Toward quantum sensing of chiral induced spin selectivity: Probing donor-bridge-acceptor molecules with NV centers in diamond

被引:4
|
作者
Voelker, Laura A. [1 ]
Herb, Konstantin [1 ]
Janitz, Erika [1 ]
Degen, Christian L. [1 ]
Abendroth, John M. [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Phys, Otto Stern Weg 1, CH-8093 Zurich, Switzerland
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 158卷 / 16期
基金
瑞士国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
NUCLEAR-MAGNETIC-RESONANCE; ELECTRON-TRANSFER; SPECTROSCOPY; COHERENCE; PROTEINS; NMR;
D O I
10.1063/5.0145466
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photoexcitable donor-bridge-acceptor (D-B-A) molecules that support intramolecular charge transfer are ideal platforms to probe the influence of chiral induced spin selectivity (CISS) in electron transfer and resulting radical pairs. In particular, the extent to which CISS influences spin polarization or spin coherence in the initial state of spin-correlated radical pairs following charge transfer through a chiral bridge remains an open question. Here, we introduce a quantum sensing scheme to measure directly the hypothesized spin polarization in radical pairs using shallow nitrogen-vacancy (NV) centers in diamond at the single- to few-molecule level. Importantly, we highlight the perturbative nature of the electron spin-spin dipolar coupling within the radical pair and demonstrate how Lee-Goldburg decoupling can preserve spin polarization in D-B-A molecules for enantioselective detection by a single NV center. The proposed measurements will provide fresh insight into spin selectivity in electron transfer reactions.
引用
收藏
页数:12
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