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An exact solution in the theory of fluorescence resonance energy transfer with vibrational relaxation

机译:振动松弛荧光共振能量转移理论的精确解决方案

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摘要

The elegant expression of Forster that predicts the well-known 1/R-6 distance (R) dependence of the rate of energy transfer, although widely used, was derived using several approximations. Notable among them is the neglect of the vibrational relaxation in the reactant (donor) and product (acceptor) manifolds. Vibrational relaxation can play an important role when the energy transfer rate is faster than the vibrational relaxation rate. Under such conditions, donor to acceptor energy transfer can occur from the excited vibrational states. This phenomenon is not captured by the usual formulation based on the overlap of donor emission and acceptor absorption spectra. Here, we develop a Green's function-based generalized formalism and obtain an exact solution for the excited state population relaxation and the rate of energy transfer in the presence of vibrational relaxation. We find that the application of the well-known Forster's expression might lead to overestimation of R.
机译:Forster的优雅表达式预测了众所周知的能量转移率的1/R-6距离(R)依赖性,尽管被广泛使用,但它是通过几种近似方法推导出来的。其中值得注意的是忽略了反应物(施主)和产物(受主)流形中的振动弛豫。当能量传递速率快于振动弛豫速率时,振动弛豫可以发挥重要作用。在这种条件下,施主到受主的能量转移可以从激发态发生。基于施主发射光谱和受主吸收光谱重叠的通常公式无法捕捉到这种现象。在这里,我们发展了一种基于格林函数的广义形式主义,得到了振动弛豫下激发态布居弛豫和能量转移速率的精确解。我们发现,应用著名的福斯特表达式可能会导致高估R。

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