). Whereas the second oxidation led to a perceived green color at 715 nm with the extinction of the NIR absorbing IVCT. Owing to the dissymmetry of the fluorophore along with its two unique oxidation sites, the IVCT gives rise to a mixed valence transfer charge (MVCT). The coloration efficiency of the fluorophore in both solution and a device was 1433 and 200 cm2 C-1, respectively. The fluorescence intensity could be reversibly modulated electrochemically. The photoemission intensity of the fluorophore was modulated with applied potential in an operating electrochromic/electrofluorochromic device. Both the dual electrochromic and the electrofluorochromic behavior of the fluorophore were demonstrated.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Alemania