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首页> 外文期刊>The Journal of Chemical Physics >MICROSCOPIC FORMULATION OF MARCUS THEORY OF ELECTRON TRANSFER
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MICROSCOPIC FORMULATION OF MARCUS THEORY OF ELECTRON TRANSFER

机译:电子转移马尔科斯理论的微观形式

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A microscopic theory for the rate of nonadiabatic electron transfer is developed and its relation to classical Marcus theory is analyzed. The focus is on how the nonlinear response of a molecular solvent to a change in the charge distribution of the donor-acceptor pair influences the rate; quantum mechanical and solvent dynamical effects are ignored. Under these restrictions, the rate is determined by the probability density of the energy gap, which is defined as the instantaneous change in solvation energy upon moving an electron from the donor to the acceptor. It is shown how this probability density can be obtained from the free energies of transferring varying amounts of charge between the donor and acceptor (as specified by a charging parameter). A simple algorithm is proposed for calculating these free-energy changes (and hence the energy gap probability density) from computer simulations on just three states: the reactant, the product, and an ''anti''-product formed by transferring a positive unit charge from the donor to the acceptor. Microscopic generalizations of the Marcus nonequilibrium free-energy surfaces for the reactant and the product, constructed as functions of the charging parameter, are presented. Their relation to surfaces constructed as functions of the energy gap is also established. The Marcus relation (i.e., the activation energy as a parabolic function of the free-energy change of reaction) is derived in a way that clearly shows that it is a good approximation in the normal region even when the solvent response is significantly nonlinear. A simple generalization of this relation, in which the activation energy is given by parabolic functions with different curvatures in the normal and inverted regions, is proposed. These curvatures are inversely proportional to the reorganization energies of the product and the antiproduct, respectively. Computer simulations of a simple model system are performed to illustrate and test these results and procedures. [References: 33]
机译:建立了非绝热电子传递速率的微观理论,并分析了其与经典马库斯理论的关系。重点是分子溶剂对供体-受体对电荷分布变化的非线性响应如何影响速率。量子力学和溶剂动力学效应被忽略。在这些限制下,速率由能隙的概率密度确定,该能隙的密度定义为电子从供体移动到受体时溶剂化能量的瞬时变化。它显示了如何通过在供体和受体之间转移不同量的电荷的自由能(由充电参数指定)可以得到这种概率密度。提出了一种简单的算法,用于通过仅在以下三种状态下的计算机模拟来计算这些自由能的变化(以及能隙概率密度):反应物,产物和通过转移正单元形成的“反”产物从捐赠者向接受者收取费用。给出了反应物和产物的马库斯非平衡自由能面的微观概括,并构造为加料参数的函数。还确定了它们与构造为能隙的表面的关系。马库斯关系(即活化能作为反应自由能变化的抛物线函数)的推导方式清楚地表明,即使溶剂响应明显非线性,它在正常区域也是很好的近似值。提出了这种关系的简单概括,其中,激活能量由在法向和反向区域中具有不同曲率的抛物线函数给出。这些曲率分别与产物和反产物的重组能成反比。执行简单模型系统的计算机仿真以说明和测试这些结果和过程。 [参考:33]

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