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SOLVENT FREE ENERGY CURVES FOR ELECTRON TRANSFER REACTIONS - A NONLINEAR SOLVENT RESPONSE MODEL

机译:电子转移反应的溶剂自由能曲线-非线性溶剂反应模型

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Marcus theory for electron transfer assumes a linear response of the solvent so that both the reactant and product free energy curves are parabolic functions of the solvent polarization, each with the same solvent force constant k characterizing the curvature. Simulation data by other workers indicate that the assumption of parabolic free energy curves is good for the Fe2+-Fe3+ self-exchange reaction but that the k of the reactant and product free energy curves are different for the reaction D-0 + A(0) --> D1- + A(1+). However, the fluctuations sampled in these simulations were not large enough to reach the activation barrier region, which was thus treated either by umbrella sampling or by parabolic extrapolation. Here, we present free energy curves calculated from a simple model of ionic solvation developed in an earlier paper by Hyun, Babu, and Ichiye, which we refer to here as the HBI model. The HBI model describes the nonlinearity of the solvent response due to the orientation of polar solvent molecules. Since it is a continuum model, it may be considered the first-order nonlinear correction to the linear response Born model. Moreover, in the limit of zero charge or infinite radius, the Born model and the Marcus relations are recovered. Here, the full free energy curves are calculated using analytic expressions from the HBI model. The HBI reactant and product curves have different k for D-0 + A(0) --> D1- + A(1+) as in the simulations, but examining the full curves shows they are nonparabolic due to the nonlinear response of the solvent. On the other hand, the HBI curves are close to parabolic for the Fe2+-Fe3+ reaction, also in agreement with simulations, while those for another self-exchange reaction D-0-A(1+) show greater deviations from parabolic behavior than the Fe2+-Fe3+ reaction. This indicates that transitions from neutral to charged species will have the largest deviations. Thus, the second moment of the polarization is shown to be a measure of the deviation from Marcus theory. Finally, since the HBI expressions for the free energy curves are not simple, the ABI curves are compared with various approximate parabolic descriptions of the curves, including Marcus parabolas. (C) 1996 American Institute of Physics. [References: 24]
机译:马库斯关于电子转移的理论假设溶剂具有线性响应,因此反应物和产物自由能曲线都是溶剂极化的抛物线函数,每条函数具有相同的溶剂力常数k表征曲率。其他工作人员的模拟数据表明,抛物线自由能曲线的假设对Fe2 + -Fe3 +自交换反应有好处,但反应D-0 + A(0)的反应物和产物自由能曲线的k不同-> D1- + A(1+)。但是,在这些模拟中采样的波动不足以到达激活屏障区域,因此可以通过伞状采样或抛物线外推法对其进行处理。在这里,我们展示了由Hyun,Babu和Ichiye在较早的论文中开发的离子化溶剂的简单模型计算出的自由能曲线,在此我们将其称为HBI模型。 HBI模型描述了由于极性溶剂分子的取向而引起的溶剂响应的非线性。由于它是一个连续模型,因此可以认为它是线性响应Born模型的一阶非线性校正。而且,在零电荷或无限半径的极限下,恢复了伯恩模型和马库斯关系。在这里,使用HBI模型的解析表达式来计算完整的自由能曲线。与模拟中一样,D-0 + A(0)-> D1- + A(1+)的HBI反应物和产物曲线具有不同的k,但检查整个曲线表明它们是非抛物线的,这是由于模拟的溶剂。另一方面,Fe2 + -Fe3 +反应的HBI曲线接近于抛物线,也与模拟一致,而另一种自交换反应D-0-A(1+)的HBI曲线则显示出与抛物线行为相比更大的偏差。 Fe2 + -Fe3 +反应。这表明从中性到带电物种的过渡将具有最大的偏差。因此,极化的第二矩显示为偏离Marcus理论的量度。最后,由于自由能曲线的HBI表达式并不简单,因此将ABI曲线与曲线的各种近似抛物线描述进行比较,包括Marcus抛物线。 (C)1996年美国物理研究所。 [参考:24]

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