Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208-3113, USA.
J Phys Chem A. 2010 Jan 14;114(1):162-71. doi: 10.1021/jp907476q.
This paper expands the established four-state model of spin-correlated radical pairs (SCRPs) to include local nuclear spins which are ubiquitous in real-world systems and essential for the radical pair intersystem crossing (RP-ISC) mechanism. These nuclei are coupled to the unpaired electron spins by hyperfine interaction and split their electron paramagnetic resonance (EPR) lines. Rather than enumerating all possible nuclear states, an algorithm is devised to sort out the net hyperfine offset 2Q, which, along with the electron spin-spin coupling 2J, characterizes the behavior of SCRPs. Using this algorithm, the EPR spectra of SCRPs coupled to arbitrary nuclear spins can be efficiently simulated with only 2J and the EPR spectra of individual radicals as the inputs. Particularly illustrative is the case of a SCRP resulting from photoinduced electron transfer comprised of a spectrally narrow anion radical signal having small hyperfine splittings and a broad cation radical signal having many large hyperfine splittings and a Gaussian width sigma, where the EPR peak of the anion radical exhibits an effective splitting of 2(1/2)J(2)/sigma. For SCRPs having singlet and triplet pathways for charge recombination, their kinetic behavior is obtained concisely by considering the decay rate constants k(S) and k(T) as imaginary energies, while adhering to the existing derivation of the four-state model. These models are employed to interpret the diverse array of spectral and kinetic modulation patterns observed in the experimental EPR spectra of photogenerated SCRPs and to extract the 2J value, which reflects the donor-acceptor electronic coupling. During the first several hundred nanoseconds following photoexcitation, the spectral and time domain characteristics of the measured time-resolved EPR spectra manifest the consequences of the Uncertainty Principle, and the modulation patterns in either domain result from hyperfine splittings between the unpaired electron and the nuclear spins.
本文将已建立的四态自旋相关自由基对(SCRP)模型扩展到包括普遍存在于实际系统中的局部核自旋,这对于自由基对系间交叉(RP-ISC)机制至关重要。这些核自旋通过超精细相互作用与未配对的电子自旋耦合,并分裂它们的电子顺磁共振(EPR)谱线。本文没有枚举所有可能的核态,而是设计了一种算法来整理净超精细偏移 2Q,它与电子自旋-自旋耦合 2J 一起,表征 SCRP 的行为。使用该算法,可以仅使用 2J 和单个自由基的 EPR 谱作为输入,有效地模拟与任意核自旋耦合的 SCRP 的 EPR 谱。特别说明的是,光诱导电子转移产生的 SCRP 情况,它由具有小超精细分裂的光谱窄的阴离子自由基信号和具有许多大超精细分裂和高斯宽度 sigma 的宽阳离子自由基信号组成,其中阴离子自由基的 EPR 峰表现出有效分裂为 2(1/2)J(2)/sigma。对于具有单重态和三重态电荷复合途径的 SCRP,通过将衰减速率常数 k(S)和 k(T)视为虚能,同时遵守四态模型的现有推导,可以简洁地获得它们的动力学行为。这些模型用于解释在光生 SCRP 的实验 EPR 光谱中观察到的各种光谱和动力学调制模式,并提取 2J 值,该值反映了供体-受体电子耦合。在光激发后的最初几百纳秒内,测量的时间分辨 EPR 光谱的光谱和时域特征表现出测不准原理的结果,并且两个域中的调制模式都源自未配对电子与核自旋之间的超精细分裂。