Runeson Johan E, Manolopoulos David E
Physical and Theoretical Chemistry Laboratory, Department of Chemistry, University of Oxford, OX1 3QZ Oxford, UK.
Sci Adv. 2025 Jun 6;11(23):eadw4798. doi: 10.1126/sciadv.adw4798.
We assess how quantum-mechanical effects associated with high-frequency chromophore vibrations influence excitation energy transfer in biological light-harvesting complexes. After defining a classical nuclear limit that is consistent with the quantum-classical equilibrium, we include nuclear quantum effects through a variational polaron transformation of the high-frequency vibrational modes. This approach is validated by comparison with fully quantum-mechanical benchmark calculations and applied to three prototypical light-harvesting complexes. For light-harvesting complex 2 of purple bacteria, the inter-ring transfer is 1.5 times slower in the quantum treatment than in the classical treatment. For the Fenna-Matthews-Olson complex, the transfer rate is the same in both cases, whereas for light-harvesting complex II of spinach, the transfer is 1.7 times slower in the quantum treatment. The effect is most pronounced for systems with large excitonic energy gaps and strong vibronic coupling to high-frequency modes. In all cases, nuclear quantum effects are found to be unimportant for the directionality of energy transfer.
我们评估了与高频发色团振动相关的量子力学效应如何影响生物光捕获复合物中的激发能量转移。在定义了与量子 - 经典平衡相一致的经典核极限之后,我们通过高频振动模式的变分极化子变换纳入核量子效应。通过与完全量子力学基准计算进行比较验证了该方法,并将其应用于三种典型的光捕获复合物。对于紫色细菌的光捕获复合物2,量子处理中的环间转移比经典处理慢1.5倍。对于费纳 - 马修斯 - 奥尔森复合物,两种情况下的转移速率相同,而对于菠菜的光捕获复合物II,量子处理中的转移慢1.7倍。对于具有大激子能隙和与高频模式强振动耦合的系统,这种效应最为明显。在所有情况下,发现核量子效应对于能量转移的方向性并不重要。