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PEO/LiClO_4复合体系电解质膜的固体NMR研究 被引量:1

SOLID-STATE NMR STUDY ON THE STRUCTURES OF PEO/LiClO_4 POLYMER ELECTROLYTE SYSTEM
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摘要 Lithium perchlorate/poly(ethylene oxide)complex,as potential polymer electrolytes,has attracted much research interests in the past decades,due to its great applicational significance.However,despite of great efforts,the mechanism of ion conducting of the system is still a topic with debates.In this work,the()13C CP/MAS spectra of a series of PEO/LiClO4 complexes were measured with different compositions.It is found that for the extensively dried samples,the()13C CP/MAS spectrum can exhibit up to 11 narrow peaks and the characteristics of the spectrum varies greatly with the composition.The()13C spin-lattice relaxation time(T1)of these narrow peaks are found to be comparable to that of the neat PEO crystalline region,indicating these narrow peaks are corresponding to the complexed crystalline structures.On the other hand,the()1H T1ρ of the narrow peaks are much longer than that of the neat PEO crystalline region,suggesting that the chain motion of PEO in the complex is greatly restricted due to the interaction between the oxygen of PEO and Li+.The aforementioned 11 peaks are assigned to three complexed crystalline structures.The conductivity of the complex sample decreases greatly when [O]∶ molar ratio decreases to 4∶1,while half of the ()13C peaks that are attributed to one crystalline structure varnish,indicating that there should exist certain kind of correlation between the complexed crystalline structure and the conductivity. Lithium perchlorate/poly(ethylene oxide)complex, as potential polymer electrolytes, has attracted much research interests in the past decades, due to its great applicational significance. However, despite of great efforts, the mechanism of ion conducting of the system is still a topic with debates. In this work, the ^13 C CP/MAS spectra of a series of PEO/LiClO4 complexes were measured with different compositions. It is found that for the extensively dried samples, the ^13C CP/MAS spectrum can exhibit up to 11 narrow peaks and the characteristics of the spectrum varies greatly with the composition. The ^13C spin-lattice relaxation time ( T1 ) of these narrow peaks are found to be comparable to that of the neat PEO crystalline region, indicating these narrow peaks are corresponding to the complexed crystalline structures. On the other hand, the ^1H T1ρ of the narrow peaks are much longer than that of the neat PEO crystalline region, suggesting that the chain motion of PEO in the complex is greatly restricted due to the interaction between the oxygen of PEO and Li^+ . The aforementioned 11 peaks are assigned to three complexed crystalline structures. The conductivity of the complex sample decreases greatly when [ O ] : [Li ] molar ratio decreases to 4 : 1, while half of the ^13C peaks that are attributed to one crystalline structure varnish, indicating that there should exist certain kind of correlation between the complexed crystalline structure and the conductivity.
出处 《高分子学报》 SCIE CAS CSCD 北大核心 2007年第12期1196-1200,共5页 Acta Polymerica Sinica
基金 国家自然科学基金(基金号20474019) 上海市科委重大基础研究(项目号04DZ14002)资助项目
关键词 聚合物固体电解质 PEO/HClO4复合物 固体高分辨核磁共振碳谱 电导率 结晶结构 Polymer electrolyte, PEO/LiClO4 complex, Solid-state high-resolution ^13C-NMR, Conductivity, Crystalline structures
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  • 1刘廷栋,许晓秋.淀粉类高吸水性树脂[J].精细化工,1993,10(5):45-50. 被引量:33
  • 2Wieczorck W,Such K,Chung S H.[J].J Phs Chem,1994,98:9047-9054.
  • 3Croce F,Persi L,Scrosati B,et al.[J].Electrochimica Acta,2001,46:2456-2461.
  • 4Wieczorek W,Siekierski M A.[J].J Appl Phys,1994,76:2220-2226.
  • 5Li T,Balbuena P B J.[J].Electrochem Soc,1999,146:3613.
  • 6Clancy S,Shriver D F,et al.[J].Macromolecules,1986,19(3):606.
  • 7Wright P V.[J].Electrochim Acta,1998,43:1137-1143.
  • 8Armand M B,Chabano J M,Duclot M J.Fast Ion Transport in Solids[M].New York:North Holland,1979.131.
  • 9Christian V,Nicholas,David J,et al.[J].Brit Polym J,1988,20:289-292.
  • 10Berthier C,Gorecki W,Minier M.Solid State Ionics,1983,11:91~95

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