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首页> 外文期刊>The Journal of Chemical Physics >Dynamics of sodium ions in NaClO4 complexed in poly(propylene-oxide): A Na-23 nuclear magnetic resonance study [Review]
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Dynamics of sodium ions in NaClO4 complexed in poly(propylene-oxide): A Na-23 nuclear magnetic resonance study [Review]

机译:聚环氧丙烷中NaClO4中钠离子的动力学:Na-23核磁共振研究[综述]

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Amorphous poly(propylene oxide), PPO (molecular weights, 425 and similar to 10(6)), complexed with NaClO4 salt has ionic conductivities as high as 10(-5) S/cm at room temperature. In an attempt to directly study the dynamics of the Na+ ions, (I=3/2) nuclear magnetic resonance (NMR) spin-lattice relaxation times, T-1, and spin-spin relaxation times, T-2, at a resonance frequency of 77.0 MHz have been measured over the temperature range from 150 to 390 K. A range of salt compositions [(PPO)(n)NaClO4; n=8-30] have been investigated. In addition, the glass transition temperature for each sample is reported. The recovery of equilibrium magnetization following a pi/2 pulse is biexponential as expected for a spin I=3/2 system in the viscous liquid region. Below T-g a better fit to the magnetization recovery curve can be obtained if Kohlrausch-Williams-Watts (KWW) functions are used in place of the exponential functions. At low temperature the molecular motion has slowed to the point where a common spin temperature is not achieved by ionic diffusion. Two T-2 values are observed over a limited temperature region near the T1 minimum. In the remaining low temperature region only the T-2 associated with the central transition could be determined because the large Na-23 quadrupole coupling constant made detection of the satellite transitions impossible. There is no evidence from the NMR relaxation time data for two Na+ populations. The experimental spin-lattice relaxation times can be analyzed to determine the correlation time for the ionic motion as a function of reciprocal temperature. The correlation time data display a distinct change in behavior at T-g which is interpreted as an indication of a crossover between two ionic transport mechanisms. Plots of T-1 as a function of T-g/T indicate that dynamics for T>T-g are largely determined by the flexibility of the polymer host (the alpha process) whereas a different process dominates for T>T-g (presumably the beta process). A comparison of correlation times derived from NMR relaxation times and ionic conductivities show a marked difference especially in the region of T-g. The conductivity decreases rapidly while the sodium ion motion continues with a correlation time similar to 10(-6) s through the glass transition. (C) 1998 American Institute of Physics. [References: 102]
机译:与NaClO4盐络合的非晶态聚环氧丙烷PPO(分子量425,与10(6)相似)在室温下的离子电导率高达10(-5)S / cm。为了直接研究Na +离子的动力学,共振时(I = 3/2)核磁共振(NMR)自旋晶格弛豫时间T-1和自旋自旋弛豫时间T-2在150至390 K的温度范围内已测得77.0 MHz的频率。一系列盐组成[[PPO](n)NaClO4; n = 8-30]已被研究。另外,报告了每个样品的玻璃化转变温度。 pi / 2脉冲后,平衡磁化强度的恢复是双指数的,这对于粘性液体区域中的自旋I = 3/2系统是预期的。如果使用Kohlrausch-Williams-Watts(KWW)函数代替指数函数,则在T-g以下可更好地拟合磁化恢复曲线。在低温下,分子运动已减慢到无法通过离子扩散实现普通自旋温度的程度。在接近T1最小值的有限温度区域内观察到两个T-2值。在其余的低温区域中,只能确定与中央过渡有关的T-2,因为较大的Na-23四极耦合常数使得无法检测卫星过渡。从NMR弛豫时间数据来看,没有两个Na +族群的证据。可以分析实验的自旋晶格弛豫时间,以确定离子运动的相关时间与倒数温度的关系。相关时间数据显示了T-g行为的明显变化,这被解释为两种离子传输机制之间交叉的指示。 T-1作为T-g / T的函数图表明,T> T-g的动力学很大程度上取决于聚合物主体的柔韧性(α过程),而T> T-g的不同过程占主导地位(大概是β过程)。由NMR弛豫时间和离子电导率得出的相关时间的比较显示出明显的差异,尤其是在T-g区域。电导率迅速降低,而钠离子运动继续通过玻璃化转变的相关时间类似于10(-6)s。 (C)1998美国物理研究所。 [参考:102]

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