Photogenerated Spin-Correlated Radical Pairs: From Photosynthetic Energy Transduction to Quantum Information Science

化学 未成对电子 自旋(空气动力学) 化学物理 抗磁性 电子顺磁共振 自旋工程 自旋态 自旋极化 原子物理学 电子 激进的 核磁共振 物理 量子力学 磁场 有机化学 热力学 无机化学
作者
Samantha M. Harvey,Michael R. Wasielewski
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:143 (38): 15508-15529 被引量:127
标识
DOI:10.1021/jacs.1c07706
摘要

More than a half century ago, the NMR spectra of diamagnetic products resulting from radical pair reactions were observed to have strongly enhanced absorptive and emissive resonances. At the same time, photogenerated radical pairs were discovered to exhibit unusual electron paramagnetic resonance spectra that also had such resonances. These non-Boltzmann, spin-polarized spectra were observed in both chemical systems as well as in photosynthetic reaction center proteins following photodriven charge separation. Subsequent studies of these phenomena led to a variety of chemical electron donor-acceptor model systems that provided a broad understanding of the spin dynamics responsible for these spectra. When the distance between the two radicals is restricted, these observations result from the formation of spin-correlated radical pairs (SCRPs) in which the spin-spin exchange and dipolar interactions between the two unpaired spins play an important role in the spin dynamics. Early on, it was recognized that SCRPs photogenerated by ultrafast electron transfer are entangled spin pairs created in a well-defined spin state. These SCRPs can serve as spin qubit pairs (SQPs), whose spin dynamics can be manipulated to study a wide variety of quantum phenomena intrinsic to the field of quantum information science. This Perspective highlights the role of SCRPs as SQPs, gives examples of possible quantum manipulations using SQPs, and provides some thoughts on future directions.
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