Entangled spin-polarized excitons from singlet fission in a rigid dimer

被引:30
作者
Dill, Ryan D. D. [1 ]
Smyser, Kori E. E. [1 ]
Rugg, Brandon K. K. [2 ]
Damrauer, Niels H. H. [1 ,3 ]
Eaves, Joel D. D. [1 ,3 ]
机构
[1] Univ Colorado Boulder, Dept Chem, Boulder, CO 80309 USA
[2] Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA
[3] Univ Colorado Boulder, Renewable & Sustainable Energy Inst, Boulder, CO 80309 USA
基金
美国能源部; 美国国家科学基金会;
关键词
TRANSIENT NUTATION; TRIPLET EXCITONS; TIME; SPECTROSCOPY; EPR;
D O I
10.1038/s41467-023-36529-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Singlet fission is recognized as an enabling process for next-generation solar cells. Here the authors design a molecular system where specific spin sub-levels can be initialized to produce a highly entangled state and demonstrate that the coherence between magnetic sub-levels of that state is preserved at higher temperatures than those encountered in conventional superconducting quantum hardware. Singlet fission, a process that splits a singlet exciton into a biexciton, has promise in quantum information. We report time-resolved electron paramagnetic resonance measurements on a conformationally well-defined acene dimer molecule, TIPS-BP1', designed to exhibit strongly state-selective relaxation to specific magnetic spin sublevels. The resulting optically pumped spin polarization is a nearly pure initial state from the ensemble. The long-lived spin coherences modulate the signal intrinsically, allowing a measurement scheme that substantially removes noise and uncertainty in the magnetic resonance spectra. A nonadiabatic transition theory with a minimal number of spectroscopic parameters allows the quantitative assignment and interpretation of the spectra. In this work, we show that the rigid dimer TIPS-BP1' supports persistent spin coherences at temperatures far higher than those used in conventional superconducting quantum hardware.
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页数:7
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