کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1294738 1498332 2011 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
K+-doped poly(ε-caprolactone)/siloxane biohybrid electrolytes for electrochromic devices
موضوعات مرتبط
مهندسی و علوم پایه شیمی الکتروشیمی
پیش نمایش صفحه اول مقاله
K+-doped poly(ε-caprolactone)/siloxane biohybrid electrolytes for electrochromic devices
چکیده انگلیسی

Sol–gel derived KCF3SO3-doped di-urethane cross-linked poly(ε-caprolactone) (PCL(530))/siloxane ormolytes with ∞ > n ≥ 0.5 (n indicates the number of (C(= O)(CH2)5O) repeat units per K+ ion) have been studied. Xerogel samples with n ≥ 1 are thermally stable up to 235 °C. A small amount of PCL crystallites are formed in some dilute-to-concentrated samples. At n ≤ 4 a crystalline PCL(530)/siloxane–KCF3SO3 complex with unknown stoichiometry emerges. At n ≤ 2 this complex coexists with pure salt. At temperatures greater than 40 °C the composition which exhibits the highest ionic conductivity is n = 21. “Free” anions, coordinated CF3SO3− ions, contact ion pairs and several higher ionic aggregates are present in all the samples. The K+ ions bond to the oxygen atoms of the carbonyl groups of the urethane and ester groups, of the PCL (530) ether chain and of the triflate ions, at all salt concentrations. The ormolytes were successfully used in the assembly of prototype electrochromic devices (ECDs) that exhibit fast switching time and good open circuit memory. The ECD incorporating the ormolyte with n = 21 displays an average transmittance in the visible region of ca. 55% in the colored state and 76% in the bleached state.


► Potassium triflate-doped poly(ε-caprolactone)/siloxane network biohybrid were prepared.
► The electrolytes were used in the assembly of prototype electrochromic devices.
► The devices exhibit fast switching time and good open circuit memory.
► Average transmittances in the VIS region were 55 (colored) and 76% (bleached).

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Solid State Ionics - Volumes 204–205, 12 December 2011, Pages 129–139
نویسندگان
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