کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7019664 | 1455936 | 2018 | 34 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Molecular engineering of organic-inorganic interface towards high-performance polyelectrolyte membrane via amphiphilic block copolymer
ترجمه فارسی عنوان
مهندسی مولکولی واسط آلی-معدنی نسبت به غشاء پلی الکترولیتی با عملکرد بالا از طریق کوپلیمر بلوک آمفیفیلی
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
تصفیه و جداسازی
چکیده انگلیسی
Fast proton transport, good stability and high fuel-blocking property in solid polyelectrolytes is of critical significance for a number of energy-conversion devices. However, the simultaneous enhancement of these properties has proved to be extremely challenging. Herein, we report a novel strategy to remarkably increase the comprehensive properties of Nafion-based mixed-matrix polyelectrolyte membranes through engineering organic-inorganic interfaces using amphiphilic block copolymer functionalized nanoparticles, SiO2 nanoparticles grafted with sulfonated polystyrene-b-polyperfluroallylbenzene. The amphiphilic block copolymer on nanoparticles imparts favorable interactions between the nanoparticles and amphiphilic Nafion, and thus facilitates the dispersion of nanoparticles and the reorganization of ion clusters. As a result, the mixed-matrix polyelectrolyte membrane with 2.5â¯wt% filler loading exhibits proton conductivities of 327â¯mSâ¯cmâ1 at 80â¯Â°C, 100% RH, and 63â¯mSâ¯cmâ1 at 80â¯Â°C, 50% RH, which is one of the highest proton conductivities ever reported. Moreover, the membrane also shows pronounced enhancements in thermal stability, dimensional stability, methanol-blocking property, and mechanical strength, in comparison with those of Nafion.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Membrane Science - Volume 563, 1 October 2018, Pages 1-9
Journal: Journal of Membrane Science - Volume 563, 1 October 2018, Pages 1-9
نویسندگان
Guangwei He, Jing Zhao, Chaoyi Chang, Mingzhao Xu, Shaofei Wang, Shengtao Jiang, Zhen Li, Xueyi He, Xingyu Wu, Zhongyi Jiang,