کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1289005 973280 2010 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Oligo(ethylene glycol)-functionalized disiloxanes as electrolytes for lithium-ion batteries
موضوعات مرتبط
مهندسی و علوم پایه شیمی الکتروشیمی
پیش نمایش صفحه اول مقاله
Oligo(ethylene glycol)-functionalized disiloxanes as electrolytes for lithium-ion batteries
چکیده انگلیسی

Functionalized disiloxane compounds were synthesized by attaching oligo(ethylene glycol) chains, –(CH2CH2O)–n, n = 2–7, via hydrosilation, dehydrocoupling, and nucleophilic substitution reactions and were examined as non-aqueous electrolyte solvents in lithium-ion cells. The compounds were fully characterized by 1H, 13C, and 29Si nuclear magnetic resonance (NMR) spectroscopy. Upon doping with lithium bis(oxalato)borate (LiBOB) or LiPF6, the disiloxane electrolytes showed conductivities up to 6.2 × 10−4 S cm−1 at room temperature. The thermal behavior of the electrolytes was studied by differential scanning calorimetry, which revealed very low glass transition temperatures before and after LiBOB doping and much higher thermal stability compared to organic carbonate electrolytes. Cyclic voltammetry measurements showed that disiloxane-based electrolytes with 0.8 M LiBOB salt concentration are stable to 4.7 V. The LiBOB/disiloxane combinations were found to be good electrolytes for lithium-ion cells; unlike LiPF6, LiBOB can provide a good passivation film on the graphite anode. The LiPF6/disiloxane electrolyte was enabled in lithium-ion cells by adding 1 wt% vinyl ethylene carbonate (VEC). Full cell performance tests with LiNi0.80Co0.15Al0.05O2 as the cathode and mesocarbon microbead (MCMB) graphite as the anode show stable cyclability. The results demonstrate that disiloxane-based electrolytes have considerable potential as electrolytes for use in lithium-ion batteries.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Power Sources - Volume 195, Issue 18, 15 September 2010, Pages 6062–6068
نویسندگان
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